Afrin Lawrence B, Khoruts Alexander
Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Division of Gastroenterology and Center for Immunology, BioTechnology Institute, University of Minnesota, Minneapolis, Minnesota.
Clin Ther. 2015 May 1;37(5):941-53. doi: 10.1016/j.clinthera.2015.02.008. Epub 2015 Mar 12.
This article reviews the diagnostically challenging presentation of mast cell activation disease (MCAD) and current thoughts regarding interactions between microbiota and MCs.
A search for all studies on interactions between mast cells, mast cell activation disease, and microbiota published on pubmed.gov and scholar.google.com between 1960 and 2015 was conducted using the search terms mast cell, mastocyte, mastocytosis, mast cell activation, mast cell activation disease, mast cell activation syndrome, microbiome, microbiota. A manual review of the references from identified studies was also conducted. Studies were excluded if they were not accessible electronically or by interlibrary loan.
Research increasingly is revealing essential involvement of MCs in normal human biology and in human disease. Via many methods, normal MCs-present sparsely in every tissue-sense their environment and reactively exert influences that, directly and indirectly, locally and remotely, improve health. The dysfunctional MCs of the "iceberg" of MCAD, on the other hand, sense abnormally, react abnormally, activate constitutively, and sometimes (in mastocytosis, the "tip" of the MCAD iceberg) even proliferate neoplastically. MCAD causes chronic multisystem illness generally, but not necessarily, of an inflammatory ± allergic theme and with great variability in behavior among patients and within any patient over time. Furthermore, the range of signals to which MCs respond and react include signals from the body's microbiota, and regardless of whether an MCAD patient has clonal mastocytosis or the bulk of the iceberg now known as MC activation syndrome (also suspected to be clonal but without significant MC proliferation), dysfunctional MCs interact as dysfunctionally with those microbiota as they interact with other human tissues, potentially leading to many adverse consequences.
Interactions between microbiota and MCs are complex at baseline. The potential for both pathology and benefit may be amplified when compositionally variant microbiota interact with aberrant MCs in various types of MCAD. More research is needed to better understand and leverage these interactions.
本文综述肥大细胞活化疾病(MCAD)具有诊断挑战性的表现以及目前关于微生物群与肥大细胞(MC)之间相互作用的观点。
使用搜索词肥大细胞、肥大细胞、肥大细胞增多症、肥大细胞活化、肥大细胞活化疾病、肥大细胞活化综合征、微生物组、微生物群,在pubmed.gov和scholar.google.com上搜索1960年至2015年间发表的关于肥大细胞、肥大细胞活化疾病和微生物群之间相互作用的所有研究。还对已识别研究的参考文献进行了人工查阅。如果研究无法通过电子方式获取或通过馆际互借获取,则将其排除。
研究越来越多地揭示了MC在正常人类生物学和人类疾病中的重要作用。通过多种方式,正常的MC(稀疏地存在于每个组织中)感知其环境并做出反应性影响,直接和间接、局部和远程地改善健康。另一方面,MCAD“冰山”中功能失调的MC感知异常、反应异常、持续激活,有时(在肥大细胞增多症中,MCAD冰山的“顶端”)甚至发生肿瘤性增殖。MCAD通常会导致慢性多系统疾病,但不一定具有炎症±过敏主题,并且患者之间以及任何患者在不同时间的行为差异很大。此外,MC响应和反应的信号范围包括来自身体微生物群的信号,并且无论MCAD患者是患有克隆性肥大细胞增多症还是现在被称为MC激活综合征的冰山主体(也怀疑是克隆性的,但没有明显的MC增殖),功能失调的MC与这些微生物群的相互作用与它们与其他人体组织的相互作用一样功能失调,可能导致许多不良后果。
微生物群与MC之间的相互作用在基线时很复杂。当组成不同的微生物群与各种类型的MCAD中的异常MC相互作用时,病理和益处的可能性可能会放大。需要更多的研究来更好地理解和利用这些相互作用。