Evidence map›Paper›PMID 25486415›Full record

Trial reportAIDS (London, England)2015

TB-IRIS, T-cell activation, and remodeling of the T-cell compartment in highly immunosuppressed HIV-infected patients with TB.

Viraga Haridas, Polidy Pean, Luke D Jasenosky, Yoann Madec, Didier Laureillard, Thim Sok, Sun Sath, Laurence Borand, Olivier Marcy, Sarin Chan and 5 more

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in AIDS (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Phenotypic Profile ofOpen forum infectious diseases · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Observational
  11. Review
  12. Observational
  13. High Activation of γδ T Cells and the γδ2Frontiers in immunology · 2019
    Article
  14. Article
  15. Article
  16. Immune reconstitution inflammatory syndrome associated with pulmonary pathogens.European respiratory review : an official journal of the European Respiratory Society · 2017
    Review
  17. Article
  18. Review
  19. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 3 countries.

Viraga HaridasaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA bImmunology Platform, Institut Pasteur du Cambodge, Phnom Penh, Cambodia cInstitut Pasteur, Emerging Diseases Epidemiology Unit, Paris, France dCambodian Health Committee, Phnom Penh, Cambodia eInstitut Pasteur du Cambodge, Epidemiology and Public Health Unit, Phnom Penh, Cambodia fDepartment of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA gFrench National Agency for Research on AIDS and Viral Hepatitis (ANRS), Paris hAssistance Publique - Hôpitaux de Paris, Bicêtre Hospital, Le Kremlin-Bicêtre, France. *Viraga Haridas, Polidy Pean, and Luke D. Jasenosky contributed equally to the writing of this article. †Current address: Univ. Montpellier, INSERM U1058, Department of Infectious and Tropical Diseases, CHRU Nimes, Nimes, France. ‡Current Address: Univ. Bordeaux, Centre INSERM U897, Epidemiologie-Biostatisque, Bordeaux, France. §Current address: Calmette Hospital, Phnom Penh, Cambodia. ¶Current address: UMR INSERM 1087, CNRS UMR_6291, l'Institut du Thorax, Nantes University, Nantes, France.
Polidy Pean
Luke D Jasenosky
Yoann Madec
Didier Laureillard
Thim Sok
Sun Sath
Laurence Borand
Olivier Marcy
Sarin Chan
Erdyni Tsitsikov
Jean-François Delfraissy
François-Xavier Blanc
Anne E Goldfeld
CAPRI-T (ANRS 12164) Study Team
Cambodian Institute for Cooperation and Peace · KHBoston Children's Museum · USInstitut Pasteur du Cambodge · KHAgence Nationale de la Recherche · FRBicêtre Hospital · FRHarvard University · USInstitut Pasteur · FR

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
The Asia-Pacific HIV Research CollaborationU01AI069907 · NIAID · FOUNDATION FOR AIDS RESEARCH · PI ANNETTE H SOHN · 2006 to 2026
$44.8M
T CELL SUBSETS AND THEIR FUNCTION IN TB/HIV PARADOXICAL REACTIONSR21AI076023 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 2009 to 2010
$575k
NCATS NIH HHS UL1 TR001102NIAID NIH HHS R21 AI076023NIAID NIH HHS R21AI076023NIAID NIH HHS U01 AI069907NIAID NIH HHS U01AI069907-07
6 · The paper itself

Abstract

objectiveTo investigate the impact of tuberculosis-associated immune reconstitution inflammatory syndrome (TB-IRIS) upon immunological recovery and the T-cell compartment after initiation of TB and antiretroviral therapy (ART). DESIGN AND

methodsWe prospectively evaluated T-cell immunophenotypes by flow cytometry and cytokines by Luminex assays in a subset (n = 154) of highly immunosuppressed HIV-infected patients with TB from the Cambodian Early versus Late Introduction of Antiretrovirals randomized clinical trial. We compared findings from patients who developed TB-IRIS with findings from patients who did not develop TB-IRIS. Data were evaluated with mixed-effect linear regression, Kaplan-Meier estimates, and Wilcoxon rank-sum tests, and q-values were calculated to control for multiple comparisons.

resultsDevelopment of TB-IRIS was associated with significantly greater pre-ART frequencies of HLA-DRCD45ROCD4, CCR5CD4, OX40CD4, and Fas effector memory CD8 T cells, and significantly elevated levels of plasma interleukin (IL)-6, IL-1β, IL-8, and IL-10, and viral load. Post-ART initiation, effector memory CD4 and Fas effector memory CD4 T-cell frequencies significantly expanded, and central memory CD4 T-cell frequencies significantly contracted in patients who experienced TB-IRIS. By week 34 post-TB treatment initiation, effector memory/central memory CD4 T-cell ratios were markedly higher in TB-IRIS versus non-TB-IRIS patients.

conclusionsA distinct pattern of pre-ART T-cell and cytokine markers appear to poise the immune response of certain patients to develop TB-IRIS. Experience of TB-IRIS is then associated with long-term remodeling of the CD4 T-cell memory compartment towards an effector memory-dominated phenotype. We speculate that these pre and post-ART TB-IRIS-associated immune parameters may contribute to superior immune control of TB/HIV co-infection and better clinical outcome.

Indexed as

AdultAnti-Retroviral AgentsAntitubercular AgentsCambodiaCytokinesFemaleFlow CytometryHIV InfectionsHumansImmune Reconstitution Inflammatory SyndromeImmunophenotypingMaleProspective StudiesT-LymphocytesTreatment OutcomeTuberculosisAnti-Retroviral AgentsAntitubercular AgentsCytokines

Identifiers

PMID25486415
PMCPMC4649949
OpenAlexW2028841565

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.