Low levels of SIV-specific CD8+ T cells in germinal centers characterizes acute SIV infection.
Shengbin LiJoy M FolkvordKatalin J KovacsReece K WagstaffGwantwa MwakalundwaAaron K RendahlEva G RakaszElizabeth ConnickPamela J SkinnerPublished in: PLoS pathogens (2019)
CD8+ T cells play an important role in controlling of HIV and SIV infections. However, these cells are largely excluded from B cell follicles where HIV and SIV producing cells concentrate during chronic infection. It is not known, however, if antigen-specific CD8+ T cells are excluded gradually as pathogenesis progresses from early to chronic phase, or this phenomenon occurs from the beginning infection. In this study we determined that SIV-specific CD8+ T cells were largely excluded from follicles during early infection, we also found that within follicles, they were entirely absent in 60% of the germinal centers (GCs) examined. Furthermore, levels of SIV-specific CD8+ T cells in follicular but not extrafollicular areas significantly correlated inversely with levels of viral RNA+ cells. In addition, subsets of follicular SIV-specific CD8+ T cells were activated and proliferating and expressed the cytolytic protein perforin. These studies suggest that a paucity of SIV-specific CD8+ T cells in follicles and complete absence within GCs during early infection may set the stage for the establishment of persistent chronic infection.
Keyphrases
- induced apoptosis
- hiv infected
- antiretroviral therapy
- human immunodeficiency virus
- hiv positive
- hepatitis c virus
- endoplasmic reticulum stress
- intensive care unit
- hiv testing
- small molecule
- liver failure
- drug induced
- oxidative stress
- extracorporeal membrane oxygenation
- respiratory failure
- peripheral blood
- mechanical ventilation