{"title":"Tumour-Reactive Plasma Cells in Antitumour Immunity: Current Insights and Future Prospects","authors":"Peng Chen, Yiwei Chu, Ronghua Liu","doi":"10.1093/immadv/ltae003","DOIUrl":null,"url":null,"abstract":"\n Tumour-reactive plasma cells (TRPCs) have been reported to be positively associated with the long-term survival of patients with various cancers. However, unlike tumour-specific antigen (TSA)-induced T cells which have precise effects against tumours, plasma cells require TSA to obtain specific responses. Therefore, the search for a TSA suitable for B cell recognition is urgent. In this review, we discuss the functions of tumour-reactive plasma cells. Further, this review also explores the concept of screening for neoantigen-reactive plasma cells, drawing inspiration from T-cell screening methods. While challenges exist, such as epitope prediction and efficient screening, the development of novel techniques may lead to the discovery of highly specific plasma cells for adoptive cell therapy. In conclusion, tumour-reactive plasma cells are emerging as powerful players in cancer immunotherapy. Their ability to produce antibodies against a variety of antigens, especially neoantigens, opens new avenues for personalized treatments. Overcoming challenges in epitope prediction and screening will be crucial in harnessing the full potential of these plasma cells for the benefit of cancer patients.","PeriodicalId":73353,"journal":{"name":"Immunotherapy advances","volume":null,"pages":null},"PeriodicalIF":4.1000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunotherapy advances","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/immadv/ltae003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Tumour-reactive plasma cells (TRPCs) have been reported to be positively associated with the long-term survival of patients with various cancers. However, unlike tumour-specific antigen (TSA)-induced T cells which have precise effects against tumours, plasma cells require TSA to obtain specific responses. Therefore, the search for a TSA suitable for B cell recognition is urgent. In this review, we discuss the functions of tumour-reactive plasma cells. Further, this review also explores the concept of screening for neoantigen-reactive plasma cells, drawing inspiration from T-cell screening methods. While challenges exist, such as epitope prediction and efficient screening, the development of novel techniques may lead to the discovery of highly specific plasma cells for adoptive cell therapy. In conclusion, tumour-reactive plasma cells are emerging as powerful players in cancer immunotherapy. Their ability to produce antibodies against a variety of antigens, especially neoantigens, opens new avenues for personalized treatments. Overcoming challenges in epitope prediction and screening will be crucial in harnessing the full potential of these plasma cells for the benefit of cancer patients.
据报道,肿瘤反应性浆细胞(TRPCs)与各种癌症患者的长期存活率呈正相关。然而,与肿瘤特异性抗原(TSA)诱导的 T 细胞对肿瘤有精确作用不同,浆细胞需要 TSA 才能获得特异性反应。因此,寻找适合 B 细胞识别的 TSA 已迫在眉睫。在这篇综述中,我们讨论了肿瘤反应性浆细胞的功能。此外,本综述还从 T 细胞筛选方法中汲取灵感,探讨了筛选新抗原反应性浆细胞的概念。虽然存在表位预测和高效筛选等挑战,但新技术的开发可能会导致发现高度特异性的浆细胞,用于采用细胞疗法。总之,肿瘤反应性浆细胞正在成为癌症免疫疗法中的强大角色。它们能够产生针对各种抗原(尤其是新抗原)的抗体,为个性化治疗开辟了新途径。要充分利用这些浆细胞的潜力造福癌症患者,克服表位预测和筛选方面的挑战至关重要。