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5. Biofilm-derived oxylipin 10-HOME-mediated immune response in women with breast implants

Author

Khan, Imran, Minto, Robert E., Kelley-Patteson, Christine, Singh, Kanhaiya, Timsina, Lava, Suh, Lily J., Rinne, Ethan, Van Natta, Bruce W., Neumann, Colby R., Mohan, Ganesh, Lester, Mary, Von Der Haar, R. Jason, German, Rana, Marino, Natascia, Hassanein, Aladdin H., Gordillo, Gayle M., Kaplan, Mark H., Sen, Chandan K., Kadin, Marshall E., and Sinha, Mithun

Subjects
Complications and side effects, Physiological aspects, Development and progression, Risk factors, Health aspects, Causes of, Unsaturated fatty acids -- Physiological aspects -- Health aspects, Breast implants -- Complications and side effects, Microbial mats -- Health aspects -- Causes of, Immunologic diseases -- Risk factors -- Development and progression, Breast prosthesis -- Complications and side effects
Abstract

Introduction Breast implants were first introduced in 1962. Nearly 60 years later, their safety has continued to be controversial in the medical field, including a period of FDA-mandated restrictions on [...], This study investigates a mechanistic link of bacterial biofilm-mediated host-pathogen interaction leading to immunological complications associated with breast implant illness (BII). Over 10 million women worldwide have breast implants. In recent years, women have described a constellation of immunological symptoms believed to be related to their breast implants. We report that periprosthetic breast tissue of participants with symptoms associated with BII had increased abundance of biofilm and biofilm-derived oxylipin 10-HOME compared with participants with implants who are without symptoms (non-BII) and participants without implants. S. epidermidis biofilm was observed to be higher in the BII group compared with the non-BII group and the normal tissue group. Oxylipin 10-HOME was found to be immunogenically capable of polarizing naive [CD4.sup.+] T cells with a resulting Th1 subtype in vitro and in vivo. Consistently, an abundance of [CD4.sup.+]Th1 subtype was observed in the periprosthetic breast tissue and blood of people in the BII group. Mice injected with 10-HOME also had increased Th1 subtype in their blood, akin to patients with BII, and demonstrated fatigue-like symptoms. The identification of an oxylipinmediated mechanism of immune activation induced by local bacterial biofilm provides insight into the possible pathogenesis of the implant-associated immune symptoms of BII.

Published
2024
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6. OxymiRs in Regenerative Medicine

Author

Neumann, Colby R., primary, Khan, Imran, additional, Mohan, Ganesh, additional, Ghatak, Subhadip, additional, Sen, Chandan K., additional, and Sinha, Mithun, additional

Published
2023
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7. Contributors

Author

Abouhashem, Ahmed Safwat, primary, Ahmad, Aamir, additional, Ahmad, Shazia, additional, Ali, Saira R., additional, Anderson, Tyler, additional, Avitabile, Daniele, additional, Balakrishnan, Asha, additional, Balkhi, Mumtaz Yaseen, additional, Bao, Bin, additional, Bastaki, Nasma, additional, Beclin, Christophe, additional, Ben-Aicha, Soumaya, additional, Bosio, Andreas, additional, Bruch, Emily, additional, Calin, George A., additional, Cao, Yang, additional, Capogrossi, Maurizio C., additional, Caporali, Andrea, additional, Chan, Derryn Xin Hui, additional, Chan, Yuk Cheung, additional, Chavali, Pavithra L., additional, Chavali, Sreenivas, additional, Chen, Alex F., additional, Chen, Xiaona, additional, Cook, Charles, additional, Cremer, Harold, additional, Czeisler, Catherine, additional, Dakhlallah, Duaa, additional, Das, Amitava, additional, Delany, Anne M., additional, Dolezalova, Dasa, additional, Domínguez-Bendala, Juan, additional, EI Naggar, Manar A., additional, Emanueli, Costanza, additional, Ezzie, Michael, additional, Fathallah, Sara T., additional, Franceschetti, Tiziana, additional, Gambari, Roberto, additional, Ghatak, Subhadip, additional, Gleadle, Jonathan M., additional, Guan, Le Luo, additional, Guttridge, Denis C., additional, Gygli, Patrick Edwin, additional, Haider, Khawaja H., additional, Hampl, Aleš, additional, Han, Sen, additional, Harmsen, Martin C., additional, Hasegawa, Yoshinori, additional, Hashish, Sara A., additional, Hesse, Eric, additional, Houlé, John D., additional, Inoue, Kazuki, additional, Jagdeo, Jared, additional, Khan, Imran, additional, Khan, Mahmood, additional, Khorsandi, Shirin Elizabeth, additional, Klein, Dagmar, additional, Kong, Dejuan, additional, Krenning, Guido, additional, Kusumanchi, Praveen, additional, Li, Yiwei, additional, Li, Zhigang, additional, Liangpunsakul, Suthat, additional, Liechty, Kenneth W., additional, Louiselle, Amanda, additional, Lu, Leina, additional, Magenta, Alessandra, additional, Malmuthuge, Nilusha, additional, Mamalis, Andrew, additional, Marsh, Clay B., additional, Möbus, Selina, additional, Mohan, Ganesh, additional, Mohler, Peter J., additional, Moldovan, Leni, additional, Monroig, Paloma del C., additional, Mraz, Marek, additional, Nana-Sinkam, S. Patrick, additional, Neumann, Colby R., additional, Niemiec, Stephen, additional, Otero, José Javier, additional, Pal, Durba, additional, Pastori, Ricardo L., additional, Piper, Melissa G., additional, Pompilio, Giulio, additional, Qadir, Mirza Muhammed Fahd, additional, Ramsamy, Srinivas, additional, Rojas-Canales, Darling, additional, Rossini, Alessandra, additional, Roy, Sashwati, additional, Rustagi, Yashika, additional, Salama, Alaa A., additional, Salama, Mohamed, additional, Sampath, Prabha, additional, Sarkar, Fazlul H., additional, Sato, Mitsuo, additional, Sen, Chandan K., additional, Shames, David S., additional, Sharma, Amar Deep, additional, Singh, Anjali Kumari, additional, Singh, Kanhaiya, additional, Sinha, Mithun, additional, Srivastava, Prashant, additional, Sun, Hao, additional, Sun, Yeqing, additional, Tahara, Hidetoshi, additional, Taipaleenmäki, Hanna, additional, Trgovich, Joanne, additional, Tucker, Elise J., additional, Wang, Huating, additional, Wang, Jie-Mei, additional, Wang, Lijun, additional, Wang, Yijie, additional, Watson, Brandon, additional, Xu, Dan, additional, Xu, Junwang, additional, Xuan, Yi, additional, Yang, Dakai, additional, Yang, Zhihong, additional, Yonis, Nouran, additional, Zambrotta, Marina E., additional, Zgheib, Carlos, additional, Zhang, Ting, additional, Zhao, Baohong, additional, Zhao, Yu, additional, and Zhou, Liang, additional

Published
2023
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8. Oxylipins in Breast Implant Associated Systemic Symptoms

Author

Khan, Imran, primary, Timsina, Lava, additional, Chauhan, Ruvi, additional, Ingersol, Christopher, additional, Wang, David R, additional, Rinne, Ethan, additional, Muraru, Rodica, additional, Mohan, Ganesh, additional, Minto, Robert E, additional, Van Natta, Bruce W, additional, Hassanein, Aladdin H, additional, Kelley-Patteson, Christine, additional, and Sinha, Mithun, additional

Published
2024
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9. Prophylactic absorbable antibiotic beads for prepectoral implant-based breast reconstruction: A single institution early experience.

Author

Ahmed, Shahnur, Hajj, John P., VonDerHaar, R. Jason, Bamba, Ravinder, Danforth, Rachel M., Sinha, Mithun, Fisher, Carla S., Ludwig, Kandice K., Lester, Mary E., and Hassanein, Aladdin H.

Abstract

Infection after implant-based breast reconstruction remains challenging, with infection rates up to 24%. Best clinical practice indicates prophylactic oral antibiotics are ineffective at preventing infection. Absorbable antibiotic beads have been routinely used in other surgical subspecialties such as orthopedic and vascular procedures for continuous local antibiotic delivery to the surgical site when implants are placed. Biodegradable calcium sulfate antibiotic beads have been shown to normalize incidence of infection when used prophylactically for a high-risk prepectoral patient population. The purpose of this study is to evaluate the effect of prophylactic biodegradable antibiotic beads when used non-selectively for all prepectoral immediate tissue expander (TE) reconstruction. Patients who underwent mastectomy and immediate prepectoral TE reconstruction on the same day between 2018 and 2024 were reviewed. Patients were divided into two groups: those who received antibiotic beads (Group 1) and those who did not (Group 2). Absorbable calcium-sulfate beads were reconstituted with 1 g vancomycin and 240 mg gentamicin. There were 33 patients (63 TEs) in Group 1 and 330 patients (545 TEs) in Group 2. TE loss was present in 1.5% (1/65 TEs) Group 1 compared to 9.4% (51/545 TEs) in Group 2 (p = 0.032). The mean follow-up time was 178 days (range 93–266 days). Prophylactic biodegradable antibiotic beads used during immediate tissue expander reconstruction decreased implant loss rate. There was one occurrence of SSI in the antibiotic bead group. Antibiotic beads may potentially decrease complications in immediate TE reconstruction when used non-selectively for all patients. [ABSTRACT FROM AUTHOR]

Published
2024
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14. MicroRNA Interaction network in human: implications of clustered microRNA in biological pathways and genetic diseases

Author

Mookherjee, Sushmita, Sinha, Mithun, Mukhopadhyay, Saikat, Bhattacharyya, Nitai P., and Mohanty, P. K.

Subjects
Quantitative Biology - Genomics, Quantitative Biology - Molecular Networks
Abstract

A novel group of small non-coding RNA, known as microRNA (miRNA) is predicted to regulate as high as 90% of the coding genes in human. The diversity and abundance of miRNA targets offer an enormous level of combinatorial possibilities and suggest that miRNAs and their targets form a complex regulatory network. In the present study, we analyzed 711 miRNAs and their 34, 525 predicted targets in the miRBase database which generate a complex bipartite network having numerous numbers of genes forming the hub. Genes at the hub (total 9877) are significantly over represented in genes with specific molecular functions, biological processes and biological pathways as revealed from the analysis using PANTHER. We further construct a miRNA co-target network by linking every pair of miRNAs which co-target at least one gene. The weight of the link, which is taken to be the number of co-targets of the pair of miRNAs vary widely, and we could erase several links while keeping the relevant features of the network intact. The largest connected sub-graph, thus obtained, contains 479 miRNAs. More than 75% of the miRNAs deregulated in 15 different diseases collected from published data are found to be in this largest sub graph. We further analyze this sub-graph to obtain 70 small clusters containing total 330 miRNAs of 479. We identified the biological pathways where the co-targeted genes in the clusters are significantly over- represented in comparison to that obtained with that are not co-targeted by the miRNAs in the cluster. Using published data, we identified that specific clusters of miRNAs are associated with specific diseases by altering particular pathways. We propose that instead of single miRNA, clusters of miRNA that co-targets the genes are important for the regulation of miRNA in diseases., Comment: 11 pages, 7 eps figures (Supplementary material is available on request)

Published
2009

15. Quantification of Lymphangiogenesis in the Murine Lymphedema Tail Model Using Intravital Microscopy.

Author

Mohan, Ganesh, Khan, Imran, Diaz, Stephanie M., Kamocka, Malgorzata M., Hulsman, Luci A., Ahmed, Shahnur, Neumann, Colby R., Jorge, Miguel D., Gordillo, Gayle M., Sen, Chandan K., Sinha, Mithun, and Hassanein, Aladdin H.

Abstract

Background: Lymphedema is chronic limb swelling resulting from lymphatic dysfunction. It affects an estimated five million Americans. There is no cure for this disease. Assessing lymphatic growth is essential in developing novel therapeutics. Intravital microscopy (IVM) is a powerful imaging tool for investigating various biological processes in live animals. Tissue nanotransfection technology (TNT) facilitates a direct, transcutaneous nonviral vector gene delivery using a chip with nanochannel poration in a rapid (<100 ms) focused electric field. TNT was used in this study to deliver the genetic cargo in the murine tail lymphedema to assess the lymphangiogenesis. The purpose of this study is to experimentally evaluate the applicability of IVM to visualize and quantify lymphatics in the live mice model. Methods and Results: The murine tail model of lymphedema was utilized. TNT was applied to the murine tail (day 0) directly at the surgical site with genetic cargo loaded into the TNT reservoir: TNTpCMV6 group receives pCMV6 (expression vector backbone alone) (n = 6); TNTProx1 group receives pCMV6-Prox1 (n = 6). Lymphatic vessels (fluorescein isothiocyanate [FITC]-dextran stained) and lymphatic branch points (indicating lymphangiogenesis) were analyzed with the confocal/multiphoton microscope. The experimental group TNTProx1 exhibited reduced postsurgical tail lymphedema and increased lymphatic distribution compared to TNTpCMV6 group. More lymphatic branching points (>3-fold) were observed at the TNT site in TNTProx1 group. Conclusions: This study demonstrates a novel, powerful imaging tool for investigating lymphatic vessels in live murine tail model of lymphedema. IVM can be utilized for functional assessment of lymphatics and visualization of lymphangiogenesis following gene-based therapy. [ABSTRACT FROM AUTHOR]

Published
2024
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17. CD30 Lateral Flow and Enzyme-Linked Immunosorbent Assays for Detection of BIA-ALCL: A Pilot Study

Author

Zeyl, Victoria G., primary, Xu, Haiying, additional, Khan, Imran, additional, Machan, Jason T., additional, Clemens, Mark W., additional, Hu, Honghua, additional, Deva, Anand, additional, Glicksman, Caroline, additional, McGuire, Patricia, additional, Adams, William P., additional, Sieber, David, additional, Sinha, Mithun, additional, and Kadin, Marshall E., additional

Published
2023
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22. Contributors

Author

Abas, Motaz, primary, Agarwal, Mangilal, additional, Ajo, Alessandro, additional, Arany, Praveen, additional, Atway, Said A., additional, Azeltine, Mark, additional, Bagchi, Debasis, additional, Balaji, Swathi, additional, Banerjee, Jaideep, additional, Barman, Pijus K., additional, Basson, Rubinder, additional, Bayat, Ardeshir, additional, Biswas, Nirupam, additional, Campbell, Amy, additional, Chan, Yuk Cheung Cyrus, additional, Clark, Andrew, additional, Daneshkhah, Ali, additional, Das, Amitava, additional, denDekker, Aaron D., additional, Desai, Karishma, additional, Dhall, Sandeep, additional, DiMassa, Nicholas V., additional, Dutta, Dibyendu, additional, El Masry, Mohamed, additional, Elgharably, Haytham, additional, Gallagher, Katherine A., additional, Ghatak, Subhadip, additional, Ghosh, Nandini, additional, Grice, Elizabeth A., additional, Grover, Komel, additional, Herman, Ira M., additional, Kaul, Aditya, additional, Khan, Imran, additional, Khandelwal, Puneet, additional, Khanna, Savita, additional, Khona, Dolly, additional, Koh, Timothy J., additional, Li, Hui, additional, Liechty, Kenneth W., additional, Louiselle, Amanda E., additional, Madeshiya, Amit Kumar, additional, Maitra, Sayantan, additional, Martins-Green, Manuela, additional, Masri, Leighanne, additional, Mathew-Steiner, Shomita S., additional, Medina-Cruz, David, additional, Miao, Qi, additional, Mohnacky, Jennifer, additional, Mosca, Rodrigo, additional, Narmoneva, Daria A., additional, Neumann, Colby, additional, Niemiec, Stephen M., additional, Niranjan, Priya, additional, Pal, Durba, additional, Parikh, Umang, additional, Pattarayan, Dhamotharan, additional, Ponnusamy, Sasikumar, additional, Rawat, Atul, additional, Rijal, Nava P., additional, Roy, Amit K., additional, Roy, Sashwati, additional, Saeed, Shayan, additional, Saleh, Bahram, additional, Santra, Suman, additional, Saravanan, Swetha, additional, Sen, Abhishek, additional, Sen, Chandan K., additional, Siegel, Amanda P., additional, Singh, Kanhaiya, additional, Sinha, Mithun, additional, Strang, Harrison, additional, Uberoi, Aayushi, additional, Vernet-Crua, Ada, additional, Webster, Thomas J., additional, Wijesinghe, Dayanjan S., additional, Wilgus, Traci A., additional, Xu, Junwang, additional, and Zgheib, Carlos, additional

Published
2020
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26. Abstract 111: Allogeneic Mesenchymal Stromal Cells Significantly Increase Type 1 Regulatory T-cells, Decrease Effector Th17 Cells, And Decrease Aneurysm Volume In A Dose Dependent Fashion In Patients With Small Abdominal Aortic Aneurysms - Results Of The Phase I Aneurysm Repression With Mesenchymal Stromal Cells (the Arrest Trial)

Author

Samra, Humraaz, primary, Ingram, Michael, additional, Leckie, Katherin, additional, Moldovan, Leni, additional, Wanczyk, Kristen, additional, Timsina, Lava, additional, Sinha, Mithun, additional, Mohammed, Imran Khan, additional, Mylvaganam, Ravi, additional, Motaganahalli, Anush, additional, Territo, Paul, additional, GUTWEIN, Ashley, additional, Motaganahalli, Raghunandan, additional, and Murphy, Michael P, additional

Published
2023
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29. Topical tissue nano-transfection mediates non-viral stroma reprogramming and rescue

Author

Gallego-Perez, Daniel, Pal, Durba, Ghatak, Subhadip, Malkoc, Veysi, Higuita-Castro, Natalia, Gnyawali, Surya, Chang, Lingqian, Liao, Wei-Ching, Shi, Junfeng, Sinha, Mithun, Singh, Kanhaiya, Steen, Erin, Sunyecz, Alec, Stewart, Richard, Moore, Jordan, Ziebro, Thomas, Northcutt, Robert G., Homsy, Michael, Bertani, Paul, Lu, Wu, Roy, Sashwati, Khanna, Savita, Rink, Cameron, Sundaresan, Vishnu Baba, Otero, Jose J., Lee, L. James, and Sen, Chandan K.

Published
2017
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31. Allogeneic Mesenchymal Stromal Cells Significantly Increase Type 1 Regulatory T Cells, Decrease Effector Th17 Cells, and Decrease Aneurysm Volume in a Dose-dependent Fashion in Patients With Small Abdominal Aortic Aneurysms: Results of the Phase I Aneurysm Repression With Mesenchymal Stromal Cells (the Arrest Trial)

Author

Samra, Humraaz, primary, Leckie, Katherin, additional, Moldovan, Leni, additional, Wanczyk, Kristen, additional, Timsina, Lava, additional, Sinha, Mithun, additional, Mohammed, Imran Khan, additional, Mylvaganam, Ravi, additional, Motaganahalli, Anush, additional, Territo, Paul, additional, Gutwein, Ashley, additional, Motaganahalli, Raghunandan, additional, and Murphy, Michael P., additional

Published
2023
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36. Initial Results of a Lateral Flow Assay for Diagnosis of Breast Implant Associated-Anaplastic Large Cell Lymphoma (BIA-ALCL) in Peri-Implant Seromas

Author

Zeyl, Victoria G., primary, Mohammed, Imran Khan, additional, Xu, Haiying, additional, Adams, William P., additional, Clemens, Mark, additional, Glicksman, Caroline A., additional, Hunsicker, Lisa M., additional, McGuire, Patricia A., additional, Sinha, Mithun, additional, and Kadin, Marshall, additional

Published
2022
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37. Immunomodulatory Effects of Oxylipin 10-HOME Produced by Biofilm Results in Host-Biofilm Interaction in Breast Implant Illness

Author

Khan Mohammed, Imran, primary, Minto, Robert, additional, Kelley-Patteson, Christine, additional, Timsina, Lava, additional, Singh, Kanhaiya, additional, Van Natta, Bruce W., additional, Mohan, Ganesh, additional, Chauhan, Ruvi, additional, Lester, Mary, additional, Hassanein, Al, additional, Gordillo, Gayle M., additional, Sen, Chandan, additional, Kadin, Marshall, additional, and Sinha, Mithun, additional

Published
2022
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41. Laser Capture Microdissection in the Spatial Analysis of Epigenetic Modifications in Skin: A Comprehensive Review

Author

Bhamidipati, Theja, Sinha, Mithun, Sen, Chandan K., and Singh, Kanhaiya

Subjects
Article Subject
Abstract

Each cell in the body contains an intricate regulation for the expression of its relevant DNA. While every cell in a multicellular organism contains identical DNA, each tissue-specific cell expresses a different set of active genes. This organizational property exists in a paradigm that is largely controlled by forces external to the DNA sequence via epigenetic regulation. DNA methylation and chromatin modifications represent some of the classical epigenetic modifications that control gene expression. Complex tissues like skin consist of heterogeneous cell types that are spatially distributed and mixed. Furthermore, each individual skin cell has a unique response to physiological and pathological cues. As such, it is difficult to classify skin tissue as homogenous across all cell types and across different environmental exposures. Therefore, it would be prudent to isolate targeted tissue elements prior to any molecular analysis to avoid a possibility of confounding the sample with unwanted cell types. Laser capture microdissection (LCM) is a powerful technique used to isolate a targeted cell group with extreme microscopic precision. LCM presents itself as a solution to tackling the problem of tissue heterogeneity in molecular analysis. This review will cover an overview of LCM technology, the principals surrounding its application, and benefits of its application to the newly defined field of epigenomics, in particular of cutaneous pathology. This presents a comprehensive review about LCM and its use in the spatial analysis of skin epigenetics. Within the realm of skin pathology, this ability to isolate tissues under specific environmental stresses, such as oxidative stress, allows a far more focused investigation.

Published
2022
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42. Pseudomonas Aeruginosa Theft Biofilm Require Host Lipids of Cutaneous Wound.

Author

Sinha, Mithun, Ghosh, Nandini, Wijesinghe, Dayanjan S., Mathew-Steiner, Shomita S., Das, Amitava, Singh, Kanhaiya, El Masry, Mohamed, Khanna, Savita, Inoue, Hiroyuki, Yamazaki, Katsuhisa, Kawada, Manabu, Gordillo, Gayle M., Roy, Sashwati, and Sen, Chandan K.

Abstract

Objective: This work addressing complexities in wound infection, seeks to test the reliance of bacterial pathogen Pseudomonas aeruginosa (PA) on host skin lipids to form biofilm with pathological consequences. Background: PA biofilm causes wound chronicity. Both CDC as well as NIH recognizes biofilm infection as a threat leading to wound chronicity. Chronic wounds on lower extremities often lead to surgical limb amputation. Methods: An established preclinical porcine chronic wound biofilm model, infected with PA or Pseudomonas aeruginosa ceramidase mutant (PA∆Cer), was used. Results: We observed that bacteria drew resource from host lipids to induce PA ceramidase expression by three orders of magnitude. PA utilized product of host ceramide catabolism to augment transcription of PA ceramidase. Biofilm formation was more robust in PA compared to PA∆Cer. Downstream products of such metabolism such as sphingosine and sphingosine-1-phosphate were both directly implicated in the induction of ceramidase and inhibition of peroxisome proliferator-activated receptor (PPAR)δ, respectively. PA biofilm, in a ceram-idastin-sensitive manner, also silenced PPARδ via induction of miR-106b. Low PPARδ limited ABCA12 expression resulting in disruption of skin lipid homeostasis. Barrier function of the wound-site was thus compromised. Conclusions: This work demonstrates that microbial pathogens must co-opt host skin lipids to unleash biofilm pathogenicity. Anti-biofilm strategies must not necessarily always target the microbe and targeting host lipids at risk of infection could be productive. This work may be viewed as a first step, laying fundamental mechanistic groundwork, toward a paradigm change in biofilm management. [ABSTRACT FROM AUTHOR]

Published
2023
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44. Contributors

Author

Ahmad, Aamir, primary, Alemdehy, Mir Farshid, additional, Anderson, Tyler, additional, Awad, Hamdy, additional, Balakrishnan, Asha, additional, Balkhi, Mumtaz Yaseen, additional, Bally-Cuif, Laure, additional, Banerjee, Jaideep, additional, Bao, Bin, additional, Barry, Christopher Taylor, additional, Beclin, Christophe, additional, Boison, Detlev, additional, Bosio, Andreas, additional, Brandi, Maria Luisa, additional, Brown, Melissa, additional, Calin, George A., additional, Cao, Yang, additional, Capogrossi, Maurizio C., additional, Caporali, Andrea, additional, Carulli, Christian, additional, Chan, Yuk Cheung, additional, Chavali, Pavithra L., additional, Chavali, Sreenivas, additional, Chen, Alex F., additional, Chen, Xiaona, additional, Cook, Charles, additional, Coolen, Marion, additional, Cremer, Harold, additional, Czeisler, Catherine, additional, Dakhlallah, Duaa, additional, Das, Amitava, additional, Delany, Anne M., additional, Dolezalova, Dasa, additional, Domínguez-Bendala, Juan, additional, Emanueli, Costanza, additional, Erkeland, Stefan J., additional, Ezzie, Michael, additional, Fasanaro, Pasquale, additional, Foinquinos, Ariana, additional, Franceschetti, Tiziana, additional, Gambari, Roberto, additional, Ahmad, Shazia, additional, Ghatak, Subhadip, additional, Guan, Le Luo, additional, Guttridge, Denis C., additional, Gygli, Patrick Edwin, additional, Haider, Khawaja H., additional, Hampl, Aleš, additional, Harmsen, Martin C., additional, Hasegawa, Yoshinori, additional, Hindges, Robert, additional, Hinsdale, Myron, additional, Houlé, John D., additional, Howard, Lynsey, additional, Hui Chan, Derryn Xin, additional, Ichi, Shunsuke, additional, Innocenti, Massimo, additional, Jagdeo, Jared, additional, Kagele, Dominique A., additional, Khan, Mahmood, additional, Klein, Dagmar, additional, Kobayashi, Tatsuya, additional, Kong, Dejuan, additional, Krenning, Guido, additional, Li, Yiwei, additional, Liechty, Kenneth W., additional, Lisse, Thomas, additional, Liu, Lin, additional, Lloyd, Pamela, additional, Lu, Leina, additional, Lusardi, Theresa A., additional, Luzi, Ettore, additional, Macera, Armando, additional, Magenta, Alessandra, additional, Maiorano, Nicola Antonio, additional, Malik, Obaid, additional, Mamalis, Andrew, additional, Mania-Farnell, Barbara, additional, Marsh, Clay B., additional, Mayanil, C. Shekhar, additional, McLone, David, additional, Möbus, Selina, additional, Mohler, Peter J., additional, Moldovan, Leni, additional, Monroig, Paloma del C., additional, Mraz, Marek, additional, Nana-Sinkam, S. Patrick, additional, Nguyen, Laurent, additional, O’Connell, Ryan M., additional, Otero, José Javier, additional, Pal, Durba, additional, Papaioannou, Garyfallia, additional, Pastori, Ricardo L., additional, Piper, Melissa G., additional, Pirotte, Sophie, additional, Pompilio, Giulio, additional, Ramsamy, Srinivas, additional, Romao, Josue Moura, additional, Rossini, Alessandra, additional, Roy, Sashwati, additional, Sampath, Prabha, additional, Sarkar, Fazlul H., additional, Sato, Mitsuo, additional, Sen, Chandan K., additional, Shames, David S., additional, Shantikumar, Saran, additional, Sharma, Amar Deep, additional, Siddiqui, M. Rizwan, additional, Sinha, Mithun, additional, Sun, Hao, additional, Sun, Yeqing, additional, Tahara, Hidetoshi, additional, Thum, Thomas, additional, Tili, Esmerina, additional, Tomita, Tadanori, additional, Trgovich, Joanne, additional, Viereck, Janika, additional, Volvert, Marie-Laure, additional, Wang, Jie-Mei, additional, Wang, Lijun, additional, Wang, Huating, additional, Wang, Yijie, additional, Xu, Dan, additional, Xu, Junwang, additional, Yang, Dakai, additional, Zambrotta, Marina E., additional, Zgheib, Carlos, additional, Zhao, Yu, additional, and Zhou, Liang, additional

Published
2015
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49. QS9: Host Biofilm Interaction In Breast Implant Illness

Author

Khan, Imran, primary, Minto, Robert E., additional, Kelley-Patteson, Christine, additional, Van Natta, Bruce, additional, Mohan, Ganesh, additional, Suh, Lily, additional, Singh, Kanhaiya, additional, Lester, Mary, additional, Jason VonDerHaar, R, additional, Gordillo, Gayle M., additional, Hassanein, Aladdin, additional, Sen, Chandan K., additional, Kadin, Marshall E., additional, and Sinha, Mithun, additional

Published
2021
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