231 results on '"Butchar, Jonathan P."'
Search Results
2. Fluorescent nanodiamonds engage innate immune effector cells: A potential vehicle for targeted anti-tumor immunotherapy
- Author
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Suarez-Kelly, Lorena P., Campbell, Amanda R., Rampersaud, Isaac V., Bumb, Ambika, Wang, Min S., Butchar, Jonathan P., Tridandapani, Susheela, Yu, Lianbo, Rampersaud, Arfaan A., and Carson, William E., III
- Published
- 2017
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3. Active Hexose-Correlated Compound Shows Direct and Indirect Effects against Chronic Lymphocytic Leukemia.
- Author
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Merchand-Reyes, Giovanna, Santhanam, Ramasamy, Valencia-Pena, Maria L., Kumar, Krishan, Mo, Xiaokui, Belay, Tesfaye, Woyach, Jennifer A., Mundy-Bosse, Bethany, Tridandapani, Susheela, and Butchar, Jonathan P.
- Abstract
Chronic lymphocytic leukemia (CLL) is a disease characterized by the accumulation of mature CD19
+ CD5+ CD23+ B cells in the bloodstream and in lymphoid organs. It usually affects people over 70 years of age, which limits the options for treatments. The disease is typically well-managed, but to date is still incurable. Hence, the need for novel therapeutic strategies remains. Nurse-like cells (NLCs) are major components of the microenvironment for CLL, supporting tumor cell survival, proliferation, and even drug resistance. They are of myeloid lineage, guided toward differentiating into their tumor-supportive role by the CLL cells themselves. As such, they are analogous to tumor-associated macrophages and represent a major therapeutic target. Previously, it was found that a mushroom extract, Active Hexose-Correlated Compound (AHCC), promoted the death of acute myeloid leukemia cells while preserving normal monocytes. Given these findings, it was asked whether AHCC might have a similar effect on the abnormally differentiated myeloid-lineage NLCs in CLL. CLL-patient PBMCs were treated with AHCC, and it was found that AHCC treatment showed a direct toxic effect against isolated CLL cells. In addition, it significantly reduced the number of tumor-supportive NLCs and altered their phenotype. The effects of AHCC were then tested in the Eµ-TCL1 mouse model of CLL and the MllPTD/WT Flt3ITD/WT model of AML. Results showed that AHCC not only reduced tumor load and increased survival in the CLL and AML models, but it also enhanced antitumor antibody treatment in the CLL model. These results suggest that AHCC has direct and indirect effects against CLL and that it may be of benefit when combined with existing treatments. [ABSTRACT FROM AUTHOR]- Published
- 2023
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4. Targeting BET Proteins Decreases Hyaluronidase-1 in Pancreatic Cancer
- Author
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Kumar, Krishan, primary, Kanojia, Deepak, additional, Bentrem, David J., additional, Hwang, Rosa F., additional, Butchar, Jonathan P., additional, Tridandapani, Susheela, additional, and Munshi, Hidayatullah G., additional
- Published
- 2023
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5. Inhibition of BET Proteins Regulates Fcγ Receptor Function and Reduces Inflammation in Rheumatoid Arthritis
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Shankar, Divya, primary, Merchand-Reyes, Giovanna, additional, Buteyn, Nathaniel J., additional, Santhanam, Ramasamy, additional, Fang, Huiqing, additional, Kumar, Krishan, additional, Mo, Xiaokui, additional, Ganesan, Latha P., additional, Jarjour, Wael, additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2023
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6. Data from NK Cell–Mediated Antitumor Effects of a Folate-Conjugated Immunoglobulin Are Enhanced by Cytokines
- Author
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Jaime-Ramirez, Alena C., primary, McMichael, Elizabeth L., primary, Kondadasula, SriVidya, primary, Skinner, Cassandra C., primary, Mundy-Bosse, Bethany L., primary, Luedke, Eric, primary, Jones, Natalie B., primary, Mani, Aruna, primary, Roda, Julie, primary, Karpa, Volodymyr, primary, Li, Hong, primary, Li, Jilong, primary, Elavazhagan, Saranya, primary, La Perle, Krista M., primary, Schmitt, Alessandra C., primary, Lu, Yanhui, primary, Zhang, Xiaoli, primary, Pan, Xueliang, primary, Mao, Hsaioyin, primary, Davis, Melanie, primary, Jarjoura, David, primary, Butchar, Jonathan P., primary, Poi, Ming, primary, Phelps, Mitch, primary, Tridandapani, Susheela, primary, Byrd, John C., primary, Caligiuri, Michael A., primary, Lee, Robert J., primary, and Carson, William E., primary
- Published
- 2023
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7. Supplemental Figures 1-3 from NK Cell–Mediated Antitumor Effects of a Folate-Conjugated Immunoglobulin Are Enhanced by Cytokines
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Jaime-Ramirez, Alena C., primary, McMichael, Elizabeth L., primary, Kondadasula, SriVidya, primary, Skinner, Cassandra C., primary, Mundy-Bosse, Bethany L., primary, Luedke, Eric, primary, Jones, Natalie B., primary, Mani, Aruna, primary, Roda, Julie, primary, Karpa, Volodymyr, primary, Li, Hong, primary, Li, Jilong, primary, Elavazhagan, Saranya, primary, La Perle, Krista M., primary, Schmitt, Alessandra C., primary, Lu, Yanhui, primary, Zhang, Xiaoli, primary, Pan, Xueliang, primary, Mao, Hsaioyin, primary, Davis, Melanie, primary, Jarjoura, David, primary, Butchar, Jonathan P., primary, Poi, Ming, primary, Phelps, Mitch, primary, Tridandapani, Susheela, primary, Byrd, John C., primary, Caligiuri, Michael A., primary, Lee, Robert J., primary, and Carson, William E., primary
- Published
- 2023
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8. Supplementary Figure Legends from NK Cell–Mediated Antitumor Effects of a Folate-Conjugated Immunoglobulin Are Enhanced by Cytokines
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Jaime-Ramirez, Alena C., primary, McMichael, Elizabeth L., primary, Kondadasula, SriVidya, primary, Skinner, Cassandra C., primary, Mundy-Bosse, Bethany L., primary, Luedke, Eric, primary, Jones, Natalie B., primary, Mani, Aruna, primary, Roda, Julie, primary, Karpa, Volodymyr, primary, Li, Hong, primary, Li, Jilong, primary, Elavazhagan, Saranya, primary, La Perle, Krista M., primary, Schmitt, Alessandra C., primary, Lu, Yanhui, primary, Zhang, Xiaoli, primary, Pan, Xueliang, primary, Mao, Hsaioyin, primary, Davis, Melanie, primary, Jarjoura, David, primary, Butchar, Jonathan P., primary, Poi, Ming, primary, Phelps, Mitch, primary, Tridandapani, Susheela, primary, Byrd, John C., primary, Caligiuri, Michael A., primary, Lee, Robert J., primary, and Carson, William E., primary
- Published
- 2023
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9. Generation of monocyte-derived tumor-associated macrophages using tumor-conditioned media provides a novel method to study tumor-associated macrophages in vitro
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Benner, Brooke, Scarberry, Luke, Suarez-Kelly, Lorena P., Duggan, Megan C., Campbell, Amanda R., Smith, Emily, Lapurga, Gabriella, Jiang, Kallie, Butchar, Jonathan P., Tridandapani, Susheela, Howard, John Harrison, Baiocchi, Robert A., Mace, Thomas A., and Carson, III, William E.
- Published
- 2019
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10. Disruption of Nurse-like Cell Differentiation as a Therapeutic Strategy for Chronic Lymphocytic Leukemia
- Author
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Merchand-Reyes, Giovanna, primary, Santhanam, Ramasamy, additional, Robledo-Avila, Frank H., additional, Weigel, Christoph, additional, Ruiz-Rosado, Juan de Dios, additional, Mo, Xiaokui, additional, Partida-Sánchez, Santiago, additional, Woyach, Jennifer A., additional, Oakes, Christopher C., additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2022
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11. Abstract LB050: Targeting cells in the microenvironment as a novel therapeutic strategy for chronic lymphocytic leukemia
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Reyes, Giovanna Merchand, primary, Santhanam, Ramasamy, additional, Avila, Frank H. Robledo, additional, Weigel, Christoph, additional, Rosado, Juan D. Ruiz, additional, Mo, Xiaokui, additional, Sanchez, Santiago Partida, additional, Woyach, Jennifer A., additional, Oakes, Christopher C., additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2022
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12. miR-155 regulates IFN-γ production in natural killer cells
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Trotta, Rossana, Chen, Li, Ciarlariello, David, Josyula, Srirama, Mao, Charlene, Costinean, Stefan, Yu, Lianbo, Butchar, Jonathan P., Tridandapani, Susheela, Croce, Carlo M., and Caligiuri, Michael A.
- Published
- 2012
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13. CD19 targeting of chronic lymphocytic leukemia with a novel Fc-domain–engineered monoclonal antibody
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Awan, Farrukh T., Lapalombella, Rosa, Trotta, Rossana, Butchar, Jonathan P., Yu, Bo, Benson, Don M., Jr, Roda, Julie M., Cheney, Carolyn, Mo, Xiaokui, Lehman, Amy, Jones, Jeffrey, Flynn, Joseph, Jarjoura, David, Desjarlais, John R., Tridandapani, Susheela, Caligiuri, Michael A., Muthusamy, Natarajan, and Byrd, John C.
- Published
- 2010
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14. Lenalidomide down-regulates the CD20 antigen and antagonizes direct and antibody-dependent cellular cytotoxicity of rituximab on primary chronic lymphocytic leukemia cells
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Lapalombella, Rosa, Yu, Bo, Triantafillou, Georgia, Liu, Qing, Butchar, Jonathan P., Lozanski, Gerard, Ramanunni, Asha, Smith, Lisa L., Blum, William, Andritsos, Leslie, Wang, Da-Sheng, Lehman, Amy, Chen, Ching-Shih, Johnson, Amy J., Marcucci, Guido, Lee, Robert J., Lee, L. James, Tridandapani, Susheela, Muthusamy, Natarajan, and Byrd, John C.
- Published
- 2008
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15. NKp46 identifies an NKT cell subset susceptible to leukemic transformation in mouse and human
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Yu, Jianhua, Mitsui, Takeki, Wei, Min, Mao, Hsiaoyin, Butchar, Jonathan P., Shah, Mithun Vinod, Zhang, Jianying, Mishra, Anjali, Alvarez-Breckenridge, Christopher, Liu, Xingluo, Liu, Shujun, Yokohama, Akihiko, Trotta, Rossana, Marcucci, Guido, Benson, Jr., Don M., Loughran, Jr., Thomas P., Tridandapani, Susheela, and Caligiuri, Michael A.
- Subjects
T cells -- Health aspects ,Gene expression -- Research ,Leukemia -- Genetic aspects -- Care and treatment ,Health care industry - Abstract
IL-15 may have a role in the development of T cell large granular lymphocyte (T-LGL) or NKT leukemias. However, the mechanisms of action and the identity of the cell subset that undergoes leukemic transformation remain elusive. Here we show that in both mice and humans, NKp46 expression marks a minute population of WT NKT cells with higher activity and potency to become leukemic. Virtually 100% of T-LGL leukemias in IL-15 transgenic mice expressed NKp46, as did a majority of human T-LGL leukemias. The minute [NKp46.sup.+] NKT population, but not the NKp46 NKT population, was selectively expanded by overexpression of endogenous IL-15. Importantly, IL-15 transgenic NKp46 NKT cells did not become [NKp46.sup.+] in vivo, suggesting that [NKp46.sup.+] T-LGL leukemia cells were the malignant counterpart of the minute WT [NKp46.sup.+] NKT population. Mechanistically, [NKp46.sup.+] NKT cells possessed higher responsiveness to IL-15 in vitro and in vivo compared with that of their NKp46 NKT counterparts. Furthermore, interruption of IL-15 signaling using a neutralizing antibody could prevent LGL leukemia in IL-15 transgenic mice. Collectively, our data demonstrate that NKp46 identifies a functionally distinct NKT subset in mice and humans that appears to be directly susceptible to leukemic transformation when IL-15 is overexpressed. Thus, IL-15 signaling and NKp46 maybe useful targets in the treatment of patients with T-LGL or NKT leukemia., Introduction NKT cells are defined as a subset of T cells that share some characteristics with NK cells, particularly expression of the NK1.1 or DX5 antigen in mice and CD56 [...]
- Published
- 2011
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16. Francisella gains a survival advantage within mononuclear phagocytes by suppressing the host IFNγ response
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Parsa, Kishore V.L., Butchar, Jonathan P., Rajaram, Murugesan V.S., Cremer, Thomas J., Gunn, John S., Schlesinger, Larry S., and Tridandapani, Susheela
- Published
- 2008
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17. The tyrosine kinase Syk promotes phagocytosis of Francisella through the activation of Erk
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Parsa, Kishore V.L., Butchar, Jonathan P., Rajaram, Murugesan V.S., Cremer, Thomas J., and Tridandapani, Susheela
- Published
- 2008
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18. Activation of plasmacytoid dendritic cells promotes AML-cell fratricide
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Fatehchand, Kavin, primary, Mehta, Payal, additional, Colvin, Christopher B., additional, Buteyn, Nathaniel J., additional, Santhanam, Ramasamy, additional, Merchand-Reyes, Giovanna, additional, Inshaar, Hafza, additional, Shen, Brenda, additional, Mo, Xiaokui, additional, Mundy-Bosse, Bethany, additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2021
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19. Antibody Conjugation of Fluorescent Nanodiamonds for Targeted Innate Immune Cell Activation
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Suarez-Kelly, Lorena P., primary, Sun, Steven H., additional, Ren, Casey, additional, Rampersaud, Isaac V., additional, Albertson, David, additional, Duggan, Megan C., additional, Noel, Tiffany C., additional, Courtney, Nicholas, additional, Buteyn, Nathaniel J., additional, Moritz, Charles, additional, Yu, Lianbo, additional, Yildiz, Vedat O., additional, Butchar, Jonathan P., additional, Tridandapani, Susheela, additional, Rampersaud, Arfaan A., additional, and Carson, William E., additional
- Published
- 2021
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20. Fcγ Receptor Signaling in Phagocytes
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Joshi, Trupti, Butchar, Jonathan P., and Tridandapani, Susheela
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- 2006
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21. Decoding protein-protein interactions through combinatorial chemistry: Sequence specificity of SHP-1, SHP-2, and SHIP SH2 domains
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Sweeney, Michael C., Wavreille, Anne-Sophie, Park, Junguk, Butchar, Jonathan P., Tridandapani, Susheela, and Pei, Dehua
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Tyrosine -- Chemical properties ,Phosphatases -- Chemical properties ,Proteins -- Chemical properties ,Biological sciences ,Chemistry - Abstract
The validity of combinatorial library method was demonstrated by determining the sequence specificity of four Src homology 2 (SH2) domains derived from protein tyrosine phosphatase SHP-1 and SHP-2 and inositol phosphatase SHIP. The result shows that several proteins are found to bind to the SH2 domains of SHP-1 and SHP-2 through a new, nonclassical ITIM motif, (V/I/L)XpY(M/L/F)XP, which corresponds to class IV peptides selected from pY library.
- Published
- 2005
22. Glycovariant anti-CD37 monospecific protein therapeutic exhibits enhanced effector cell-mediated cytotoxicity against chronic and acute B cell malignancies
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Rafiq, Sarwish, Siadak, Anthony, Butchar, Jonathan P., Cheney, Carolyn, Lozanski, Gerard, Jacob, Naduparambil K., Lapalombella, Rosa, McGourty, Jackie, Moledor, Meghan, Lowe, Richard, Setter, Ben, Jones, Jeffrey, Flynn, Joseph M., Andritsos, Leslie, Devine, Steven, Mo, Xiaokui, Jarjoura, David, Tridandapani, Susheela, Algate, Paul, Byrd, John C., and Muthusamy, Natarajan
- Published
- 2013
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23. Elucidating nurse-like cell development as a new therapeutic strategy for chronic lymphocytic leukemia
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Reyes, Giovanna Merchand, primary, Santhanam, Ramasamy, additional, Weigel, Christoph, additional, Woyach, Jennifer, additional, Tridandapani, Susheela, additional, Oakes, Christopher, additional, and Butchar, Jonathan P, additional
- Published
- 2020
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24. Activation of the Intracellular Pattern Recognition Receptor NOD2 Promotes Acute Myeloid Leukemia (AML) Cell Apoptosis and Provides a Survival Advantage in an Animal Model of AML
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Buteyn, Nathaniel J., primary, Santhanam, Ramasamy, additional, Merchand-Reyes, Giovanna, additional, Murugesan, Rakesh A., additional, Dettorre, Gino M., additional, Byrd, John C., additional, Sarkar, Anasuya, additional, Vasu, Sumithira, additional, Mundy-Bosse, Bethany L., additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2020
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25. CD31 Acts as a Checkpoint Molecule and Is Modulated by FcγR-Mediated Signaling in Monocytes
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Merchand-Reyes, Giovanna, primary, Robledo-Avila, Frank H., additional, Buteyn, Nathaniel J., additional, Gautam, Shalini, additional, Santhanam, Ramasamy, additional, Fatehchand, Kavin, additional, Mo, Xiaokui, additional, Partida-Sanchez, Santiago, additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2019
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26. Evidence for interaction of the NLRP3 inflammasome and Bruton’s tyrosine kinase in tumor-associated macrophages: implications for myeloid cell production of interleukin-1beta
- Author
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Benner, Brooke, primary, Scarberry, Luke, additional, Stiff, Andrew, additional, Duggan, Megan C., additional, Good, Logan, additional, Lapurga, Gabriella, additional, Butchar, Jonathan P., additional, Tridandapani, Susheela, additional, and Carson, William E., additional
- Published
- 2019
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27. CD31 acts as a checkpoint molecule and is modulated by FcγR-mediated signaling in monocytes
- Author
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Butchar, Jonathan P, primary, Merchand-Reyes, Giovanna, additional, Robledo-Avila, Frank, additional, Buteyn, Nathaniel, additional, Gautam, Shalini, additional, Santhanam, Ramasamy, additional, Fatehchand, Kavin, additional, Partida-Sanchez, Santiago, additional, and Tridandapani, Susheela, additional
- Published
- 2019
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28. Generation of monocyte-derived tumorassociated macrophages using tumorconditioned media provides a novel method to study tumor-associated macrophages in vitro.
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Benner, Brooke, Scarberry, Luke, Suarez-Kelly, Lorena P., Duggan, Megan C., Campbell, Amanda R., Smith, Emily, Lapurga, Gabriella, Jiang, Kallie, Butchar, Jonathan P., Tridandapani, Susheela, Howard, John Harrison, Baiocchi, Robert A., Mace, Thomas A., and Carson III, William E.
- Subjects
KILLER cells ,TRANSFORMING growth factors ,MACROPHAGES ,CELL physiology ,INHIBITION of cellular proliferation - Abstract
Background: Tumor-associated macrophages (TAM) are expanded and exhibit tumor-promoting properties within the tumor microenvironment. Current methods to study TAM have not been replicated across cancer types and often do not include exogenous growth factors from the tumor, a key factor in TAM differentiation in vivo. Methods: In this study, an in vitro method to generate monocyte- derived TAM using tumor- conditioned media (TCM) and a cytokine cocktail containing IL-4, IL-10, and M-CSF was utilized to study the phenotype, morphology, and function of TAM across multiple cancer types. TCM was generated from two breast cancer cell lines and an Epstein-Barr virus-positive lymphoma cell line. The properties of in vitro generated TAM were compared to in vitro generated M1 and M2- like macrophages and TAM isolated from patients with cancer. Results: TAM generated in this fashion displayed an increase in CD163/CD206 co-expression compared to M2- like macrophages (87 and 36%, respectively). TAM generated in vitro exhibited increased transcript levels of the functional markers IL-6, IL-10, CCL2, c-Myc, iNOS, and arginase compared to in vitro generated M2-like macrophages. Functionally, in vitro generated TAM inhibited the proliferation of T cells (47% decrease from M1-like macrophages) and the production of IFN-γ by natural killer cells was inhibited (44%) when co-cultured with TAM. Furthermore, in vitro generated TAM secreted soluble factors that promote the growth and survival of tumor cells. Conclusions: Limited access to patient TAM highlights the need for methods to generate TAM in vitro. Our data confirm that monocyte-derived TAM can be generated reliably using TCM plus the cytokine cocktail of IL-4, IL-10, and M-CSF. Given the ability of TAM to inhibit immune cell function, continued study of methods to deplete or deactivate TAM in the setting of cancer are warranted. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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29. Anti-leukemic effects of all-trans retinoic acid in combination with Daratumumab in acute myeloid leukemia
- Author
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Buteyn, Nathaniel J, primary, Fatehchand, Kavin, additional, Santhanam, Ramasamy, additional, Fang, Huiqing, additional, Dettorre, Gino M, additional, Gautam, Shalini, additional, Harrington, Bonnie K, additional, Henderson, Sally E, additional, Merchand-Reyes, Giovanna, additional, Mo, Xiaokui, additional, Benson, Don M, additional, Carson, William E, additional, Vasu, Sumithira, additional, Byrd, John C, additional, Butchar, Jonathan P, additional, and Tridandapani, Susheela, additional
- Published
- 2018
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30. Active Hexose-Correlated Compound Restores Gene Expression and Protein Secretion of Protective Cytokines of Immune Cells in a Murine Stress Model during Chlamydia muridarumGenital Infection
- Author
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Belay, Tesfaye, Sahu, Rajnish, Martin, Elisha, Brown, Kristin, Rolen, Courtney, Hankins, Shomonique, Punturi, Brianna, Patterson, Maya, Chambers, Chase, Kirby, Brandon, and Butchar, Jonathan
- Abstract
Chlamydia trachomatisgenital infection is the most common bacterial sexually transmitted disease worldwide. Previously, we reported that cold-induced stress results in immune suppression of mice that subsequently leads to increased intensity of Chlamydia muridarumgenital infection.
- Published
- 2021
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31. Active hexose-correlated compound enhances extrinsic-pathway-mediated apoptosis of Acute Myeloid Leukemic cells
- Author
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Fatehchand, Kavin, primary, Santhanam, Ramasamy, additional, Shen, Brenda, additional, Erickson, Ericka L., additional, Gautam, Shalini, additional, Elavazhagan, Saranya, additional, Mo, Xiaokui, additional, Belay, Tesfaye, additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2017
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32. Interferon-γ Promotes Antibody-mediated Fratricide of Acute Myeloid Leukemia Cells
- Author
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Fatehchand, Kavin, primary, McMichael, Elizabeth L., additional, Reader, Brenda F., additional, Fang, Huiqing, additional, Santhanam, Ramasamy, additional, Gautam, Shalini, additional, Elavazhagan, Saranya, additional, Mehta, Payal, additional, Buteyn, Nathaniel J., additional, Merchand-Reyes, Giovanna, additional, Vasu, Sumithira, additional, Mo, Xiaokui, additional, Benson, Don M., additional, Blachly, James S., additional, Carson, William E., additional, Byrd, John C., additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2016
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33. Reprogramming Nurse-like Cells with Interferon γ to Interrupt Chronic Lymphocytic Leukemia Cell Survival
- Author
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Gautam, Shalini, primary, Fatehchand, Kavin, additional, Elavazhagan, Saranya, additional, Reader, Brenda F., additional, Ren, Li, additional, Mo, Xiaokui, additional, Byrd, John C., additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2016
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34. Lipopolysaccharide downregulates FcγRIIb via MARCH3-mediated ubiquitination
- Author
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Butchar, Jonathan P, primary, Fatehchand, Kavin, additional, Ren, Li, additional, Elavazhagan, Saranya, additional, Fang, Huiqing, additional, Mo, Xiaokui, additional, Vasilakos, John P, additional, Dietsch, Gregory N, additional, Hershberg, Robert M, additional, and Tridandapani, Susheela, additional
- Published
- 2016
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35. NK Cell–Mediated Antitumor Effects of a Folate-Conjugated Immunoglobulin Are Enhanced by Cytokines
- Author
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Jaime-Ramirez, Alena C., primary, McMichael, Elizabeth L., additional, Kondadasula, SriVidya, additional, Skinner, Cassandra C., additional, Mundy-Bosse, Bethany L., additional, Luedke, Eric, additional, Jones, Natalie B., additional, Mani, Aruna, additional, Roda, Julie, additional, Karpa, Volodymyr, additional, Li, Hong, additional, Li, Jilong, additional, Elavazhagan, Saranya, additional, La Perle, Krista M., additional, Schmitt, Alessandra C., additional, Lu, Yanhui, additional, Zhang, Xiaoli, additional, Pan, Xueliang, additional, Mao, Hsaioyin, additional, Davis, Melanie, additional, Jarjoura, David, additional, Butchar, Jonathan P., additional, Poi, Ming, additional, Phelps, Mitch, additional, Tridandapani, Susheela, additional, Byrd, John C., additional, Caligiuri, Michael A., additional, Lee, Robert J., additional, and Carson, William E., additional
- Published
- 2016
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36. Toll-like Receptor 4 Ligands Down-regulate Fcγ Receptor IIb (FcγRIIb) via MARCH3 Protein-mediated Ubiquitination
- Author
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Fatehchand, Kavin, primary, Ren, Li, additional, Elavazhagan, Saranya, additional, Fang, Huiqing, additional, Mo, Xiaokui, additional, Vasilakos, John P., additional, Dietsch, Gregory N., additional, Hershberg, Robert M., additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2016
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37. Analysis of the Effects of the Bruton's tyrosine kinase (Btk) Inhibitor Ibrutinib on Monocyte Fcγ Receptor (FcγR) Function
- Author
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Ren, Li, primary, Campbell, Amanda, additional, Fang, Huiqing, additional, Gautam, Shalini, additional, Elavazhagan, Saranya, additional, Fatehchand, Kavin, additional, Mehta, Payal, additional, Stiff, Andrew, additional, Reader, Brenda F., additional, Mo, Xiaokui, additional, Byrd, John C., additional, Carson, William E., additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2016
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38. Effects of the Btk Inhibitor Ibrutinib on Monocyte Responses to Antibodies
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Ren, Li, primary, Campbell, Amanda, additional, Gautam, Shalini, additional, Fang, Huiqing, additional, Fatehchand, Kavin, additional, Stiff, Andrew, additional, Mehta, Payal, additional, Mo, Xiaokui, additional, Fang, Xuexun, additional, Byrd, John C., additional, Carson, William, additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2015
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39. Anti–BAFF-R antibody VAY-736 demonstrates promising preclinical activity in CLL and enhances effectiveness of ibrutinib
- Author
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McWilliams, Emily M., Lucas, Christopher R., Chen, Timothy, Harrington, Bonnie K., Wasmuth, Ronni, Campbell, Amanda, Rogers, Kerry A., Cheney, Carolyn M., Mo, Xiaokui, Andritsos, Leslie A., Awan, Farrukh T., Woyach, Jennifer, Carson, William E., Butchar, Jonathan, Tridandapani, Susheela, Hertlein, Erin, Castro, Carlos E., Muthusamy, Natarajan, and Byrd, John C.
- Abstract
The Bruton tyrosine kinase inhibitor (BTKi) ibrutinib has transformed chronic lymphocytic leukemia (CLL) therapy but requires continuous administration. These factors have spurred interest in combination treatments. Unlike with chemotherapy, CD20-directed antibody therapy has not improved the outcome of BTKi treatment. Whereas CD20 antigen density on CLL cells decreases during ibrutinib treatment, the B-cell activating factor (BAFF) and its receptor (BAFF-R) remain elevated. Furthermore, BAFF signaling via noncanonical NF-κB remains elevated with BTKi treatment. Blocking BAFF interaction with BAFF-R by using VAY-736, a humanized defucosylated engineered antibody directed against BAFF-R, antagonized BAFF-mediated apoptosis protection and signaling at the population and single-cell levels in CLL cells. Furthermore, VAY-736 showed superior antibody-dependent cellular cytotoxicity compared with CD20- and CD52-directed antibodies used in CLL. VAY-736 exhibited in vivo activity as a monotherapy and, when combined with ibrutinib, produced prolonged survival compared with either therapy alone. The in vivo activity of VAY-736 is dependent upon immunoreceptor tyrosine–based activation motif (ITAM)–mediated activation of effector cells as shown by using an ITAM-deficient mouse model. Collectively, our findings support targeting the BAFF signaling pathway with VAY-736 to more effectively treat CLL as a single agent and in combination with ibrutinib.
- Published
- 2019
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40. Granzyme B Expression Is Enhanced in Human Monocytes by TLR8 Agonists and Contributes to Antibody-Dependent Cellular Cytotoxicity
- Author
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Elavazhagan, Saranya, primary, Fatehchand, Kavin, additional, Santhanam, Vikram, additional, Fang, Huiqing, additional, Ren, Li, additional, Gautam, Shalini, additional, Reader, Brenda, additional, Mo, Xiaokui, additional, Cheney, Carolyn, additional, Briercheck, Edward, additional, Vasilakos, John P., additional, Dietsch, Gregory N., additional, Hershberg, Robert M., additional, Caligiuri, Michael, additional, Byrd, John C., additional, Butchar, Jonathan P., additional, and Tridandapani, Susheela, additional
- Published
- 2015
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41. Targeting Interleukin-2-inducible T-cell Kinase (ITK) and Resting Lymphocyte Kinase (RLK) Using a Novel Covalent Inhibitor PRN694
- Author
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Zhong, Yiming, primary, Dong, Shuai, additional, Strattan, Ethan, additional, Ren, Li, additional, Butchar, Jonathan P., additional, Thornton, Kelsey, additional, Mishra, Anjali, additional, Porcu, Pierluigi, additional, Bradshaw, J. Michael, additional, Bisconte, Angelina, additional, Owens, Timothy D., additional, Verner, Erik, additional, Brameld, Ken A., additional, Funk, Jens Oliver, additional, Hill, Ronald J., additional, Johnson, Amy J., additional, and Dubovsky, Jason A., additional
- Published
- 2015
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42. Virulent Type A Francisella tularensis actively suppresses cytokine responses in human monocytes
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Gillette, Devyn D., primary, Curry, Heather M., additional, Cremer, Thomas, additional, Ravneberg, David, additional, Fatehchand, Kavin, additional, Shah, Prexy A., additional, Wewers, Mark D., additional, Schlesinger, Larry S., additional, Butchar, Jonathan P., additional, Tridandapani, Susheela, additional, and Gavrilin, Mikhail A., additional
- Published
- 2014
- Full Text
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43. A novel immunomodulatory function of PHLPP1: inhibition of iNOS via attenuation of STAT1 ser727 phosphorylation in mouse macrophages
- Author
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Alamuru, Neeraja P, primary, Behera, Soma, additional, Butchar, Jonathan P, additional, Tridandapani, Susheela, additional, Kaimal Suraj, Sasidhara, additional, Babu, P Prakash, additional, Hasnain, Seyed E, additional, Ehtesham, Nasreen Z, additional, and Parsa, Kishore V L, additional
- Published
- 2014
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44. Monocyte/macrophage inflammatory response pathways to combat Francisella infection: possible therapeutic targets?
- Author
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Gillette, Devyn D., primary, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2014
- Full Text
- View/download PDF
45. Guidelines for the use and interpretation of assays for monitoring autophagy.
- Author
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Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group) [research center], Klionsky, Daniel J., Abdalla, Fabio C., Abeliovich, Hagai, Abraham, Robert T., Acevedo-Arozena, Abraham, Adeli, Khosrow, Agholme, Lotta, Agnello, Maria, Agostinis, Patrizia, Aguirre-Ghiso, Julio A., Ahn, Hyung Jun, Ait-Mohamed, Ouardia, Ait-Si-Ali, Slimane, Akematsu, Takahiko, Akira, Shizuo, Al-Younes, Hesham M., Al-Zeer, Munir A., Albert, Matthew L., Albin, Roger L., Alegre-Abarrategui, Javier, Aleo, Maria Francesca, Alirezaei, Mehrdad, Almasan, Alexandru, Almonte-Becerril, Maylin, Amano, Atsuo, Amaravadi, Ravi, Amarnath, Shoba, Amer, Amal O., Andrieu-Abadie, Nathalie, Anantharam, Vellareddy, Ann, David K., Anoopkumar-Dukie, Shailendra, Aoki, Hiroshi, Apostolova, Nadezda, Arancia, Giuseppe, Aris, John P., Asanuma, Katsuhiko, Asare, Nana Y. O., Ashida, Hisashi, Askanas, Valerie, Askew, David S., Auberger, Patrick, Baba, Misuzu, Backues, Steven K., Baehrecke, Eric H., Bahr, Ben A., Bai, Xue-Yuan, Bailly, Yannick, Baiocchi, Robert, Baldini, Giulia, Balduini, Walter, Ballabio, Andrea, Bamber, Bruce A., Bampton, Edward T. W., Banhegyi, Gabor, Bartholomew, Clinton R., Bassham, Diane C., Bast, Robert C. Jr, Batoko, Henri, Bay, Boon-Huat, Beau, Isabelle, Bechet, Daniel M., Begley, Thomas J., Behl, Christian, Behrends, Christian, Bekri, Soumeya, Bellaire, Bryan, Bendall, Linda J., Benetti, Luca, Berliocchi, Laura, Bernardi, Henri, Bernassola, Francesca, Besteiro, Sebastien, Bhatia-Kissova, Ingrid, Bi, Xiaoning, Biard-Piechaczyk, Martine, Blum, Janice S., Boise, Lawrence H., Bonaldo, Paolo, Boone, David L., Bornhauser, Beat C., Bortoluci, Karina R., Bossis, Ioannis, Bost, Frederic, Bourquin, Jean-Pierre, Boya, Patricia, Boyer-Guittaut, Michael, Bozhkov, Peter V., Brady, Nathan R., Brancolini, Claudio, Brech, Andreas, Brenman, Jay E., Brennand, Ana, Bresnick, Emery H., Brest, Patrick, Bridges, Dave, Bristol, Molly L., Brookes, Paul S., Brown, Eric J., Brumell, John H., Brunetti-Pierri, Nicola, Brunk, Ulf T., Bulman, Dennis E., Bultman, Scott J., Bultynck, Geert, Burbulla, Lena F., Bursch, Wilfried, Butchar, Jonathan P., Buzgariu, Wanda, Bydlowski, Sergio P., Cadwell, Ken, Cahova, Monika, Cai, Dongsheng, Cai, Jiyang, Cai, Qian, Calabretta, Bruno, Calvo-Garrido, Javier, Camougrand, Nadine, Campanella, Michelangelo, Campos-Salinas, Jenny, Candi, Eleonora, Cao, Lizhi, Caplan, Allan B., Carding, Simon R., Cardoso, Sandra M., Carew, Jennifer S., Carlin, Cathleen R., Carmignac, Virginie, Carneiro, Leticia A. M., Carra, Serena, Caruso, Rosario A., Casari, Giorgio, Casas, Caty, Castino, Roberta, Cebollero, Eduardo, Cecconi, Francesco, Celli, Jean, Chaachouay, Hassan, Chae, Han-Jung, Chai, Chee-Yin, Chan, David C., Chan, Edmond Y., Chang, Raymond Chuen-Chung, Che, Chi-Ming, Chen, Ching-Chow, Chen, Guang-Chao, Chen, Guo-Qiang, Chen, Min, Chen, Quan, Chen, Steve S.-L., Chen, Wenli, Chen, Xihui, Chen, Xiangmei, Chen, Xiequn, Chen, Ye-Guang, Chen, Yingyu, Chen, Yongqiang, Chen, Yu-Jen, Chen, Zhixiang, Cheng, Alan, Cheng, Christopher H. K., Cheng, Yan, Cheong, Heesun, Cheong, Jae-Ho, Cherry, Sara, Chess-Williams, Russ, Cheung, Zelda H., Chevet, Eric, Chiang, Hui-Ling, Chiarelli, Roberto, Chiba, Tomoki, Chin, Lih-Shen, Chiou, Shih-Hwa, Chisari, Francis V., Cho, Chi Hin, Cho, Dong-Hyung, Choi, Augustine M. K., Choi, Dooseok, Choi, Kyeong Sook, Choi, Mary E., Chouaib, Salem, Choubey, Divaker, Choubey, Vinay, Chu, Charleen T., Chuang, Tsung-Hsien, Chueh, Sheau-Huei, Chun, Taehoon, Chwae, Yong-Joon, Chye, Mee-Len, Ciarcia, Roberto, Ciriolo, Maria R., Clague, Michael J., Clark, Robert S. B., Clarke, Peter G. H., Clarke, Robert, Codogno, Patrice, Coller, Hilary A., Colombo, Maria I., Comincini, Sergio, Condello, Maria, Condorelli, Fabrizio, Cookson, Mark R., Coombs, Graham H., Coppens, Isabelle, Corbalan, Ramon, Cossart, Pascale, Costelli, Paola, Costes, Safia, Coto-Montes, Ana, Couve, Eduardo, Coxon, Fraser P., Cregg, James M., Crespo, Jose L., Cronje, Marianne J., Cuervo, Ana Maria, Cullen, Joseph J., Czaja, Mark J., D'Amelio, Marcello, Darfeuille-Michaud, Arlette, Davids, Lester M., Davies, Faith E., De Felici, Massimo, de Groot, John F., de Haan, Cornelis A. M., De Martino, Luisa, De Milito, Angelo, De Tata, Vincenzo, Debnath, Jayanta, Degterev, Alexei, Dehay, Benjamin, Delbridge, Lea M. D., Demarchi, Francesca, Deng, Yi Zhen, Dengjel, Jorn, Dent, Paul, Denton, Donna, Deretic, Vojo, Desai, Shyamal D., Devenish, Rodney J., Di Gioacchino, Mario, Di Paolo, Gilbert, Di Pietro, Chiara, Diaz-Araya, Guillermo, Diaz-Laviada, Ines, Diaz-Meco, Maria T., Diaz-Nido, Javier, Dikic, Ivan, Dinesh-Kumar, Savithramma P., Ding, Wen-Xing, Distelhorst, Clark W., Diwan, Abhinav, Djavaheri-Mergny, Mojgan, Dokudovskaya, Svetlana, Dong, Zheng, Dorsey, Frank C., Dosenko, Victor, Dowling, James J., Doxsey, Stephen, Dreux, Marlene, Drew, Mark E., Duan, Qiuhong, Duchosal, Michel A., Duff, Karen, Dugail, Isabelle, Durbeej, Madeleine, Duszenko, Michael, Edelstein, Charles L., Edinger, Aimee L., Egea, Gustavo, Eichinger, Ludwig, Eissa, N. Tony, Ekmekcioglu, Suhendan, El-Deiry, Wafik S., Elazar, Zvulun, Elgendy, Mohamed, Ellerby, Lisa M., Eng, Kai Er, Engelbrecht, Anna-Mart, Engelender, Simone, Erenpreisa, Jekaterina, Escalante, Ricardo, Esclatine, Audrey, Eskelinen, Eeva-Liisa, Espert, Lucile, Espina, Virginia, Fan, Huizhou, Fan, Jia, Fan, Qi-Wen, Fan, Zhen, Fang, Shengyun, Fang, Yongqi, Fanto, Manolis, Fanzani, Alessandro, Farkas, Thomas, Farre, Jean-Claude, Faure, Mathias, Fechheimer, Marcus, Feng, Carl G., Feng, Jian, Feng, Qili, Feng, Youji, Fesus, Laszlo, Feuer, Ralph, Figueiredo-Pereira, Maria E., Fimia, Gian Maria, Fingar, Diane C., Finkbeiner, Steven, Finkel, Toren, Finley, Kim D., Fiorito, Filomena, Fisher, Edward A., Fisher, Paul B., Flajolet, Marc, Florez-McClure, Maria L., Florio, Salvatore, Fon, Edward A., Fornai, Francesco, Fortunato, Franco, Fotedar, Rati, Fowler, Daniel H., Fox, Howard S., Franco, Rodrigo, Frankel, Lisa B., Fransen, Marc, Fuentes, Jose M., Fueyo, Juan, Fujii, Jun, Fujisaki, Kozo, Fujita, Eriko, Fukuda, Mitsunori, Furukawa, Ruth H., Gaestel, Matthias, Gailly, Philippe, Gajewska, Malgorzata, Galliot, Brigitte, Galy, Vincent, Ganesh, Subramaniam, Ganetzky, Barry, Ganley, Ian G., Gao, Fen-Biao, Gao, George F., Gao, Jinming, Garcia, Lorena, Garcia-Manero, Guillermo, Garcia-Marcos, Mikel, Garmyn, Marjan, Gartel, Andrei L., Gatti, Evelina, Gautel, Mathias, Gawriluk, Thomas R., Gegg, Matthew E., Geng, Jiefei, Germain, Marc, Gestwicki, Jason E., Gewirtz, David A., Ghavami, Saeid, Ghosh, Pradipta, Giammarioli, Anna M., Giatromanolaki, Alexandra N., Gibson, Spencer B., Gilkerson, Robert W., Ginger, Michael L., Ginsberg, Henry N., Golab, Jakub, Goligorsky, Michael S., Golstein, Pierre, Gomez-Manzano, Candelaria, Goncu, Ebru, Gongora, Celine, Gonzalez, Claudio D., Gonzalez, Ramon, Gonzalez-Estevez, Cristina, Gonzalez-Polo, Rosa Ana, Gonzalez-Rey, Elena, Gorbunov, Nikolai V., Gorski, Sharon, Goruppi, Sandro, Gottlieb, Roberta A., Gozuacik, Devrim, Granato, Giovanna Elvira, Grant, Gary D., Green, Kim N., Gregorc, Ales, Gros, Frederic, Grose, Charles, Grunt, Thomas W., Gual, Philippe, Guan, Jun-Lin, Guan, Kun-Liang, Guichard, Sylvie M., Gukovskaya, Anna S., Gukovsky, Ilya, Gunst, Jan, Gustafsson, Asa B., Halayko, Andrew J., Hale, Amber N., Halonen, Sandra K., Hamasaki, Maho, Han, Feng, Han, Ting, Hancock, Michael K., Hansen, Malene, Harada, Hisashi, Harada, Masaru, Hardt, Stefan E., Harper, J. 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A., Hussey, Patrick J., Hwang, Jung Jin, Hwang, Seungmin, Ichihara, Atsuhiro, Ilkhanizadeh, Shirin, Inoki, Ken, Into, Takeshi, Iovane, Valentina, Iovanna, Juan L., Ip, Nancy Y., Isaka, Yoshitaka, Ishida, Hiroyuki, Isidoro, Ciro, Isobe, Ken-Ichi, Iwasaki, Akiko, Izquierdo, Marta, Izumi, Yotaro, Jaakkola, Panu M., Jaattela, Marja, Jackson, George R., Jackson, William T., Janji, Bassam, Jendrach, Marina, Jeon, Ju-Hong, Jeung, Eui-Bae, Jiang, Hong, Jiang, Hongchi, Jiang, Jean X., Jiang, Ming, Jiang, Qing, Jiang, Xuejun, Jimenez, Alberto, Jin, Meiyan, Jin, Shengkan, Joe, Cheol O., Johansen, Terje, Johnson, Daniel E., Johnson, Gail V. W., Jones, Nicola L., Joseph, Bertrand, Joseph, Suresh K., Joubert, Annie M., Juhasz, Gabor, Juillerat-Jeanneret, Lucienne, Jung, Chang Hwa, Jung, Yong-Keun, Kaarniranta, Kai, Kaasik, Allen, Kabuta, Tomohiro, Kadowaki, Motoni, Kagedal, Katarina, Kamada, Yoshiaki, Kaminskyy, Vitaliy O., Kampinga, Harm H., Kanamori, Hiromitsu, Kang, Chanhee, Kang, Khong Bee, Kang, Kwang Il, Kang, Rui, Kang, Yoon-A., Kanki, Tomotake, Kanneganti, Thirumala-Devi, Kanno, Haruo, Kanthasamy, Anumantha G., Kanthasamy, Arthi, Karantza, Vassiliki, Kaushal, Gur P., Kaushik, Susmita, Kawazoe, Yoshinori, Ke, Po-Yuan, Kehrl, John H., Kelekar, Ameeta, Kerkhoff, Claus, Kessel, David H., Khalil, Hany, Kiel, Jan A. K. 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J., Sanchez-Alcazar, Jose A., Sanchez-Prieto, Ricardo, Sandri, Marco, Sankar, Uma, Sansanwal, Poonam, Santambrogio, Laura, Saran, Shweta, Sarkar, Sovan, Sarwal, Minnie, Sasakawa, Chihiro, Sasnauskiene, Ausra, Sass, Miklos, Sato, Ken, Sato, Miyuki, Schapira, Anthony H. 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Lindsay, Whitworth, Alexander J., Wileman, Tom, Wiley, John W., Wilkinson, Simon, Willbold, Dieter, Williams, Roger L., Williamson, Peter R., Wouters, Bradly G., Wu, Chenghan, Wu, Dao-Cheng, Wu, William K. 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D., Demarchi, Francesca, Deng, Yi Zhen, Dengjel, Jorn, Dent, Paul, Denton, Donna, Deretic, Vojo, Desai, Shyamal D., Devenish, Rodney J., Di Gioacchino, Mario, Di Paolo, Gilbert, Di Pietro, Chiara, Diaz-Araya, Guillermo, Diaz-Laviada, Ines, Diaz-Meco, Maria T., Diaz-Nido, Javier, Dikic, Ivan, Dinesh-Kumar, Savithramma P., Ding, Wen-Xing, Distelhorst, Clark W., Diwan, Abhinav, Djavaheri-Mergny, Mojgan, Dokudovskaya, Svetlana, Dong, Zheng, Dorsey, Frank C., Dosenko, Victor, Dowling, James J., Doxsey, Stephen, Dreux, Marlene, Drew, Mark E., Duan, Qiuhong, Duchosal, Michel A., Duff, Karen, Dugail, Isabelle, Durbeej, Madeleine, Duszenko, Michael, Edelstein, Charles L., Edinger, Aimee L., Egea, Gustavo, Eichinger, Ludwig, Eissa, N. 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W., Jones, Nicola L., Joseph, Bertrand, Joseph, Suresh K., Joubert, Annie M., Juhasz, Gabor, Juillerat-Jeanneret, Lucienne, Jung, Chang Hwa, Jung, Yong-Keun, Kaarniranta, Kai, Kaasik, Allen, Kabuta, Tomohiro, Kadowaki, Motoni, Kagedal, Katarina, Kamada, Yoshiaki, Kaminskyy, Vitaliy O., Kampinga, Harm H., Kanamori, Hiromitsu, Kang, Chanhee, Kang, Khong Bee, Kang, Kwang Il, Kang, Rui, Kang, Yoon-A., Kanki, Tomotake, Kanneganti, Thirumala-Devi, Kanno, Haruo, Kanthasamy, Anumantha G., Kanthasamy, Arthi, Karantza, Vassiliki, Kaushal, Gur P., Kaushik, Susmita, Kawazoe, Yoshinori, Ke, Po-Yuan, Kehrl, John H., Kelekar, Ameeta, Kerkhoff, Claus, Kessel, David H., Khalil, Hany, Kiel, Jan A. K. W., Kiger, Amy A., Kihara, Akio, Kim, Deok Ryong, Kim, Do-Hyung, Kim, Dong-Hou, Kim, Eun-Kyoung, Kim, Hyung-Ryong, Kim, Jae-Sung, Kim, Jeong Hun, Kim, Jin Cheon, Kim, John K., Kim, Peter K., Kim, Seong Who, Kim, Yong-Sun, Kim, Yonghyun, Kimchi, Adi, Kimmelman, Alec C., King, Jason S., Kinsella, Timothy J., Kirkin, Vladimir, Kirshenbaum, Lorrie A., Kitamoto, Katsuhiko, Kitazato, Kaio, Klein, Ludger, Klimecki, Walter T., Klucken, Jochen, Knecht, Erwin, Ko, Ben C. B., Koch, Jan C., Koga, Hiroshi, Koh, Jae-Young, Koh, Young Ho, Koike, Masato, Komatsu, Masaaki, Kominami, Eiki, Kong, Hee Jeong, Kong, Wei-Jia, Korolchuk, Viktor I., Kotake, Yaichiro, Koukourakis, Michael I., Kouri Flores, Juan B., Kovacs, Attila L., Kraft, Claudine, Krainc, Dimitri, Kramer, Helmut, Kretz-Remy, Carole, Krichevsky, Anna M., Kroemer, Guido, Krüger, Rejko, Krut, Oleg, Ktistakis, Nicholas T., Kuan, Chia-Yi, Kucharczyk, Roza, Kumar, Ashok, Kumar, Raj, Kumar, Sharad, Kundu, Mondira, Kung, Hsing-Jien, Kurz, Tino, Kwon, Ho Jeong, La Spada, Albert R., Lafont, Frank, Lamark, Trond, Landry, Jacques, Lane, Jon D., Lapaquette, Pierre, Laporte, Jocelyn F., Laszlo, Lajos, Lavandero, Sergio, Lavoie, Josee N., Layfield, Robert, Lazo, Pedro A., Le, Weidong, Le Cam, Laurent, Ledbetter, Daniel J., Lee, Alvin J. 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- Abstract
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused o
- Published
- 2012
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46. Guidelines for the use and interpretation of assays for monitoring autophagy
- Author
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Paul, Denton, Donna, Deretic, Vojo, Desai, Shyamal D, Devenish, Rodney J, Di Gioacchino, Mario, Di Paolo, Gilbert, Di Pietro, Chiara, Díaz-Araya, Guillermo, Díaz-Laviada, Inés, Diaz-Meco, Maria T, Diaz-Nido, Javier, Dikic, Ivan, Dinesh-Kumar, Savithramma P, Ding, Wen-Xing, Distelhorst, Clark W, Diwan, Abhinav, Djavaheri-Mergny, Mojgan, Dokudovskaya, Svetlana, Dong, Zheng, Dorsey, Frank C, Dosenko, Victor, Dowling, James J, Doxsey, Stephen, Dreux, Marlène, Drew, Mark E, Duan, Qiuhong, Duchosal, Michel A, Duff, Karen, Dugail, Isabelle, Durbeej, Madeleine, Duszenko, Michael, Edelstein, Charles L, Edinger, Aimee L, Egea, Gustavo, Eichinger, Ludwig, Eissa, N Tony, Ekmekcioglu, Suhendan, El-Deiry, Wafik S, Elazar, Zvulun, Elgendy, Mohamed, Ellerby, Lisa M, Eng, Kai Er, Engelbrecht, Anna-Mart, Engelender, Simone, Erenpreisa, Jekaterina, Escalante, Ricardo, Esclatine, Audrey, Eskelinen, Eeva-Liisa, Espert, Lucile, Espina, Virginia, Fan, Huizhou, Fan, Jia, Fan, Qi-Wen, Fan, Zhen, Fang, Shengyun, Fang, Yongqi, Fanto, Manolis, Fanzani, Alessandro, Farkas, Thomas, Farré, Jean-Claude, Faure, Mathias, Fechheimer, Marcus, Feng, Carl G, Feng, Jian, Feng, Qili, Feng, Youji, Fésüs, László, Feuer, Ralph, Figueiredo-Pereira, Maria E, Fimia, Gian Maria, Fingar, Diane C, Finkbeiner, Steven, Finkel, Toren, Finley, Kim D, Fiorito, Filomena, Fisher, Edward A, Fisher, Paul B, Flajolet, Marc, Florez-McClure, Maria L, Florio, Salvatore, Fon, Edward A, Fornai, Francesco, Fortunato, Franco, Fotedar, Rati, Fowler, Daniel H, Fox, Howard S, Franco, Rodrigo, Frankel, Lisa B, Fransen, Marc, Fuentes, José M, Fueyo, Juan, Fujii, Jun, Fujisaki, Kozo, Fujita, Eriko, Fukuda, Mitsunori, Furukawa, Ruth H, Gaestel, Matthias, Gailly, Philippe, Gajewska, Malgorzata, Galliot, Brigitte, Galy, Vincent, Ganesh, Subramaniam, Ganetzky, Barry, Ganley, Ian G, Gao, Fen-Biao, Gao, George F, Gao, Jinming, Garcia, Lorena, Garcia-Manero, Guillermo, Garcia-Marcos, Mikel, Garmyn, Marjan, Gartel, Andrei L, Gatti, Evelina, Gautel, Mathias, Gawriluk, Thomas R, Gegg, Matthew E, Geng, Jiefei, Germain, Marc, Gestwicki, Jason E, Gewirtz, David A, Ghavami, Saeid, Ghosh, Pradipta, Giammarioli, Anna M, Giatromanolaki, Alexandra N, Gibson, Spencer B, Gilkerson, Robert W, Ginger, Michael L, Goncu, Ebru, Gongora, Céline, Gonzalez, Claudio D, Gonzalez, Ramon, González-Estévez, Cristina, González-Polo, Rosa Ana, Gonzalez-Rey, Elena, Gorbunov, Nikolai V, Gorski, Sharon, Goruppi, Sandro, Gottlieb, Roberta A, Gozuacik, Devrim, Granato, Giovanna Elvira, Grant, Gary D, Green, Kim N, Gregorc, Aleš, Gros, Frédéric, Grose, Charles, Grunt, Thomas W, Gual, Philippe, Guan, Jun-Lin, Guan, Kun-Liang, Guichard, Sylvie M, Gukovskaya, Anna S, Gukovsky, Ilya, Gunst, Jan, Gustafsson, Asa B, Halayko, Andrew J, Hale, Amber N, Halonen, Sandra K, Hamasaki, Maho, Han, Feng, Han, Ting, Hancock, Michael K, Hansen, Malene, Harada, Hisashi, Harada, Masaru, Hardt, Stefan E, Harper, J Wade, Harris, Adrian L, Harris, James, Harris, Steven D, Hébert, Marie-Joseé, Heidenreich, Kim A, Helfrich, Miep H, Helgason, Gudmundur V, Henske, Elizabeth P, Herman, Brian, Herman, Paul K, Hetz, Claudio, Hilfiker, Sabine, Hill, Joseph A, Hocking, Lynne J, Hofman, Paul, Hofmann, Thomas G, Höhfeld, Jörg, Holyoake, Tessa L, Hong, Ming-Huang, Hood, David A, Hotamisligil, Gökhan S, Houwerzijl, Ewout J, Høyer-Hansen, Maria, Hu, Bingren, Hu, Chien-An A, Hu, Hong-Ming, Hua, Ya, Huang, Canhua, Huang, Ju, Huang, Shengbing, Huang, Wei-Pang, Huber, Tobias B, Huh, Won-Ki, Hung, Tai-Ho, Hupp, Ted R, Hur, Gang Min, Hurley, James B, Hussain, Sabah N A, Hussey, Patrick J, Hwang, Jung Jin, Hwang, Seungmin, Ichihara, Atsuhiro, Ilkhanizadeh, Shirin, Inoki, Ken, Into, Takeshi, Iovane, Valentina, Iovanna, Juan L, Ip, Nancy Y, Isaka, Yoshitaka, Ishida, Hiroyuki, Isidoro, Ciro, Isobe, Ken-ichi, Iwasaki, Akiko, Izquierdo, Marta, Izumi, Yotaro, Jaakkola, Panu M, Jäättelä, Marja, Jackson, George R, Jackson, William T, Janji, Bassam, Jendrach, Marina, Jeon, Ju-Hong, Jeung, Eui-Bae, Jiang, Hong, Jiang, Hongchi, Jiang, Jean X, Jiang, Ming, Jiang, Qing, Jiang, Xuejun, Jiménez, Alberto, Jin, Meiyan, Jin, Shengkan, Joe, Cheol O, Johansen, Terje, Johnson, Daniel E, Johnson, Gail V W, Jones, Nicola L, Joseph, Bertrand, Joseph, Suresh K, Joubert, Annie M, Juhász, Gábor, Juillerat-Jeanneret, Lucienne, Jung, Chang Hwa, Jung, Yong-Keun, Kaarniranta, Kai, Kaasik, Allen, Kabuta, Tomohiro, Kadowaki, Motoni, Kågedal, Katarina, Kamada, Yoshiaki, Kaminskyy, Vitaliy O, Kampinga, Harm H, Kanamori, Hiromitsu, Kang, Chanhee, Kang, Khong Bee, Kang, Kwang Il, Kang, Rui, Kang, Yoon-A, Kanki, Tomotake, Kanneganti, Thirumala-Devi, Kanno, Haruo, Kanthasamy, Anumantha G, Kanthasamy, Arthi, Karantza, Vassiliki, Kaushal, Gur P, Kaushik, Susmita, Kawazoe, Yoshinori, Ke, Po-Yuan, Kehrl, John H, Kelekar, Ameeta, Kerkhoff, Claus, Kessel, David H, Khalil, Hany, Kiel, Jan A K W, Kiger, Amy A, Kihara, Akio, Kim, Deok Ryong, Kim, Do-Hyung, Kim, Dong-Hou, Kim, Eun-Kyoung, Kim, Hyung-Ryong, Kim, Jae-Sung, Kim, Jeong Hun, Kim, Jin Cheon, Kim, John K, Kim, Peter K, Kim, Seong Who, Kim, Yong-Sun, Kim, Yonghyun, Kimchi, Adi, Kimmelman, Alec C, King, Jason S, Kinsella, Timothy J, Kirkin, Vladimir, Kirshenbaum, Lorrie A, Kitamoto, Katsuhiko, Kitazato, Kaio, Klein, Ludger, Klimecki, Walter T, Klucken, Jochen, Knecht, Erwin, Ko, Ben C B, Koch, Jan C, Koga, Hiroshi, Koh, Jae-Young, Koh, Young Ho, Koike, Masato, Komatsu, Masaaki, Kominami, Eiki, Kong, Hee Jeong, Kong, Wei-Jia, Korolchuk, Viktor I, Kotake, Yaichiro, Koukourakis, Michael I, Kouri Flores, Juan B, Kovács, Attila L, Kraft, Claudine, Krainc, Dimitri, Krämer, Helmut, Kretz-Remy, Carole, Krichevsky, Anna M, Kroemer, Guido, Krüger, Rejko, Krut, Oleg, Ktistakis, Nicholas T, Kuan, Chia-Yi, Kucharczyk, Roza, Kumar, Ashok, Kumar, Raj, Kumar, Sharad, Kundu, Mondira, Kung, Hsing-Jien, Kurz, Tino, Kwon, Ho Jeong, La Spada, Albert R, Lafont, Frank, Lamark, Trond, Landry, Jacques, Lane, Jon D, Lapaquette, Pierre, 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Liu, Kaiyu, Liu, Leyuan, Liu, Qiong A, Liu, Wei, Liu, Young-Chau, Liu, Yule, Lockshin, Richard A, Lok, Chun-Nam, Lonial, Sagar, Loos, Benjamin, Lopez-Berestein, Gabriel, López-Otín, Carlos, Lossi, Laura, Lotze, Michael T, Lőw, Peter, Lu, Binfeng, Lu, Bingwei, Lu, Bo, Lu, Zhen, Luciano, Frédéric, Lukacs, Nicholas W, Lund, Anders H, Lynch-Day, Melinda A, Ma, Yong, Macian, Fernando, MacKeigan, Jeff P, Macleod, Kay F, Madeo, Frank, Maiuri, Luigi, Maiuri, Maria Chiara, Malagoli, Davide, Malicdan, May Christine V, Malorni, Walter, Man, Na, Mandelkow, Eva-Maria, Manon, Stéphen, Manov, Irena, Mao, Kai, Mao, Xiang, Mao, Zixu, Marambaud, Philippe, Marazziti, Daniela, Marcel, Yves L, Marchbank, Katie, Marchetti, Piero, Marciniak, Stefan J, Marcondes, Mateus, Mardi, Mohsen, Marfe, Gabriella, Mariño, Guillermo, Markaki, Maria, Marten, Mark R, Martin, Seamus J, Martinand-Mari, Camille, Martinet, Wim, Martinez-Vicente, Marta, Masini, Matilde, Matarrese, Paola, Matsuo, Saburo, Matteoni, Raffaele, 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Yoshikawa, Yuko, Yoshimori, Tamotsu, Yoshimoto, Kohki, You, Ho Jin, Youle, Richard J, Younes, Anas, Yu, Li, Yu, Long, Yu, Seong-Woon, Yu, Wai Haung, Yuan, Zhi-Min, Yue, Zhenyu, Yun, Cheol-Heui, Yuzaki, Michisuke, Zabirnyk, Olga, Silva-Zacarin, Elaine, Zacks, David, Zacksenhaus, Eldad, Zaffaroni, Nadia, Zakeri, Zahra, Zeh, Herbert J, Zeitlin, Scott O, Zhang, Hong, Zhang, Hui-Ling, Zhang, Jianhua, Zhang, Jing-Pu, Zhang, Lin, Zhang, Long, Zhang, Ming-Yong, Zhang, Xu Dong, Zhao, Mantong, Zhao, Yi-Fang, Zhao, Ying, Zhao, Zhizhuang J, Zheng, Xiaoxiang, Zhivotovsky, Boris, Zhong, Qing, Zhou, Cong-Zhao, Zhu, Changlian, Zhu, Wei-Guo, Zhu, Xiao-Feng, Zhu, Xiongwei, Zhu, Yuangang, Zoladek, Teresa, Zong, Wei-Xing, Zorzano, Antonio, Zschocke, Jürgen, and Zuckerbraun, Brian
- Abstract
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused o
- Published
- 2012
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47. Ibrutinib (PCI-32765) Antagonizes Rituximab-Dependent NK-Cell Mediated Cytotoxicity
- Author
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Kohrt, Holbrook E, primary, Sagiv-Barfi, Idit, additional, Rafiq, Sarwish, additional, Herman, Sarah E.M., additional, Butchar, Jonathan P, additional, Cheney, Carolyn, additional, Zhang, Xiaoli, additional, Buggy, Joseph J., additional, Muthusamy, Natarajan, additional, Levy, Ronald, additional, Johnson, Amy J, additional, and Byrd, John C., additional
- Published
- 2013
- Full Text
- View/download PDF
48. Fcγ Receptor-induced Soluble Vascular Endothelial Growth Factor Receptor-1 (VEGFR-1) Production Inhibits Angiogenesis and Enhances Efficacy of Anti-tumor Antibodies
- Author
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Justiniano, Steven E., primary, Elavazhagan, Saranya, additional, Fatehchand, Kavin, additional, Shah, Prexy, additional, Mehta, Payal, additional, Roda, Julie M., additional, Mo, Xiaokui, additional, Cheney, Carolyn, additional, Hertlein, Erin, additional, Eubank, Timothy D., additional, Marsh, Clay, additional, Muthusamy, Natarajan, additional, Butchar, Jonathan P., additional, Byrd, John C., additional, and Tridandapani, Susheela, additional
- Published
- 2013
- Full Text
- View/download PDF
49. Toll-like Receptor 2 Ligands Regulate Monocyte Fcγ Receptor Expression and Function
- Author
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Shah, Prexy, primary, Fatehchand, Kavin, additional, Patel, Hemal, additional, Fang, Huiqing, additional, Justiniano, Steven E., additional, Mo, Xiaokui, additional, Jarjoura, David, additional, Tridandapani, Susheela, additional, and Butchar, Jonathan P., additional
- Published
- 2013
- Full Text
- View/download PDF
50. Comparative Assessment of Clinically Utilized CD20-Directed Antibodies in Chronic Lymphocytic Leukemia Cells Reveals Divergent NK Cell, Monocyte, and Macrophage Properties
- Author
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Rafiq, Sarwish, primary, Butchar, Jonathan P., additional, Cheney, Carolyn, additional, Mo, Xiaokui, additional, Trotta, Rossana, additional, Caligiuri, Michael, additional, Jarjoura, David, additional, Tridandapani, Susheela, additional, Muthusamy, Natarajan, additional, and Byrd, John C., additional
- Published
- 2013
- Full Text
- View/download PDF
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