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A comprehensive analysis of the binding of anti-KIR antibodies to activating KIRs.

机译:对抗KIR抗体与活化KIR结合的全面分析。

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Analysis of killer cell immunoglobulin-like receptor (KIR) expression has been notoriously difficult because of the cross-reactivity of available antibodies, in particular between activating and inhibitory isoforms. We undertook a comprehensive study of available anti-KIR antibodies binding to activating KIRs (a-KIRs). Using cell lines stably transfected with a-KIRs (KIR2DS1-S5 and KIR3DS1), we confirmed documented binding specificities. In addition, we show that clones HPMA4 and 143211-previously assumed to be specific for KIR2DS1/L1 and KIR2DL1, respectively-bind KIR2DS5 and KIR2DS3 (HPMA4), and KIR2DS5 (143211). Other antibodies with previously undocumented binding were JJC11.6 (recognizing KIR2DS3) and 5.133 (recognizing all a-KIRs except KIR2DS1 and KIR2DS3). The novel KIR2DS5 reactivities were confirmed by blocking with soluble KIR-Fc fusion proteins, and by reverse transcriptase-PCR analysis of sorted primary natural killer cells. In conclusion, we show formerly undocumented binding properties of anti-KIR antibodies. These cross-reactivities should be taken into account when analyzing KIR expression.
机译:众所周知,杀伤细胞免疫球蛋白样受体(KIR)表达的分析非常困难,因为可用抗体之间存在交叉反应,特别是在激活和抑制同工型之间。我们对与激活KIR(a-KIR)结合的可用抗KIR抗体进行了全面研究。使用稳定转染了a-KIR的细胞系(KIR2DS1-S5和KIR3DS1),我们证实了已记录的结合特异性。此外,我们显示以前假定克隆HPMA4和143211特定于KIR2DS1 / L1和KIR2DL1,分别将KIR2DS5和KIR2DS3(HPMA4)和KIR2DS5(143211)绑定。具有先前未记录的结合的其他抗体是JJC11.6(可识别KIR2DS3)和5.133(可识别除KIR2DS1和KIR2DS3以外的所有a-KIR)。通过用可溶性KIR-Fc融合蛋白阻断,以及通过对分类的初级自然杀伤细胞进行逆转录酶-PCR分析,证实了新的KIR2DS5反应性。总之,我们显示了以前未记录的抗KIR抗体的结合特性。分析KIR表达时,应考虑这些交叉反应性。

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