Evidence map›Paper›PMID 26857467›Full record

ArticleLeukemia2016

Proteogenomic-based discovery of minor histocompatibility antigens with suitable features for immunotherapy of hematologic cancers.

D P Granados, A Rodenbrock, J-P Laverdure, C Côté, O Caron-Lizotte, C Carli, H Pearson, V Janelle, C Durette, E Bonneil and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 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

15 authors at 2 institutions in 1 country.

D P GranadosInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
A RodenbrockInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
J-P LaverdureInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
C CôtéInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
O Caron-LizotteInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
C CarliCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Hôpital Maisonneuve-Rosemont, Montréal, QC, Canada.
H PearsonInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
V JanelleCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Hôpital Maisonneuve-Rosemont, Montréal, QC, Canada.
C DuretteInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
E BonneilInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
D C RoyDepartment of Medicine, Université de Montréal, Montréal, QC, Canada.
J-S DelisleDepartment of Medicine, Université de Montréal, Montréal, QC, Canada.
S LemieuxInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
P ThibaultInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
C PerreaultInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.ORCID 0000-0001-9453-7383
Institute for Research in Immunology and Cancer · CAHôpital Maisonneuve-Rosemont · CA

Funding

CIHR
6 · The paper itself

Abstract

Pre-clinical studies have shown that injection of allogeneic T cells primed against a single minor histocompatibility antigen (MiHA) could cure hematologic cancers (HC) without causing any toxicity to the host. However, translation of this approach in humans has been hampered by the paucity of molecularly defined human MiHAs. Using a novel proteogenomic approach, we have analyzed cells from 13 volunteers and discovered a vast repertoire of MiHAs presented by the most common HLA haplotype in European Americans: HLA-A*02:01;B*44:03. Notably, out of >6000 MiHAs, we have identified a set of 39 MiHAs that share optimal features for immunotherapy of HCs. These 'optimal MiHAs' are coded by common alleles of genes that are preferentially expressed in hematopoietic cells. Bioinformatic modeling based on MiHA allelic frequencies showed that the 39 optimal MiHAs would enable MiHA-targeted immunotherapy of practically all HLA-A*02:01;B*44:03 patients. Further extension of this strategy to a few additional HLA haplotypes would allow treatment of almost all patients.

Indexed as

Cells, CulturedFemaleHaplotypesHematologic NeoplasmsHLA-A2 AntigenHLA-B44 AntigenHumansImmunotherapyMaleMinor Histocompatibility AntigensProteogenomicsHLA-A*02:01 antigenHLA-A2 AntigenHLA-B44 AntigenMinor Histocompatibility Antigens

Identifiers

PMID26857467
OpenAlexW2259492344

What OpenQuestion holds

Textmetadata
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.