The impact of viral evolution and frequency of variant epitopes on primary and memory human immunodeficiency virus type 1-specific CD8⁺ T cell responses.
Identifieur interne : 000D25 ( Main/Exploration ); précédent : 000D24; suivant : 000D26The impact of viral evolution and frequency of variant epitopes on primary and memory human immunodeficiency virus type 1-specific CD8⁺ T cell responses.
Auteurs : Nada M. Melhem [Liban] ; Kellie N. Smith [États-Unis] ; Xiao-Li Huang [États-Unis] ; Bonnie A. Colleton [États-Unis] ; Weimin Jiang [États-Unis] ; Robbie B. Mailliard [États-Unis] ; James I. Mullins [États-Unis] ; Charles R. Rinaldo [États-Unis]Source :
- Virology [ 1096-0341 ] ; 2014.
Descripteurs français
- KwdFr :
- Adulte, Agents antiVIH (usage thérapeutique), Antigènes d'histocompatibilité de classe I (génétique), Antigènes d'histocompatibilité de classe I (immunologie), Déterminants antigéniques des lymphocytes T (génétique), Déterminants antigéniques des lymphocytes T (immunologie), Humains, Infections à VIH (génétique), Infections à VIH (immunologie), Infections à VIH (traitement médicamenteux), Infections à VIH (virologie), Lymphocytes T (immunologie), Lymphocytes T (virologie), Lymphocytes T CD8+ (immunologie), Mâle, Protéines virales (génétique), Protéines virales (immunologie), VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (génétique), VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (immunologie), VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (isolement et purification), Études de cohortes, Évolution moléculaire.
- MESH :
- génétique : Antigènes d'histocompatibilité de classe I, Déterminants antigéniques des lymphocytes T, Infections à VIH, Protéines virales, VIH-1 (Virus de l'Immunodéficience Humaine de type 1).
- immunologie : Antigènes d'histocompatibilité de classe I, Déterminants antigéniques des lymphocytes T, Infections à VIH, Lymphocytes T, Lymphocytes T CD8+, Protéines virales, VIH-1 (Virus de l'Immunodéficience Humaine de type 1).
- isolement et purification : VIH-1 (Virus de l'Immunodéficience Humaine de type 1).
- traitement médicamenteux : Infections à VIH.
- usage thérapeutique : Agents antiVIH.
- virologie : Infections à VIH, Lymphocytes T.
- Adulte, Humains, Mâle, Études de cohortes, Évolution moléculaire.
English descriptors
- KwdEn :
- Adult, Anti-HIV Agents (therapeutic use), CD8-Positive T-Lymphocytes (immunology), Cohort Studies, Epitopes, T-Lymphocyte (genetics), Epitopes, T-Lymphocyte (immunology), Evolution, Molecular, HIV Infections (drug therapy), HIV Infections (genetics), HIV Infections (immunology), HIV Infections (virology), HIV-1 (genetics), HIV-1 (immunology), HIV-1 (isolation & purification), Histocompatibility Antigens Class I (genetics), Histocompatibility Antigens Class I (immunology), Humans, Male, T-Lymphocytes (immunology), T-Lymphocytes (virology), Viral Proteins (genetics), Viral Proteins (immunology).
- MESH :
- chemical , genetics : Epitopes, T-Lymphocyte, Histocompatibility Antigens Class I, Viral Proteins.
- chemical , immunology : Epitopes, T-Lymphocyte, Histocompatibility Antigens Class I, Viral Proteins.
- chemical , therapeutic use : Anti-HIV Agents.
- drug therapy : HIV Infections.
- genetics : HIV Infections, HIV-1.
- immunology : CD8-Positive T-Lymphocytes, HIV Infections, HIV-1, T-Lymphocytes.
- isolation & purification : HIV-1.
- virology : HIV Infections, T-Lymphocytes.
- Adult, Cohort Studies, Evolution, Molecular, Humans, Male.
Abstract
It is unclear if HIV-1 variants lose the ability to prime naïve CD8(+) cytotoxic T lymphocytes (CTL) during progressive, untreated infection. We conducted a comprehensive longitudinal analysis of viral evolution and its impact on primary and memory CD8(+) T cell responses pre-seroconversion (SC), post-SC, and during combination antiretroviral therapy (cART). Memory T cell responses targeting autologous virus variants reached a nadir by 8 years post-SC with development of AIDS, followed by a transient enhancement of anti-HIV-1 CTL responses upon initiation of cART. We show broad and high magnitude primary T cell responses to late variants in pre-SC T cells, comparable to primary anti-HIV-1 responses induced in T cells from uninfected persons. Despite evolutionary changes, CD8(+) T cells could still be primed to HIV-1 variants. Hence, vaccination against late, mutated epitopes could be successful in enhancing primary reactivity of T cells for control of the residual reservoir of HIV-1 during cART.
DOI: 10.1016/j.virol.2013.10.015
PubMed: 24503065
Affiliations:
- Liban, États-Unis
- Pennsylvanie, Washington (État)
- Pittsburgh, Seattle, University Park (Pennsylvanie)
- Université d'État de Pennsylvanie, Université de Pittsburgh, Université de Washington
Links toward previous steps (curation, corpus...)
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- to stream Ncbi, to step Curation: 001006
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Le document en format XML
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<term>Anti-HIV Agents (therapeutic use)</term>
<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Cohort Studies</term>
<term>Epitopes, T-Lymphocyte (genetics)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
<term>Evolution, Molecular</term>
<term>HIV Infections (drug therapy)</term>
<term>HIV Infections (genetics)</term>
<term>HIV Infections (immunology)</term>
<term>HIV Infections (virology)</term>
<term>HIV-1 (genetics)</term>
<term>HIV-1 (immunology)</term>
<term>HIV-1 (isolation & purification)</term>
<term>Histocompatibility Antigens Class I (genetics)</term>
<term>Histocompatibility Antigens Class I (immunology)</term>
<term>Humans</term>
<term>Male</term>
<term>T-Lymphocytes (immunology)</term>
<term>T-Lymphocytes (virology)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (immunology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Agents antiVIH (usage thérapeutique)</term>
<term>Antigènes d'histocompatibilité de classe I (génétique)</term>
<term>Antigènes d'histocompatibilité de classe I (immunologie)</term>
<term>Déterminants antigéniques des lymphocytes T (génétique)</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
<term>Humains</term>
<term>Infections à VIH (génétique)</term>
<term>Infections à VIH (immunologie)</term>
<term>Infections à VIH (traitement médicamenteux)</term>
<term>Infections à VIH (virologie)</term>
<term>Lymphocytes T (immunologie)</term>
<term>Lymphocytes T (virologie)</term>
<term>Lymphocytes T CD8+ (immunologie)</term>
<term>Mâle</term>
<term>Protéines virales (génétique)</term>
<term>Protéines virales (immunologie)</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (génétique)</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (immunologie)</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (isolement et purification)</term>
<term>Études de cohortes</term>
<term>Évolution moléculaire</term>
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<term>Histocompatibility Antigens Class I</term>
<term>Viral Proteins</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Anti-HIV Agents</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>HIV Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>HIV Infections</term>
<term>HIV-1</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Antigènes d'histocompatibilité de classe I</term>
<term>Déterminants antigéniques des lymphocytes T</term>
<term>Infections à VIH</term>
<term>Protéines virales</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Antigènes d'histocompatibilité de classe I</term>
<term>Déterminants antigéniques des lymphocytes T</term>
<term>Infections à VIH</term>
<term>Lymphocytes T</term>
<term>Lymphocytes T CD8+</term>
<term>Protéines virales</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>CD8-Positive T-Lymphocytes</term>
<term>HIV Infections</term>
<term>HIV-1</term>
<term>T-Lymphocytes</term>
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<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>HIV-1</term>
</keywords>
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</keywords>
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<term>Lymphocytes T</term>
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<keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>HIV Infections</term>
<term>T-Lymphocytes</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Cohort Studies</term>
<term>Evolution, Molecular</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Humains</term>
<term>Mâle</term>
<term>Études de cohortes</term>
<term>Évolution moléculaire</term>
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<front><div type="abstract" xml:lang="en">It is unclear if HIV-1 variants lose the ability to prime naïve CD8(+) cytotoxic T lymphocytes (CTL) during progressive, untreated infection. We conducted a comprehensive longitudinal analysis of viral evolution and its impact on primary and memory CD8(+) T cell responses pre-seroconversion (SC), post-SC, and during combination antiretroviral therapy (cART). Memory T cell responses targeting autologous virus variants reached a nadir by 8 years post-SC with development of AIDS, followed by a transient enhancement of anti-HIV-1 CTL responses upon initiation of cART. We show broad and high magnitude primary T cell responses to late variants in pre-SC T cells, comparable to primary anti-HIV-1 responses induced in T cells from uninfected persons. Despite evolutionary changes, CD8(+) T cells could still be primed to HIV-1 variants. Hence, vaccination against late, mutated epitopes could be successful in enhancing primary reactivity of T cells for control of the residual reservoir of HIV-1 during cART.</div>
</front>
</TEI>
<affiliations><list><country><li>Liban</li>
<li>États-Unis</li>
</country>
<region><li>Pennsylvanie</li>
<li>Washington (État)</li>
</region>
<settlement><li>Pittsburgh</li>
<li>Seattle</li>
<li>University Park (Pennsylvanie)</li>
</settlement>
<orgName><li>Université d'État de Pennsylvanie</li>
<li>Université de Pittsburgh</li>
<li>Université de Washington</li>
</orgName>
</list>
<tree><country name="Liban"><noRegion><name sortKey="Melhem, Nada M" sort="Melhem, Nada M" uniqKey="Melhem N" first="Nada M" last="Melhem">Nada M. Melhem</name>
</noRegion>
</country>
<country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Smith, Kellie N" sort="Smith, Kellie N" uniqKey="Smith K" first="Kellie N" last="Smith">Kellie N. Smith</name>
</region>
<name sortKey="Colleton, Bonnie A" sort="Colleton, Bonnie A" uniqKey="Colleton B" first="Bonnie A" last="Colleton">Bonnie A. Colleton</name>
<name sortKey="Huang, Xiao Li" sort="Huang, Xiao Li" uniqKey="Huang X" first="Xiao-Li" last="Huang">Xiao-Li Huang</name>
<name sortKey="Jiang, Weimin" sort="Jiang, Weimin" uniqKey="Jiang W" first="Weimin" last="Jiang">Weimin Jiang</name>
<name sortKey="Mailliard, Robbie B" sort="Mailliard, Robbie B" uniqKey="Mailliard R" first="Robbie B" last="Mailliard">Robbie B. Mailliard</name>
<name sortKey="Mullins, James I" sort="Mullins, James I" uniqKey="Mullins J" first="James I" last="Mullins">James I. Mullins</name>
<name sortKey="Rinaldo, Charles R" sort="Rinaldo, Charles R" uniqKey="Rinaldo C" first="Charles R" last="Rinaldo">Charles R. Rinaldo</name>
</country>
</tree>
</affiliations>
</record>
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