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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
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.
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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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