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Integrative Analysis of Immunological Data to Explore Chronic Immune T-Cell Activation in Successfully Treated HIV Patients.

Identifieur interne : 001236 ( PubMed/Corpus ); précédent : 001235; suivant : 001237

Integrative Analysis of Immunological Data to Explore Chronic Immune T-Cell Activation in Successfully Treated HIV Patients.

Auteurs : Marie-Quitterie Picat ; Isabelle Pellegrin ; Juliette Bitard ; Linda Wittkop ; Cécile Proust-Lima ; Benoît Liquet ; Jean-François Moreau ; Fabrice Bonnet ; Patrick Blanco ; Rodolphe Thiébaut

Source :

RBID : pubmed:28046052

English descriptors

Abstract

To unravel the complex relationships between cytomegalovirus-induced-, autoimmune-induced responses, microbial translocation and chronic immune activation (CIA) in successfully treated HIV-infected patients and to explore the mediating role of alpha-interferon in these processes.

DOI: 10.1371/journal.pone.0169164
PubMed: 28046052

Links to Exploration step

pubmed:28046052

Le document en format XML

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<term>Antigens, CD38 (metabolism)</term>
<term>Autoimmunity (immunology)</term>
<term>CD4-Positive T-Lymphocytes (immunology)</term>
<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Chronic Disease</term>
<term>Cohort Studies</term>
<term>Cross-Sectional Studies</term>
<term>Cytomegalovirus</term>
<term>Female</term>
<term>France</term>
<term>HIV Infections (immunology)</term>
<term>HIV Infections (therapy)</term>
<term>HLA-DR Antigens (metabolism)</term>
<term>Humans</term>
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<term>Male</term>
<term>Middle Aged</term>
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<term>Algorithms</term>
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<term>Cohort Studies</term>
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<term>Lymphocyte Activation</term>
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<front>
<div type="abstract" xml:lang="en">To unravel the complex relationships between cytomegalovirus-induced-, autoimmune-induced responses, microbial translocation and chronic immune activation (CIA) in successfully treated HIV-infected patients and to explore the mediating role of alpha-interferon in these processes.</div>
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<DateCreated>
<Year>2017</Year>
<Month>01</Month>
<Day>03</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>09</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>11</Month>
<Day>16</Day>
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<ISSN IssnType="Electronic">1932-6203</ISSN>
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<Volume>12</Volume>
<Issue>1</Issue>
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<Year>2017</Year>
</PubDate>
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<Title>PloS one</Title>
<ISOAbbreviation>PLoS ONE</ISOAbbreviation>
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<ArticleTitle>Integrative Analysis of Immunological Data to Explore Chronic Immune T-Cell Activation in Successfully Treated HIV Patients.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.pone.0169164</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To unravel the complex relationships between cytomegalovirus-induced-, autoimmune-induced responses, microbial translocation and chronic immune activation (CIA) in successfully treated HIV-infected patients and to explore the mediating role of alpha-interferon in these processes.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">Cross-sectional study nested in the ANRS CO3 Aquitaine Cohort, a prospective hospital-based cohort of HIV-1-infected patients in South-Western France.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Patients initiated antiretroviral therapy between 2005 and 2008 and were treated with sustained virological suppression for at least two years. CIA was defined by the percentage of HLA-DR+/CD38+ among CD8+T-cells. Integrative analyses were performed using structural equation modelling (SEM).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The main analysis was performed in 57 HLA-A*0201 positive patients, due to availability of percentages of actin-, vimentin-, lamin-specific CD8+T-cells (HLA-A2-restricted tests) to further characterize autoimmune response. Cytomegalovirus-induced response was assessed by Quantiferon and pp-65 ELISPOT. SEM revealed a direct effect of cytomegalovirus-induced response on CIA (standardized estimate βstd = 0.56, p-value = 0.0004). The effect of autoimmune-induced response on CIA was indirect through alpha-interferon pathway, assessed by expression levels of 5 alpha-interferon-stimulated genes ADAR, ISG15, IFIT1, Mx1 and OAS1 (effect of autoimmune response on alpha-interferon: βstd = 0.36, p-value = 0.0401; effect of alpha-interferon on CIA: βstd = 0.39, p-value = 0.0044). There was no direct effect of autoimmune-induced response on CIA (p-value = 0.3169). Microbial translocation as measured by 16SrDNA and sCD14 in plasma was not associated with CIA. Results were consistent in 142 patients in whom cytomegalovirus and auto-immunity responses were measured by Quantiferon and anti-nuclear antibodies, respectively. All analyses performed in HLA-A*0201 positive patients and in the overall population revealed a significant effect of IFN-α latent variable on CIA.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The role of cytomegalovirus-induced response on CIA was confirmed as well as the involvement of alpha-interferon on CIA. The indirect effect of auto-immunity response on CIA revealed through the alpha-interferon pathway requires further investigation to confirm the potential role of auto-immunity for CIA in HIV-infected patients.</AbstractText>
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<LastName>Picat</LastName>
<ForeName>Marie-Quitterie</ForeName>
<Initials>MQ</Initials>
<AffiliationInfo>
<Affiliation>Centre INSERM U1219 Bordeaux Population Health, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Univ. Bordeaux, ISPED, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Service d'Information Médicale, USMR, CHU de Bordeaux - Pôle de Santé Publique, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>INRIA, Team SISTM, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Pellegrin</LastName>
<ForeName>Isabelle</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>Laboratoire d'Immunologie-Immunogénétique, Pôle de Biologie, CHU Bordeaux, Bordeaux, France.</Affiliation>
</AffiliationInfo>
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<LastName>Bitard</LastName>
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<ForeName>Linda</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Univ. Bordeaux, ISPED, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Service d'Information Médicale, USMR, CHU de Bordeaux - Pôle de Santé Publique, Bordeaux, France.</Affiliation>
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<Affiliation>INRIA, Team SISTM, Bordeaux, France.</Affiliation>
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<Affiliation>Centre INSERM U1219 Bordeaux Population Health, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>Univ. Bordeaux, ISPED, Bordeaux, France.</Affiliation>
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<LastName>Liquet</LastName>
<ForeName>Benoît</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>ARC Centre of Excellence for Mathematical and Statistical Frontiers, Queensland University of Technology (QUT), Brisbane, Australia.</Affiliation>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Univ. Bordeaux, Bordeaux, France.</Affiliation>
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<Affiliation>CNRS, UMR 5164, Bordeaux, France.</Affiliation>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Univ. Bordeaux, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Service de Médecine Interne et maladies Infectieuses, CHU de Bordeaux, Bordeaux, France.</Affiliation>
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<LastName>Blanco</LastName>
<ForeName>Patrick</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Laboratoire d'Immunologie-Immunogénétique, Pôle de Biologie, CHU Bordeaux, Bordeaux, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Univ. Bordeaux, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>CNRS, UMR 5164, Bordeaux, France.</Affiliation>
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<ForeName>Rodolphe</ForeName>
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<Affiliation>Centre INSERM U1219 Bordeaux Population Health, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>Univ. Bordeaux, ISPED, Bordeaux, France.</Affiliation>
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<Affiliation>Service d'Information Médicale, USMR, CHU de Bordeaux - Pôle de Santé Publique, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>INRIA, Team SISTM, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.</Affiliation>
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<CoiStatement>The authors have declared that no competing interests exist.</CoiStatement>
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