Evidence map›Paper›PMID 30364159›Full record

ReviewFrontiers in immunology2018

Determining the Quantitative Principles of T Cell Response to Antigenic Disparity in Stem Cell Transplantation.

Ali Salman, Vishal Koparde, Charles E Hall, Max Jameson-Lee, Catherine Roberts, Myrna Serrano, Badar AbdulRazzaq, Jeremy Meier, Caleb Kennedy, Masoud H Manjili and 8 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. HLA Haplotypes and Relapse After Hematopoietic Cell Transplantation.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  2. Review
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  7. Immune escape and immunotherapy of acute myeloid leukemia.The Journal of clinical investigation · 2020
    Review
  8. Article
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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

18 authors.

Ali SalmanBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Vishal KopardeVirginia Commonwealth University Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, VA, United States.
Charles E HallBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Max Jameson-LeeBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Catherine RobertsBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Myrna SerranoVirginia Commonwealth University Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, VA, United States.
Badar AbdulRazzaqBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Jeremy MeierBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.
Caleb KennedyCenter for International Blood and Marrow Transplant Research, Minneapolis, MN, United States.
Masoud H ManjiliDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, United States.
Stephen R SpellmanCenter for International Blood and Marrow Transplant Research, Minneapolis, MN, United States.
Dayanjan WijesingheSchool of Pharmacy, Virginia Commonwealth University, Richmond, VA, United States.
Shahrukh HashmiMayo Clinic, Rochester Minnesota and King Faisal Research Hospital, Riyadh, Saudi Arabia.
Greg BuckVirginia Commonwealth University Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, VA, United States.
Rehan QayyumDepartment of Internal Medicine, Virginia Commonwealth University, Richmond, VA, United States.
Michael NealeDepartment of Psychiatry & Statistical Genomics, Virginia Commonwealth University, Richmond, VA, United States.
Jason ReedDepartment of Physics, Virginia Commonwealth University, Richmond, VA, United States.
Amir A ToorBone Marrow Transplant, Virginia Commonwealth University Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, United States.

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
(PQD5) Mass Profiling Melanoma Responses to Improve Therapy Choices and PrognosisR01CA185189 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REED, JASON C, TEITELL, MICHAEL A · 2014 to 2017
$1.9M
NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA185189
6 · The paper itself

Abstract

Alloreactivity compromising clinical outcomes in stem cell transplantation is observed despite HLA matching of donors and recipients. This has its origin in the variation between the exomes of the two, which provides the basis for minor histocompatibility antigens (mHA). The mHA presented on the HLA class I and II molecules and the ensuing T cell response to these antigens results in graft vs. host disease. In this paper, results of a whole exome sequencing study are presented, with resulting alloreactive polymorphic peptides and their HLA class I and HLA class II (DRB1) binding affinity quantified. Large libraries of potentially alloreactive recipient peptides binding both sets of molecules were identified, with HLA-DRB1 generally presenting a greater number of peptides. These results are used to develop a quantitative framework to understand the immunobiology of transplantation. A tensor-based approach is used to derive the equations needed to determine the alloreactive donor T cell response from the mHA-HLA binding affinity and protein expression data. This approach may be used in future studies to simulate the magnitude of expected donor T cell response and determine the risk for alloreactive complications in HLA matched or mismatched hematopoietic cell and solid organ transplantation.

Indexed as

Stem Cell TransplantationAlgorithmsAntigen PresentationAntigen-Presenting CellsAntigensGraft vs Host DiseaseHistocompatibilityHLA AntigensHumansIsoantigensModels, TheoreticalPeptidesProtein BindingTissue DonorsT-LymphocytesAntigensHLA AntigensIsoantigensPeptidesantigen responseGVHDHLAmatricesstem cell transplantationT cell responsetensorsvectors and operators

Identifiers

PMID30364159
PMCPMC6193078

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.