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T-cell responses to sequentially emerging viral escape mutants shape long-term HIV-1 population dynamics.
- Source :
-
PLoS pathogens [PLoS Pathog] 2020 Dec 28; Vol. 16 (12), pp. e1009177. Date of Electronic Publication: 2020 Dec 28 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- HIV-1 strains harboring immune escape mutations can persist in circulation, but the impact of selection by multiple HLA alleles on population HIV-1 dynamics remains unclear. In Japan, HIV-1 Reverse Transcriptase codon 135 (RT135) is under strong immune pressure by HLA-B*51:01-restricted and HLA-B*52:01-restricted T cells that target a key epitope in this region (TI8; spanning RT codons 128-135). Major population-level shifts have occurred at HIV-1 RT135 during the Japanese epidemic, which first affected hemophiliacs (via imported contaminated blood products) and subsequently non-hemophiliacs (via domestic transmission). Specifically, threonine accumulated at RT135 (RT135T) in hemophiliac and non-hemophiliac HLA-B*51:01+ individuals diagnosed before 1997, but since then RT135T has markedly declined while RT135L has increased among non-hemophiliac individuals. We demonstrated that RT135V selection by HLA-B*52:01-restricted TI8-specific T-cells led to the creation of a new HLA-C*12:02-restricted epitope TN9-8V. We further showed that TN9-8V-specific HLA-C*12:02-restricted T cells selected RT135L while TN9-8T-specific HLA-C*12:02-restricted T cells suppressed replication of the RT135T variant. Thus, population-level accumulation of the RT135L mutation over time in Japan can be explained by initial targeting of the TI8 epitope by HLA-B*52:01-restricted T-cells, followed by targeting of the resulting escape mutant by HLA-C*12:02-restricted T-cells. We further demonstrate that this phenomenon is particular to Japan, where the HLA-B*52:01-C*12:02 haplotype is common: RT135L did not accumulate over a 15-year longitudinal analysis of HIV sequences in British Columbia, Canada, where this haplotype is rare. Together, our observations reveal that T-cell responses to sequentially emerging viral escape mutants can shape long-term HIV-1 population dynamics in a host population-specific manner.<br />Competing Interests: The authors have declared that no competing interests exist.
- Subjects :
- Cells, Cultured
Clonal Evolution immunology
Epitopes, T-Lymphocyte genetics
HIV Seropositivity
HeLa Cells
Host Adaptation immunology
Host-Pathogen Interactions genetics
Host-Pathogen Interactions immunology
Humans
Molecular Typing
Mutation
T-Lymphocytes, Cytotoxic metabolism
Viral Load immunology
Virus Replication genetics
Virus Replication immunology
Antigenic Variation immunology
HIV Infections immunology
HIV Infections virology
HIV-1 classification
HIV-1 genetics
HIV-1 immunology
Immune Evasion genetics
T-Lymphocytes, Cytotoxic immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1553-7374
- Volume :
- 16
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- PLoS pathogens
- Publication Type :
- Academic Journal
- Accession number :
- 33370400
- Full Text :
- https://doi.org/10.1371/journal.ppat.1009177