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α4 Integrin blockade impairs CD8+ T cell neuroimmune surveillance following SIV infection
Pabitra B. Pal, Sonny R. Elizaldi, Giovanne B. Diniz, Ravi Prakash Rai, Yashavanth Shaan Lakshmanappa, Anil Verma, Daniel Rossmiller, Jesse Kaufman, Rahul Srivastava, Sean Ott, Carissa T. Erices, Kayla Schwartz, Danielle Beckman, Zhong-Min Ma, Alex Petkov, Daniel Newhouse, Dhivyaa Rajasundaram, John H. Morrison, Reben Raeman, Smita S. Iyer
Pabitra B. Pal, Sonny R. Elizaldi, Giovanne B. Diniz, Ravi Prakash Rai, Yashavanth Shaan Lakshmanappa, Anil Verma, Daniel Rossmiller, Jesse Kaufman, Rahul Srivastava, Sean Ott, Carissa T. Erices, Kayla Schwartz, Danielle Beckman, Zhong-Min Ma, Alex Petkov, Daniel Newhouse, Dhivyaa Rajasundaram, John H. Morrison, Reben Raeman, Smita S. Iyer
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Research Article AIDS/HIV Immunology

α4 Integrin blockade impairs CD8+ T cell neuroimmune surveillance following SIV infection

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Abstract

Integrin-targeted therapies are under investigation for HIV-associated neuroinflammation, yet their effect on CNS antiviral immunity remains undefined. We examined the role of α4 integrin in T cell–mediated neuroimmune surveillance using SIV-infected macaques with α4 blockade and T cell–specific α4-deficient mice. In macaques, α4 blockade preserved CD4+ Th1 cell access to the brain parenchyma but impaired CD8 effector recruitment, disrupting antiviral control. Despite stable cerebrospinal fluid viral loads, hippocampal SIV RNA increased under blockade. Single-cell analyses revealed α4 enrichment in CD8 effector memory (Tem) cells; blockade reduced inferred CD8+ Tem-monocyte interactions and heightened innate immune activation in the hippocampus. Microscopy demonstrated persistent SIV-induced microglial simplification despite treatment. Th1 CD4 effectors correlated positively with gray matter viral RNA, whereas α4β7+ CD8+ T cells correlated inversely, implicating impaired CD8+ Tem recruitment in elevated parenchymal viral burden. In mice, α4 proved dispensable for CD4 trafficking to inflamed brain but essential for CD8 effector access across CNS compartments and for both subsets to reach skull marrow. These findings establish that α4 integrin governs CD8-mediated neuroimmune surveillance through coordinated cellular positioning, with blockade enabling viral seeding while disrupting spatially organized antiviral defense.

Authors

Pabitra B. Pal, Sonny R. Elizaldi, Giovanne B. Diniz, Ravi Prakash Rai, Yashavanth Shaan Lakshmanappa, Anil Verma, Daniel Rossmiller, Jesse Kaufman, Rahul Srivastava, Sean Ott, Carissa T. Erices, Kayla Schwartz, Danielle Beckman, Zhong-Min Ma, Alex Petkov, Daniel Newhouse, Dhivyaa Rajasundaram, John H. Morrison, Reben Raeman, Smita S. Iyer

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Figure 2

Single-cell transcriptomics reveals disrupted immune coordination and altered antiviral signaling in the brain following α4 blockade.

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Single-cell transcriptomics reveals disrupted immune coordination and al...
(A) Single-cell RNA-seq workflow. UMAP of brain and spleen CD45+ cells show leukocyte enrichment by PTPRC expression. (B) Brain immune cluster annotation using Blueprint and ENCODE references identifies CD4+/CD8+ T cells, NK cells, and myeloid subsets. (C) ITGA4 expression across brain immune clusters. (D) Dot plots comparing α4-treated, IgG-treated, and SIV– control (Ctrl) groups: (top) CD8+ Tem gene expression, (middle) CD4+ Tcm gene expression, (bottom) Myeloid gene expression. (E) CellChat shows preserved interaction number but reduced strength for secreted signaling between CD8+ Tem and monocytes under α4-blockade. (F) Cytokine pathways enriched in IgG-treated brains (IL-1, BAFF, APRIL, BAG) versus α4-treated brains (IL-2, TNF-α, CSF), with altered CD8+ Tem-monocyte directionality. (G) Aggregate signaling shows reduced cytokine output and increased receptor input in α4-treated monocytes. (H) Ligand-receptor analysis shows increased NAMPT and reduced MIF-CD74/CD44 and TGFβ1-TGFβR1/TGFβR2 interactions with α4-blockade. (I and J) CD6 signaling is diminished in CD8+ Tem cells while LCK signaling is preserved. CD80, SELPLG, NECTIN, and SEMA7 pathways are maintained or increased. (K) SIV RNA+ cell frequencies in CD4+ T cell and monocyte clusters.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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