多发性骨髓瘤中的自然杀伤细胞生物学和疗法:挑战与机遇。

IF 9.4 1区 医学 Q1 HEMATOLOGY Experimental Hematology & Oncology Pub Date : 2024-11-13 DOI:10.1186/s40164-024-00578-4
Kamlesh Bisht, Aimee Merino, Rob Igarashi, Laurent Gauthier, Marielle Chiron, Alexandre Desjonqueres, Eric Smith, Edward Briercheck, Rizwan Romee, Evren Alici, Eric Vivier, Michael O'Dwyer, Helgi van de Velde
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引用次数: 0

摘要

尽管在治疗方面取得了进展,但多发性骨髓瘤(MM)仍然无法治愈。NK 细胞已成为治疗多发性骨髓瘤的一种有前途的选择。NK 细胞具有异质性,通常根据其表面标志物(如 CD56 和 CD16a)的相对表达进行分类。这些细胞通过种系编码的激活受体和抑制受体(可识别 MM 细胞上存在的转化标记),在突变负荷低且无新抗原呈递的情况下激发抗肿瘤反应。较高的 NK 细胞活性与生存和预后的改善有关,而较低的活性则与 MM 的临床分期和疾病进展有关。此外,并非所有 NK 细胞表型对抗 MM 的作用都相同;某些 NK 细胞表型的比例越高,预后越好。在 MM 中,NK 细胞的比例、表型和功能在不同疾病阶段有很大差异;这还受到骨髓微环境、NK 细胞上激活受体和抑制受体的比例、归宿受体的表达以及骨髓缺氧的影响。自体干细胞移植、免疫调节、蛋白酶体抑制和检查点抑制等抗骨髓瘤疗法会进一步调节患者体内的NK细胞状况。因此,NK细胞自然可以与抗骨髓瘤疗法协同作用,并通过策略性调节提高抗骨髓瘤效果。这篇综述文章介绍了NK细胞的免疫型和表型差异以及在平衡状态和恶性状态下的功能变化,并就如何利用NK细胞的潜力改善MM预后的策略提供了专家见解。
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Natural killer cell biology and therapy in multiple myeloma: challenges and opportunities.

Despite therapeutic advancements, multiple myeloma (MM) remains incurable. NK cells have emerged as a promising option for the treatment of MM. NK cells are heterogenous and typically classified based on the relative expression of their surface markers (e.g., CD56 and CD16a). These cells elicit an antitumor response in the presence of low mutational burden and without neoantigen presentation via germline-encoded activating and inhibitory receptors that identify the markers of transformation present on the MM cells. Higher NK cell activity is associated with improved survival and prognosis, whereas lower activity is associated with advanced clinical stage and disease progression in MM. Moreover, not all NK cell phenotypes contribute equally toward the anti-MM effect; higher proportions of certain NK cell phenotypes result in better outcomes. In MM, the proportion, phenotype, and function of NK cells are drastically varied between different disease stages; this is further influenced by the bone marrow microenvironment, proportion of activating and inhibitory receptors on NK cells, expression of homing receptors, and bone marrow hypoxia. Antimyeloma therapies, such as autologous stem cell transplant, immunomodulation, proteasome inhibition, and checkpoint inhibition, further modulate the NK cell landscape in the patients. Thus, NK cells can naturally work in tandem with anti-MM therapies and be strategically modulated for improved anti-MM effect. This review article describes immunotypic and phenotypic differences in NK cells along with the functional changes in homeostatic and malignant states and provides expert insights on strategies to harness the potential of NK cells for improving outcomes in MM.

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来源期刊
CiteScore
12.60
自引率
7.30%
发文量
97
审稿时长
6 weeks
期刊介绍: Experimental Hematology & Oncology is an open access journal that encompasses all aspects of hematology and oncology with an emphasis on preclinical, basic, patient-oriented and translational research. The journal acts as an international platform for sharing laboratory findings in these areas and makes a deliberate effort to publish clinical trials with 'negative' results and basic science studies with provocative findings. Experimental Hematology & Oncology publishes original work, hypothesis, commentaries and timely reviews. With open access and rapid turnaround time from submission to publication, the journal strives to be a hub for disseminating new knowledge and discussing controversial topics for both basic scientists and busy clinicians in the closely related fields of hematology and oncology.
期刊最新文献
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