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Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity
Human immunodeficiency virus type 1 (HIV-1) infection causes a progressive depletion of CD4 + T cells. Despite its importance for HIV-1 pathogenesis, the precise mechanisms underlying CD4 + T-cell depletion remain incompletely understood. Here we make the surprising observation that antibody-depende...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739418/ https://www.ncbi.nlm.nih.gov/pubmed/26870823 http://dx.doi.org/10.1016/j.ebiom.2015.12.004 |
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author | Richard, Jonathan Veillette, Maxime Ding, Shilei Zoubchenok, Daria Alsahafi, Nirmin Coutu, Mathieu Brassard, Nathalie Park, Jongwoo Courter, Joel R. Melillo, Bruno Smith, Amos B. Shaw, George M. Hahn, Beatrice H. Sodroski, Joseph Kaufmann, Daniel E. Finzi, Andrés |
author_facet | Richard, Jonathan Veillette, Maxime Ding, Shilei Zoubchenok, Daria Alsahafi, Nirmin Coutu, Mathieu Brassard, Nathalie Park, Jongwoo Courter, Joel R. Melillo, Bruno Smith, Amos B. Shaw, George M. Hahn, Beatrice H. Sodroski, Joseph Kaufmann, Daniel E. Finzi, Andrés |
author_sort | Richard, Jonathan |
collection | PubMed |
description | Human immunodeficiency virus type 1 (HIV-1) infection causes a progressive depletion of CD4 + T cells. Despite its importance for HIV-1 pathogenesis, the precise mechanisms underlying CD4 + T-cell depletion remain incompletely understood. Here we make the surprising observation that antibody-dependent cell-mediated cytotoxicity (ADCC) mediates the death of uninfected bystander CD4 + T cells in cultures of HIV-1-infected cells. While HIV-1-infected cells are protected from ADCC by the action of the viral Vpu and Nef proteins, uninfected bystander CD4 + T cells bind gp120 shed from productively infected cells and are efficiently recognized by ADCC-mediating antibodies. Thus, gp120 shedding represents a viral mechanism to divert ADCC responses towards uninfected bystander CD4 + T cells. Importantly, CD4-mimetic molecules redirect ADCC responses from uninfected bystander cells to HIV-1-infected cells; therefore, CD4-mimetic compounds might have therapeutic utility in new strategies aimed at specifically eliminating HIV-1-infected cells. |
format | Online Article Text |
id | pubmed-4739418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47394182016-02-11 Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity Richard, Jonathan Veillette, Maxime Ding, Shilei Zoubchenok, Daria Alsahafi, Nirmin Coutu, Mathieu Brassard, Nathalie Park, Jongwoo Courter, Joel R. Melillo, Bruno Smith, Amos B. Shaw, George M. Hahn, Beatrice H. Sodroski, Joseph Kaufmann, Daniel E. Finzi, Andrés EBioMedicine Research Paper Human immunodeficiency virus type 1 (HIV-1) infection causes a progressive depletion of CD4 + T cells. Despite its importance for HIV-1 pathogenesis, the precise mechanisms underlying CD4 + T-cell depletion remain incompletely understood. Here we make the surprising observation that antibody-dependent cell-mediated cytotoxicity (ADCC) mediates the death of uninfected bystander CD4 + T cells in cultures of HIV-1-infected cells. While HIV-1-infected cells are protected from ADCC by the action of the viral Vpu and Nef proteins, uninfected bystander CD4 + T cells bind gp120 shed from productively infected cells and are efficiently recognized by ADCC-mediating antibodies. Thus, gp120 shedding represents a viral mechanism to divert ADCC responses towards uninfected bystander CD4 + T cells. Importantly, CD4-mimetic molecules redirect ADCC responses from uninfected bystander cells to HIV-1-infected cells; therefore, CD4-mimetic compounds might have therapeutic utility in new strategies aimed at specifically eliminating HIV-1-infected cells. Elsevier 2015-12-09 /pmc/articles/PMC4739418/ /pubmed/26870823 http://dx.doi.org/10.1016/j.ebiom.2015.12.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Richard, Jonathan Veillette, Maxime Ding, Shilei Zoubchenok, Daria Alsahafi, Nirmin Coutu, Mathieu Brassard, Nathalie Park, Jongwoo Courter, Joel R. Melillo, Bruno Smith, Amos B. Shaw, George M. Hahn, Beatrice H. Sodroski, Joseph Kaufmann, Daniel E. Finzi, Andrés Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title | Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title_full | Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title_fullStr | Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title_full_unstemmed | Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title_short | Small CD4 Mimetics Prevent HIV-1 Uninfected Bystander CD4 + T Cell Killing Mediated by Antibody-dependent Cell-mediated Cytotoxicity |
title_sort | small cd4 mimetics prevent hiv-1 uninfected bystander cd4 + t cell killing mediated by antibody-dependent cell-mediated cytotoxicity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739418/ https://www.ncbi.nlm.nih.gov/pubmed/26870823 http://dx.doi.org/10.1016/j.ebiom.2015.12.004 |
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