Evidence map›Paper›PMID 26315539›Full record

ArticleBMC immunology2015

Proportions of CD4+, CD8+ and B cell subsets are not affected by exposure to HIV or to Cotrimoxazole prophylaxis in Malawian HIV-uninfected but exposed children.

Herbert Longwe, Kamija S Phiri, Nyanyiwe M Mbeye, Thandile Gondwe, Kondwani C Jambo, Wilson L Mandala

Abstract read
In one paragraph

Article in BMC immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Immunomodulatory effect of propolisOpen veterinary journal · 2024
    Article
  2. Article
  3. Article
  4. Circulating β cell-specific CD8Clinical and experimental immunology · 2020
    Article
  5. Observational
  6. Article
  7. 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

6 authors.

Herbert LongweDepartment of Basic Medical Sciences, College of Medicine, University of Malawi, Blantyre, Malawi. herbert.longwe@gmail.com.
Kamija S PhiriTropical Haematology Research Unit, College of Medicine, University of Malawi, Blantyre, Malawi. kamijaphiri@gmail.com.
Nyanyiwe M MbeyeTropical Haematology Research Unit, College of Medicine, University of Malawi, Blantyre, Malawi.
Thandile GondweDepartment of Public Health, College of Medicine, University of Malawi, Blantyre, Malawi. thandile_nkosi@yahoo.com.
Kondwani C JamboMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi. K.Jambo@liverpool.ac.uk.
Wilson L MandalaDepartment of Basic Medical Sciences, College of Medicine, University of Malawi, Blantyre, Malawi. wmandala2002@gmail.com.

Funding

Wellcome Trust 087547/Z/08/Z
6 · The paper itself

Abstract

backgroundAs a result of successful PMTCT programs, children born from HIV-infected mothers are now effectively protected from contracting the infection. However, it is not well known whether in utero exposure to the virus and the subsequent exposure to Cotrimoxazole (CTX) prophylaxis affect the cell mediated immune system of the children. This observational prospective study was aimed at determining how CD4(+) T, CD8(+) T and B cell subsets varied in HIV-exposed but uninfected (HEU) children at different ages.

methodsWe recruited HEU and HIV-unexposed and uninfected (HUU) children from 6 months of age and followed them up until they were 18 months old. HEU children received daily CTX prophylaxis beginning at 6 weeks of age until when 12 months of age. Venous blood samples were collected 6 monthly and analysed for different subsets of CD8(+) T, B cells and totalCD4(+) T cells.

resultsAt 6 months of age, HEU children had a lower percentage of total CD4(+) T cells compared to HUU children and a lower proportion of naïve CD8(+) T cells but higher percentage of effector memory CD8(+) T cells compared to HUU children. HEU and HUU children had similar proportions of all B cell subsets at all ages.

conclusionsThe study showed that the subtle variations in CD4(+) and CD8(+) T cell subsets observed at 6 months do not last beyond 12 months of age, suggesting that HEU children have a robust cell-mediated immune system during first year of life.

trial registrationThis article report is not based on results of a controlled health-care intervention.

Indexed as

B-Lymphocyte SubsetsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesHIV-1HIV InfectionsHumansInfantLymphocyte CountMalawiTrimethoprim, Sulfamethoxazole Drug CombinationTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID26315539
PMCPMC4552147

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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.