Evidence map›Paper›PMID 24781195›Full record

ReviewImmunologic research2014

Clinical impact of H-Y alloimmunity.

Rakesh Popli, Bita Sahaf, Hideki Nakasone, Joyce Yeuk Yu Lee, David B Miklos

Open access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.4field-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

42 citing papers in PubMed, 66 citations in OpenAlex.

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  6. [The importance of sex/gender for graft and patient survival].Innere Medizin (Heidelberg, Germany) · 2025
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  10. Sex as a biological variable: Mechanistic insights and clinical relevance in solid organ transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Review
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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

5 authors at 1 institution in 1 country.

Rakesh PopliDivision of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Bita Sahaf
Hideki Nakasone
Joyce Yeuk Yu Lee
David B Miklos
Stanford University · US

Funding

TUMOR SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN BONE MARROW TRANSPLANTATIONP01CA049605 · NCI · STANFORD UNIVERSITY · PI David B. Miklos · 1989 to 2026
$73.3M
Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
Identification of Minor Histocompatibility AntigensK08HL069132 · NHLBI · STANFORD UNIVERSITY · PI MIKLOS, DAVID B. · 2002 to 2006
$647k
Microarray Analysis of H-Y Antibodies in Human TransplantationR21HL084318 · NHLBI · STANFORD UNIVERSITY · PI MIKLOS, DAVID B. · 2007 to 2008
$434k
NCI NIH HHS 1P030CA124435-01NCI NIH HHS P01 CA049605NCI NIH HHS P30 CA124435NHLBI NIH HHS K08 HL069132NHLBI NIH HHS R21 HL084318
6 · The paper itself

Abstract

H-Y antigens are a group of minor histocompatibility antigens encoded on the Y-chromosome with homologous H-X antigens on the X-chromosome. The disparate regions of the H-Y antigens are highly immunogenic and play an important role in understanding human alloimmunity. In this review, we investigate the history of H-Y antigen discovery along with their critical contributions in transplantation and pregnancy. In hematopoietic cell transplantation, male recipients with female donors who become seropositive for B-cell responses as H-Y antibodies following transplantation have increased rates of chronic graft-versus-host disease and decreased rates of relapse. Conversely, female patients who receive male kidney allografts are more likely than other gender combinations to develop H-Y antibodies and reject their allografts. Finally, in the setting of pregnancy, mothers who initially gave birth to boys are more likely to have subsequent pregnancy complications, including miscarriages, in association with H-Y antibody development. H-Y antigens continue to serve as a model for alloimmunity in new clinical scenarios. Our development of more sensitive antibody detection and next-generation DNA sequencing promises to further advance our understanding and better predict the clinical consequences of alloimmunity.

Indexed as

Abortion, HabitualAnimalsB-LymphocytesFemaleGraft RejectionGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHistocompatibilityHumansH-Y AntigenIsoantibodiesMaleOrgan TransplantationPregnancySex FactorsT-LymphocytesH-Y antibodyH-Y AntigenIsoantibodies

Identifiers

PMID24781195
PMCPMC4380433
OpenAlexW2095376778

What OpenQuestion holds

Textmetadata
LicenceTDM
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.