Donor-recipient incompatibility at CD31-codon 563 is a major risk factor for acute graft-versus-host disease after allogeneic bone marrow transplantation from a human leucocyte antigen-matched donor

被引:19
作者
Balduini, CL
Frassoni, F
Noris, P
Klersy, C
Iannone, AM
Bacigalupo, A
Giorgiani, G
Di Pumpo, M
Locatelli, F
机构
[1] Univ Pavia, IRCCS San Matteo, Dept Internal Med, I-27100 Pavia, Italy
[2] Hosp San Martino, Div Haematol, Genoa, Italy
[3] Univ Pavia, IRCCS San Matteo, Immunohaematol & Transfus Ctr, I-27100 Pavia, Italy
[4] Univ Pavia, IRCCS San Matteo, Dept Paediat, I-27100 Pavia, Italy
关键词
minor histocompatibility antigens; bone marrow transplantation; acute graft-versus-host disease; CD31; HA-1;
D O I
10.1046/j.1365-2141.2001.03035.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Disparities at minor histocompatibility antigens (mHA) are thought to be responsible for acute graft-versus-host disease (aGVHD) in patients receiving bone marrow transplantation (BMT) from a human leucocyte antigen (BLA)-matched donor. Although some mHA have been identified in humans, their role in aGVHD has not. Patients (n = 150) receiving a BMT from an HLA-matched donor were investigated for a correlation between aGVHD and donor/recipient incompatibility for seven polymorphisms previously proposed for mHA (HA-1, H-Y, CD31-codon 125, CD31-codon 563, HPA-1, HPA-3 and HPA-5). Only mismatch at CD31-codon 563 predicted grade II-IV aGVHD. The risk derived from CD31-codon 563 mismatch was the same as that derived from the use of bone marrow from an un elated donor. We suggest that donor/recipient compatibility at CD31-codon 563 should be added to HLA-typing for donor selection and/or adjustment of aGVHD prophylaxis.
引用
收藏
页码:951 / 953
页数:3
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