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人外周血细胞软琼脂培养中的抗体形成灶

Antibody-forming foci in soft-agar cultures of human peripheral blood cells.

作者信息

Villa M L, Clerici E

出版信息

J Immunol Methods. 1981;45(2):129-36. doi: 10.1016/0022-1759(81)90207-6.

Abstract

Human peripheral blood lymphocytes (PBL) from healthy blood donors were grown in soft-agar gel with sheep red blood cells (SRBC) and autologous plasma as a source of complement. After 4--6 days incubation, foci of proliferating hemolysin-forming cells, surrounded by a lytic area of 0.2--0.5 mm, were detected on the surface of the plates. The response was antigen specific, since new hemolytic areas were observed on pouring a fresh agar-SRBC mixture over the surface of primary cultures, but not on pouring a mixture containing rat or rabbit erythrocytes. The antibody response was significantly increased by addition to the cultures of polyethylene glycol 6000 (PEG), 8% final concentration. The mean number of foci was 8.4 +/- 2.2 in cultures without PEG and 36.2 +/- 2.3 in PEG+ cultures, both containing 9 X 10(6) lymphocytes. This finding is in agreement with observations on the frequency of precursors of antibody-forming cells among lymphoid populations. The explanation of the mechanism by which PEG 6000 modified the immune reactivity of PBL is not clear. However, we think, that this technique provides a reliable methodology for PBL antigenic stimulation in vitro.

摘要

将来自健康献血者的人外周血淋巴细胞(PBL)与绵羊红细胞(SRBC)及作为补体来源的自体血浆一起在软琼脂凝胶中培养。培养4 - 6天后,在平板表面检测到增殖性溶血素形成细胞的集落,其周围有0.2 - 0.5毫米的溶解区域。该反应具有抗原特异性,因为在原代培养物表面倒入新鲜的琼脂 - SRBC混合物时可观察到新的溶血区域,而倒入含有大鼠或兔红细胞的混合物时则未观察到。通过向培养物中添加终浓度为8%的聚乙二醇6000(PEG),抗体反应显著增强。在不含PEG的培养物中,集落的平均数量为8.4±2.2,在含PEG的培养物中为36.2±2.3,两种培养物均含有9×10⁶个淋巴细胞。这一发现与关于淋巴群体中抗体形成细胞前体频率的观察结果一致。PEG 6000改变PBL免疫反应性的机制尚不清楚。然而,我们认为,该技术为体外PBL抗原刺激提供了一种可靠的方法。

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