Abstract

Class I Human Leukocyte Antigen (HLA) evolutionary divergence (HED) is a metric which reflects immunopeptidome diversity and has been associated with immune checkpoint inhibitor responses in solid tumors. Its impact and interest in allogeneic hematopoietic stem cell transplantation (HCT) have not yet been thoroughly studied. This study analyzed the clinical and immune impact of class I and II HED in 492 acute myeloid leukemia (AML) recipients undergoing HCT. The overall cohort was divided into a training (n=338) and a testing (n=132) set. Univariate cox screening found a positive impact of a high class I HED and a negative impact of a high class II HED on both disease-free (DFS) and overall survival (OS). These results were combined in a unique marker, class I/class II HED ratio, and assessed in the testing cohort. The final multivariate cox model confirmed the positive impact of a high versus low class I/class II HED ratio on both DFS (Hazard Ratio (HR) 0.41 [95% CI 0.2-0.83]; p=0.01) and OS (HR 0.34 [0.19-0.59]; p<0.001), independently of HLA matching and other HCT parameters. No significant association was found between the ratio and graft-versus-host disease (GvHD) nor with neutrophil and platelet recovery. A high class I HED was associated with a tendency for an increase in NK, CD8 T-cell, and B cell recovery at 12 months. These results introduce HED as an original and independent prognosis marker reflecting immunopeptidome diversity and alloreactivity after HCT.

Highlights

  • Allogeneic hematopoietic stem cell transplantation (HCT) is the only curative therapy for several malignant hematological diseases and acute myeloid leukemia (AML)

  • Most patients were in complete remission (n=350, 75%) and received a single HCT (n=429, 91.3%)

  • As a higher class I Human Leukocyte Antigen (HLA) diversity is theoretically associated with a broader antigenic repertoire, we investigated whether the overall favorable prognosis associated with class I HLA evolutionary divergence (HED) translated into differences in the immune reconstitution profile after HCT

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Summary

Introduction

Allogeneic hematopoietic stem cell transplantation (HCT) is the only curative therapy for several malignant hematological diseases and acute myeloid leukemia (AML). The success of this therapy partly relies on the recognition of cancer cell antigens by alloreactive T cells, leading to the so-called graftversus-leukemia (GVL) effect [1]. When recognized antigens are present on normal tissue, this effect is counterbalanced by graftversus-host disease (GVHD), one of the main sources of morbidity and death after HCT [2]. In addition to HLA main alleles, recognition of minor-histocompatibility antigens which represent non-HLA self-peptides that can be recognized by allogeneic T-cells, is an additional source of alloreactivity [4, 5]. No other markers of T-cells alloreactivity exist to complement HLA matching

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