Evidence map›Paper›PMID 25945792›Full record

ArticlePloS one2015

HLA Class II Antigens and Their Interactive Effect on Perinatal Mother-To-Child HIV-1 Transmission.

Ma Luo, Joanne Embree, Suzie Ramdahin, Thomas Bielawny, Tyler Laycock, Jeffrey Tuff, Darren Haber, Mariel Plummer, Francis A Plummer

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. CCR2 polymorphism and HIV: mutation in both mother and child is associated with higher transmission.International journal of biochemistry and molecular biology · 2019
    Article
  3. Review
  4. 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

9 authors at 1 institution in 1 country.

Ma LuoDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada; National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Joanne EmbreeDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Suzie RamdahinDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Thomas BielawnyNational Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Tyler LaycockDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Jeffrey TuffNational Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Darren HaberDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Mariel PlummerDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Francis A PlummerDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada; National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
University of Manitoba · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

HLA class II antigens are central in initiating antigen-specific CD4+ T cell responses to HIV-1. Specific alleles have been associated with differential responses to HIV-1 infection and disease among adults. This study aims to determine the influence of HLA class II genes and their interactive effect on mother-child perinatal transmission in a drug naïve, Mother-Child HIV transmission cohort established in Kenya, Africa in 1986. Our study showed that DRB concordance between mother and child increased risk of perinatal HIV transmission by three fold (P = 0.00035/Pc = 0.0014, OR: 3.09, 95%CI, 1.64-5.83). Whereas, DPA1, DPB1 and DQB1 concordance between mother and child had no significant influence on perinatal HIV transmission. In addition, stratified analysis showed that DRB1*15:03+ phenotype (mother or child) significantly increases the risk of perinatal HIV-1 transmission. Without DRB1*15:03, DRB1 discordance between mother and child provided 5 fold protection (P = 0.00008, OR: 0.186, 95%CI: 0.081-0.427). However, the protective effect of DRB discordance was diminished if either the mother or the child was DRB1*15:03+ phenotype (P = 0.49-0.98, OR: 0.7-0.99, 95%CI: 0.246-2.956). DRB3+ children were less likely to be infected perinatally (P = 0.0006, Pc = 0.014; OR:0.343, 95%CI:0.183-0.642). However, there is a 4 fold increase in risk of being infected at birth if DRB3+ children were born to DRB1*15:03+ mother compared to those with DRB1*15:03- mother. Our study showed that DRB concordance/discordance, DRB1*15:03, children's DRB3 phenotype and their interactions play an important role in perinatal HIV transmission. Identification of genetic factors associated with protection or increased risk in perinatal transmission will help develop alternative prevention and treatment methods in the event of increases in drug resistance of ARV.

Indexed as

Histocompatibility Antigens Class IIHIV-1Infectious Disease Transmission, VerticalAdolescentAdultCohort StudiesFemaleGene FrequencyGenes, MHC Class IIGenetic Predisposition to DiseaseGenotypeHIV InfectionsHLA-DRB1 ChainsHLA-DRB3 ChainsHumansInfantHistocompatibility Antigens Class IIHLA-DRB1*15 antigenHLA-DRB1 ChainsHLA-DRB3 Chains

Identifiers

PMID25945792
PMCPMC4422511
OpenAlexW2340936363

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.