Abstract B102: Pre-existing citrulline-specific CD4 T-cells can be efficiently harnessed for tumor therapy

Victoria A Brentville, P. Symonds, K. Cook, I. Daniels, Suha Atabani, R. Choudhury, Poonam M Vaghela, R. Metheringham, Mohamed Gijon, W. Xue, L. Durrant
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Abstract

Citrullination is the post-translational modification of arginine to citrulline mediated by Peptidylarginine deiminases (PADs), which are a family of calcium dependent enzymes found in a variety of tissues. Citrullinated proteins are known to play a significant role in the pathogenesis of autoimmune diseases and are presented in complex with MHC class II. We have previously shown that citrullinated peptides from vimentin and α-enolase are presented on HLA-DR4 in tumor cells and mediate strong anti-tumor responses (Brentville et al., 2016; Cook et al., 2017). Here we show that responses to these peptides are also restricted through HLA-DP4. These responses can be detected within 2 days of vaccination and can mediate rapid regression of tumors within 4 days in mice suggesting evidence of a pre-existing repertoire of T-cells specific for these citrullinated peptides. Evidence of CD4 T-cells specific to citrullinated antigens have been identified in a number of autoimmune disease patients in particular rheumatoid arthritis patients. These patients show an increase in frequency and change in phenotype of citrulline specific CD4 T-cells compared to healthy individuals (James et al., 2014). In this report we also demonstrate that a repertoire of CD4 T-cell responses to citrullinated peptides exists in healthy individuals and that this can be uncovered/enhanced by removal of CD25+ T-cells thus suggesting the existence of a regulatory mechanism keeping these responses in check. The responding populations appear to be oligoclonal and show an increase in effector memory and Temra phenotype. This suggests that a repertoire of CD4 T-cells exists to citrullinated peptides that could be targeted for cancer therapy. Citation Format: Victoria A. Brentville, Peter Symonds, Katherine W. Cook, Ian Daniels, Suha Atabani, Ruhul Choudhury, Poonam Vaghela, Rachael L. Metheringham, Mohamed Gijon, Wei Xue, Lindy G. Durrant. Pre-existing citrulline-specific CD4 T-cells can be efficiently harnessed for tumor therapy [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 B102.
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摘要:预先存在的瓜氨酸特异性CD4 t细胞可以有效地用于肿瘤治疗
瓜氨酸化是由肽精氨酸脱亚胺酶(pad)介导的精氨酸转化为瓜氨酸的翻译后修饰,pad是存在于多种组织中的钙依赖性酶家族。瓜氨酸化蛋白已知在自身免疫性疾病的发病机制中发挥重要作用,并与MHC II类复合物呈现。我们之前的研究表明,来自vimentin和α-烯醇化酶的瓜氨酸肽存在于肿瘤细胞的HLA-DR4上,并介导强烈的抗肿瘤反应(Brentville等人,2016;Cook et al., 2017)。在这里,我们表明对这些肽的反应也通过HLA-DP4受到限制。这些反应可以在接种后2天内检测到,并且可以在小鼠体内介导肿瘤在4天内的快速消退,这表明存在针对这些瓜氨酸化肽的预先存在的t细胞库的证据。有证据表明,在许多自身免疫性疾病患者,特别是类风湿性关节炎患者中,已经发现了针对瓜氨酸化抗原的CD4 t细胞。与健康个体相比,这些患者显示瓜氨酸特异性CD4 t细胞的频率和表型变化增加(James et al., 2014)。在本报告中,我们还证明了健康个体中存在CD4 t细胞对瓜氨酸化肽的反应库,并且可以通过去除CD25+ t细胞来发现/增强,从而表明存在一种调节机制来控制这些反应。响应的群体似乎是寡克隆的,并显示出效应记忆和Temra表型的增加。这表明CD4 t细胞库存在瓜氨酸化肽,可以靶向癌症治疗。引文格式:Victoria A. Brentville, Peter Symonds, Katherine W. Cook, Ian Daniels, Suha Atabani, Ruhul Choudhury, Poonam Vaghela, Rachael L. Metheringham, Mohamed Gijon, Wei Xue, Lindy G. Durrant。预先存在的瓜氨酸特异性CD4 t细胞可以有效地用于肿瘤治疗[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 B102。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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