新表面分子参与人类NK细胞活化和触发的裂解机制。

A Moretta, C Bottino, G Tripodi, M Vitale, D Pende, L Morelli, R Augugliaro, M Barbaresi, E Ciccone, R Millo
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引用次数: 0

摘要

用CD3- CD16+ NK克隆免疫小鼠后,分离到3种新的单克隆抗体7A6、PP35和A6/143。筛选程序是基于单克隆抗体在针对P815小鼠肥大细胞瘤细胞系的重定向杀伤试验中触发免疫克隆的细胞溶解活性的能力。7A6单抗与58 kDa表面分子反应,这些分子似乎属于与先前描述的nk亚群特异性GL183和EB6单抗定义的相同分子家族。然而,与这些单抗不同的是,7A6单抗与所有CD3- NK淋巴细胞反应(并激活),独立于它们的亚群分配(基于EB6、GL183和CD16的表达或缺乏表达)。PP35单抗与所有CD3- NK细胞、TCR γ / δ +细胞和一小部分TCR α / β + CD8+淋巴细胞上表达的70 kDa表面分子反应。PP35 MAb诱导了几乎所有NK细胞的活化,尽管克隆分析显示在不同克隆中引起的细胞溶解反应的大小存在定量差异。最后,A6/143单抗与所有人PBL表达的一个115 kDa分子反应。与7A6和PP35单抗类似,A6/143单抗可激活克隆NK细胞的所有亚群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel surface molecules involved in human NK cell activation and triggering of the lytic machinery.

Three new monoclonal antibodies (MAbs) termed 7A6, PP35 and A6/143 were isolated after mouse immunization with CD3- CD16+ NK clones. The screening procedure was based on the ability of MAbs to trigger cytolytic activity of the immunizing clones in a re-directed killing assay against the P815 murine mastocytoma cell line. The 7A6 MAb reacts with 58 kDa surface molecules that appear to belong to the same molecular family defined by the previously described NK-sub-set-specific GL183 and EB6 MAbs. However, unlike from these MAbs, the 7A6 MAb reacted with (and activated) all CD3- NK lymphocytes, independent of their sub-set assignment (based on the expression or lack of expression of EB6, GL183 and CD16). The PP35 MAb reacted with a 70 kDa surface molecule expressed on all CD3- NK cells, as well as on TCR gamma/delta + cells and on a small sub-set of TCR alpha/beta + CD8+ lymphocytes. The PP35 MAb induced activation of essentially all NK cells, although clonal analysis revealed quantitative differences in the magnitude of the cytolytic responses elicited in different clones. Finally, the A6/143 MAb reacted with a molecule of 115 kDa expressed by all human PBL. Similarly to 7A6 and PP35 MAbs, the A6/143 MAb activated all sub-sets of cloned NK cells.

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