Impact of Early Versus Late Antiretroviral Treatment Initiation on Naive T Lymphocytes in HIV-1-Infected Children and Adolescents - The-ANRS-EP59-CLEAC Study.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 01 02 2021
accepted: 24 03 2021
entrez: 10 5 2021
pubmed: 11 5 2021
medline: 21 10 2021
Statut: epublish

Résumé

The early initiation of antiretroviral therapy (ART) in HIV-1-infected infants reduces mortality and prevents early CD4 T-cell loss. However, the impact of early ART on the immune system has not been thoroughly investigated in children over five years of age or adolescents. Here, we describe the levels of naive CD4 and CD8 T lymphocytes (CD4/CD8T The ANRS-EP59-CLEAC study enrolled 27 children (5-12 years of age) and nine adolescents (13-17 years of age) in the early-treatment group, and 19 children (L-Ch) and 21 adolescents (L-Ado) in the late-treatment group. T lymphocytes were analyzed by flow cytometry and plasma markers were analyzed by ELISA. Linear regression analysis was performed with univariate and multivariate models. At the time of evaluation, all patients were on ART and had a good immunovirological status: 83% had HIV RNA loads below 50 copies/mL and the median CD4 T-cell count was 856 cells/µL (interquartile range: 685-1236 cells/µL). In children, early ART was associated with higher CD8T In children and adolescents, the benefits of early ART for CD8T ClinicalTrials.gov, identifier NCT02674867.

Sections du résumé

Background
The early initiation of antiretroviral therapy (ART) in HIV-1-infected infants reduces mortality and prevents early CD4 T-cell loss. However, the impact of early ART on the immune system has not been thoroughly investigated in children over five years of age or adolescents. Here, we describe the levels of naive CD4 and CD8 T lymphocytes (CD4/CD8T
Methods
The ANRS-EP59-CLEAC study enrolled 27 children (5-12 years of age) and nine adolescents (13-17 years of age) in the early-treatment group, and 19 children (L-Ch) and 21 adolescents (L-Ado) in the late-treatment group. T lymphocytes were analyzed by flow cytometry and plasma markers were analyzed by ELISA. Linear regression analysis was performed with univariate and multivariate models.
Results
At the time of evaluation, all patients were on ART and had a good immunovirological status: 83% had HIV RNA loads below 50 copies/mL and the median CD4 T-cell count was 856 cells/µL (interquartile range: 685-1236 cells/µL). In children, early ART was associated with higher CD8T
Conclusion
In children and adolescents, the benefits of early ART for CD8T
Clinical Trial Registration
ClinicalTrials.gov, identifier NCT02674867.

Identifiants

pubmed: 33968064
doi: 10.3389/fimmu.2021.662894
pmc: PMC8100053
doi:

Banques de données

ClinicalTrials.gov
['NCT02674867']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

662894

Informations de copyright

Copyright © 2021 Frange, Montange, Le Chenadec, Batalie, Fert, Dollfus, Faye, Blanche, Chacé, Fourcade, Hau, Levine, Mahlaoui, Marcou, Tabone, Veber, Hoctin, Wack, Avettand-Fenoël, Warszawski and Buseyne.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Pierre Frange (P)

Immunologie, hématologie et rhumatologie pédiatrique, hôpital Necker-Enfants malades, AP-HP- Centre - Université de Paris, Paris, France.
Laboratoire de microbiologie clinique, hôpital Necker-Enfants malades, AP-HP-Centre - Université de Paris, Paris, France.
EHU 7328 PACT, Institut Imagine, Université de Paris, Paris, France.

Thomas Montange (T)

Unité Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, Paris, France.
Département de Virologie, UMR CNRS 3569 Institut Pasteur, Paris, France.

Jérôme Le Chenadec (J)

Départment d'épidémiologie, Centre de Recherche en Épidémiologie et Santé des Populations, INSERM U1018, Le Kremlin-Bicêtre, Villejuif, France.

Damien Batalie (D)

Unité Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, Paris, France.
Département de Virologie, UMR CNRS 3569 Institut Pasteur, Paris, France.

Ingrid Fert (I)

Unité Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, Paris, France.
Département de Virologie, UMR CNRS 3569 Institut Pasteur, Paris, France.

Catherine Dollfus (C)

Hémato-oncologie pédiatrique, Hôpital Trousseau, AP-HP, Paris, France.

Albert Faye (A)

Pédiatrie Générale, Hôpital Robert Debré, AP-HP, Paris, France.

Stéphane Blanche (S)

Immunologie, hématologie et rhumatologie pédiatrique, hôpital Necker-Enfants malades, AP-HP- Centre - Université de Paris, Paris, France.

Anne Chacé (A)

Pédiatrie et néonatologie, Centre hospitalier intercommunal de Villeuneuve-Saint-Georges, Villeuneuve-Saint-Georges, France.

Corine Fourcade (C)

Pédiatrie Générale, Hôpital Bicêtre, AP-HP, Paris, France.

Isabelle Hau (I)

Pédiatrie Générale, Centre hospitalier intercommunal de Créteil, Créteil, France.

Martine Levine (M)

Immuno-hématologie pédiatrique, Hôpital Robert Debré, AP-HP, Paris, France.

Nizar Mahlaoui (N)

Immunologie, hématologie et rhumatologie pédiatrique, hôpital Necker-Enfants malades, AP-HP- Centre - Université de Paris, Paris, France.

Valérie Marcou (V)

Médecine et réanimation néonatale, Hôpital Cochin, AP-HP-Centre - Université de Paris, Paris, France.

Marie-Dominique Tabone (MD)

Hémato-oncologie pédiatrique, Hôpital Trousseau, AP-HP, Paris, France.

Florence Veber (F)

Immunologie, hématologie et rhumatologie pédiatrique, hôpital Necker-Enfants malades, AP-HP- Centre - Université de Paris, Paris, France.

Alexandre Hoctin (A)

Départment d'épidémiologie, Centre de Recherche en Épidémiologie et Santé des Populations, INSERM U1018, Le Kremlin-Bicêtre, Villejuif, France.

Thierry Wack (T)

Départment d'épidémiologie, Centre de Recherche en Épidémiologie et Santé des Populations, INSERM U1018, Le Kremlin-Bicêtre, Villejuif, France.

Véronique Avettand-Fenoël (V)

Laboratoire de microbiologie clinique, hôpital Necker-Enfants malades, AP-HP-Centre - Université de Paris, Paris, France.
CNRS 8104/INSERM U1016, Institut Cochin, Université Paris Descartes, Paris, France.

Josiane Warszawski (J)

Départment d'épidémiologie, Centre de Recherche en Épidémiologie et Santé des Populations, INSERM U1018, Le Kremlin-Bicêtre, Villejuif, France.
INED, Université Paris Sud, Le Kremlin-Bicêtre, Orsay, France.

Florence Buseyne (F)

Unité Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, Paris, France.
Département de Virologie, UMR CNRS 3569 Institut Pasteur, Paris, France.

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