Dirección de Innovación y Transferencia de Conocimiento, Benemérita Universidad Autónoma de Puebla, Puebla CP, México.
Laboratorio de Biología Celular, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Metepec, Puebla CP, México.
Expert Opin Drug Discov. 2022 Dec;17(12):1341-1355. doi: 10.1080/17460441.2022.2148652. Epub 2022 Nov 24.
LAG-3 is considered to be the third point of immunological control in relation to clinical trials that address cancer treatment, only behind PD-1 and CTLA-4, due to its role as a suppressor of the immune response and enhancer of differentiation of Treg cells.
The authors focus on emphasizing the strategy of development of LAG-3 inhibitors to develop anticancer therapeutics, especially from the perspective of designing new monoclonal and bispecific antibodies against LAG-3. This article also covers details of patents and clinical trials of LAG-3 inhibitors reported in the literature. In addition, we highlight as future research challenges the design and development of peptides and small molecules as inhibitors of LAG-3 function.
Three approaches have been used for the development of LAG-3 inhibitors, and they include inhibitory LAG-3 binding peptides and antagonist monoclonal and multispecific antibodies. These approaches include more than 100 clinical trials of 21 molecules that bind to LAG-3 and block its binding to MHC II. However, these approaches do not cover the design and development of peptides and small molecules that could inhibit the function of LAG-3, for which it is necessary to develop new alternatives that cover this gap.
在涉及癌症治疗的临床试验中,LAG-3 被认为是免疫控制的第三点,仅次于 PD-1 和 CTLA-4,因为它作为免疫反应的抑制剂和 Treg 细胞分化的增强剂发挥作用。
作者专注于强调开发 LAG-3 抑制剂的策略,以开发抗癌疗法,特别是从设计针对 LAG-3 的新型单克隆和双特异性抗体的角度。本文还涵盖了文献中报道的 LAG-3 抑制剂的专利和临床试验的详细信息。此外,我们强调设计和开发作为 LAG-3 功能抑制剂的肽和小分子作为未来的研究挑战。
已经使用了三种方法来开发 LAG-3 抑制剂,包括抑制 LAG-3 结合肽以及拮抗剂单克隆和多特异性抗体。这些方法包括超过 100 项针对 21 种与 LAG-3 结合并阻断其与 MHC II 结合的分子的临床试验。然而,这些方法并未涵盖可抑制 LAG-3 功能的肽和小分子的设计和开发,为此有必要开发新的替代品来填补这一空白。