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Deep analysis of CD4 T cells in the rhesus CNS during SIV infection.
Elizaldi, Sonny R; Verma, Anil; Ma, Zhong-Min; Ott, Sean; Rajasundaram, Dhivyaa; Hawes, Chase E; Lakshmanappa, Yashavanth Shaan; Cottrell, Mackenzie L; Kashuba, Angela D M; Ambrose, Zandrea; Lifson, Jeffrey D; Morrison, John H; Iyer, Smita S.
Afiliación
  • Elizaldi SR; Graduate Group in Immunology, UC Davis, California, United States of America.
  • Verma A; Department of Pathology, School of Medicine, University of Pittsburgh, Pennsylvania, United States of America.
  • Ma ZM; California National Primate Research Center, UC Davis, California, United States of America.
  • Ott S; California National Primate Research Center, UC Davis, California, United States of America.
  • Rajasundaram D; Department of Pediatrics, School of Medicine, University of Pittsburgh, Pennsylvania, United States of America.
  • Hawes CE; Graduate Group in Immunology, UC Davis, California, United States of America.
  • Lakshmanappa YS; California National Primate Research Center, UC Davis, California, United States of America.
  • Cottrell ML; Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Kashuba ADM; Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Ambrose Z; Department of Microbiology and Molecular Genetics, School of Medicine, University of Pittsburgh, Pennsylvania, United States of America.
  • Lifson JD; AIDS and Cancer Virus Program, Frederick National Laboratory, Frederick, Maryland, United States of America.
  • Morrison JH; California National Primate Research Center, UC Davis, California, United States of America.
  • Iyer SS; Department of Neurology, School of Medicine, UC Davis, California, United States of America.
PLoS Pathog ; 19(12): e1011844, 2023 Dec.
Article en En | MEDLINE | ID: mdl-38060615
Virologic suppression with antiretroviral therapy (ART) has significantly improved health outcomes for people living with HIV, yet challenges related to chronic inflammation in the central nervous system (CNS)-known as Neuro-HIV- persist. As primary targets for HIV-1 with the ability to survey and populate the CNS and interact with myeloid cells to co-ordinate neuroinflammation, CD4 T cells are pivotal in Neuro-HIV. Despite their importance, our understanding of CD4 T cell distribution in virus-targeted CNS tissues, their response to infection, and potential recovery following initiation of ART remain limited. To address these gaps, we studied ten SIVmac251-infected rhesus macaques using an ART regimen simulating suboptimal adherence. We evaluated four macaques during the acute phase pre-ART and six during the chronic phase. Our data revealed that HIV target CCR5+ CD4 T cells inhabit both the brain parenchyma and adjacent CNS tissues, encompassing choroid plexus stroma, dura mater, and the skull bone marrow. Aligning with the known susceptibility of CCR5+ CD4 T cells to viral infection and their presence within the CNS, high levels of viral RNA were detected in the brain parenchyma and its border tissues during acute SIV infection. Single-cell RNA sequencing of CD45+ cells from the brain revealed colocalization of viral transcripts within CD4 clusters and significant activation of antiviral molecules and specific effector programs within T cells, indicating CNS CD4 T cell engagement during infection. Acute infection led to marked imbalance in the CNS CD4/CD8 ratio which persisted into the chronic phase. These observations underscore the functional involvement of CD4 T cells within the CNS during SIV infection, enhancing our understanding of their role in establishing CNS viral presence. Our findings offer insights for potential T cell-focused interventions while underscoring the challenges in eradicating HIV from the CNS, particularly in the context of sub-optimal ART.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Síndrome de Inmunodeficiencia Adquirida del Simio / Virus de la Inmunodeficiencia de los Simios Límite: Animals / Humans Idioma: En Revista: PLoS Pathog Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Síndrome de Inmunodeficiencia Adquirida del Simio / Virus de la Inmunodeficiencia de los Simios Límite: Animals / Humans Idioma: En Revista: PLoS Pathog Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos