Evidence map›Paper›PMID 38289184›Full record

ArticleTransfusion2024

RH genotypes and red cell alloimmunization rates in chronically transfused patients with sickle cell disease: A multisite study in the USA.

Narek Israelyan, Sunitha Vege, David F Friedman, Zhe Zhang, Stacey Uter, Ross M Fasano, Marianne Yee, Connie Piccone, Shannon Kelly, Jane S Hankins and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Transfusion, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 7 institutions in 1 country.

Narek IsraelyanDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-0974-6952
Sunitha VegeImmunohematology and Genomics Laboratory, New York Blood Center Enterprise, Long Island City, New York, USA.ORCID 0000-0003-0243-266X
David F FriedmanDivision of Hematology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0001-7422-6676
Zhe ZhangDepartment of Biomedical Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-4771-0697
Stacey UterDivision of Hematology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Ross M FasanoCenter for Transfusion Medicine and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0001-8692-4041
Marianne YeeAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.ORCID 0000-0001-6082-8385
Connie PicconePediatric Hematology, Carle Foundation Hospital, Carle Illinois College of Medicine, Urbana, Illinois, USA.
Shannon KellyDepartment of Pediatric Hematology and Oncology, UCSF Benioff Children's Hospital Oakland, Oakland, California, USA.
Jane S HankinsDepartment of Global Pediatric Medicine and Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0003-4439-7321
Yan ZhengDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0001-7254-7564
Connie M WesthoffImmunohematology and Genomics Laboratory, New York Blood Center Enterprise, Long Island City, New York, USA.ORCID 0000-0002-1929-4593
Stella T ChouDivision of Hematology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-4333-6965
Children's Hospital of Philadelphia · USEmory University · USNew York Blood Center · USSt. Jude Children's Research Hospital · USCarle Foundation Hospital · USHospital of the University of Pennsylvania · USUCSF Benioff Children's Hospital · US

Funding

Improving transfusion therapy for patients with sickle cell disease with pluripotent stem cell-derived red cellsU01HL134696 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHOU, STELLA T · 2016 to 2022
$8.3M
RH genotype matched red cell transfusions for patients with sickle cell diseaseR01HL147879 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHOU, STELLA T · 2019 to 2022
$3.4M
Kinetics of Red Blood Cell Clearance in Chronically Transfused Children with Sickle Cell DiseaseK23HL146904 · NHLBI · EMORY UNIVERSITY · PI YEE, MARIANNE ELAINE MCPHERSON · 2020 to 2024
$853k
Doris Duke Charitable FoundationNHLBI NIH HHS R01 HL147879NHLBI NIH HHS U01 HL134696
6 · The paper itself

Abstract

backgroundRed cell alloimmunization remains a challenge for individuals with sickle cell disease (SCD) and contributes to increased risk of hemolytic transfusion reactions and associated comorbidities. Despite prophylactic serological matching for ABO, Rh, and K, red cell alloimmunization persists, in part, due to a high frequency of variant RH alleles in patients with SCD and Black blood donors. STUDY DESIGN AND

methodsWe compared RH genotypes and rates of alloimmunization in 342 pediatric and young adult patients with SCD on chronic transfusion therapy exposed to >90,000 red cell units at five sites across the USA. Genotyping was performed with RHD and RHCE BeadChip arrays and targeted assays.

resultsPrevalence of overall and Rh-specific alloimmunization varied among institutions, ranging from 5% to 41% (p = .0035) and 5%-33% (p = .0002), respectively. RH genotyping demonstrated that 33% RHD and 57% RHCE alleles were variant in this cohort. Patients with RHCE alleles encoding partial e antigens had higher rates of anti-e identified than those encoding at least one conventional e antigen (p = .0007). There was no difference in anti-D, anti-C, or anti-E formation among patients with predicted partial or altered antigen expression compared to those with conventional antigens, suggesting that variant Rh on donor cells may also stimulate alloimmunization to these antigens. DISCUSSION: These results highlight variability in alloimmunization rates and suggest that a molecular approach to Rh antigen matching may be necessary for optimal prevention of alloimmunization given the high prevalence of variant RH alleles among both patients and Black donors.

Indexed as

Anemia, Hemolytic, AutoimmuneAnemia, Sickle CellBlood Group AntigensChildErythrocytesErythrocyte TransfusionGenotypeHumansIsoantibodiesRh-Hr Blood-Group SystemYoung AdultBlood Group AntigensIsoantibodiesRh-Hr Blood-Group Systemalloimmunizationblood group genomicsimmunohematology (RBC serology, blood groups)Rh blood group systemsickle cell disease

Identifiers

PMID38289184
PMCPMC10947898
OpenAlexW4391348914

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.