Evidence map›Paper›PMID 26417433›Full record

ArticleImmunity, inflammation and disease2015

Differences in antigen-specific CD4+ responses to opportunistic infections in HIV infection.

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

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
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 Department of Respiratory Medicine, National Heart and Lung Institute, Imperial College London London, UK.
Damien J Montamat-SicotteTuberculosis Research Centre Department of Respiratory Medicine, National Heart and Lung Institute, Imperial College London London, UK.
Graham S CookeSection of Infectious Diseases, Department of Medicine, Imperial College London London, UK.
Moses S KapembwaDepartment of GU and HIV Medicine, The North West London Hospitals NHS Trust London, UK.
Onn M KonTuberculosis Service, St Mary's Hospital, Imperial College Healthcare NHS Trust London, UK.
Lisa GrassTuberculosis Research Centre Department of Respiratory Medicine, National Heart and Lung Institute, Imperial College London London, UK.
Robert D SampsonCentre for Respiratory Infection, Flow Cytometry Facility, National Heart and Lung Institute, Imperial College London London, UK.
Graham P TaylorSection of Infectious Diseases, Department of Medicine, Imperial College London London, UK.
Ajit LalvaniTuberculosis Research Centre Department of Respiratory Medicine, National Heart and Lung Institute, Imperial College London London, UK.
Imperial College London · GBImperial College Healthcare NHS Trust · GBLondon North West Healthcare NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV-infected individuals with severe immunodeficiency are at risk of opportunistic infection (OI). Tuberculosis (TB) may occur without substantial immune suppression suggesting an early and sustained adverse impact of HIV on Mycobacterium tuberculosis (MTB)-specific cell mediated immunity (CMI). This prospective observational cohort study aimed to observe differences in OI-specific and MTB-specific CMI that might underlie this. Using polychromatic flow cytometry, we compared CD4+ responses to MTB, cytomegalovirus (CMV), Epstein-Barr virus (EBV) and Candida albicans in individuals with and without HIV infection. MTB-specific CD4+ T-cells were more polyfunctional than virus specific (CMV/EBV) CD4+ T-cells which predominantly secreted IFN-gamma (IFN-γ) only. There was a reduced frequency of IFN-γ and IL-2 (IL-2)-dual-MTB-specific cells in HIV-infected individuals, which was not apparent for the other pathogens. MTB-specific cells were less differentiated especially compared with CMV-specific cells. CD127 expression was relatively less frequent on MTB-specific cells in HIV co-infection. MTB-specific CD4+ T-cells PD-1 expression was infrequent in contrast to EBV-specific CD4+ T-cells. The variation in the inherent quality of these CD4+ T-cell responses and impact of HIV co-infection may contribute to the timing of co-infectious diseases in HIV infection.

Indexed as

Candida albicanscytomegalovirusEpstein-Barr virusHIVMycobacterium tuberculosis

Identifiers

PMID26417433
PMCPMC4578516
OpenAlexW1502231050

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.