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用新型重组抗体阻断B7-H4通路可增强T细胞介导的抗肿瘤反应。

Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses.

作者信息

Dangaj Denarda, Scholler Nathalie

机构信息

Department of Oncology; Ludwig Cancer Research Center; University of Lausanne; Lausanne, Switzerland.

出版信息

Oncoimmunology. 2013 Aug 1;2(8):e25913. doi: 10.4161/onci.25913. Epub 2013 Jul 31.

Abstract

B7-H4 inhibits T-cell activation and is widely expressed by solid neoplasms. We have recently demonstrated that the expression of B7-H4 on the surface of malignant cells in vivo is inducible, and that novel anti-B7-H4 recombinant antibodies can reverse the inhibition of tumor-specific T cells. Thus, antibodies targeting the B7-H4 pathways may extend the survival of cancer patients by restoring T cell-mediated antitumor responses.

摘要

B7-H4抑制T细胞活化,在实体瘤中广泛表达。我们最近证明,体内恶性细胞表面B7-H4的表达是可诱导的,并且新型抗B7-H4重组抗体可逆转对肿瘤特异性T细胞的抑制作用。因此,靶向B7-H4通路的抗体可能通过恢复T细胞介导的抗肿瘤反应来延长癌症患者的生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f452/3782523/33a50bc7c9b2/onci-2-e25913-g1.jpg

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