TCGF体外扩增可促进有限数量淋巴细胞的HLA分型和核型。

Diagnostic immunology Pub Date : 1985-01-01
J L Blank, J A Hank, J Molenda, W Borcherding, L Meisner, P M Sondel
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引用次数: 0

摘要

通常很难从骨髓移植受者获得足够数量的白细胞用于移植后的免疫监测和移植评估。我们已经开发了一种细胞培养扩增技术,可以在有限数量(少于10(7))淋巴细胞上进行HLA-A,B和DR分型以及核型。来自健康对照供体的淋巴细胞被体外同种异体激活,并通过t细胞生长因子(TCGF)培养进一步扩增。培养14天后,将这些细胞送去进行HLA-A、B和DR盲分型和核型。表面标记研究表明,90%的生长因子扩增t细胞为OK-la阳性。这些携带dr的体外扩增t细胞的HLA分型与新鲜未扩增淋巴细胞的HLA分型具有良好的相关性。扩增的t细胞核型显示正常的男性或女性细胞。当检测淋巴细胞计数非常低的儿童或成人患者时,这项技术可能特别有价值。
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HLA typing and karyotyping of limited numbers of lymphocytes is facilitated by in vitro expansion with TCGF.

It is often difficult to obtain sufficient quantities of leukocytes from bone marrow (BM) transplant recipients for post-transplant immunological monitoring and evaluation of engraftment. We have developed a cell culture expansion technique that allows HLA-A,B, and DR typing as well as karyotyping on limited numbers (less than 10(7)) of lymphocytes. Lymphocytes from healthy control donors were allo-activated in vitro and further expanded by culturing in T-cell growth factor (TCGF). After 14 days of culture, these cells were sent for blind HLA-A,B and DR typing and for karyotyping. Surface marker studies showed that 90% of the T-cells expanded in growth factor are OK-la positive. HLA typing with these DR-bearing in vitro expanded T-cells showed excellent correlation with HLA typing on fresh unexpanded lymphocytes. Karyotyping of expanded T-cells showed normal male or female cells as expected. This technique may be especially valuable when testing pediatric or adult patients with very low lymphocyte counts.

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