Salmon Hélène, Idoyaga Juliana, Rahman Adeeb, Leboeuf Marylène, Remark Romain, Jordan Stefan, Casanova-Acebes Maria, Khudoynazarova Makhzuna, Agudo Judith, Tung Navpreet, Chakarov Svetoslav, Rivera Christina, Hogstad Brandon, Bosenberg Marcus, Hashimoto Daigo, Gnjatic Sacha, Bhardwaj Nina, Palucka Anna Karolina, Brown Brian D, Brody Joshua, Ginhoux Florent, Merad Miriam
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Immunity. 2016 Apr 19;44(4):924-38. doi: 10.1016/j.immuni.2016.03.012.
Large numbers of melanoma lesions develop resistance to targeted inhibition of mutant BRAF or fail to respond to checkpoint blockade. We explored whether modulation of intratumoral antigen-presenting cells (APCs) could increase responses to these therapies. Using mouse melanoma models, we found that CD103(+) dendritic cells (DCs) were the only APCs transporting intact antigens to the lymph nodes and priming tumor-specific CD8(+) T cells. CD103(+) DCs were required to promote anti-tumoral effects upon blockade of the checkpoint ligand PD-L1; however, PD-L1 inhibition only led to partial responses. Systemic administration of the growth factor FLT3L followed by intratumoral poly I:C injections expanded and activated CD103(+) DC progenitors in the tumor, enhancing responses to BRAF and PD-L1 blockade and protecting mice from tumor rechallenge. Thus, the paucity of activated CD103(+) DCs in tumors limits checkpoint-blockade efficacy and combined FLT3L and poly I:C therapy can enhance tumor responses to checkpoint and BRAF blockade.
大量黑色素瘤病灶对突变型BRAF的靶向抑制产生耐药性,或对检查点阻断无反应。我们探究了肿瘤内抗原呈递细胞(APC)的调节是否能增强对这些疗法的反应。利用小鼠黑色素瘤模型,我们发现CD103(+)树突状细胞(DC)是唯一能将完整抗原转运至淋巴结并启动肿瘤特异性CD8(+) T细胞的APC。在阻断检查点配体PD-L1时,需要CD103(+) DC来促进抗肿瘤作用;然而,PD-L1抑制仅导致部分反应。全身给予生长因子FLT3L,随后瘤内注射聚肌胞苷酸(poly I:C),可扩增并激活肿瘤内的CD103(+) DC祖细胞,增强对BRAF和PD-L1阻断的反应,并保护小鼠免受肿瘤再次攻击。因此,肿瘤中活化的CD103(+) DC数量稀少限制了检查点阻断的疗效,联合FLT3L和聚肌胞苷酸疗法可增强肿瘤对检查点和BRAF阻断的反应。