Evidence map›Paper›PMID 26756579›Full record

ArticlePloS one2016

PD-1 Expression and Cytokine Secretion Profiles of Mycobacterium tuberculosis-Specific CD4+ T-Cell Subsets; Potential Correlates of Containment in HIV-TB Co-Infection.

Katrina M Pollock, Damien J Montamat-Sicotte, Lisa Grass, Graham S Cooke, Moses S Kapembwa, Onn M Kon, Robert D Sampson, Graham P Taylor, Ajit Lalvani

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Pathogens (Basel, Switzerland) · 2025
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  14. Immune checkpoint blockade in infectious diseases.Nature reviews. Immunology · 2018
    Review
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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

9 authors at 3 institutions in 1 country.

Katrina M PollockTuberculosis Research Centre, Respiratory Infections Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Damien J Montamat-SicotteTuberculosis Research Centre, Respiratory Infections Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Lisa GrassTuberculosis Research Centre, Respiratory Infections Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Graham S CookeSection of Virology, Department of Medicine, Imperial College London, London, United Kingdom.
Moses S KapembwaDepartment of GU and HIV Medicine, The North West London Hospitals NHS Trust, London, United Kingdom.
Onn M KonTuberculosis Service, St Mary's Hospital, Imperial College Healthcare Trust, London, United Kingdom.
Robert D SampsonCentre for Respiratory Infection, Flow Cytometry Facility, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Graham P TaylorSection of Virology, Department of Medicine, Imperial College London, London, United Kingdom.
Ajit LalvaniTuberculosis Research Centre, Respiratory Infections Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Imperial College London · GBLondon North West Healthcare NHS Trust · GBSt Mary's Hospital · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

HIV co-infection is an important risk factor for tuberculosis (TB) providing a powerful model in which to dissect out defective, protective and dysfunctional Mycobacterium tuberculosis (MTB)-specific immune responses. To identify the changes induced by HIV co-infection we compared MTB-specific CD4+ responses in subjects with active TB and latent TB infection (LTBI), with and without HIV co-infection. CD4+ T-cell subsets producing interferon-gamma (IFN-γ), interleukin-2 (IL-2) and tumour necrosis factor-alpha (TNF-α) and expressing CD279 (PD-1) were measured using polychromatic flow-cytometry. HIV-TB co-infection was consistently and independently associated with a reduced frequency of CD4+ IFN-γ and IL-2-dual secreting T-cells and the proportion correlated inversely with HIV viral load (VL). The impact of HIV co-infection on this key MTB-specific T-cell subset identifies them as a potential correlate of mycobacterial immune containment. The percentage of MTB-specific IFN-γ-secreting T-cell subsets that expressed PD-1 was increased in active TB with HIV co-infection and correlated with VL. This identifies a novel correlate of dysregulated immunity to MTB, which may in part explain the paucity of inflammatory response in the face of mycobacterial dissemination that characterizes active TB with HIV co-infection.

Indexed as

Mycobacterium tuberculosisAdultAntigens, BacterialCD4-Positive T-LymphocytesCoinfectionFemaleGene Expression RegulationHIV InfectionsHumansImmunophenotypingInterferon-gammaInterleukin-2Latent TuberculosisLymphocyte SubsetsMaleMiddle AgedAntigens, BacterialInterferon-gammaInterleukin-2PDCD1 protein, humanProgrammed Cell Death 1 ReceptorTumor Necrosis Factor-alpha

Identifiers

PMID26756579
PMCPMC4710462
OpenAlexW2235293951

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.