Division of Rheumatology and Connective Tissue Research, Departments of Medicine, Pediatrics, and Molecular Genetics & Microbiology, University of Medicine and Dentistry of New Jersey - Robert Wood Johnson Medical School, New Brunswick, NJ 08903-001, USA.
J Clin Rheumatol. 2012 Sep;18(6):316-8. doi: 10.1097/RHU.0b013e318269446b.
In evolutionary terms, IgG is the most recent addition to the human humoral immune response, the most recent of the 5 isotypes (classes). The IgG 4 subclasses and their multiple receptors, each with a unique structure and functions, speak to their broad repertoire of often overlapping functions. The IgG subclasses differ only slightly in structure, but therein lies their unique qualities. Focusing solely on the clinical niches filled by each and the clinical correlations thereof allows one to clearly see nature in its abhorrence of, and skill in filling, vacuums. One of the IgG subclasses, IgG4, the least in serum concentration, has recently become the topic of intense interest, as the linkage of certain diseases with IgG4 becomes apparent. As this association is studied, the molecular biology at the root of these diseases becomes the predominant cytokines explaining the pattern of histopathology.
从进化角度来看,IgG 是人 5 种同种型(类)抗体中最晚出现的一种,也是最“新”的一种。IgG4 亚类及其多种受体,各具有独特的结构和功能,说明它们具有广泛的重叠功能。这些 IgG 亚类在结构上只有细微的差异,但正是这些差异造就了它们独特的性质。仅关注每种 IgG 亚类所占据的临床利基及其临床相关性,就可以清楚地看到自然界对填补空白的厌恶和技巧。IgG4 是血清浓度最低的 IgG 亚类之一,最近成为人们关注的焦点,因为某些疾病与 IgG4 的关联变得明显。随着对这种关联的研究,这些疾病的分子生物学基础成为解释组织病理学模式的主要细胞因子。