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增强对多发性骨髓瘤的免疫力。

Boosting Immunity against Multiple Myeloma.

作者信息

Lopes Raquel, Ferreira Bruna Velosa, Caetano Joana, Barahona Filipa, Carneiro Emilie Arnault, João Cristina

机构信息

Lymphoma and Myeloma Research Programme, Champalimaud Centre for the Unknown, 1400-038 Lisbon, Portugal.

Faculty of Medicine, University of Lisbon, 1649-028 Lisbon, Portugal.

出版信息

Cancers (Basel). 2021 Mar 11;13(6):1221. doi: 10.3390/cancers13061221.

Abstract

Despite the improvement of patient's outcome obtained by the current use of immunomodulatory drugs, proteasome inhibitors or anti-CD38 monoclonal antibodies, multiple myeloma (MM) remains an incurable disease. More recently, the testing in clinical trials of novel drugs such as anti-BCMA CAR-T cells, antibody-drug conjugates or bispecific antibodies broadened the possibility of improving patients' survival. However, thus far, these treatment strategies have not been able to steadily eliminate all malignant cells, and the aim has been to induce a long-term complete response with minimal residual disease (MRD)-negative status. In this sense, approaches that target not only myeloma cells but also the surrounding microenvironment are promising strategies to achieve a sustained MRD negativity with prolonged survival. This review provides an overview of current and future strategies used for immunomodulation of MM focusing on the impact on bone marrow (BM) immunome.

摘要

尽管目前使用免疫调节药物、蛋白酶体抑制剂或抗CD38单克隆抗体可改善患者预后,但多发性骨髓瘤(MM)仍然是一种无法治愈的疾病。最近,抗BCMA嵌合抗原受体T细胞(CAR-T细胞)、抗体药物偶联物或双特异性抗体等新型药物的临床试验拓宽了提高患者生存率的可能性。然而,到目前为止,这些治疗策略尚无法稳定地清除所有恶性细胞,目标是诱导长期完全缓解并达到微小残留病(MRD)阴性状态。从这个意义上讲,不仅靶向骨髓瘤细胞而且靶向周围微环境的方法是实现持续MRD阴性并延长生存期的有前景的策略。本综述概述了目前及未来用于MM免疫调节的策略,重点关注对骨髓免疫组的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8cc/8001641/76c551357222/cancers-13-01221-g001.jpg

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