Upregulation of PD-1 expression on HIV-specific CD8+ T cells leads to reversible immune dysfunction
By L. Trautmann, L. Janbazian, N. Chomont, E. Said, S. Gimmig, B. Bessette, M. Boulassel, E. Delwart, H. Sepulveda, R. Balderas and 3 more. Nature Medicine, 2006
1,643 citations recorded by the source corpus.
Subfields: Epidemiology, Immunology, Virology
View Paper: https://www.semanticscholar.org/paper/79d8cd6dc8f8c55162612d4ce38da626c3d91ed2
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Citations in the corpus
- Emerging Concepts in the Immunopathogenesis of AIDS (2009, neutral): “The efficacy of ART in 474 Douek · Roederer · Koup A nn u.”
- Targeting Tim-3 and PD-1 pathways to reverse T cell exhaustion and restore anti-tumor immunity (2010, background): “CD8+ T cells in humans chronically infected with HIV (Day et al., 2006; Petrovas et al., 2006; Trautmann et al., 2006), hepatitis B virus (Boettler et al.”
- Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production (2013, background): “…Vol. 210, No. 1 Article 151 Because PD-1, which was coexpressed with Ki-67, may define cells with reduced proliferation capacity (Day et al., 2006; Trautmann et al., 2006), the four sorted purified memory CD4 T cell populations were stimulated with anti-CD3 plus anti-CD28 antibodies and cell…”
- PD-1 is a regulator of virus-specific CD8+ T cell survival in HIV infection (2006, result): “We did not see a correlation between plasma viral load and PD-1 expression on HIV-specifi c CD8+ T cells in this small group of subjects (unpublished data), although in larger cohort studies such an association has been clearly demonstrated (34, 35 ).”
- PD-1 and its ligands in tolerance and immunity. (2008, background): “Blocking PD1:PD-L interactions in vitro reverses the exhaustion of HIV-specific, HBV-specific (92), HCV-specific, and SIV-specific (97) CD8 and CD4 T cells and restores proliferation and cytokine production (23, 89, 90, 93).”