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CD32 + CD4 + T Cells Sharing B Cell Properties Increase With Simian Immunodeficiency Virus Replication in Lymphoid Tissues.
- Source :
-
Frontiers in immunology [Front Immunol] 2021 Jun 16; Vol. 12, pp. 695148. Date of Electronic Publication: 2021 Jun 16 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- CD4 T cell responses constitute an important component of adaptive immunity and are critical regulators of anti-microbial protection. CD4 <superscript>+</superscript> T cells expressing CD32a have been identified as a target for HIV. CD32a is an Fcγ receptor known to be expressed on myeloid cells, granulocytes, B cells and NK cells. Little is known about the biology of CD32 <superscript>+</superscript> CD4 <superscript>+</superscript> T cells. Our goal was to understand the dynamics of CD32 <superscript>+</superscript> CD4 <superscript>+</superscript> T cells in tissues. We analyzed these cells in the blood, lymph nodes, spleen, ileum, jejunum and liver of two nonhuman primate models frequently used in biomedical research: African green monkeys (AGM) and macaques. We studied them in healthy animals and during viral (SIV) infection. We performed phenotypic and transcriptomic analysis at different stages of infection. In addition, we compared CD32+CD4+ T cells in tissues with well-controlled (spleen) and not efficiently controlled (jejunum) SIV replication in AGM. The CD32 <superscript>+</superscript> CD4 <superscript>+</superscript> T cells more frequently expressed markers associated with T cell activation and HIV infection (CCR5, PD-1, CXCR5, CXCR3) and had higher levels of actively transcribed SIV RNA than CD32 <superscript>-</superscript> CD4 <superscript>+</superscript> T cells. Furthermore, CD32 <superscript>+</superscript> CD4 <superscript>+</superscript> T cells from lymphoid tissues strongly expressed B-cell-related transcriptomic signatures, and displayed B cell markers at the cell surface, including immunoglobulins CD32+CD4+ T cells were rare in healthy animals and blood but increased strongly in tissues with ongoing viral replication. CD32 <superscript>+</superscript> CD4 <superscript>+</superscript> T cell levels in tissues correlated with viremia. Our results suggest that the tissue environment induced by SIV replication drives the accumulation of these unusual cells with enhanced susceptibility to viral infection.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Huot, Rascle, Planchais, Contreras, Passaes, Le Grand, Beignon, Kornobis, Legendre, Varet, Saez-Cirion, Mouquet, Jacquelin and Müller-Trutwin.)
- Subjects :
- Animals
B-Lymphocytes immunology
B-Lymphocytes metabolism
CD4-Positive T-Lymphocytes immunology
CD4-Positive T-Lymphocytes metabolism
Chlorocebus aethiops
Disease Models, Animal
Host-Pathogen Interactions
Jejunum immunology
Jejunum metabolism
Jejunum virology
Lymphocyte Activation
Lymphoid Tissue immunology
Lymphoid Tissue metabolism
Macaca fascicularis
Phenotype
Simian Acquired Immunodeficiency Syndrome immunology
Simian Acquired Immunodeficiency Syndrome metabolism
Simian Immunodeficiency Virus immunology
Spleen immunology
Spleen metabolism
Spleen virology
Viral Load
B-Lymphocytes virology
CD4-Positive T-Lymphocytes virology
Lymphoid Tissue virology
Receptors, IgG metabolism
Simian Acquired Immunodeficiency Syndrome virology
Simian Immunodeficiency Virus growth & development
Virus Replication
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 34220857
- Full Text :
- https://doi.org/10.3389/fimmu.2021.695148