Evidence map›Paper›PMID 25048802›Full record

ArticlePloS one2014

A subset of circulating blood mycobacteria-specific CD4 T cells can predict the time to Mycobacterium tuberculosis sputum culture conversion.

Catherine Riou, Clive M Gray, Masixole Lugongolo, Thabisile Gwala, Agano Kiravu, Pamela Deniso, Lynsey Stewart-Isherwood, Shaheed Vally Omar, Martin P Grobusch, Gerrit Coetzee and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. CD4Frontiers in immunology · 2019
    Article
  8. High Frequencies of Caspase-3 ExpressingFrontiers in immunology · 2018
    Article
  9. Review
  10. Human Immunology of Tuberculosis.Microbiology spectrum · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
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

14 authors at 5 institutions in 3 countries.

Catherine RiouDivision of Immunology, Institute of Infectious Disease and Molecular Medicine and National Health Laboratory Services, University of Cape Town, Cape Town, South Africa.
Clive M GrayDivision of Immunology, Institute of Infectious Disease and Molecular Medicine and National Health Laboratory Services, University of Cape Town, Cape Town, South Africa.
Masixole LugongoloNational Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
Thabisile GwalaNational Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
Agano KiravuDivision of Immunology, Institute of Infectious Disease and Molecular Medicine and National Health Laboratory Services, University of Cape Town, Cape Town, South Africa.
Pamela DenisoRight to Care and the Clinical HIV Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Lynsey Stewart-IsherwoodRight to Care and the Clinical HIV Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Shaheed Vally OmarNational Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
Martin P GrobuschCenter of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Division of Internal Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Gerrit CoetzeeNational Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
Francesca ConradieRight to Care and the Clinical HIV Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Nazir IsmailNational Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
Gilla KaplanLaboratory of Mycobacterial Immunity and Pathogenesis, Public Health Research Institute at the International Center for Public Health, Newark, New Jersey, United States of America.
Dorothy FallowsLaboratory of Mycobacterial Immunity and Pathogenesis, Public Health Research Institute at the International Center for Public Health, Newark, New Jersey, United States of America.
National Health Laboratory Service · ZAUniversity of the Witwatersrand · ZAInternational Center for Public Health · USUniversity of Cape Town · ZAUniversity of Amsterdam · NL

Funding

Emerging XDR-TB: Host and Pathogen ContributionsR01AI080737 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FALLOWS, DOROTHY A. · 2009 to 2013
$2.9M
Analysis of XDR-TB and MDR-TB strains: safety, diagnosis and pathogenesisD43TW008264 · FIC · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KREISWIRTH, BARRY NEAL · 2009 to 2013
$741k
FIC NIH HHS D43 TW008264FIC NIH HHS D43TW008264NIAID NIH HHS R01 AI080737NIAID NIH HHS R01 AI80737
6 · The paper itself

Abstract

We investigated 18 HIV-negative patients with MDR-TB for M. tuberculosis (Mtb)- and PPD-specific CD4 T cell responses and followed them over 6 months of drug therapy. Twelve of these patients were sputum culture (SC) positive and six patients were SC negative upon enrollment. Our aim was to identify a subset of mycobacteria-specific CD4 T cells that would predict time to culture conversion. The total frequency of mycobacteria-specific CD4 T cells at baseline could not distinguish patients showing positive or negative SC. However, a greater proportion of late-differentiated (LD) Mtb- and PPD-specific memory CD4 T cells was found in SC positive patients than in those who were SC negative (p = 0.004 and p = 0.0012, respectively). Similarly, a higher co-expression of HLA-DR+ Ki67+ on Mtb- and PPD-specific CD4 T cells could also discriminate between sputum SC positive versus SC negative (p = 0.004 and p = 0.001, respectively). Receiver operating characteristic (ROC) analysis revealed that baseline levels of Ki67+ HLA-DR+ Mtb- and PPD-specific CD4 T cells were predictive of the time to sputum culture conversion, with area-under-the-curve of 0.8 (p = 0.027). Upon treatment, there was a significant decline of these Ki67+ HLA-DR+ T cell populations in the first 2 months, with a progressive increase in mycobacteria-specific polyfunctional IFNγ+ IL2+ TNFα+ CD4 T cells over 6 months. Thus, a subset of activated and proliferating mycobacterial-specific CD4 T cells (Ki67+ HLA-DR+) may provide a valuable marker in peripheral blood that predicts time to sputum culture conversion in TB patients at the start of treatment.

Indexed as

AdultCD4 Lymphocyte CountCD4-Positive T-LymphocytesCohort StudiesFemaleHIVHIV InfectionsHumansMaleMiddle AgedMycobacterium tuberculosisSputumTuberculosis

Identifiers

PMID25048802
PMCPMC4105550
OpenAlexW2080430019

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.