摘要:MDSCs诱导的翻译后修饰的同瓜氨酸可作为CD4 t细胞的有效抗肿瘤靶点

K. Cook, W. Xue, P. Symonds, Mohamed Gijon, Sabaria Shah, Suha Atabani, Poonam M Vaghela, R. Choudhury, R. Metheringham, I. Daniels, Victoria A Brentville, L. Durrant
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引用次数: 0

摘要

翻译后修饰如瓜氨酸化和磷酸化已被证明为癌症疫苗提供了新的靶点。修饰蛋白的表位允许产生能够靶向肿瘤的细胞毒性CD4细胞。在这项研究中,我们发现,当赖氨酸被氨基甲酰化过程翻译后修饰时产生的氨基酸高胱甘氨酸可以成为有效的肿瘤免疫靶点。根据MHC-II结合算法,从细胞骨架蛋白vimentin和糖酵解酶醛缩酶中选择同丘氨酸化的表位。用三种同源肽段(一种来自vimentin,另一种来自醛缩酶A)免疫HLA转基因小鼠,可诱导受HLA- dr4、DR1或DP4限制的强效IFNγ应答。反应是特异性的同硝化肽,不与未修饰的肽交叉反应。这些反应被描述为cd4介导的th1型反应,产生少量的IL-10或IL-17。在人类中,我们也发现健康的供体和癌症患者都有CD4 t细胞库来识别这些同卵氨酸化肽。在B16黑色素瘤模型中,接种同卵氨酸肽可提高转基因HLA-DR4(存活率70%,p=0.0042)和HHDII/DR1(存活率50%,p)的存活率。引用形式:Katherine W. Cook, Wei Xue, Peter Symonds, Mohamed Gijon, Sabaria Shah, Suha Atabani, Poonam Vaghela, Ruhul Choudhury, Rachael L. Metheringham, Ian Daniels, Victoria Brentville, Lindy Durrant。由MDSCs诱导的翻译后修饰的同瓜氨酸可作为CD4 t细胞的有效抗肿瘤靶点[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 B104。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract B104: Post-translationally modified homocitrulline induced by MDSCs can be an effective antitumor target for CD4 T-cells
Post-translational modifications such as citrullination and phosphorylation have been shown to provide novel target for cancer vaccines. Epitopes from modified proteins allow the generation of cytotoxic CD4 cells capable of targeting tumor. In this study we show that homocitrulline, an amino acid produced when lysine is post translationally modified by the process of carbamylation, can be a target for effective tumor immunity. Homocitrullinated epitopes from the cytoskeletal protein vimentin and the glycolytic enzyme aldolase were selected based upon MHC-II binding algorithms. Immunization of HLA transgenic mice with three homocitrullinated peptides, one from vimentin and two from aldolase A, induced potent IFNγ responses restricted via HLA-DR4, DR1 or DP4. Responses are specific to the homocitrullinated peptides and did not cross react with unmodified peptides. The responses have been characterized as CD4-mediated, Th1-type responses with minimal IL-10 or IL-17 production. In humans, we have also shown that healthy donors and cancer patients both have a CD4 T-cell repertoire recognizing these homocitrullinated peptides. In B16 melanoma tumor models, vaccination with homocitrullinated peptides increases survival in transgenic HLA-DR4 (survival 70%, p=0.0042), HHDII/DR1 (survival 50%, p Citation Format: Katherine W. Cook, Wei Xue, Peter Symonds, Mohamed Gijon, Sabaria Shah, Suha Atabani, Poonam Vaghela, Ruhul Choudhury, Rachael L. Metheringham, Ian Daniels, Victoria Brentville, Lindy Durrant. Post-translationally modified homocitrulline induced by MDSCs can be an effective antitumor target for CD4 T-cells [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 B104.
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