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Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help
The inherent molecular complexity of human pathogens requires that mammals evolved an adaptive immune system equipped to handle presentation of non-conventional MHC ligands derived from disease-causing agents, such as HIV-1 envelope (Env) glycoprotein. Here, we report that a CD4(+) T cell repertoire...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242320/ https://www.ncbi.nlm.nih.gov/pubmed/32439962 http://dx.doi.org/10.1038/s41467-020-16319-0 |
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author | Sun, Lina Paschall, Amy V. Middleton, Dustin R. Ishihara, Mayumi Ozdilek, Ahmet Wantuch, Paeton L. Aceil, Javid Duke, Jeremy A. LaBranche, Celia C. Tiemeyer, Michael Avci, Fikri Y. |
author_facet | Sun, Lina Paschall, Amy V. Middleton, Dustin R. Ishihara, Mayumi Ozdilek, Ahmet Wantuch, Paeton L. Aceil, Javid Duke, Jeremy A. LaBranche, Celia C. Tiemeyer, Michael Avci, Fikri Y. |
author_sort | Sun, Lina |
collection | PubMed |
description | The inherent molecular complexity of human pathogens requires that mammals evolved an adaptive immune system equipped to handle presentation of non-conventional MHC ligands derived from disease-causing agents, such as HIV-1 envelope (Env) glycoprotein. Here, we report that a CD4(+) T cell repertoire recognizes a glycopeptide epitope on gp120 presented by MHCII pathway. This glycopeptide is strongly immunogenic in eliciting glycan-dependent cellular and humoral immune responses. The glycopeptide specific CD4(+) T cells display a prominent feature of Th2 and Th17 differentiation and exert high efficacy and potency to help Env trimer humoral immune responses. Glycopeptide-induced CD4(+) T cell response prior to Env trimer immunization elicits neutralizing antibody development and production of antibodies facilitating uptake of immunogens by antigen-presenting cells. Our identification of gp120 glycopeptide–induced, T cell–specific immune responses offers a foundation for developing future knowledge-based vaccines that elicit strong and long-lasting protective immune responses against HIV-1 infection. |
format | Online Article Text |
id | pubmed-7242320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72423202020-05-29 Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help Sun, Lina Paschall, Amy V. Middleton, Dustin R. Ishihara, Mayumi Ozdilek, Ahmet Wantuch, Paeton L. Aceil, Javid Duke, Jeremy A. LaBranche, Celia C. Tiemeyer, Michael Avci, Fikri Y. Nat Commun Article The inherent molecular complexity of human pathogens requires that mammals evolved an adaptive immune system equipped to handle presentation of non-conventional MHC ligands derived from disease-causing agents, such as HIV-1 envelope (Env) glycoprotein. Here, we report that a CD4(+) T cell repertoire recognizes a glycopeptide epitope on gp120 presented by MHCII pathway. This glycopeptide is strongly immunogenic in eliciting glycan-dependent cellular and humoral immune responses. The glycopeptide specific CD4(+) T cells display a prominent feature of Th2 and Th17 differentiation and exert high efficacy and potency to help Env trimer humoral immune responses. Glycopeptide-induced CD4(+) T cell response prior to Env trimer immunization elicits neutralizing antibody development and production of antibodies facilitating uptake of immunogens by antigen-presenting cells. Our identification of gp120 glycopeptide–induced, T cell–specific immune responses offers a foundation for developing future knowledge-based vaccines that elicit strong and long-lasting protective immune responses against HIV-1 infection. Nature Publishing Group UK 2020-05-21 /pmc/articles/PMC7242320/ /pubmed/32439962 http://dx.doi.org/10.1038/s41467-020-16319-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sun, Lina Paschall, Amy V. Middleton, Dustin R. Ishihara, Mayumi Ozdilek, Ahmet Wantuch, Paeton L. Aceil, Javid Duke, Jeremy A. LaBranche, Celia C. Tiemeyer, Michael Avci, Fikri Y. Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title | Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title_full | Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title_fullStr | Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title_full_unstemmed | Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title_short | Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help |
title_sort | glycopeptide epitope facilitates hiv-1 envelope specific humoral immune responses by eliciting t cell help |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242320/ https://www.ncbi.nlm.nih.gov/pubmed/32439962 http://dx.doi.org/10.1038/s41467-020-16319-0 |
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