HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells

Even with sustained antiretroviral therapy, resting CD4 + T cells remain a persistent reservoir of HIV infection, representing a critical barrier to curing HIV. Here, we demonstrate that CD8 + T cells recognize infected, non-activated CD4 + T cells in the absence of de novo protein production, as me...

Descripción completa

Detalles Bibliográficos
Autores: Monel, Blandine, McKeon, Annmarie, Lamothe-Molina, Pedro, Jani, Priya, Boucau, Julie, Jones, R. Brad, Le Gall, Sylvie, Walker, Bruce D., Pacheco Nieva, Yovana
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2019
País:Colombia
Institución:Universidad del Rosario
Repositorio:Repositorio EdocUR - U. Rosario
Idioma:inglés
OAI Identifier:oai:repository.urosario.edu.co:10336/23642
Acceso en línea:https://doi.org/10.1016/j.celrep.2019.03.016
https://repository.urosario.edu.co/handle/10336/23642
Access Level:acceso abierto
Palabra clave:T lymphocyte receptor
Antigen presentation
Article
CD4+ T lymphocyte
CD8+ T lymphocyte
Colorimetry
Controlled study
Cytokine production
Degranulation
Flow cytometry
Fluorescence microscopy
Fluorescence resonance energy transfer
Human
Human cell
Human immunodeficiency virus 1 infection
Immune response
Immunological synapse
Long terminal repeat
Molecular recognition
Priority journal
Protein cleavage
Protein protein interaction
Synapse
Virus entry
Virus genome
Virus particle
Cytotoxic T lymphocytes
Elite controllers
Granzyme
HIV
HIV cure
HLA
Immunologic synapse
Perforin
id CO_8a2ec4c2c3ab05c9e84cedee7f4e1e11
oai_identifier_str oai:repository.urosario.edu.co:10336/23642
network_acronym_str CO
network_name_str Colombia
repository_id_str
spelling HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T CellsMonel, BlandineMcKeon, AnnmarieLamothe-Molina, PedroJani, PriyaBoucau, JulieJones, R. BradLe Gall, SylvieWalker, Bruce D.Pacheco Nieva, YovanaT lymphocyte receptorAntigen presentationArticleCD4+ T lymphocyteCD8+ T lymphocyteColorimetryControlled studyCytokine productionDegranulationFlow cytometryFluorescence microscopyFluorescence resonance energy transferHumanHuman cellHuman immunodeficiency virus 1 infectionImmune responseImmunological synapseLong terminal repeatMolecular recognitionPriority journalProtein cleavageProtein protein interactionSynapseVirus entryVirus genomeVirus particleCytotoxic T lymphocytesElite controllersGranzymeHIVHIV cureHLAImmunologic synapsePerforinEven with sustained antiretroviral therapy, resting CD4 + T cells remain a persistent reservoir of HIV infection, representing a critical barrier to curing HIV. Here, we demonstrate that CD8 + T cells recognize infected, non-activated CD4 + T cells in the absence of de novo protein production, as measured by immune synapse formation, degranulation, cytokine production, and killing of infected cells. Immune recognition is induced by HLA-I presentation of peptides derived from incoming viral particles, and recognition occurred either following cell-free virus infection or following cell-to-cell spread. CD8 + T cells from HIV controllers mediate more effective immune recognition than CD8 + T cells from progressors. These results indicate that non-activated HIV-infected CD4 + T cells can be targeted by CD8 + T cells directly after HIV entry, before reverse transcription, and thus before the establishment of latency, and suggest a mechanism whereby the immune response may reduce the size of the HIV reservoir. The cure for HIV is not achievable due to HIV reservoirs, mostly in resting CD4 + T cells. Monel et al. show that CD8 + T cells from HIV controllers are able to establish immunological synapses with HIV + resting CD4 + T cells, leading to IFN-?, MIP1-? production, degranulation, and the elimination of the target cells. © 2019 The AuthorsElsevier B.V.20192020-05-26T00:03:57Zinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.1016/j.celrep.2019.03.01622111247https://repository.urosario.edu.co/handle/10336/23642reponame:Repositorio EdocUR - U. Rosarioinstname:Universidad del Rosarioinstacron:Universidad del Rosarioenghttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85063383455&doi=10.1016%2fj.celrep.2019.03.016&partnerID=40&md5=332d50ba72513d6eed03a3e1bef75e1cinfo:eu-repo/semantics/openAccess2022-05-02T07:37:21Z
dc.title.none.fl_str_mv HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
title HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
spellingShingle HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
Monel, Blandine
T lymphocyte receptor
Antigen presentation
Article
CD4+ T lymphocyte
CD8+ T lymphocyte
Colorimetry
Controlled study
Cytokine production
Degranulation
Flow cytometry
Fluorescence microscopy
Fluorescence resonance energy transfer
Human
Human cell
Human immunodeficiency virus 1 infection
Immune response
Immunological synapse
Long terminal repeat
Molecular recognition
Priority journal
Protein cleavage
Protein protein interaction
Synapse
Virus entry
Virus genome
Virus particle
Cytotoxic T lymphocytes
Elite controllers
Granzyme
HIV
HIV cure
HLA
Immunologic synapse
Perforin
title_short HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
title_full HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
title_fullStr HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
title_full_unstemmed HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
title_sort HIV Controllers Exhibit Effective CD8 + T Cell Recognition of HIV-1-Infected Non-activated CD4 + T Cells
dc.creator.none.fl_str_mv Monel, Blandine
McKeon, Annmarie
Lamothe-Molina, Pedro
Jani, Priya
Boucau, Julie
Jones, R. Brad
Le Gall, Sylvie
Walker, Bruce D.
Pacheco Nieva, Yovana
author Monel, Blandine
author_facet Monel, Blandine
McKeon, Annmarie
Lamothe-Molina, Pedro
Jani, Priya
Boucau, Julie
Jones, R. Brad
Le Gall, Sylvie
Walker, Bruce D.
Pacheco Nieva, Yovana
author_role author
author2 McKeon, Annmarie
Lamothe-Molina, Pedro
Jani, Priya
Boucau, Julie
Jones, R. Brad
Le Gall, Sylvie
Walker, Bruce D.
Pacheco Nieva, Yovana
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv T lymphocyte receptor
Antigen presentation
Article
CD4+ T lymphocyte
CD8+ T lymphocyte
Colorimetry
Controlled study
Cytokine production
Degranulation
Flow cytometry
Fluorescence microscopy
Fluorescence resonance energy transfer
Human
Human cell
Human immunodeficiency virus 1 infection
Immune response
Immunological synapse
Long terminal repeat
Molecular recognition
Priority journal
Protein cleavage
Protein protein interaction
Synapse
Virus entry
Virus genome
Virus particle
Cytotoxic T lymphocytes
Elite controllers
Granzyme
HIV
HIV cure
HLA
Immunologic synapse
Perforin
topic T lymphocyte receptor
Antigen presentation
Article
CD4+ T lymphocyte
CD8+ T lymphocyte
Colorimetry
Controlled study
Cytokine production
Degranulation
Flow cytometry
Fluorescence microscopy
Fluorescence resonance energy transfer
Human
Human cell
Human immunodeficiency virus 1 infection
Immune response
Immunological synapse
Long terminal repeat
Molecular recognition
Priority journal
Protein cleavage
Protein protein interaction
Synapse
Virus entry
Virus genome
Virus particle
Cytotoxic T lymphocytes
Elite controllers
Granzyme
HIV
HIV cure
HLA
Immunologic synapse
Perforin
description Even with sustained antiretroviral therapy, resting CD4 + T cells remain a persistent reservoir of HIV infection, representing a critical barrier to curing HIV. Here, we demonstrate that CD8 + T cells recognize infected, non-activated CD4 + T cells in the absence of de novo protein production, as measured by immune synapse formation, degranulation, cytokine production, and killing of infected cells. Immune recognition is induced by HLA-I presentation of peptides derived from incoming viral particles, and recognition occurred either following cell-free virus infection or following cell-to-cell spread. CD8 + T cells from HIV controllers mediate more effective immune recognition than CD8 + T cells from progressors. These results indicate that non-activated HIV-infected CD4 + T cells can be targeted by CD8 + T cells directly after HIV entry, before reverse transcription, and thus before the establishment of latency, and suggest a mechanism whereby the immune response may reduce the size of the HIV reservoir. The cure for HIV is not achievable due to HIV reservoirs, mostly in resting CD4 + T cells. Monel et al. show that CD8 + T cells from HIV controllers are able to establish immunological synapses with HIV + resting CD4 + T cells, leading to IFN-?, MIP1-? production, degranulation, and the elimination of the target cells. © 2019 The Authors
publishDate 2019
dc.date.none.fl_str_mv 2019
2020-05-26T00:03:57Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://doi.org/10.1016/j.celrep.2019.03.016
22111247
https://repository.urosario.edu.co/handle/10336/23642
url https://doi.org/10.1016/j.celrep.2019.03.016
https://repository.urosario.edu.co/handle/10336/23642
identifier_str_mv 22111247
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-85063383455&doi=10.1016%2fj.celrep.2019.03.016&partnerID=40&md5=332d50ba72513d6eed03a3e1bef75e1c
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositorio EdocUR - U. Rosario
instname:Universidad del Rosario
instacron:Universidad del Rosario
instname_str Universidad del Rosario
instacron_str Universidad del Rosario
institution Universidad del Rosario
reponame_str Repositorio EdocUR - U. Rosario
collection Repositorio EdocUR - U. Rosario
_version_ 1825051768237588480
score 15,81155