Hurley C K, Wade J A, Oudshoorn M, Middleton D, Kukuruga D, Navarrete C, Christiansen F, Hegland J, Ren E C, Andersen I, Cleaver S A, Brautbar C, Raffoux C
Department of Microbiology and Immunology, Georgetown University Medical School, Washington DC., USA.
Tissue Antigens. 1999 Apr;53(4 Pt 1):394-406. doi: 10.1034/j.1399-0039.1999.530414.x.
The World Marrow Donor Association has formulated guidelines for establishing the extent and quality of histocompatibility testing for unrelated donor registries, umbilical cord blood banks, and transplant centers involved in international exchange of hematopoietic stem cells for allogeneic transplantation. Registry and cord blood bank guidelines suggest that, at a minimum, initial HLA typing should be performed for three HLA loci, HLA-A, -B, and -DR, at low resolution/split antigen level. DNA-based testing methods should be utilized for HLA-DR typing. DNA-based testing for HLA-A and -B should replace serologic testing of new volunteer donors and cord blood units as robust protocols and reagents become available to the laboratories. Transplant center guidelines for typing of patient, family and to confirm the HLA types of potential unrelated donors should include, at the minimum, typing HLA-A, B, and -DR loci using primarily DNA-based testing methods at allele level resolution for DRB1 and low resolution/ split antigen level for HLA-A and -B. It is strongly recommended that the typing of a patient and the selected donor be performed using the same set of reagents, methodology, and interpretation criteria with fresh tissue samples to ensure HLA identity. Guidelines for laboratory accreditation, approaches to quality assurance and quality control for HLA testing, and suggestions for the format of the HLA database of donor types are also outlined.
世界骨髓捐献者协会已制定指南,用于确定参与异基因造血干细胞国际移植交换的无关供者登记处、脐带血库和移植中心的组织相容性检测范围及质量。登记处和脐带血库指南建议,至少应在低分辨率/分裂抗原水平对三个HLA位点(HLA-A、-B和-DR)进行初始HLA分型。HLA-DR分型应采用基于DNA的检测方法。随着实验室可获得可靠的方案和试剂,基于DNA的HLA-A和-B检测应取代对新志愿者供者和脐带血单位的血清学检测。移植中心对患者、家属进行分型以及确认潜在无关供者HLA类型的指南应至少包括,主要采用基于DNA的检测方法,在等位基因水平对DRB1进行分辨率检测,在低分辨率/分裂抗原水平对HLA-A和-B进行检测。强烈建议使用同一套试剂、方法和解读标准,对患者和选定供者的新鲜组织样本进行分型,以确保HLA匹配。同时还概述了实验室认可指南、HLA检测的质量保证和质量控制方法以及供者类型HLA数据库格式建议。