血管生成抑制剂在免疫应答中的作用

J. Nemunaitis, Monika Devanaboyina, N. Ngo, Rakan Albalawy, L. Filipiak, H. Staats, L. Stanbery, Danae M. Hamouda
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引用次数: 2

摘要

血管生成在肿瘤生长中起着重要作用。建立的血管系统为肿瘤细胞的维持提供了营养和其他必要的生存因素。此外,具有降低免疫活性导致癌症抑制和增加抗癌反应能力的免疫因子通过VEGF刺激的血管生成提供。然而,VEGF提供的不仅仅是血管生成刺激;它本身是一种具有活性的生长因子,也可以减少对参与抗癌机制的树突状细胞(dc)和T细胞的刺激。因此,抑制VEGF提供了免疫治疗的优势。这一点在IFN- β ELISPOT试验中得到了很好的证明,在暴露于骨髓瘤裂解物负载的树突细胞后,测量了T淋巴细胞对多发性骨髓瘤细胞的抗肿瘤反应。阻断VEGF可增强T淋巴细胞抗癌免疫反应。通过刺激免疫系统,血管生成抑制剂可以与免疫疗法、化疗和/或放射疗法联合使用。最近在晚期肾细胞癌、非小细胞肺癌(NSCLC)和肝细胞癌的临床试验证明,血管生成抑制和特别是免疫检查点阻断治疗的免疫增强作用改善了结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune Response Role of Angiogenesis Inhibitors
Angiogenesis plays an important role in tumor growth. Established vasculature provides a supply of nutrients and other necessary survival factors for tumor cell maintenance. In addition, immune factors with capacity to both decrease immune activity leading to cancer suppression and to increase anticancer response are provided via VEGF stimulated angiogenesis. However, VEGF provides more than angiogenesis stimulation; it is itself a growth factor with activity to also decrease the stimulation of dendritic cells (DCs) and T cells involved in anti-cancer mechanisms. As such inhibition of VEGF provides immune therapeutic advantage. This was well demonstrated by IFN-ɣ ELISPOT assay in which T lymphocytes antitumor response was measured against multiple myeloma cells following exposure to myeloma lysate-loaded dendric cells. Block of VEGF lead to enhanced T lymphocyte anticancer immune response. Through stimulation of the immune system angiogenesis inhibitors can work in conjunction with immunotherapy, chemotherapy and/or radiation therapy. Recent clinical trials in advanced renal cell carcinoma, non-small cell lung cancer (NSCLC), and hepatocellular carcinoma have evidenced improved outcomes due to an immune enhancing effect with angiogenesis inhibition and in particular immune checkpoint blockade treatment.
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