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T 细胞免疫在单克隆丙种球蛋白病与多发性骨髓瘤中的作用:从免疫发病机制到新型治疗策略

英文原题:The Role of T Cell Immunity in Monoclonal Gammopathy and Multiple Myeloma: From Immunopathogenesis to Novel Therapeutic Approaches.

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The Role of T Cell Immunity in Monoclonal Gammopathy and Multiple Myeloma: From Immunopathogenesis to Novel Therapeutic Approaches.

PubMed 2022/05/08(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

多发性骨髓瘤(MM)是克隆性浆细胞的恶性增殖,通常由无症状前驱状态发展而来,即意义未明的单克隆丙种球蛋白病(MGUS)和冒烟型MM(SMM)。深刻的免疫功能障碍和细胞因子失调是疾病进展过程中的特征,可使肿瘤性浆细胞逃避免疫并增殖。过去数十年的多项研究显示,免疫系统能够识别MGUS和MM克隆细胞,提示可利用抗骨髓瘤T细胞免疫用于治疗。与这一观点一致,CAR-T 细胞疗法正在成为MM的新型治疗方式,尤其用于复发/难治性疾病。本文聚焦T细胞功能受损在浆细胞疾病免疫发病机制中的关键作用,特别是从MGUS进展至SMM和MM的过程,并强调在这些阶段采用T细胞免疫治疗的潜力。

展开英文摘要原文

Multiple Myeloma (MM) is a malignant growth of clonal plasma cells, typically arising from asymptomatic precursor conditions, namely monoclonal gammopathy of undetermined significance (MGUS) and smoldering MM (SMM). Profound immunological dysfunctions and cytokine deregulation are known to characterize the evolution of the disease, allowing immune escape and proliferation of neoplastic plasma cells. In the past decades, several studies have shown that the immune system can recognize MGUS and MM clonal cells, suggesting that anti-myeloma T cell immunity could be harnessed for therapeutic purposes.

In line with this notion, chimeric antigen receptor T cell (CAR-T) therapy is emerging as a novel treatment in MM, especially in the relapsed/refractory disease setting. In this review, we focus on the pivotal contribution of T cell impairment in the immunopathogenesis of plasma cell dyscrasias and, in particular, in the disease progression from MGUS to SMM and MM, highlighting the potentials of T cell-based immunotherapeutic approaches in these settings.

论文信息

作者
Lagreca I、Riva G、Nasillo V、Barozzi P、Castelli I、Basso S、Bettelli F、Giusti D
单位
Section of Hematology, Department of Surgical and Medical Sciences, University of Modena and Reggio Emilia, AOU Modena, 41124 Modena, Italy.Italy
文献类型
综述
期刊
International journal of molecular sciences2022 May 8
原文标识
PubMed 35563634 · DOI 10.3390/ijms23095242