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METHOD FOR MODULATION OF TUMOR ASSOCIATED MYELOID CELLS AND ENHANCING IMMUNE CHECKPOINT BLOCKADE

机译:调节肿瘤相关髓样细胞和增强免疫检查点封锁的方法

摘要

The present invention relates to methods for modulating immune response based on binding I-domain of CD11b on the tumor associated myeloid cells (TAMCs) in the tumor microenvironment. Particularly, binding to I-domain of CD11b with anti-CD11b-I-domain antibody triggers immunostimulatory environment that have one or more of the following effects in the tumor microenvironment: increase the inflammatory cytokine in the tumor microenvironment, decrease the population of IDO+ myeloid suppresser cells, up-regulate M1 marker over M2 marker on the tumor associated macrophage, increase M1:M2 tumor associated macrophage ratio, promote differentiation of dendritic cells (DC), nature killer dendritic cells (NKDC), and plasmacytoid dendritic cells (pDC), increase population of 4−1BB+PD−1+ neoantigen specific CD8 T cells. Converting cold (non-inflamed) to hot (inflamed) tumor by binding to I-domain of CD11b with anti-CD11b-I-domain antibody allows enhanced effectiveness of immune response modulator.
机译:本发明涉及基于CD11b在肿瘤微环境中的肿瘤相关髓样细胞(TAMC)上的结合I结构域来调节免疫应答的方法。特别地,用抗CD11b-I-结构域抗体与CD11b的I-结构域结合会触发免疫刺激环境,其在肿瘤微环境中具有以下一种或多种作用:增加肿瘤微环境中的炎性细胞因子,减少IDO +髓样细胞的数量抑制细胞,在肿瘤相关巨噬细胞上上调M1标记,使其超过M2标记,增加M1:M2肿瘤相关巨噬细胞比例,促进树突状细胞(DC),自然杀伤性树突状细胞(NKDC)和浆细胞样树突状细胞(pDC)的分化,增加4-1BB + PD-1 +新抗原特异性CD8 T细胞的数量。通过用抗CD11b-I域抗体与CD11b的I结构域结合,将冷(非发炎)肿瘤转变为热(发炎)肿瘤,可以增强免疫应答调节剂的有效性。

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