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Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility.

Authors :
Talwar JV
Laub D
Pagadala MS
Castro A
Lewis M
Luebeck GE
Gorman BR
Pan C
Dong FN
Markianos K
Teerlink CC
Lynch J
Hauger R
Pyarajan S
Tsao PS
Morris GP
Salem RM
Thompson WK
Curtius K
Zanetti M
Carter H
Source :
American journal of human genetics [Am J Hum Genet] 2023 Jul 06; Vol. 110 (7), pp. 1138-1161. Date of Electronic Publication: 2023 Jun 19.
Publication Year :
2023

Abstract

Autoimmunity and cancer represent two different aspects of immune dysfunction. Autoimmunity is characterized by breakdowns in immune self-tolerance, while impaired immune surveillance can allow for tumorigenesis. The class I major histocompatibility complex (MHC-I), which displays derivatives of the cellular peptidome for immune surveillance by CD8 <superscript>+</superscript> T cells, serves as a common genetic link between these conditions. As melanoma-specific CD8 <superscript>+</superscript> T cells have been shown to target melanocyte-specific peptide antigens more often than melanoma-specific antigens, we investigated whether vitiligo- and psoriasis-predisposing MHC-I alleles conferred a melanoma-protective effect. In individuals with cutaneous melanoma from both The Cancer Genome Atlas (n = 451) and an independent validation set (n = 586), MHC-I autoimmune-allele carrier status was significantly associated with a later age of melanoma diagnosis. Furthermore, MHC-I autoimmune-allele carriers were significantly associated with decreased risk of developing melanoma in the Million Veteran Program (OR = 0.962, p = 0.024). Existing melanoma polygenic risk scores (PRSs) did not predict autoimmune-allele carrier status, suggesting these alleles provide orthogonal risk-relevant information. Mechanisms of autoimmune protection were neither associated with improved melanoma-driver mutation association nor improved gene-level conserved antigen presentation relative to common alleles. However, autoimmune alleles showed higher affinity relative to common alleles for particular windows of melanocyte-conserved antigens and loss of heterozygosity of autoimmune alleles caused the greatest reduction in presentation for several conserved antigens across individuals with loss of HLA alleles. Overall, this study presents evidence that MHC-I autoimmune-risk alleles modulate melanoma risk unaccounted for by current PRSs.<br />Competing Interests: Declaration of interests G.P.M. receives research support from Thermo Fisher, CareDx, and PIRCHE. M.Z. is a board member of Invectys Inc.<br /> (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
110
Issue :
7
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
37339630
Full Text :
https://doi.org/10.1016/j.ajhg.2023.05.013