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HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes

Certain Major Histocompatibility-I (MHC-I) types are associated with superior immune containment of HIV-1 infection by CD8(+) cytotoxic T lymphocytes (CTLs), but the mechanisms mediating this containment are difficult to elucidate in vivo. Here we provide controlled assessments of fitness landscapes...

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Autores principales: Gorin, Aleksandr M., Du, Yushen, Liu, Franklin Y., Zhang, Tian-Hao, Ng, Hwee L., Hofmann, Christian, Cumberland, William G., Sun, Ren, Yang, Otto O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560751/
https://www.ncbi.nlm.nih.gov/pubmed/28787455
http://dx.doi.org/10.1371/journal.ppat.1006541
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author Gorin, Aleksandr M.
Du, Yushen
Liu, Franklin Y.
Zhang, Tian-Hao
Ng, Hwee L.
Hofmann, Christian
Cumberland, William G.
Sun, Ren
Yang, Otto O.
author_facet Gorin, Aleksandr M.
Du, Yushen
Liu, Franklin Y.
Zhang, Tian-Hao
Ng, Hwee L.
Hofmann, Christian
Cumberland, William G.
Sun, Ren
Yang, Otto O.
author_sort Gorin, Aleksandr M.
collection PubMed
description Certain Major Histocompatibility-I (MHC-I) types are associated with superior immune containment of HIV-1 infection by CD8(+) cytotoxic T lymphocytes (CTLs), but the mechanisms mediating this containment are difficult to elucidate in vivo. Here we provide controlled assessments of fitness landscapes and CTL-imposed constraints for immunodominant epitopes presented by two protective (B*57 and B*27) and one non-protective (A*02) MHC-I types. Libraries of HIV-1 with saturation mutagenesis of CTL epitopes are propagated with and without CTL selective pressure to define the fitness landscapes for epitope mutation and escape from CTLs via deep sequencing. Immunodominant B*57- and B*27- present epitopes are highly limited in options for fit mutations, with most viable variants recognizable by CTLs, whereas an immunodominant A*02 epitope-presented is highly permissive for mutation, with many options for CTL evasion without loss of viability. Generally, options for evasion overlap considerably between CTL clones despite highly distinct T cell receptors. Finally, patterns of variant recognition suggest population-wide CTL selection for the A*02-presented epitope. Overall, these findings indicate that these protective MHC-I types yield CTL targeting of highly constrained epitopes, and underscore the importance of blocking public escape pathways for CTL-based interventions against HIV-1.
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spelling pubmed-55607512017-08-25 HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes Gorin, Aleksandr M. Du, Yushen Liu, Franklin Y. Zhang, Tian-Hao Ng, Hwee L. Hofmann, Christian Cumberland, William G. Sun, Ren Yang, Otto O. PLoS Pathog Research Article Certain Major Histocompatibility-I (MHC-I) types are associated with superior immune containment of HIV-1 infection by CD8(+) cytotoxic T lymphocytes (CTLs), but the mechanisms mediating this containment are difficult to elucidate in vivo. Here we provide controlled assessments of fitness landscapes and CTL-imposed constraints for immunodominant epitopes presented by two protective (B*57 and B*27) and one non-protective (A*02) MHC-I types. Libraries of HIV-1 with saturation mutagenesis of CTL epitopes are propagated with and without CTL selective pressure to define the fitness landscapes for epitope mutation and escape from CTLs via deep sequencing. Immunodominant B*57- and B*27- present epitopes are highly limited in options for fit mutations, with most viable variants recognizable by CTLs, whereas an immunodominant A*02 epitope-presented is highly permissive for mutation, with many options for CTL evasion without loss of viability. Generally, options for evasion overlap considerably between CTL clones despite highly distinct T cell receptors. Finally, patterns of variant recognition suggest population-wide CTL selection for the A*02-presented epitope. Overall, these findings indicate that these protective MHC-I types yield CTL targeting of highly constrained epitopes, and underscore the importance of blocking public escape pathways for CTL-based interventions against HIV-1. Public Library of Science 2017-08-07 /pmc/articles/PMC5560751/ /pubmed/28787455 http://dx.doi.org/10.1371/journal.ppat.1006541 Text en © 2017 Gorin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gorin, Aleksandr M.
Du, Yushen
Liu, Franklin Y.
Zhang, Tian-Hao
Ng, Hwee L.
Hofmann, Christian
Cumberland, William G.
Sun, Ren
Yang, Otto O.
HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title_full HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title_fullStr HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title_full_unstemmed HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title_short HIV-1 epitopes presented by MHC class I types associated with superior immune containment of viremia have highly constrained fitness landscapes
title_sort hiv-1 epitopes presented by mhc class i types associated with superior immune containment of viremia have highly constrained fitness landscapes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560751/
https://www.ncbi.nlm.nih.gov/pubmed/28787455
http://dx.doi.org/10.1371/journal.ppat.1006541
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