贝伐单抗
细胞毒性T细胞
医学
肺癌
渗透(HVAC)
免疫系统
免疫疗法
癌症研究
PD-L1
CD8型
封锁
肿瘤科
免疫学
内科学
化疗
化学
材料科学
受体
体外
复合材料
生物化学
作者
Yanxia Liu,Tongmei Zhang,Lína Zhang,Cong Zhao,Zhiyun Zhang,Ziyu Wang,Meng Gu,Weiying Li,Baolan Li
出处
期刊:Immunotherapy
[Future Medicine]
日期:2022-05-16
卷期号:14 (9): 695-708
被引量:9
标识
DOI:10.2217/imt-2021-0196
摘要
Aim: VEGF/VEGFR inhibitors may help immune checkpoint inhibitors expand the population that will benefit from treatment. The authors investigated the efficacy of combined bevacizumab and PD-1 antibody. Materials & methods: C57BL/6J mice were injected subcutaneously with 1 × 106 Lewis lung carcinoma cells. The mice were intraperitoneally injected with 0.25 mg anti-PD-1 inhibitors and/or 15 mg/kg bevacizumab. Tumor tissues were harvested. The authors reported that a non-small cell lung cancer patient received 200 mg PD-1 antibody combined with 7.5 mg/kg bevacizumab as fourth-line treatment. Results: Bevacizumab combined with PD-1 antibody induced a strong and durable antitumor effect. Bevacizumab combined with PD-1 antibody improved abnormal tumor vessels and enhanced the cytotoxic function and infiltration of T lymphocytes. The patient's survival time was significantly prolonged. Conclusion: Bevacizumab combined with anti-PD-1 antibody induces a durable antitumor effect by increasing the infiltration and cytotoxic function of CD8+ T cells in lung cancer.
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