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使用免疫磁珠法从血液中阳性选择细胞进行HLA I类和II类分型——一种快速可靠的技术。

HLA class I and II typing using cells positively selected from blood by immunomagnetic isolation--a fast and reliable technique.

作者信息

Vartdal F, Gaudernack G, Funderud S, Bratlie A, Lea T, Ugelstad J, Thorsby E

出版信息

Tissue Antigens. 1986 Nov;28(5):301-12. doi: 10.1111/j.1399-0039.1986.tb00500.x.

DOI:10.1111/j.1399-0039.1986.tb00500.x
PMID:3469787
Abstract

This paper describes a new cell isolation and HLA typing technique, which permits cell separation and HLA class I or class II typing to be performed in 70 min. Magnetic monodisperse microspheres (Dynabeads TM) were coated with monoclonal antibodies (MAbs) specific for the CD8 T cell antigen or for HLA class II monomorphic epitopes. They could then be used to obtain HLA class I or class II positive cells directly from ACD blood in approximately 15 min by the use of magnetic separation. The cells (attached to the microspheres) were subsequently used in microcytotoxic HLA typing (total incubation time of 55 min) using acridin orange/ethidiumbromide to stain viable (yellow) and dead (red) cells. It was found that this immunomagnetic (IM) HLA typing technique was specific, has a sensitivity superior to that observed for conventional microcytotoxicity assays and gave low background staining. IM HLA-ABC typing of 50 healthy donors and 10 patients and IM HLA-DR typing of 25 healthy donors and 30 patients gave results corresponding well with that obtained independently by conventional HLA typing (concordancy rates 92-100%). Furthermore, the IM HLA typing technique permitted reliable HLA class II typing of blood cells from six patients where conventional HLA class II typing was impossible. The IM HLA typing technique also enables HLA class I and II typing to be quickly and reliably performed on cells from ACD blood of cadaveric donors.

摘要

本文描述了一种新的细胞分离和HLA分型技术,该技术可在70分钟内完成细胞分离以及HLA I类或II类分型。将磁性单分散微球(Dynabeads TM)用针对CD8 T细胞抗原或HLA II类单态性表位的单克隆抗体(MAbs)包被。然后通过磁分离,可在约15分钟内直接从ACD血中获得HLA I类或II类阳性细胞。随后,将附着在微球上的细胞用于微细胞毒性HLA分型(总孵育时间为55分钟),使用吖啶橙/溴化乙锭对活细胞(黄色)和死细胞(红色)进行染色。结果发现,这种免疫磁珠(IM)HLA分型技术具有特异性,灵敏度优于传统的微细胞毒性检测,且背景染色较低。对50名健康供者和10名患者进行IM HLA-ABC分型,以及对25名健康供者和30名患者进行IM HLA-DR分型,所得结果与通过传统HLA分型独立获得的结果高度吻合(一致性率为92%-100%)。此外,对于6名无法进行传统HLA II类分型的患者,IM HLA分型技术能够对其血细胞进行可靠的HLA II类分型。IM HLA分型技术还能够快速、可靠地对尸体供者ACD血中的细胞进行HLA I类和II类分型。

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