Christophe Viret

ORCID: 0000-0003-1874-3489
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Autophagy in Disease and Therapy
  • Mosquito-borne diseases and control
  • CAR-T cell therapy research
  • Calcium signaling and nucleotide metabolism
  • Viral Infections and Vectors
  • Adenosine and Purinergic Signaling
  • Diabetes and associated disorders
  • vaccines and immunoinformatics approaches
  • Inflammatory Bowel Disease
  • Cellular transport and secretion
  • Toxoplasma gondii Research Studies
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Immunotherapy and Biomarkers
  • Cytomegalovirus and herpesvirus research
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Phagocytosis and Immune Regulation
  • Complement system in diseases
  • Viral Infections and Outbreaks Research
  • Cell Adhesion Molecules Research
  • Vibrio bacteria research studies
  • Microscopic Colitis
  • Optimism, Hope, and Well-being

Inserm
2016-2025

Centre National de la Recherche Scientifique
2016-2025

Centre International de Recherche en Infectiologie
2016-2025

Université Claude Bernard Lyon 1
2016-2025

École Normale Supérieure de Lyon
2014-2025

Fondation pour la Recherche Médicale
2018-2022

Université Toulouse III - Paul Sabatier
2007-2015

Weatherford College
2015

Centre de Physiopathologie de Toulouse-Purpan
2007-2015

Centre Hospitalier Universitaire de Toulouse
2009

Recent studies have challenged the view that Langerhans cells (LCs) constitute exclusive antigen-presenting of skin and suggest dermal dendritic cell (DDC) network is exceedingly complex. Using knockin mice to track ablate DCs expressing langerin (CD207), we discovered dermis contains five distinct DC subsets identified their migratory counterparts in draining lymph nodes. Based on this refined classification, demonstrated quantitatively minor CD207+ CD103+ DDC subset endowed with unique...

10.1084/jem.20091964 article EN cc-by-nc-sa The Journal of Experimental Medicine 2009-12-28

Peripheral T cell maintenance requires a survival signal delivered upon receptor (TCR)-major histocompatibility complex (MHC) molecule interaction. Since self-peptides play critical role in the intrathymic positive selection of mature TCR repertoire, we hypothesized an equally important persistence. We used mice with normal expression MHC class II molecules but restricted self-peptide complexity (H-2Mα−/−) to show that II-restricted specificity displays deficient H-2Mα−/− thymus shows...

10.1016/s1074-7613(00)80055-2 article EN cc-by-nc-nd Immunity 1999-05-01

Multiple sclerosis-associated retroviral element (MSRV) is a element, the sequence of which served to define W family human endogenous retroviruses. MSRV viral particles display proinflammatory activities both in vitro mononuclear cell cultures and vivo humanized SCID mice model. To understand molecular basis such properties, we have investigated inflammatory potential surface unit envelope protein (ENV-SU), fraction that poised naturally interact with host cells. We report this study ENV-SU...

10.4049/jimmunol.176.12.7636 article EN The Journal of Immunology 2006-06-15

A cytolytic T lymphocyte (CTL) clone that lyses many HLA-A2 melanomas was derived from a population of tumor-infiltrating lymphocytes an melanoma patient. The gene coding for the antigen recognized by this CTL identified transfection cDNA library. It is which has been reported to code N-acetylglucosaminyltransferase V (GnT-V). Remarkably, antigenic peptide encoded sequence located in intron. In contrast fully spliced GnT-V mRNA, found wide range normal and tumoral tissues, mRNA containing...

10.1084/jem.183.3.1173 article EN The Journal of Experimental Medicine 1996-03-01

OBJECTIVE We have previously reported a highly diabetogenic CD8 T-cell clone, G9C8, in the nonobese diabetic (NOD) mouse, specific to low-avidity insulin peptide B15-23, and cells responsive this antigen are among earliest islet infiltrates. aimed study selection, activation, development of capacity these insulin-reactive T-cells. RESEARCH DESIGN AND METHODS generated receptor (TCR) transgenic mouse expressing cloned TCR Vα18/Vβ6 G9C8 clone. The mice were crossed TCRCα−/− so that majority...

10.2337/db08-0800 article EN cc-by-nc-nd Diabetes 2009-02-10

Autophagy is a cell autonomous process allowing each individual to fight intracellular pathogens. can destroy pathogens within the cytosol, and elicit innate adaptive immune responses against microorganisms. Nevertheless, numerous have developed molecular strategies enabling them avoid or even exploit autophagy for their own benefit. IRGM (immunity-related GTPase family M) human protein recently highlighted its contribution upon infections. The physical association of with mitochondria...

10.3389/fimmu.2012.00426 article EN cc-by Frontiers in Immunology 2013-01-01

Autophagy is a potent cell autonomous defense mechanism that engages the lysosomal pathway to fight intracellular pathogens. Several autophagy receptors can recognize invading pathogens in order target them towards for their degradation after fusion of pathogen-containing autophagosomes with lysosomes. However, numerous avoid or exploit autophagy, among which measles virus (MeV). This induces complete flux, required improve viral replication. We therefore asked how interferes during course...

10.3390/v9050123 article EN cc-by Viruses 2017-05-22

Crohn disease (CD) is an inflammatory bowel whose pathogenesis involves inappropriate immune responses toward gut microbiota on genetically predisposed backgrounds. Notably, CD associated with single-nucleotide polymorphisms affecting several genes involved in macroautophagy/autophagy, the catabolic process that ensures degradation and recycling of cytosolic components microorganisms. In a clinical translation perspective, monitoring autophagic activity patients will require some knowledge...

10.1080/15548627.2024.2338574 article EN Autophagy 2024-04-14

Viruses adapt and modulate cellular pathways to allow their replication in host cells. The catabolic pathway of macroautophagy, for simplicity referred as autophagy, is no exception. In this review, we discuss anti-viral functions both autophagy select components the machinery, how viruses have evaded them. Some use membrane remodeling ability machinery build compartments cytosol or efficiently egress from cells a non-lytic fashion. remodeled membranes can even be found viral particles...

10.1080/27694127.2025.2464986 article EN cc-by Autophagy Reports 2025-03-18

Thymus-specific serine protease (TSSP) is a novel that may contribute to the generation of peptide repertoire presented by MHC class II molecules in thymus. Although TSSP deficiency has no quantitative impact on development CD4 T cells expressing polyclonal cell receptor (TCR) repertoire, OTII and Marilyn transgenic TCRs impaired TSSP-deficient mice. In this study, we assess role shaping functional endogenous analyzing response mice several protein antigens (Ags). responded normally most Ags...

10.1084/jem.20100027 article EN The Journal of Experimental Medicine 2010-12-20

Abstract Human melanomas are infiltrated by tumor‐reactive T lymphocytes. However, the ability of these cells to elicit a specific anti‐tumor response in vivo remains be established. Because lymphokine production is critical for cell functions, we have analyzed capacity melanoma‐specific tumor‐infiltrating lymphocyte (TIL) clones produce major lymphokines: interleukin‐2 (IL‐2), interferon‐γ (IFN‐γ) and interleukin‐4 (IL‐4), as well tumor necrosis factor (TNF), direct antigen presentation...

10.1002/eji.1830240905 article EN European Journal of Immunology 1994-09-01

Type 1 diabetes is a chronic autoimmune disease in which genetic predispositions affect the immune system, leading to loss of T cell tolerance β cells and consequent cell-mediated destruction insulin-producing islet cells. Genetic studies have suggested that PRSS16 linked susceptibility locus extended HLA class I region humans. encodes what we believe be novel protease, thymus-specific serine protease (TSSP), shows predominant expression thymic epithelial suspected restricted role II...

10.1172/jci43314 article EN Journal of Clinical Investigation 2011-04-18
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