Cross-reactive microbial peptides can modulate HIV-specific CD8+ T cell responses.
Christopher W PohlmeyerSarah B LaskeySarah E BeckDaniel C XuAdam A CapoferriCaroline C GarlissMegan E MayAlison LivingstonWalt LichmiraRichard D MooreM Sue LeffellNicholas J ButlerJennifer E ThorneJohn A FlynnRobert F SilicianoJoel N BlanksonPublished in: PloS one (2018)
Heterologous immunity is an important aspect of the adaptive immune response. We hypothesized that this process could modulate the HIV-1-specific CD8+ T cell response, which has been shown to play an important role in HIV-1 immunity and control. We found that stimulation of peripheral blood mononuclear cells (PBMCs) from HIV-1-positive subjects with microbial peptides that were cross-reactive with immunodominant HIV-1 epitopes resulted in dramatic expansion of HIV-1-specific CD8+ T cells. Interestingly, the TCR repertoire of HIV-1-specific CD8+ T cells generated by ex vivo stimulation of PBMCs using HIV-1 peptide was different from that of cells stimulated with cross-reactive microbial peptides in some HIV-1-positive subjects. Despite these differences, CD8+ T cells stimulated with either HIV-1 or cross-reactive peptides effectively suppressed HIV-1 replication in autologous CD4+ T cells. These data suggest that exposure to cross-reactive microbial antigens can modulate HIV-1-specific immunity.
Keyphrases
- hiv positive
- antiretroviral therapy
- men who have sex with men
- hiv testing
- hiv infected
- south africa
- human immunodeficiency virus
- hiv aids
- hepatitis c virus
- immune response
- microbial community
- electronic health record
- bone marrow
- induced apoptosis
- inflammatory response
- signaling pathway
- cell therapy
- regulatory t cells