An integrated database of experimentally validated major histocompatibility complex epitopes for antigen-specific cancer therapy.

Q2 Medicine Antibody Therapeutics Pub Date : 2024-06-17 eCollection Date: 2024-04-01 DOI:10.1093/abt/tbae011
Satoru Kawakita, Aidan Shen, Cheng-Chi Chao, Zhaohui Wang, Siliangyu Cheng, Bingbing Li, Chongming Jiang
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Abstract

Cancer immunotherapy represents a paradigm shift in oncology, offering a superior anti-tumor efficacy and the potential for durable remission. The success of personalized vaccines and cell therapies hinges on the identification of immunogenic epitopes capable of eliciting an effective immune response. Current limitations in the availability of immunogenic epitopes restrict the broader application of such therapies. A critical criterion for serving as potential cancer antigens is their ability to stably bind to the major histocompatibility complex (MHC) for presentation on the surface of tumor cells. To address this, we have developed a comprehensive database of MHC epitopes, experimentally validated for their MHC binding and cell surface presentation. Our database catalogs 451 065 MHC peptide epitopes, each with experimental evidence for MHC binding, along with detailed information on human leukocyte antigen allele specificity, source peptides, and references to original studies. We also provide the grand average of hydropathy scores and predicted immunogenicity for the epitopes. The database (MHCepitopes) has been made available on the web and can be accessed at https://github.com/jcm1201/MHCepitopes.git. By consolidating empirical data from various sources coupled with calculated immunogenicity and hydropathy values, our database offers a robust resource for selecting actionable tumor antigens and advancing the design of antigen-specific cancer immunotherapies. It streamlines the process of identifying promising immunotherapeutic targets, potentially expediting the development of effective antigen-based cancer immunotherapies.

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用于抗原特异性癌症治疗的经实验验证的主要组织相容性复合体表位综合数据库。
癌症免疫疗法代表着肿瘤学的范式转变,具有卓越的抗肿瘤疗效和持久缓解的潜力。个性化疫苗和细胞疗法的成功与否取决于能否鉴定出能引起有效免疫反应的免疫原表位。目前,免疫原表位的可用性有限,限制了此类疗法的广泛应用。作为潜在癌症抗原的一个关键标准是它们能稳定地与主要组织相容性复合体(MHC)结合,从而呈现在肿瘤细胞表面。为了解决这个问题,我们开发了一个全面的 MHC 表位数据库,通过实验验证了它们的 MHC 结合能力和细胞表面呈现能力。我们的数据库收录了 451065 个 MHC 多肽表位,每个表位都有与 MHC 结合的实验证据,以及有关人类白细胞抗原等位基因特异性、源肽和原始研究参考文献的详细信息。我们还提供了表位的水病评分总平均值和预测免疫原性。该数据库(MHCepitopes)已在网上公布,可通过 https://github.com/jcm1201/MHCepitopes.git 访问。通过整合各种来源的经验数据以及计算出的免疫原性和水病值,我们的数据库为选择可行的肿瘤抗原和推进抗原特异性癌症免疫疗法的设计提供了强大的资源。它简化了确定有前景的免疫治疗靶点的过程,有可能加快基于抗原的有效癌症免疫疗法的开发。
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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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
AI-based antibody discovery platform identifies novel, diverse, and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains. FcRider: a recombinant Fc nanoparticle with endogenous adjuvant activities for hybrid immunization. A pan-allelic human SIRPα-blocking antibody, ES004-B5, promotes tumor killing by enhancing macrophage phagocytosis and subsequently inducing an effective T-cell response. Correction to: A case study of a bispecific antibody manufacturability assessment and optimization during discovery stage and its implications. The process using a synthetic library that generates multiple diverse human single domain antibodies.
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