Evidence map›Paper›PMID 28618268›Full record

Trial reportCell host & microbe2017

Antigen Availability Shapes T Cell Differentiation and Function during Tuberculosis.

Albanus O Moguche, Munyaradzi Musvosvi, Adam Penn-Nicholson, Courtney R Plumlee, Helen Mearns, Hennie Geldenhuys, Erica Smit, Deborah Abrahams, Virginie Rozot, One Dintwe and 17 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Cell host & microbe, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

131 citing papers in PubMed, 181 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Antigen-experienced airway CD8Science advances · 2026
    Article
  5. Article
  6. Tuberculosis treatment and cytotoxic immune signatures: a longitudinal study.Journal of clinical tuberculosis and other mycobacterial diseases · 2026
    Article
  7. Article
  8. Review
  9. HowVaccines · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Observational

71 more citing papers are in PubMed but not listed here.

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

27 authors at 7 institutions in 3 countries.

Albanus O MogucheCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Munyaradzi MusvosviSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Adam Penn-NicholsonSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Courtney R PlumleeCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA.
Helen MearnsSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Hennie GeldenhuysSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Erica SmitSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Deborah AbrahamsSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Virginie RozotSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
One DintweSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Søren T HoffStatens Serum Institut (SSI), 2300 Copenhagen, Denmark.
Ingrid KromannStatens Serum Institut (SSI), 2300 Copenhagen, Denmark.
Morten RuhwaldStatens Serum Institut (SSI), 2300 Copenhagen, Denmark.
Peter BangStatens Serum Institut (SSI), 2300 Copenhagen, Denmark.
Ryan P LarsonCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA.
Shahin ShafianiCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA.
Shuyi MaCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA.
David R ShermanCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA.
Alessandro SetteDepartment of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla 92037, USA.
Cecilia S Lindestam ArlehamnDepartment of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla 92037, USA.
Denise M McKinneyDepartment of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla 92037, USA.
Holden MaeckerInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA 94305, USA.
Willem A HanekomSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Mark HatherillSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa.
Peter AndersenStatens Serum Institut (SSI), 2300 Copenhagen, Denmark.
Thomas J ScribaSouth African Tuberculosis Vaccine Initiative (SATVI), University of Cape Town, Cape Town 7925, South Africa; Institute of Infectious Disease and Molecular Medicine (IDM), University of Cape Town, Cape Town 7925, South Africa; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town 7925, South Africa. Electronic address: thomas.scriba@uct.ac.za.
Kevin B UrdahlCenter for Infectious Disease Research (CIDR), Seattle, WA 98109, USA; Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address: kevin.urdahl@cidresearch.org.
South African Tuberculosis Vaccine Initiative · ZACenter for Infectious Disease Research · USStatens Serum Institut · DKUniversity of Cape Town · ZALa Jolla Institute for Immunology · USInfectious Disease Research Institute · USStanford University · US

Funding

Technology CoreU19AI106761 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI SHERMAN, DAVID R, ZAK, DANIEL E · 2013 to 2017
$18.9M
Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
T regulatory cells and immunity in tuberculosisR01AI076327 · NIAID · UNIVERSITY OF WASHINGTON · PI URDAHL, KEVIN B · 2009 to 2018
$4.5M
Host determinants of protection against tuberculosis in adolescentsR01AI087915 · NIAID · UNIVERSITY OF CAPE TOWN · PI SCRIBA, THOMAS JENS · 2011 to 2015
$3.3M
BASIC IMMUNOLOGYT32CA009537 · NCI · UNIVERSITY OF WASHINGTON · PI GOVERMAN, JOAN M · 1986 to 2012
$3.1M
FACSAria II Cell SorterS10RR027366 · NCRR · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2011 to 2011
$514k
NCI NIH HHS T32 CA009537NIAID NIH HHS HHSN272201300006CNIAID NIH HHS R01 AI076327NIAID NIH HHS R01 AI087915NIAID NIH HHS T32 AI007509NIAID NIH HHS U19 AI106761
6 · The paper itself

Abstract

CD4 T cells are critical for protective immunity against Mycobacterium tuberculosis (Mtb), the cause of tuberculosis (TB). Yet to date, TB vaccine candidates that boost antigen-specific CD4 T cells have conferred little or no protection. Here we examined CD4 T cell responses to two leading TB vaccine antigens, ESAT-6 and Ag85B, in Mtb-infected mice and in vaccinated humans with and without underlying Mtb infection. In both species, Mtb infection drove ESAT-6-specific T cells to be more differentiated than Ag85B-specific T cells. The ability of each T cell population to control Mtb in the lungs of mice was restricted for opposite reasons: Ag85B-specific T cells were limited by reduced antigen expression during persistent infection, whereas ESAT-6-specific T cells became functionally exhausted due to chronic antigenic stimulation. Our findings suggest that different vaccination strategies will be required to optimize protection mediated by T cells recognizing antigens expressed at distinct stages of Mtb infection.

Indexed as

AcyltransferasesAdolescentAnimalsAntigens, BacterialAntigens, Differentiation, T-LymphocyteBacterial ProteinsCD4-Positive T-LymphocytesCell DifferentiationCytokinesFemaleHumansInterferon-gammaLungLymphocyte ActivationMaleMiceAcyltransferasesantigen 85B, Mycobacterium tuberculosisAntigens, BacterialAntigens, Differentiation, T-LymphocyteBacterial ProteinsCytokinesESAT-6 protein, Mycobacterium tuberculosisIFNG protein, mouseInterferon-gammaRNA, MessengerTuberculosis VaccinesAg85BantigensCD4 T celleffector T cellESAT-6memory T cellMycobacterium tuberculosisT cell differentiationvaccines

Identifiers

PMID28618268
PMCPMC5533182
OpenAlexW2625798606

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.