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Accumulation of follicular CD8+ T cells in pathogenic SIV infection
Sara Ferrando-Martinez, … , Constantinos Petrovas, Richard A. Koup
Sara Ferrando-Martinez, … , Constantinos Petrovas, Richard A. Koup
Published April 16, 2018
Citation Information: J Clin Invest. 2018;128(5):2089-2103. https://doi.org/10.1172/JCI96207.
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Research Article AIDS/HIV Immunology Article has an altmetric score of 2

Accumulation of follicular CD8+ T cells in pathogenic SIV infection

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Abstract

LN follicles constitute major reservoir sites for HIV/SIV persistence. Cure strategies could benefit from the characterization of CD8+ T cells able to access and eliminate HIV-infected cells from these areas. In this study, we provide a comprehensive analysis of the phenotype, frequency, localization, and functionality of follicular CD8+ T cells (fCD8+) in SIV-infected nonhuman primates. Although disorganization of follicles was a major factor, significant accumulation of fCD8+ cells during chronic SIV infection was also observed in intact follicles, but only in pathogenic SIV infection. In line with this, tissue inflammatory mediators were strongly associated with the accumulation of fCD8+ cells, pointing to tissue inflammation as a major factor in this process. These fCD8+ cells have cytolytic potential and can be redirected to target and kill HIV-infected cells using bispecific antibodies. Altogether, our data support the use of SIV infection to better understand the dynamics of fCD8+ cells and to develop bispecific antibodies as a strategy for virus eradication.

Authors

Sara Ferrando-Martinez, Eirini Moysi, Amarendra Pegu, Sarah Andrews, Krystelle Nganou Makamdop, David Ambrozak, Adrian B. McDermott, David Palesch, Mirko Paiardini, George N. Pavlakis, Jason M. Brenchley, Daniel Douek, John R. Mascola, Constantinos Petrovas, Richard A. Koup

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Figure 4

cART has a modest effect on the frequency of fCD8+ T cells.

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cART has a modest effect on the frequency of fCD8+ T cells.
(A) Pooled d...
(A) Pooled data showing the relative frequency of total LN CD8+ T cells before and after cART from RMs treated during early (n = 5) or late (n = 8) chronic SIV infection. The relative frequency of bulk memory LN CCR7loCD95hi CD8+ T cells (B) and fCD8+ T cells (C) is also shown. *P < 0.05 and **P < 0.001, by Mann-Whitney U test for unpaired comparisons and Wilcoxon test for paired comparisons. (D) Pooled data showing the relative frequency of GrzB+ non-fCD8+ and fCD8+ T cells from RMs treated during early (n = 5) or late (n = 8) chronic SIV infection. Mann-Whitney U test for unpaired comparisons and Wilcoxon test for paired comparisons.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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