首页> 美国卫生研究院文献>International Journal of Nanomedicine >Multifunctional Immunoliposomes Combining Catalase and PD-L1 Antibodies Overcome Tumor Hypoxia and Enhance Immunotherapeutic Effects Against Melanoma
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Multifunctional Immunoliposomes Combining Catalase and PD-L1 Antibodies Overcome Tumor Hypoxia and Enhance Immunotherapeutic Effects Against Melanoma

机译:结合过氧化氢酶和PD-L1抗体的多功能免疫脂质体可克服肿瘤缺氧并增强针对黑素瘤的免疫治疗效果

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摘要

Immune checkpoint blockades (ICBs) are a promising treatment for cancers such as melanoma by blocking important inhibitory pathways that enable tumor cells to evade immune attack. Programmed death ligand 1 monoclonal antibodies (aPDL1s) can be used as an ICB to significantly enhance the effectiveness of tumor immunotherapy by blocking the PD-1/PD-L1 inhibitory pathway. However, the effectiveness of aPDL1s may be limited by low selectivity in vivo and immunosuppressed tumor microenvironment including hypoxia.
机译:免疫检查站封锁(ICBs)通过阻止重要的抑制性途径(使肿瘤细胞能够逃避免疫攻击),成为治疗诸如黑色素瘤等癌症的有前途的疗法。程序性死亡配体1单克隆抗体(aPDL1s)可以用作ICB,通过阻断PD-1 / PD-L1抑制途径来显着增强肿瘤免疫疗法的有效性。但是,aPDL1s的有效性可能受到体内低选择性和免疫抑制的肿瘤微环境(包括缺氧)的限制。

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