TY - JOUR
T1 - Characterization of CD4+ T cell subsets and HIV susceptibility in the inner and outer foreskin of Ugandan men
AU - Galiwango, Ronald Moses
AU - Yegorov, Sergey
AU - Joag, Vineet
AU - Prodger, Jessica
AU - Shahabi, Kamnoosh
AU - Huibner, Sanja
AU - Muyanja, Enoch
AU - Kabuubi, Brian Roy
AU - Namuniina, Annmarie
AU - Nalutaaya, Annet
AU - Ssemaganda, Aloysius
AU - Lutwama, Fredrick
AU - Kitandwe, Paul Kato
AU - Nanvubya, Annet
AU - Mpendo, Juliet
AU - Bagaya, Bernard
AU - Kiwanuka, Noah
AU - Kaul, Rupert
N1 - Funding Information:
This work was supported by the Fogarty HIV Research Training Program of the National Institutes of Health (4D43TW009578-04; RMG), and the Canadian Institutes for Health Research (TMI-138656; RK). RK is supported by the University of Toronto/OHTN Endowed Chair in HIV Research. The authors would like to thank the study participants, staff of Entebbe General Hospital (Dr. Moses Muwanga, Margaret Otim, Josephine Nakaweesa, Juliet Ayikoru, and Ben Nsereko) and acknowledge STTARR at the Toronto MaRS Discovery district and Dr. Olga Rojas of the University of Toronto for assistance with CD3 image analysis.
Funding Information:
This work was supported by the Fogarty HIV Research Training Program of the National Institutes of Health (4D43TW009578‐04; RMG), and the Canadian Institutes for Health Research (TMI‐138656; RK). RK is supported by the University of Toronto/OHTN Endowed Chair in HIV Research. The authors would like to thank the study par‐ ticipants, staff of Entebbe General Hospital (Dr. Moses Muwanga, Margaret Otim, Josephine Nakaweesa, Juliet Ayikoru, and Ben Nsereko) and acknowledge STTARR at the Toronto MaRS Discovery district and Dr. Olga Rojas of the University of Toronto for assistance with CD3 image analysis.
Funding Information:
Fogarty HIV Research Training Program of the National Institutes of Health, Grant/ Award Number: 4D43TW009578‐04; Canadian Institutes for Health Research, Grant/Award Number: TMI‐138656; RK; University of Toronto/OHTN Endowed Chair in HIV Research
Publisher Copyright:
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
PY - 2019/7
Y1 - 2019/7
N2 - Problem: Biological mechanisms of foreskin HIV acquisition are poorly defined. The inner foreskin is preferentially infected in explant models, so we hypothesized that this site would be enriched for HIV-susceptible CD4+ T cells and proinflammatory/chemoattractant cytokines. Method of study: A total of 42 HIV-uninfected Ugandan men without genital symptoms provided foreskin tissues and swabs at the time of elective penile circumcision. The immune phenotype of foreskin-derived CD4+ T cells and entry of a CCR5-tropic HIV pseudovirus was characterized, and specific cytokine levels assayed by multiplexed chemiluminescent ELISA. Results: Unexpectedly, outer foreskin CD4+ T cells more frequently expressed CCR5 (median 29.2% vs 22.9%, P = 0.01) and CD69 (median 36.5% vs 15%, P < 0.01), and on a per-cell basis, HIV entry was higher. However, overall CD4+ T cell density was approximately twofold higher in the inner foreskin, and several highly susceptible T cell subsets were increased at this site, including Th17 cells (20.0% vs 14.1%, P = 0.0021). Specific pro-inflammatory cytokine levels were also higher on the inner foreskin surface (IL-17, IL-8, RANTES and IL-1β; all P < 0.05). Conclusion: There was marked heterogeneity in CD4+ T cell populations and immune milieu between inner and outer foreskin tissues. Despite higher per-cell viral entry into CD4+ T cells from the outer foreskin, the higher target cell density and enriched pro-inflammatory cytokines of the inner foreskin suggest that this may be a preferential site for HIV acquisition.
AB - Problem: Biological mechanisms of foreskin HIV acquisition are poorly defined. The inner foreskin is preferentially infected in explant models, so we hypothesized that this site would be enriched for HIV-susceptible CD4+ T cells and proinflammatory/chemoattractant cytokines. Method of study: A total of 42 HIV-uninfected Ugandan men without genital symptoms provided foreskin tissues and swabs at the time of elective penile circumcision. The immune phenotype of foreskin-derived CD4+ T cells and entry of a CCR5-tropic HIV pseudovirus was characterized, and specific cytokine levels assayed by multiplexed chemiluminescent ELISA. Results: Unexpectedly, outer foreskin CD4+ T cells more frequently expressed CCR5 (median 29.2% vs 22.9%, P = 0.01) and CD69 (median 36.5% vs 15%, P < 0.01), and on a per-cell basis, HIV entry was higher. However, overall CD4+ T cell density was approximately twofold higher in the inner foreskin, and several highly susceptible T cell subsets were increased at this site, including Th17 cells (20.0% vs 14.1%, P = 0.0021). Specific pro-inflammatory cytokine levels were also higher on the inner foreskin surface (IL-17, IL-8, RANTES and IL-1β; all P < 0.05). Conclusion: There was marked heterogeneity in CD4+ T cell populations and immune milieu between inner and outer foreskin tissues. Despite higher per-cell viral entry into CD4+ T cells from the outer foreskin, the higher target cell density and enriched pro-inflammatory cytokines of the inner foreskin suggest that this may be a preferential site for HIV acquisition.
KW - HIV susceptibility
KW - T cells
KW - Uganda
KW - cytokines
KW - foreskin
KW - immunology
KW - men
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U2 - 10.1111/aji.13143
DO - 10.1111/aji.13143
M3 - Article
C2 - 31081958
AN - SCOPUS:85066916437
SN - 1046-7408
VL - 82
JO - American Journal of Reproductive Immunology
JF - American Journal of Reproductive Immunology
IS - 1
M1 - e13143
ER -