Evidence map›Paper›PMID 26476208›Full record

ArticleHuman immunology2016

Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease.

Zohreh Tatari-Calderone, Heather Gordish-Dressman, Ross Fasano, Michael Riggs, Catherine Fortier, Andrew D Campbell, Dominique Charron, Victor R Gordeuk, Naomi L C Luban, Stanislav Vukmanovic and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Human immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Zohreh Tatari-CalderoneSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Health System, 111 Michigan Avenue, N.W., Washington, DC, United States; Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States. Electronic address: ztataricalderone@sidra.org.
Heather Gordish-DressmanIntegrative Systems Biology, George Washington University School of Medicine and Health Sciences, Washington, DC, United States; Center for Genetic Medicine Research, Children's National Health System, Washington, DC, United States.
Ross FasanoDepartment of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States; Division of Hematology and Oncology, Children's National Health System, Washington, DC, United States; Division of Laboratory Medicine, Children's National Medical Center, Washington, DC, United States.
Michael RiggsDepartment of Biostatistics, Cato Research, Durham, NC, United States.
Catherine FortierLaboratoire Jean Dausset and LabEx Transplantex, INSERM UMRS 1160, Monacord and ESH, Hôpital Saint-Louis, Paris, France.
Andrew D CampbellDivision of Pediatric Hematology/Oncology, University of Michigan Health System, Ann Arbor, MI, United States.
Dominique CharronLaboratoire Jean Dausset and LabEx Transplantex, INSERM UMRS 1160, Monacord and ESH, Hôpital Saint-Louis, Paris, France.
Victor R GordeukSection of Hematology/Oncology, University of Illinois Comprehensive Sickle Cell Center, Chicago, IL, United States.
Naomi L C LubanDepartment of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States; Division of Hematology and Oncology, Children's National Health System, Washington, DC, United States; Division of Laboratory Medicine, Children's National Medical Center, Washington, DC, United States.
Stanislav VukmanovicSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Health System, 111 Michigan Avenue, N.W., Washington, DC, United States; Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Ryad TamouzaLaboratoire Jean Dausset and LabEx Transplantex, INSERM UMRS 1160, Monacord and ESH, Hôpital Saint-Louis, Paris, France. Electronic address: Tamouza.ryad@gmail.com.
George Washington University · USChildren's National · USInserm · FRHôpital Saint-Louis · FRMichigan Medicine · USUniversity of Illinois Chicago · US

Funding

Sickle Cell ScholarU54HL090503 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOGG, NEIL · 2008 to 2011
$3.0M
Washington Area Comprehensive Sickle Cell CenterU54HL090508 · NHLBI · HOWARD UNIVERSITY · PI GORDEUK, VICTOR R · 2008 to 2011
$1.9M
NHLBI NIH HHS U54 HL090503NHLBI NIH HHS U54 HL090508
6 · The paper itself

Abstract

backgroundAlloimmunization or the development of alloantibodies to Red Blood Cell (RBC) antigens is considered one of the major complications after RBC transfusions in patients with sickle cell disease (SCD) and can lead to both acute and delayed hemolytic reactions. It has been suggested that polymorphisms in HLA genes, may play a role in alloimmunization. We conducted a retrospective study analyzing the influence of HLA-DRB1 and DQB1 genetic diversity on RBC-alloimmunization. STUDY

designTwo-hundred four multi-transfused SCD patients with and without RBC-alloimmunization were typed at low/medium resolution by PCR-SSO, using IMGT-HLA Database. HLA-DRB1 and DQB1 allele frequencies were analyzed using logistic regression models, and global p-value was calculated using multiple logistic regression.

resultsWhile only trends towards associations between HLA-DR diversity and alloimmunization were observed, analysis of HLA-DQ showed that HLA-DQ2 (p=0.02), -DQ3 (p=0.02) and -DQ5 (p=0.01) alleles were significantly higher in non-alloimmunized patients, likely behaving as protective alleles. In addition, multiple logistic regression analysis showed both HLA-DQ2/6 (p=0.01) and HLA-DQ5/5 (p=0.03) combinations constitute additional predictor of protective status.

conclusionOur data suggest that particular HLA-DQ alleles influence the clinical course of RBC transfusion in patients with SCD, which could pave the way towards predictive strategies.

Indexed as

Erythrocyte TransfusionAdolescentAnemia, Sickle CellChildFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHLA-DQ beta-ChainsHLA-DRB1 ChainsHumansImmunizationIsoantibodiesIsoantigensMalePolymorphism, GeneticHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DRB1 ChainsIsoantibodiesIsoantigensAlloimmunizationHLA-DQB1HLA-DRB1Red Blood Cell transfusionSickle cell disease

Identifiers

PMID26476208
PMCPMC4747802
OpenAlexW1816832019

What OpenQuestion holds

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Registered trials

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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.