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Qualitative, rather than quantitative, differences between HLA‐DQ alleles affect HLA‐DQ immunogenicity in organ transplantation.

Authors :
Maguire, Chelsea
Crivello, Pietro
Fleischhauer, Katharina
Isaacson, Dylan
Casillas, Aurora
Kramer, Cynthia S. M.
Copley, Hannah C.
Heidt, Sebastiaan
Kosmoliaptsis, Vasilis
Meneghini, Maria
Gmeiner, Michael
Schold, Jesse
Louzoun, Yoram
Tambur, Anat R.
Source :
HLA: Immune Response Genetics. Apr2024, Vol. 103 Issue 4, p1-20. 20p.
Publication Year :
2024

Abstract

Prolonging the lifespan of transplanted organs is critical to combat the shortage of this life‐saving resource. Chronic rejection, with irreversible demise of the allograft, is often caused by the development of donor‐specific HLA antibodies. Currently, enumerating molecular (amino acid) mismatches between recipient and donor is promoted to identify patients at higher risk of developing HLA antibodies, for use in organ allocation, and immunosuppression‐minimization strategies. We have counseled against the incorporation of such approaches into clinical use and hypothesized that not all molecular mismatches equally contribute to generation of donor‐specific immune responses. Herein, we document statistical shortcomings in previous study design: for example, use of individuals who lack the ability to generate donor‐specific‐antibodies (HLA identical) as part of the negative cohort. We provide experimental evidence, using CRISPR‐Cas9‐edited cells, to rebut the claim that the HLAMatchmaker eplets represent "functional epitopes." We further used unique sub‐cohorts of patients, those receiving an allograft with two HLA‐DQ mismatches yet developing antibodies only to one mismatch (2MM1DSA), to interrogate differential immunogenicity. Our results demonstrate that mismatches of DQα05‐heterodimers exhibit the highest immunogenicity. Additionally, we demonstrate that the DQα chain critically contributes to the overall qualities of DQ molecules. Lastly, our data proposes that an augmented risk to develop donor‐specific HLA‐DQ antibodies is dependent on qualitative (evolutionary and functional) divergence between recipient and donor, rather than the mere number of molecular mismatches. Overall, we propose an immunological mechanistic rationale to explain differential HLA‐DQ immunogenicity, with potential ramifications for other pathological processes such as autoimmunity and infections. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20592302
Volume :
103
Issue :
4
Database :
Academic Search Index
Journal :
HLA: Immune Response Genetics
Publication Type :
Academic Journal
Accession number :
176869552
Full Text :
https://doi.org/10.1111/tan.15455