| Literature DB >> 33633734 |
Yanmin Zhao1,2,3, Fei Gao1,2,3, Yibo Wu1,2,3, Jimin Shi1,2,3, Yi Luo1,2,3, Yamin Tan1,2,3, Jian Yu1,2,3, Xiaoyu Lai1,2,3, Mingming Zhang1,2,3, Wei Zhang4, He Huang1,2,3.
Abstract
Hematopoietic stem cell transplantation (HSCT) is a curative therapy for patients with malignant hematologic diseases. Killer immunoglobin-like receptor (KIR) expressed by NK cells is closely associated with the transplant outcomes, and it has been widely explored and debated for a few decades. Recently published studies have revealed that inhibitory KIRs (iKIRs) are educated by their cognate human lymphocyte antigen (HLA) ligands, and that decreased iKIR-HLA pairs post-transplantation may indicate a reduced NK cell function and impaired control of the primary disease. However, this theory still needs to be validated by additional clinical studies. Here we conducted a retrospective analysis of 246 patients who received haploidentical (haplo)-HSCT at our treatment center between January 2015 and June 2018. Our data suggests that decreased iKIR-HLA C pair post-HSCT correlated with a significantly higher risk of relapse [hazard risk (HR) = 2.95, p = 0.019] and reduced overall survival (OS) (HR = 3.74, p = 0.001) and disease-free survival (DFS) (HR = 4.05, p = 0.0004) in patients with myeloid disease. In conclusion, decreased iKIR-HLA C pair should be avoided during anti-thymocyte globulin (ATG)-based haplo-HSCT, especially for patients with myeloid disease.Entities:
Keywords: KIR; hematopoietic stem cell transplantation; iKIR-HLA model; relapse; survival
Year: 2021 PMID: 33633734 PMCID: PMC7901980 DOI: 10.3389/fimmu.2020.614488
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561