Shakib F, Powell-Richards A
Department of Immunology, University Hospital, Queen's Medical Centre, Nottingham, UK.
Int Arch Allergy Appl Immunol. 1991;95(2-3):102-8. doi: 10.1159/000235413.
IgG autoanti-IgE is detectable in a large proportion of individuals with allergic asthma, where it is suggested to be potentially involved in modulating IgE-mediated hypersensitivity. Using a series of overlapping recombinant human epsilon-chain peptides, we have shown that circulating IgG anti-IgE antibodies recognise at least 2 epitopes located within the C epsilon 2 and the C epsilon 4 domains, respectively. The C epsilon 2 recognition site is located within the C-terminal portion of the C epsilon 2 domain (i.e. aa301-339) which is thought to contribute residues to the Fc epsilon RI-binding site on IgE. The recognition by autoanti-IgE of an effector function site of such pivotal importance in IgE-mediated hypersensitivity suggests that it plays a possible modulatory role during mast cell and basophil activation.
在大部分过敏性哮喘患者中可检测到IgG自身抗IgE,提示其可能参与调节IgE介导的超敏反应。我们利用一系列重叠的重组人ε链肽,证明循环中的IgG抗IgE抗体分别识别位于Cε2和Cε4结构域内的至少2个表位。Cε2识别位点位于Cε2结构域的C末端部分(即氨基酸301 - 339),该部分被认为对IgE上的FcεRI结合位点有贡献。自身抗IgE对IgE介导的超敏反应中如此关键的效应功能位点的识别,表明其在肥大细胞和嗜碱性粒细胞活化过程中可能发挥调节作用。