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调控多发性骨髓瘤(MM)肿瘤免疫抑制中的调节分子。

Regulating the regulators in cancer-immunosuppression in multiple myeloma (MM).

机构信息

Transplant Immunology Group, Academic Department of Haematology & Oncology, University of Leeds, UK.

出版信息

Blood Rev. 2013 May;27(3):155-64. doi: 10.1016/j.blre.2013.04.004. Epub 2013 Apr 25.

Abstract

An effective immune response requires a prompt but measured action against the pathological insult, to prevent over-zealous inflammatory-mediated tissue destruction. In cancer, defective or incompetent immune responses may paradoxically result in disease progression despite an immune attempt at elimination. Tumour-induced immunosuppression may not only result from soluble factors and altered antigenicity, but also from cellular-mediated tumour-induced immune evasion. Multiple myeloma (MM) is associated with both cellular and humoral immune deficiencies and increased T(Reg) cells. In vitro modelling has indicated that the tumour cells directly induce functional T(Reg) cells. In light of this recent evidence, it now seems that the most promising and synergistic approaches for cancer immunotherapy would involve specific anti-tumour immunity and simultaneous reduction of tumour-induced immune-regulation. This review sets out the basic understanding of the human immune response, its dysregulation in cancer and proposes how this knowledge may influence future treatment strategies to maximise the anti-tumour immune response.

摘要

有效的免疫反应需要对病理损伤迅速但适度地采取行动,以防止过度活跃的炎症介导的组织破坏。在癌症中,有缺陷或功能不全的免疫反应可能会导致疾病进展,尽管免疫系统试图消除肿瘤。肿瘤诱导的免疫抑制不仅可能源于可溶性因子和抗原性改变,还可能源于细胞介导的肿瘤诱导的免疫逃逸。多发性骨髓瘤(MM)与细胞和体液免疫缺陷以及增加的 T(Reg)细胞有关。体外模型表明,肿瘤细胞直接诱导功能性 T(Reg)细胞。鉴于这一新的证据,目前看来,最有前途和协同作用的癌症免疫治疗方法将涉及针对肿瘤的特异性免疫和同时减少肿瘤诱导的免疫调节。这篇综述阐述了对人类免疫反应的基本理解,以及其在癌症中的失调,并提出了如何利用这些知识来影响未来的治疗策略,以最大限度地提高抗肿瘤免疫反应。

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