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计算性癌症新抗原预测:现状与最新进展

Computational cancer neoantigen prediction: current status and recent advances.

作者信息

Fotakis G, Trajanoski Z, Rieder D

机构信息

Institute of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.

出版信息

Immunooncol Technol. 2021 Nov 20;12:100052. doi: 10.1016/j.iotech.2021.100052. eCollection 2021 Dec.

Abstract

Over the last few decades, immunotherapy has shown significant therapeutic efficacy in a broad range of cancer types. Antitumor immune responses are contingent on the recognition of tumor-specific antigens, which are termed neoantigens. Tumor neoantigens are ideal targets for immunotherapy since they can be recognized as non-self antigens by the host immune system and thus are able to elicit an antitumor T-cell response. There are an increasing number of studies that highlight the importance of tumor neoantigens in immunoediting and in the sensitivity to immune checkpoint blockade. Therefore, one of the most fundamental tasks in the field of immuno-oncology research is the identification of patient-specific neoantigens. To this end, a plethora of computational approaches have been developed in order to predict tumor-specific aberrant peptides and quantify their likelihood of binding to patients' human leukocyte antigen molecules in order to be recognized by T cells. In this review, we systematically summarize and present the most recent advances in computational neoantigen prediction, and discuss the challenges and novel methods that are being developed to resolve them.

摘要

在过去几十年中,免疫疗法在多种癌症类型中显示出显著的治疗效果。抗肿瘤免疫反应取决于对肿瘤特异性抗原(即新抗原)的识别。肿瘤新抗原是免疫疗法的理想靶点,因为它们可被宿主免疫系统识别为非自身抗原,从而能够引发抗肿瘤T细胞反应。越来越多的研究强调了肿瘤新抗原在免疫编辑和对免疫检查点阻断的敏感性中的重要性。因此,免疫肿瘤学研究领域最基本的任务之一是识别患者特异性新抗原。为此,已经开发了大量的计算方法,以预测肿瘤特异性异常肽,并量化它们与患者人类白细胞抗原分子结合以便被T细胞识别的可能性。在这篇综述中,我们系统地总结并介绍了计算新抗原预测的最新进展,并讨论了为解决这些问题而正在开发的挑战和新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c883/9216660/bf4c0c9ec7aa/gr1.jpg

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