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肥大细胞增多症:从分子角度看。

Mastocytosis: from a Molecular Point of View.

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Immunology, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Clin Rev Allergy Immunol. 2018 Jun;54(3):397-411. doi: 10.1007/s12016-017-8619-2.

Abstract

Mast cells (MCs) are physiologically activated by binding of stem cell factor (SCF) to the extracellular domains of the Kit receptor. This binding increases the proliferation and prolongs the survival of normal mature MCs, as well as intensifies the release of mediators. In mastocytosis, somatic mutations of the coding Kit gene cause autocrine dysregulation and lead to constitutive KIT activation even in the absence of its ligand SCF. Clinical symptoms are caused by MC-mediator release and/or infiltration of MCs into tissues. Aberrant KIT activation may result in increased production of MCs in the skin and extracutaneous organs. Depending on the affected organ(s), the disease can be divided into cutaneous mastocytosis (CM), systemic mastocytosis (SM), and localized MC tumors. The updated classification of WHO discriminates between several distinct subvariants of CM and SM. While the prognosis in CM and indolent SM (ISM) is excellent with (almost) normal life expectancy, the prognosis in aggressive SM (ASM) and MC leukemia (MCL) is dismal. The symptoms may comprise urticaria, angioedema, flush, pruritus, abdominal pain, diarrhea, hypotension, syncope, and musculoskeletal pain and are the results of MC infiltration and mediator release into target organs, i.e., the skin, gastrointestinal tract, liver, spleen, lymph nodes, and bone marrow. Mastocytosis differs from a lot of other hematological disorders because its pathology is not only based on the lack of normal function of a specific pathway or of a specific cell type but additionally is a proliferative disease. Currently available treatments of mastocytosis include symptomatic, antimediator and cytoreductive targeted therapies.

摘要

肥大细胞(MCs)通过干细胞因子(SCF)与 Kit 受体的细胞外结构域结合而在生理上被激活。这种结合增加了正常成熟 MC 的增殖和存活时间,并增强了介质的释放。在肥大细胞增多症中,Kit 基因的体细胞突变导致自分泌失调,导致即使没有其配体 SCF 的情况下,KIT 也持续激活。临床症状是由 MC 介质释放和/或 MC 浸润组织引起的。异常的 KIT 激活可能导致皮肤和皮肤外器官中 MC 的产生增加。根据受影响的器官,该疾病可分为皮肤肥大细胞增多症(CM)、系统性肥大细胞增多症(SM)和局部 MC 肿瘤。世界卫生组织的最新分类区分了 CM 和 SM 的几个不同亚型。虽然 CM 和惰性 SM(ISM)的预后良好,几乎有正常的预期寿命,但侵袭性 SM(ASM)和 MC 白血病(MCL)的预后不佳。症状可能包括荨麻疹、血管性水肿、潮红、瘙痒、腹痛、腹泻、低血压、晕厥和肌肉骨骼疼痛,这些是 MC 浸润和介质释放到靶器官的结果,即皮肤、胃肠道、肝脏、脾脏、淋巴结和骨髓。肥大细胞增多症与许多其他血液疾病不同,因为其病理学不仅基于特定途径或特定细胞类型的正常功能缺失,而且还具有增殖性疾病。目前肥大细胞增多症的治疗方法包括对症、抗介质和细胞减少靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8628/6002427/f6bbd3b18934/12016_2017_8619_Fig1_HTML.jpg

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