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

机译:抗KIR抗体与激活KIR的结合综合分析。

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摘要

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:由于可用抗体的交叉反应性,特别是在活化和抑制同种型之间,杀手细胞免疫球蛋白样受体(KIR)表达的分析已经臭名昭着。我们对可用抗KIR抗体进行了全面的研究,该抗KIR抗体与激活KIRS(A-KIRS)有结合。使用用A-KIRS(Kir2DS1-S5和Kir3Ds1)稳定转染的细胞系,我们证实了记录的结合特异性。此外,我们表明克隆HPMA4和143211-预先假定为KIR2DS1 / L1和KIR2DL1,分别结合Kir2DS5和Kir2DS3(HPMA4),以及Kir2DS5(143211)。具有先前未记录的结合的其他抗体是JJC11.6(识别Kir2DS3)和5.133(识别除Kir2DS1和Kir2DS3外的所有A-KIR)。通过用可溶性KiR-Fc融合蛋白封闭新的Kir2DS5反应性,并通过逆转录酶-PCR分析对分选的原色天然杀伤细胞进行证实。总之,我们展示了抗KIR抗体的原始无证的结合特性。在分析KIR表达时,应考虑这些交叉反应。

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