14 results on '"Marinho, Fábio V."'
Search Results
2. Bacillus Calmette-Gué rin immunotherapy induces an efficient antitumor response to control murine melanoma depending on MyD88 signaling.
- Author
-
Borges, Vinícius M., Marinho, Fábio V., Caldeira, Christiane V. A., de Queiroz, Nina M. G. P., and Oliveira, Sergio C.
- Subjects
MYELOID differentiation factor 88 ,BCG immunotherapy ,BACILLUS (Bacteria) ,IMMUNOTHERAPY ,MELANOMA ,BLADDER cancer - Abstract
Bacillus Calmette-Gué rin (BCG) is the first line treatment for bladder cancer and it is also proposed for melanoma immunotherapy. BCG modulates the tumor microenvironment (TME) inducing an antitumor effective response, but the immune mechanisms involved still poorly understood. The immune profile of B16-F10 murine melanoma cells was assessed by infecting these cells with BCG or stimulating them with agonists for different innate immune pathways such as TLRs, inflammasome, cGAS-STING and type I IFN. B16-F10 did not respond to any of those stimuli, except for type I IFN agonists, contrasting with bone marrow-derived macrophages (BMDMs) that showed high production of proinflammatory cytokines. Additionally, we confirmed that BCG is able to infect B16-F10, which in turn can activate macrophages and spleen cells from mice in co-culture experiments. Furthermore, we established a subcutaneous B16-F10 melanoma model for intratumorally BCG treatment and compared wild type mice to TLR2
, TLR3-/- -/- , TLR4-/- , TLR7-/- , TLR3/7/9-/- , caspase 1-/- , caspase 11-/- , IL-1R-/- , cGAS-/- , STING-/- , IFNAR-/- , MyD88-/- deficient animals. These results in vivo demonstrate that MyD88 signaling is important for BCG immunotherapy to control melanoma in mice. Also, BCG fails to induce cytokine production in the co-culture experiments using B16-F10 and BMDMs or spleen cells derived from MyD88-/- compared to wild-type (WT) animals. Immunotherapy with BCG was not able to induce the recruitment of inflammatory cells in the TME from MyD88-/- mice, impairing tumor control and IFN-γ production by T cells. In conclusion, MyD88 impacts on both innate and adaptive responses to BCG leading to an efficient antitumor response against melanoma. [ABSTRACT FROM AUTHOR]- Published
- 2024
- Full Text
- View/download PDF
3. The use of gold nanorods as a new vaccine platform against schistosomiasis
- Author
-
Assis, Natan R.G., Caires, Anderson J., Figueiredo, Bárbara C., Morais, Suellen B., Mambelli, Fábio S., Marinho, Fábio V., Ladeira, Luís O., and Oliveira, Sergio C.
- Published
- 2018
- Full Text
- View/download PDF
4. The Emerging Roles of STING in Bacterial Infections
- Author
-
Marinho, Fabio V., Benmerzoug, Sulayman, Oliveira, Sergio C., Ryffel, Bernhard, and Quesniaux, V.F.J.
- Published
- 2017
- Full Text
- View/download PDF
5. Contribution of intercellular adhesion molecule 1 (ICAM-1) to control Mycobacterium avium infection
- Author
-
de Paula, Rafaella R., Marinho, Fábio V., Fahel, Julia S., and Oliveira, Sergio C.
- Published
- 2017
- Full Text
- View/download PDF
6. The role of the adaptor molecule STING during Schistosoma mansoni infection
- Author
-
Souza, Cláudia, Sanches, Rodrigo C. O., Assis, Natan R. G., Marinho, Fábio V., Mambelli, Fábio S., Morais, Suellen B., Gimenez, Enrico G. T., Guimarães, Erika S., Castro, Tiago B. R., and Oliveira, Sergio C.
- Published
- 2020
- Full Text
- View/download PDF
7. Current Understanding of Bacillus Calmette-Guérin-Mediated Trained Immunity and Its Perspectives for Controlling Intracellular Infections.
- Author
-
de Araujo, Ana Carolina V. S. C., Mambelli, Fábio, Sanches, Rodrigo O., Marinho, Fábio V., and Oliveira, Sergio C.
- Subjects
MYCOBACTERIUM bovis ,MYCOBACTERIUM tuberculosis ,BACILLUS (Bacteria) ,HEMATOPOIETIC stem cells ,IMMUNITY ,INFECTION control ,TUBERCULOSIS in cattle ,IMMUNE response - Abstract
The bacillus Calmette–Guérin (BCG) is an attenuated bacterium derived from virulent Mycobacterium bovis. It is the only licensed vaccine used for preventing severe forms of tuberculosis in children. Besides its specific effects against tuberculosis, BCG administration is also associated with beneficial non-specific effects (NSEs) following heterologous stimuli in humans and mice. The NSEs from BCG could be related to both adaptive and innate immune responses. The latter is also known as trained immunity (TI), a recently described biological feature of innate cells that enables functional improvement based on metabolic and epigenetic reprogramming. Currently, the mechanisms related to BCG-mediated TI are the focus of intense research, but many gaps are still in need of elucidation. This review discusses the present understanding of TI induced by BCG, exploring signaling pathways that are crucial to a trained phenotype in hematopoietic stem cells and monocytes/macrophages lineage. It focuses on BCG-mediated TI mechanisms, including the metabolic-epigenetic axis and the inflammasome pathway in these cells against intracellular pathogens. Moreover, this study explores the TI in different immune cell types, its ability to protect against various intracellular infections, and the integration of trained innate memory with adaptive memory to shape next-generation vaccines. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
8. TLR9 activation is required for cytotoxic response elicited by baculovirus capsid display.
- Author
-
Molinari, Paula, Crespo, María Inés, Molina, Guido N., Dho, Nicolás D., Marinho, Fábio V., Maletto, Belkys, Leclerc, Claude, Oliveira, Sergio C., Taboga, Oscar, Cebrian, Ignacio, and Morón, Gabriel
- Subjects
CYTOTOXIC T cells ,NUCLEOPOLYHEDROVIRUSES ,ALFALFA looper ,VIRAL proteins ,MAJOR histocompatibility complex - Abstract
Although the baculovirus Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) infects lepidopteran invertebrates as natural hosts, represents an efficient vector for vaccine development. Baculovirus surface display induces strong humoral responses against viruses and parasites. A novel strategy based on capsid display carrying foreign antigens in the AcMNPV particle further improved the immune response by eliciting CD8+ T cell activation. In this study, we analyze the intracellular mechanisms and signalling pathways involved in CD8+ T cell activation by capsid display. Our results show that baculovirus can attach to the cell surface, enter dendritic cells (DCs), transit within endocytic vesicles and escape to the cytosol for further degradation by the proteasome. We found that the availability of viral proteins, endosomal acidification, and proteasome activity are needed for efficient Major Histocompatibility Complex class‐I presentation by baculovirus carrying Ovalbumin in the viral capsid. Importantly, we demonstrated with this strategy that the induction of cytotoxic T cells and IL‐12 production by DCs are TLR9‐dependent and STING‐independent. Finally, our study shows differential intracellular processing for capsid and surface baculovirus proteins in DCs and highlights the role of different danger receptors during cytotoxic T cell priming through the capsid display delivery system, which could lead to improved baculovirus‐based vaccines development. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
9. The endoplasmic reticulum stress sensor IRE1α modulates macrophage metabolic function during Brucella abortus infection.
- Author
-
Guimarães, Erika S., Gomes, Marco Túlio R., Sanches, Rodrigo C. O., Matteucci, Kely Catarine, Marinho, Fábio V., and Oliveira, Sergio C.
- Subjects
BRUCELLA abortus ,ENDOPLASMIC reticulum ,UNFOLDED protein response ,MACROPHAGES ,CELL physiology ,MACROPHAGE inflammatory proteins - Abstract
Endoplasmic reticulum (ER) stress plays a major role in several inflammatory disorders. ER stress induces the unfolded protein response (UPR), a conserved response broadly associated with innate immunity and cell metabolic function in various scenarios. Brucella abortus, an intracellular pathogen, triggers the UPR via Stimulator of interferon genes (STING), an important regulator of macrophage metabolism during B. abortus infection. However, whether ER stress pathways underlie macrophage metabolic function during B. abortus infection remains to be elucidated. Here, we showed that the UPR sensor inositol-requiring enzyme 1a (IRE1α) is as an important component regulating macrophage immunometabolic function. In B. abortus infection, IRE1α supports the macrophage inflammatory profile, favoring M1-like macrophages. IRE1α drives the macrophage metabolic reprogramming in infected macrophages, contributing to the reduced oxidative phosphorylation and increased glycolysis. This metabolic reprogramming is probably associated with the IRE1α-dependent expression and stabilization of hypoxia-inducible factor-1 alpha (HIF-1α), an important molecule involved in cell metabolism that sustains the inflammatory profile in B. abortus-infected macrophages. Accordingly, we demonstrated that IRE1α favors the generation of mitochondrial reactive oxygen species (mROS) which has been described as an HIF-1α stabilizing factor. Furthermore, in infected macrophages, IRE1α drives the production of nitric oxide and the release of IL-1β. Collectively, these data unravel a key mechanism linking the UPR and the immunometabolic regulation of macrophages in Brucella infection and highlight IRE1α as a central pathway regulating macrophage metabolic function during infectious diseases. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
10. Galectin‐3 regulates proinflammatory cytokine function and favours Brucella abortus chronic replication in macrophages and mice.
- Author
-
Tana, Fernanda L., Guimarães, Erika S., Cerqueira, Daiane M., Campos, Priscila C., Gomes, Marco Túlio R., Marinho, Fábio V., and Oliveira, Sergio C.
- Subjects
BRUCELLA abortus ,GALECTINS ,CYTOKINES ,MACROPHAGES ,CELLULAR signal transduction - Abstract
In this study, we provide evidence that galectin‐3 (Gal‐3) plays an important role in Brucella abortus infection. Our results showed increased Gal‐3 expression and secretion in B. abortus infected macrophages and mice. Additionally, our findings indicate that Gal‐3 is dispensable for Brucella‐containing vacuoles disruption, inflammasome activation and pyroptosis. On the other hand, we observed that Brucella‐induced Gal‐3 expression is crucial for induction of molecules associated to type I IFN signalling pathway, such as IFN‐β: Interferon beta (IFN‐β), C‐X‐C motif chemokine ligand 10 (CXCL10) and guanylate‐binding proteins. Gal‐3 KO macrophages showed reduced bacterial numbers compared to wild‐type cells, suggesting that Gal‐3 facilitates bacterial replication in vitro. Moreover, priming Gal‐3 KO cells with IFN‐β favoured B. abortus survival in macrophages. Additionally, we also observed that Gal‐3 KO mice are more resistant to B. abortus infection and these animals showed elevated production of proinflammatory cytokines when compared to control mice. Finally, we observed an increased recruitment of macrophages, dendritic cells and neutrophils in spleens of Gal‐3 KO mice compared to wild‐type animals. In conclusion, this study demonstrated that Brucella‐induced Gal‐3 is detrimental to host and this molecule is implicated in inhibition of recruitment and activation of immune cells, which promotes B. abortus spread and aggravates the infection. Take Aways: Brucella abortus infection upregulates galectin‐3 expressionGalectin‐3 regulates guanylate‐binding proteins expression but is not required for Brucella‐containing vacuole disruptionGalectin‐3 modulates proinflammatory cytokine production during bacterial infectionGalectin‐3 favours Brucella replication [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
11. Bacterial RNA Contributes to the Down-Modulation of MHC-II Expression on Monocytes/Macrophages Diminishing CD4+ T Cell Responses.
- Author
-
Milillo, M. Ayelén, Trotta, Aldana, Serafino, Agustina, Marin Franco, José Luis, Marinho, Fábio V., Alcain, Julieta, Genoula, Melanie, Balboa, Luciana, Costa Oliveira, Sergio, Giambartolomei, Guillermo H., and Barrionuevo, Paula
- Subjects
BACTERIAL RNA ,MONOCYTES ,T cells ,MACROPHAGES ,ANTIGEN presentation - Abstract
Brucella abortus , the causative agent of brucellosis, displays many resources to evade T cell responses conducive to persist inside the host. Our laboratory has previously showed that infection of human monocytes with B. abortus down-modulates the IFN-γ-induced MHC-II expression. Brucella outer membrane lipoproteins are structural components involved in this phenomenon. Moreover, IL-6 is the soluble factor that mediated MHC-II down-regulation. Yet, the MHC-II down-regulation exerted by lipoproteins was less marked than the one observed as consequence of infection. This led us to postulate that there should be other components associated with viable bacteria that may act together with lipoproteins in order to diminish MHC-II. Our group has recently demonstrated that B. abortus RNA (PAMP related to pathogens' viability or vita -PAMP) is involved in MHC-I down-regulation. Therefore, in this study we investigated if B. abortus RNA could be contributing to the down-regulation of MHC-II. This PAMP significantly down-modulated the IFN-γ-induced MHC-II surface expression on THP-1 cells as well as in primary human monocytes and murine bone marrow macrophages. The expression of other molecules up-regulated by IFN-γ (such as co-stimulatory molecules) was stimulated on monocytes treated with B. abortus RNA. This result shows that this PAMP does not alter all IFN-γ-induced molecules globally. We also showed that other bacterial and parasitic RNAs caused MHC-II surface expression down-modulation indicating that this phenomenon is not restricted to B. abortus. Moreover, completely degraded RNA was also able to reproduce the phenomenon. MHC-II down-regulation on monocytes treated with RNA and L-Omp19 (a prototypical lipoprotein of B. abortus) was more pronounced than in monocytes stimulated with both components separately. We also demonstrated that B. abortus RNA along with its lipoproteins decrease MHC-II surface expression predominantly by a mechanism of inhibition of MHC-II expression. Regarding the signaling pathway, we demonstrated that IL-6 is a soluble factor implicated in B. abortus RNA and lipoproteins-triggered MHC-II surface down-regulation. Finally, CD4
+ T cells functionality was affected as macrophages treated with these components showed lower antigen presentation capacity. Therefore, B. abortus RNA and lipoproteins are two PAMPs that contribute to MHC-II down-regulation on monocytes/macrophages diminishing CD4+ T cell responses. [ABSTRACT FROM AUTHOR]- Published
- 2019
- Full Text
- View/download PDF
12. JVA, an isoniazid analogue, is a bioactive compound against a clinical isolate of the Mycobacterium avium complex.
- Author
-
Fahel, Júlia S., Vieira, Rafael P., Marinho, Fábio V., Santos, Viviane C., de Assis, João Vitor, Corsetti, Patrícia P., Ferreira, Rafaela S., de Almeida, Mauro V., and Oliveira, Sergio C.
- Abstract
Abstract Bacteria belonging to Mycobacterium avium complex are organisms of low pathogenicity that infect immunosuppressed individuals. Infection is treated with an antimicrobial macrolide, Clarithromycin (CAM) or Azitromycin, associated with Ethambutol and Rifabutin during 12 months. Regimen long duration and side effects hinder patient's commitment to treatment favoring emergence of antibiotic resistance. In this present study, we evaluated the activity of JVA, an Isoniazid (INH) derivative, against M. avium 2447, a clinical isolate. We demonstrated that JVA reduces M. avium 2447 growth in macrophages, more efficiently than CAM and INH. In order to explore JVA mechanism of action, we investigated compound properties and performed pH-dependent stability studies. Our results suggest an enhanced ability of JVA to cross biological membranes. Furthermore, we suggest that in acidic conditions of macrophages' phagosomes, where mycobacteria replicate, JVA would be promptly hydrolyzed to INH, delivering the adduct INH-nicotinamide adenine dinucleotide and thus inhibiting M. avium 2447 growth. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
13. B. abortus RNA is the component involved in the down-modulation of MHC-I expression on human monocytes via TLR8 and the EGFR pathway.
- Author
-
Milillo, M. Ayelén, Velásquez, Lis N., Trotta, Aldana, Delpino, M. Victoria, Marinho, Fábio V., Balboa, Luciana, Vermeulen, Mónica, Espindola, Sonia L., Rodriguez-Rodrigues, Nahuel, Fernández, Gabriela C., Oliveira, Sergio Costa, Giambartolomei, Guillermo H., and Barrionuevo, Paula
- Subjects
BRUCELLA abortus ,CHRONIC diseases ,EPIDERMAL growth factor receptors ,NEUTRALIZATION tests ,T cells ,RIBOSOMAL DNA - Abstract
Despite eliciting a potent CD8
+ T cell response, Brucella abortus is able to persist and establish a chronic infection inside its host. We have previously reported that the infection of human monocytes/macrophages with B. abortus inhibits the IFN-γ-induced MHC-I cell surface expression down-modulating cytotoxic CD8+ T cell responses. MHC-I down-modulation depends on bacterial viability and results from the capacity of B. abortus to retain the MHC-I molecules within the Golgi apparatus. Furthermore, we recently demonstrated that epidermal growth factor receptor (EGFR) pathway is involved in this phenomenon and that this is an early event during infection. However, the components and mechanisms whereby B. abortus is able to down-modulate MHC-I remained to be elucidated. In this study we demonstrated that the down-modulation of MHC-I expression is not mediated by well-known Brucella virulence factors but instead by B. abortus RNA, a PAMP associated to viability (vita-PAMP). Surprisingly, completely degraded RNA was also able to inhibit MHC-I expression to the same extent as intact RNA. Accordingly, B. abortus RNA and its degradation products were able to mimic the MHC-I intracellular retention within the Golgi apparatus observed upon infection. We further demonstrated that TLR8, a single-stranded RNA and RNA degradation products sensor, was involved in MHC-I inhibition. On the other hand, neutralization of the EGFR reversed the MHC-I inhibition, suggesting a connection between the TLR8 and EGFR pathways. Finally, B. abortus RNA-treated macrophages display diminished capacity of antigen presentation to CD8+ T cells. Overall, our results indicate that the vita-PAMP RNA as well as its degradation products constitute novel virulence factors whereby B. abortus, by a TLR8-dependent mechanism and through the EGFR pathway, inhibits the IFN-γ-induced MHC-I surface expression on human monocytes/macrophages. Thus, bacteria can hide within infected cells and avoid the immunological surveillance of cytotoxic CD8+ T cells. [ABSTRACT FROM AUTHOR]- Published
- 2017
- Full Text
- View/download PDF
14. Lack of IL-1 Receptor-Associated Kinase-4 Leads to Defective Th1 Cell Responses and Renders Mice Susceptible to Mycobacterial Infection.
- Author
-
Marinho, Fábio V., Fahel, Júlia S., Scanga, Charles A., Gomes, Marco Tulio R., Guimara?es, Gabriela, Carvalho, Gabrielle R. M., Morales, Stefanny V., Báfica, André, and Oliveira, Sergio Costa
- Subjects
- *
INTERLEUKIN-1 , *TH1 cells , *MYCOBACTERIAL diseases in animals , *INTRACELLULAR pathogens , *MYCOBACTERIA - Abstract
The Toll-like and IL-1 family receptors play critical roles in innate and adaptive immunity against intracellular pathogens. Although previous data demonstrated the importance of TLRs and IL-1R signaling events for the establishment of an effective immune response to mycobacteria, the possible function of the adaptor molecule IL-1R-associated kinase (IRAK)-4 against this pathogen has not been addressed. In this study, we determined the role of IRAK-4 in signaling pathways responsible for controlling mycobacterial infections. This kinase is important for the production of IL-12 and TNF-α by macrophages and dendritic cells exposed to mycobacteria. Moreover, Mycobacterium bovis-infected IRAK-4-knockout macrophages displayed impaired MAPK and NF-kB activation. IL-1β secretion and caspase-1 activation were also dependent on IRAK-4 signaling. Mice lacking IRAK-4 showed increased M. bovis burden in spleen, liver, and lungs and smaller liver granulomas during 60 d of infection compared with wild-type mice. Furthermore, 80% of IRAK-4-/- mice succumbed to virulent M. tuberculosis within 100 d following low-dose infection. This increased susceptibility to mycobacteria correlated with reduced IFN-γ/TNF-α recall responses by splenocytes, as well as fewer IL-12p70-producing APCs. Additionally, we observed that IRAK-4 is also important for the production of IFN-γ by CD4+ T cells from infected mice. Finally, THP-1 cells treated with an IRAK-4 inhibitor and exposed to M. bovis showed reduced TNF-α and IL-12, suggesting that the results found in mice can be extended to humans. In summary, these data demonstrate that IRAK-4 is essential for innate and adaptive immunity and necessary for efficient control of mycobacterial infections. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.