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Distinct mucosal and systemic immunological characteristics in transgender women potentially relating to HIV acquisition
Alexandra Schuetz, … , Sandhya Vasan, on behalf of the RV304/SEARCH013 Study Team
Alexandra Schuetz, … , Sandhya Vasan, on behalf of the RV304/SEARCH013 Study Team
Published July 11, 2023
Citation Information: JCI Insight. 2023;8(16):e169272. https://doi.org/10.1172/jci.insight.169272.
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Research Article AIDS/HIV Immunology

Distinct mucosal and systemic immunological characteristics in transgender women potentially relating to HIV acquisition

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Abstract

Transgender women (TGW) are disproportionally affected by HIV infection, with a global estimated prevalence of 19.9%, often attributed to behavioral risk factors, with less known about biological factors. We evaluated potential biological risk factors for HIV acquisition in TGW at the sites of viral entry by assessing immune parameters of the neovaginal surface and gut mucosa. The neovagina in TGW, compared with the vagina in cisgender women (CW), shows distinct cell composition and may pose a more inflammatory environment, evidenced by increased CD4+ T cell activation and higher levels of soluble markers of inflammation (C-reactive protein, soluble CD30). Increased inflammation may be driven by microbiome composition, as shown by a greater abundance of Prevotella and a higher Shannon Diversity Index. In addition, we have observed higher frequency of CD4+CCR5+ target cells and decreased DNA methylation of the CCR5 gene in the gut mucosa of TGW compared with CW and men who have sex with men, which was inversely correlated with testosterone levels. The rectal microbiome composition in TGW appears to favor a proinflammatory milieu as well as mucosal barrier disruption. Thus, it is possible that increased inflammation and higher frequencies of CCR5-expressing target cells at sites of mucosal viral entry may contribute to increased risk of HIV acquisition in TGW, with further validation in larger studies warranted.

Authors

Alexandra Schuetz, Michael J. Corley, Carlo Sacdalan, Yuwadee Phuang-Ngern, Thitiyanun Nakpor, Tanyaporn Wansom, Philip K. Ehrenberg, Somchai Sriplienchan, Rasmi Thomas, Nisakorn Ratnaratorn, Suchada Sukhumvittaya, Nipattra Tragonlugsana, Bonnie M. Slike, Siriwat Akapirat, Suteeraporn Pinyakorn, Rungsun Rerknimitr, Alina P.S. Pang, Eugène Kroon, Nipat Teeratakulpisan, Shelly J. Krebs, Nittaya Phanuphak, Lishomwa C. Ndhlovu, Sandhya Vasan, on behalf of the RV304/SEARCH013 Study Team

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Figure 3

Microbial profiles determined by 16s rRNA sequencing revealed distinct microbial community structures between the vagina and neovagina.

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Microbial profiles determined by 16s rRNA sequencing revealed distinct m...
(A) Bar graph of phylum rank of vaginal microbiome in cisgender women (CW; n = 10) and neovaginal microbiome in transgender women (TGW; n = 10), including Shannon Alpha Diversity displayed below bar graphs, suggesting a different microbiome composition between the vaginal and the neovaginal compartment. (B) Neovaginal samples have a unique microbiome profile compared with vaginal samples based on principal component analyses. Brown circles, vaginal; purple circles, neovaginal. (C) Heatmap of relative abundance plot of species in neovaginal/vaginal compartment highlighting differences in compositions between vaginal and neovaginal microbiome.

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