Rapid and efficient generation of T-cell receptor-like antibodies using chip-based single-cell analysis.
Rapid and efficient generation of T-cell receptor-like antibodies using chip-based single-cell analysis.
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使用基于芯片的单细胞分析快速有效地生成 T 细胞受体样抗体。
DOI:
10.1002/eji.202049083
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Kishi H
中科院分区:
文献类型:
--
作者:
Ozawa T;Kobayashi E;Hamana H;Nakamura T;Lyu F;Hayashi A;Muraguchi A;Kishi H
Non-TCR-like antibodies cannot bind biotinylated target p/MHC and signals are absent or weak (top, right), whereas the TCR-like antibody binds only to biotinylated target p/MHC, generating obvious signals (bottom, right). Keywords: ISAAC; TCR; TCR-like antibody; tumor immunotherapy EN ISAAC TCR TCR-like antibody tumor immunotherapy 1850 1853 4 07/05/21 20210701 NES 210701 Generation of TCR-like monoclonal antibodies using conventional methods is markedly laborious and inefficient. In contrast, with the blockade, eight (90%) of nine cells with FI >= 130 produced TCR-like antibodies, and none of the nine cells with FI < 130 produced TCR-like antibodies (Fig. This study demonstrates that ISAAC with blocking procedure is useful to generate TCR-like antibodies recognizing the EBV-derived BRLF1 peptide presented on HLA-A24 molecule (BRLF1p/HLA-A24).[Extracted from the article]Copyright of European Journal of Immunology is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. Copyright applies to all Abstracts.