Ibis Biosciences-Subsidiary of Abbott, Inc., Carlsbad, CA, USA.
Virulence. 2011 Sep-Oct;2(5):402-12. doi: 10.4161/viru.2.5.16342. Epub 2011 Sep 1.
The M protein coats group A streptococci (GAS) and acts as the primary antigen and determinant of type-specific immunity. M is essential for GAS virulence, providing antiphagocytic functions critical to survival in human tissues and fluids. Specific regions of M protein also serve as shared antigens, and cross-reactivity between these epitopes and human proteins may be the source of autoimmune sequelae such as rheumatic heart disease. The M protein is hypervariable, and has long served as the primary target for epidemiological typing of GAS. Though other markers or genotyping methods may be necessary to increase strain resolution when clones of a given M type differ in clinically critical ways, M typing remains the most directly informative and well-documented method for tracking outbreaks of GAS, predicting clinical outcomes during those outbreaks, and measuring the general threat presented by GAS at any given time and place.
M 蛋白包裹 A 组链球菌(GAS),并作为主要抗原和决定簇,决定特定类型的免疫反应。M 蛋白对于 GAS 的毒力至关重要,为其在人体组织和体液中的生存提供了抗吞噬作用。M 蛋白的特定区域也作为共同抗原,这些表位与人类蛋白之间的交叉反应可能是风湿性心脏病等自身免疫后遗症的来源。M 蛋白高度可变,长期以来一直是 GAS 流行病学分型的主要目标。尽管在某些情况下,当给定 M 型的克隆在临床上有显著差异时,可能需要其他标记物或基因分型方法来提高菌株分辨率,但 M 分型仍然是跟踪 GAS 爆发、预测爆发期间临床结果以及衡量特定时间和地点 GAS 一般威胁最直接、最有记录的方法。