Suppr超能文献

R707,一种针对 CXC-趋化因子受体 7 的全人源抗体,可减轻异种急性移植物抗宿主病。

R707, a fully human antibody directed against CC-chemokine receptor 7, attenuates xenogeneic acute graft-versus-host disease.

机构信息

Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

MSM Protein Technologies, Waltham, Massachusetts.

出版信息

Am J Transplant. 2019 Jul;19(7):1941-1954. doi: 10.1111/ajt.15298. Epub 2019 Mar 13.

Abstract

Acute graft-versus-host disease (aGVHD) remains a barrier to the success of allogeneic hematopoietic stem cell transplantation (HSCT). Previously, we demonstrated that CC-chemokine receptor 7 (CCR7) is critical for aGVHD pathogenesis but dispensable for beneficial graft-versus-leukemia responses. As a result, we evaluated a fully human anti-CCR7-blocking antibody as a new approach to prevent aGVHD in preclinical models. Here we report that antibody R707 is able to block human CCR7 signaling and function in vitro in response to its 2 natural ligands. The antibody was less active against the murine orthologue, however, and failed to substantially limit aGVHD in a standard murine allogeneic HSCT model. Nevertheless, R707 significantly reduced xenogeneic aGVHD induced by human peripheral blood mononuclear cells (PBMCs). R707 limited CD4 and in particular CD8 T cell expansion during the period of antibody administration. These effects were transient, however, and T cell numbers recovered after antibody cessation. R707 did not substantially impair the antitumor potential of the PBMC inoculum as antibody-treated mice retained their capacity to reject a human acute myeloid leukemia cell line. Collectively, these data indicate for the first time that an antibody directed against CCR7 might represent a viable new approach for aGVHD prevention.

摘要

急性移植物抗宿主病(aGVHD)仍然是异基因造血干细胞移植(HSCT)成功的障碍。此前,我们证明了 C 型趋化因子受体 7(CCR7)对于 aGVHD 的发病机制至关重要,但对于有益的移植物抗白血病反应是可有可无的。因此,我们评估了一种完全人源抗 CCR7 阻断抗体作为预防临床前模型中 aGVHD 的新方法。在这里,我们报告抗体 R707 能够阻断人类 CCR7 信号传导,并在体外对其 2 种天然配体做出反应。然而,该抗体对鼠同源物的活性较低,并且未能在标准的小鼠同种异体 HSCT 模型中显著限制 aGVHD。尽管如此,R707 还是显著减少了由人外周血单核细胞(PBMC)引起的异种 aGVHD。R707 在抗体给药期间限制了 CD4,特别是 CD8 T 细胞的扩增。然而,这些效果是短暂的,并且在抗体停止后 T 细胞数量恢复。R707 并没有显著损害 PBMC 接种物的抗肿瘤潜力,因为抗体治疗的小鼠保留了排斥人急性髓系白血病细胞系的能力。总的来说,这些数据首次表明,针对 CCR7 的抗体可能代表预防 aGVHD 的一种可行的新方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验