靶向CD19的T细胞接合体治疗B细胞恶性肿瘤及其他肿瘤

Xiaoqiang Yan
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摘要

版权所有:©2022 Yan X.这是一篇根据知识共享署名许可条款发布的开放获取文章,该许可允许在任何媒体上不受限制地使用,分发和复制,前提是注明原作者和来源。在过去的十年中,在开发靶向CD19的T细胞双特异性抗体(BsAbs)治疗B细胞恶性肿瘤方面取得了巨大进展。参与双特异性分子的T细胞与T细胞上的CD3和靶细胞上的肿瘤相关抗原(TAA)结合,绕过MHC限制机制,将T细胞重定向到特定靶细胞,导致T细胞与靶细胞之间形成免疫突触,靶细胞裂解[1,2]。
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T cell engagers targeting CD19 to treat B cell malignancies, and beyond
Copyright: © 2022 Yan X. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. In the past decade, a tremendous progress has been made in developing T cell engaging bispecific antibodies (BsAbs) targeting CD19 to treat B cell malignancies. The T cell engaging bispecific molecule binds to CD3 on a T cell and a tumor-associated antigen (TAA) on a target cell and redirects the T cell to a specific target cell bypassing the MHC restriction mechanism, leading to the formation of immune synapse between the T cell and target cell and target cell lysis [1,2].
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