摘要:CD56参与免疫效应细胞活化和肿瘤细胞根除:白细胞介素-15的作用

H. V. Acker, Maarten Versteven, H. D. Reu, P. Ponsaerts, Z. Berneman, V. Tendeloo, E. Smits
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引用次数: 0

摘要

肿瘤免疫学家一直在寻找更有效的免疫治疗方法,以帮助治愈癌症。在这方面,免疫细胞的参与是一个关键问题。识别抗肿瘤免疫细胞的一个特别有趣的标记是神经细胞粘附分子(NCAM),称为CD56。也就是说,CD56的造血表达似乎仅限于表现出一定程度的细胞毒性的活化免疫细胞(Van Acker等人,Frontiers in Immunology 2017)。不幸的是,目前关于CD56的表达和功能作用的知识非常分散。因此,我们试图阐明CD56表达在各种杀伤免疫细胞中的作用。首先,我们确定了高运动性NCAM-120亚型是免疫细胞上的主要亚群。接下来,通过表面CD56的中和,我们首次能够证明CD56直接参与由表达CD56的杀伤细胞(如自然杀伤细胞、γδ (γδ) t细胞和白细胞介素(IL)-15培养的树突状细胞(DCs))产生的肿瘤细胞裂解。我们还发现了一个假定的串扰机制,表明CD56在IL-15 dc和CD8 t细胞之间的相互作用中是一个共刺激分子。最后,通过分别使用曲美替尼和阿弗瑞替尼阻断丝裂原活化蛋白激酶(MAPK)途径和磷酸肌肽3激酶(PI3K) -AKT途径,我们证实了我们的假设,即IL-15刺激通过募集shc直接导致CD56上调,并结合IL-2/15Rβ链上的磷酸酪氨酸残基。总之,这些结果强调了以前被忽视的CD56在免疫细胞上表达的重要性,有利于当前和未来的免疫治疗选择。引用格式:Heleen H. Van Acker, Maarten Versteven, Hans De Reu, Peter Ponsaerts, Zwi N Berneman, Viggo F. Van Tendeloo, Evelien L. Smits。CD56参与免疫效应细胞活化和肿瘤细胞根除:白细胞介素-15的作用[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nr B192。
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Abstract B192: CD56 participation in immune effector cell activation and tumor cell eradication: A role for interleukin-15
Oncoimmunologists are in a constant search for more effective immunotherapeutic treatments, helping to cure cancer. In this respect, immune cell participation is a key issue. A particularly interesting marker to identify antitumor immune cells is the neural cell adhesion molecule (NCAM), known as CD56. Namely, hematopoietic expression of CD56 seems to be confined to activated immune cells exhibiting some level of cytotoxic properties (Van Acker et al., Frontiers in Immunology 2017). Unfortunately, the current knowledge on the expression and functional role of CD56 is very fragmented. Therefore, we sought to elucidate the role of CD56 expression on various killer immune cells. First, we identified the high motility NCAM-120 isoform to be the main subset on immune cells. Next, through neutralization of surface CD56, we were able to demonstrate for the first time a direct involvement of CD56 in tumor cell lysis exerted by CD56-expressing killer cells such as natural killer cells, gamma delta (γδ) T-cells and interleukin (IL)-15-cultured dendritic cells (DCs). We also detected a putative crosstalk mechanism, suggesting CD56 as a co-stimulatory molecule in the interaction between IL-15 DCs and CD8 T-cells. Finally, by blocking the mitogen-activated protein kinase (MAPK) pathway and the phosphoinositide 3-kinase (PI3K)–AKT pathway, with respectively trametinib and afuresertib, we confirmed our hypothesis that IL-15 stimulation directly leads to CD56 upregulation via the recruitment of shc, binding a phosphotyrosine residue on the IL-2/15Rβ chain. In conclusion, these results underscore the previously neglected importance of CD56 expression on immune cells, benefiting current and future immune therapeutic options. Citation Format: Heleen H. Van Acker, Maarten Versteven, Hans De Reu, Peter Ponsaerts, Zwi N Berneman, Viggo F. Van Tendeloo, Evelien L. Smits. CD56 participation in immune effector cell activation and tumor cell eradication: A role for interleukin-15 [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 B192.
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