Evidence map›Paper›PMID 25323824›Full record

ArticleBlood2014

HLA-C expression levels define permissible mismatches in hematopoietic cell transplantation.

Effie W Petersdorf, Theodore A Gooley, Mari Malkki, Andrea P Bacigalupo, Anne Cesbron, Ernette Du Toit, Gerhard Ehninger, Torstein Egeland, Gottfried F Fischer, Thibaut Gervais and 16 more

Abstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 4 pooled it
9.7field-weighted citation impact, top 1% 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

76 citing papers in PubMed, 4 syntheses or guidelines pooled it, 148 citations in OpenAlex.

  1. Guideline
  2. Pooled it
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  4. Pooled it
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  14. Mapping the dynamic genetic regulatory architecture ofmedRxiv : the preprint server for health sciences · 2023
    Article
  15. Review
  16. Article
  17. New strategies for mismatched unrelated donor (MMUD) hematopoietic cell transplant (HCT).Hematology. American Society of Hematology. Education Program · 2022
    Article
  18. Development of a humanized HLA-A30 transgenic mouse model.Animal models and experimental medicine · 2022
    Article
  19. Article
  20. Article

16 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 19 institutions in 14 countries.

Effie W PetersdorfDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA; Department of Medicine, University of Washington School of Medicine, Seattle, WA;
Theodore A GooleyDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA;
Mari MalkkiDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA;
Andrea P BacigalupoIstituto di Ricovero e Cura a Carattere Scientifico Azienda Ospedaliera Universitaria San Martino, Genova, Italy;
Anne CesbronLaboratoire d'Histocompatibilité et d'Immunogénétique, Etablissement Français du Sang Pays de Loire, Nantes, France;
Ernette Du ToitUniversity of Cape Town, Cape Town and South African Bone Marrow Registry, Cape Town, South Africa;
Gerhard EhningerUniversitätsklinikum Carl Gustav Carus, Dresden, Germany;
Torstein EgelandDepartment of Immunology, Oslo University Hospital, Oslo, Norway;
Gottfried F FischerDepartment for Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, Austria;
Thibaut GervaisCliniques St. Luc, Université Catholique de Louvain, Brussels, Belgium;
Michael D HaagensonCenter for International Blood and Marrow Transplant Research, Minneapolis, MN;
Mary M HorowitzCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Katharine HsuMemorial Sloan-Kettering Cancer Center, New York, NY;
Pavel JindraUniversity Hospital, Pilsen, Czech Republic;
Alejandro MadrigalAnthony Nolan Research Institute, The Royal Free Hampstead NHS Trust, London, United Kingdom;
Machteld OudshoornLeiden University Medical Center and Europdonor Foundation, Leiden, The Netherlands;
Olle RingdénDivision of Therapeutic Immunology, Center for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Huddinge, Sweden;
Marlis L SchroederCancer Care Manitoba, University of Manitoba, Winnipeg, MB, Canada;
Stephen R SpellmanCenter for International Blood and Marrow Transplant Research, Minneapolis, MN;
Jean-Marie TiercyNational Reference Laboratory for Histocompatibility, Department of Genetics and Laboratory Medicine, University Hospital Geneva, Geneva, Switzerland;
Andrea VelardiEuropean Group for Blood and Marrow Transplantation and University of Perugia, Perugia, Italy;
Campbell S WittDepartment of Clinical Immunology, Royal Perth Hospital, Perth, Australia;
Colm O'HuiginCancer and Inflammation Program, SAIC Frederick, Inc., Frederick National Laboratories for Cancer Research, Frederick, MD; and.
Richard AppsCancer and Inflammation Program, SAIC Frederick, Inc., Frederick National Laboratories for Cancer Research, Frederick, MD; and Ragon Institute of the Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA.
Mary CarringtonCancer and Inflammation Program, SAIC Frederick, Inc., Frederick National Laboratories for Cancer Research, Frederick, MD; and Ragon Institute of the Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA.
International Histocompatibility Working Group in Hematopoietic Cell Transplantation
Fred Hutch Cancer Center · USNational Marrow Donor Program · USRagon Institute of MGH, MIT and Harvard · USAnthony Nolan · GBCancerCare Manitoba · CACliniques Universitaires Saint-Luc · BEÉtablissement Français du Sang · FREuropdonor Foundation · NLKarolinska University Hospital · SEMedical College of Wisconsin · USMedical University of Vienna · ATMemorial Sloan Kettering Cancer Center · USOslo University Hospital · NOOspedale Policlinico San Martino · ITRoyal Perth Hospital · AUUniversity Hospital Carl Gustav Carus · DEUniversity Hospital of Geneva · CHUniversity of Cape Town · ZAUniversity of Perugia · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
PB vs. BMU01HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2001 to 2010
$63.3M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PAMER, ERIC G. · 1985 to 2023
$59.0M
LICI Microbiome and Genetics CoreZICBC011237 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI OHUIGIN, COLM · 2009 to 2025
$28.3M
Hematopopietic Stem Cell TransplantationU01AI069197 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Effie W Petersdorf · 2005 to 2026
$18.9M
Clinical Significance of MHC Haplotypes in Hematopoietic Cell TransplantationR01CA100019 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETERSDORF, EFFIE W · 2003 to 2025
$9.1M
CCR NIH HHS HHSN261200800001CNCI NIH HHS CA18029NCI NIH HHS CA76518NCI NIH HHS HHSN261200800001ENCI NIH HHS P01 CA018029NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA100019NCI NIH HHS U24 CA076518NCI NIH HHS U24-CA76518NHLBI NIH HHS 5U01HL069294NHLBI NIH HHS U01 HL069294NIAID NIH HHS AI069197NIAID NIH HHS U01 AI069197
6 · The paper itself

Abstract

Life-threatening graft-versus-host disease (GVHD) limits the use of HLA-C-mismatched unrelated donors in transplantation. Clinicians lack criteria for donor selection when HLA-C-mismatched donors are a patient's only option for cure. We examined the role for HLA-C expression levels to identify permissible HLA-C mismatches. The median fluorescence intensity, a proxy of HLA-C expression, was assigned to each HLA-C allotype in 1975 patients and their HLA-C-mismatched unrelated transplant donors. The association of outcome with the level of expression of patients' and donors' HLA-C allotypes was evaluated in multivariable models. Increasing expression level of the patient's mismatched HLA-C allotype was associated with increased risks of grades III to IV acute GVHD, nonrelapse mortality, and mortality. Increasing expression level among HLA-C mismatches with residue 116 or residue 77/80 mismatching was associated with increased nonrelapse mortality. The immunogenicity of HLA-C mismatches in unrelated donor transplantation is influenced by the expression level of the patient's mismatched HLA-C allotype. HLA-C expression levels provide new information on mismatches that should be avoided and extend understanding of HLA-C-mediated immune responses in human disease.

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAdultAgedAllelesFemaleGraft vs Host DiseaseHistocompatibilityHLA-C AntigensHumansLeukemiaMaleMiddle AgedMultivariate AnalysisMyelodysplastic SyndromesRetrospective StudiesHLA-C Antigens

Identifiers

PMID25323824
PMCPMC4271183
OpenAlexW2056892179

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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.