Abstract A102: Rescue of lost skin dendritic cells in melanoma is key for the resuscitation of antitumor T-cell responses

Anastasia Prokopi, Christoph H Tripp, B. Tummers, Kerstin Komenda, K. Hutter, G. Cappellano, L. Bellmann, M. Efremova, Z. Trajanoski, Suzie Chen, B. Clausen, D. Green, P. Stoitzner
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引用次数: 1

Abstract

One major characteristic of skin-related cancers is the loss of skin-resident dendritic cell populations. In the tg(Grm1)EPv mouse model, ectopic expression of the metabotropic glutamate receptor-1 in melanocytes leads to a highly proliferative and antiapoptotic phenotype, resulting in melanoma formation within the dermis. The slow progression of these tumors allows for the in depth analysis of the immune infiltrate in growing tumors. We here show that total DCs (CD11c+ cells) are gradually lost as the tumor progresses. Mainly the dermal CD11b+ DCs are affected, whereas epidermal Langerhans cells remain unchanged. We hypothesized that extrinsic cell death of the DCs may be induced within the growing tumor. Indeed, the tumor tissue upregulated the expression of Fas ligand (FasL) that can induce extrinsic apoptosis in immature DCs that express Fas (CD95). Fas-mediated apoptosis depends on the activation of caspase-8 and mice in which the autoproteolytic cleavage site D387 is mutated to alanine (casp8D387A/casp8D387A) show strong resistance to Fas-mediated death. We compared the apoptosis induction in the different DC subsets in casp8WT/casp8WT and in casp8D387A/casp8D387A upon intradermal administration of an agonistic anti-CD95 antibody and we found that, indeed, CD11b+ DCs in WT mice are susceptible to apoptosis via CD95. In order to retrieve the intratumoral DCs, we treated tg(Grm1)EPv mice carrying tumor lesions with Flt3L and the percentages of the CD11b+ subset could be restored back to the levels of tumor-free mice. At the same time, T-cells from both the tumor and the tumor-draining lymph node were able to produce more cytotoxic cytokines. Our data thus indicate that the loss of DCs in melanoma depends on induction of apoptosis within the tumor; rescue of skin DCs may be a promising strategy in order to enhance the efficacy of existing immunotherapeutic strategies against skin-related cancers. Citation Format: Anastasia Prokopi, Christoph H. Tripp, Bart Tummers, Kerstin Komenda, Katharina Hutter, Giuseppe Cappellano, Lydia Bellmann, Mirjana Efremova, Zlatko Trajanoski, Suzie Chen, Bjorn E. Clausen, Douglas R. Green, Patrizia Stoitzner. Rescue of lost skin dendritic cells in melanoma is key for the resuscitation of antitumor T-cell responses [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A102.
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摘要:修复黑色素瘤患者丢失的皮肤树突状细胞是恢复抗肿瘤t细胞反应的关键
皮肤相关癌症的一个主要特征是皮肤树突状细胞群的损失。在tg(Grm1)EPv小鼠模型中,黑色素细胞中代谢性谷氨酸受体-1的异位表达导致高增殖和抗凋亡表型,导致真皮内黑色素瘤形成。这些肿瘤的缓慢进展使得深入分析生长肿瘤中的免疫浸润成为可能。我们在这里显示,随着肿瘤的进展,总DCs (CD11c+细胞)逐渐丢失。主要是真皮CD11b+ dc受到影响,而表皮朗格汉斯细胞保持不变。我们假设树突状细胞的外源性细胞死亡可能在生长的肿瘤中被诱导。事实上,肿瘤组织上调Fas配体(FasL)的表达,FasL可以诱导表达Fas (CD95)的未成熟dc的外源性凋亡。fas介导的细胞凋亡依赖于caspase-8的激活,而自身蛋白水解裂解位点D387突变为丙氨酸(casp8D387A/casp8D387A)的小鼠对fas介导的死亡表现出强烈的抗性。我们比较了皮内给予激动性抗CD95抗体后,casp8WT/casp8WT和casp8D387A/casp8D387A不同DC亚群的凋亡诱导情况,发现WT小鼠中的CD11b+ DC确实容易通过CD95发生凋亡。为了检索肿瘤内的dc,我们用Flt3L治疗携带肿瘤病变的tg(Grm1)EPv小鼠,CD11b+亚群的百分比可以恢复到无肿瘤小鼠的水平。同时,来自肿瘤和肿瘤引流淋巴结的t细胞能够产生更多的细胞毒性细胞因子。因此,我们的数据表明,黑色素瘤中dc的丢失依赖于肿瘤内细胞凋亡的诱导;挽救皮肤dc可能是一种有前途的策略,以提高现有的免疫治疗策略对皮肤相关癌症的疗效。引文格式:Anastasia Prokopi, Christoph . Tripp, Bart Tummers, Kerstin Komenda, Katharina Hutter, Giuseppe Cappellano, Lydia Bellmann, Mirjana Efremova, Zlatko Trajanoski, Suzie Chen, Bjorn E. Clausen, Douglas R. Green, Patrizia Stoitzner。修复黑色素瘤中丢失的皮肤树突状细胞是恢复抗肿瘤t细胞反应的关键[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要1 A102。
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