Grant J A, Alam R, Lett-Brown M A
Department of Internal Medicine, University of Texas Medical Branch, Galveston 77550.
J Allergy Clin Immunol. 1991 Nov;88(5):683-93. doi: 10.1016/0091-6749(91)90170-s.
The initiation of allergic reactions with the bridging of surface-bound IgE antibodies on mast cells and basophils by allergens is well recognized. However, it is clear that other factors most likely play a role in regulating these cells. A number of cytokines have been identified that modulate the secretory response of mast cells and basophils. Among the well-characterized cytokines, interleukin-3 and connective tissue-activating peptide III (or its degradation product, neutrophil-activating peptide 2) can increase the secretory response, whereas interleukin-8 specifically inhibits the response to cytokines. Additional factors are currently under investigation. Preliminary studies suggest an important role for these histamine-releasing factors in atopic disorders, as well as in other conditions in which an IgE-dependent mechanism is not demonstrable. Furthermore, these cytokines may modulate the response of basophils and mast cells in physiologic conditions, such as tissue repair and host defense.
变应原使肥大细胞和嗜碱性粒细胞表面结合的IgE抗体桥联从而引发过敏反应,这一点已得到广泛认可。然而,很明显其他因素很可能在调节这些细胞方面发挥作用。已鉴定出多种细胞因子可调节肥大细胞和嗜碱性粒细胞的分泌反应。在特征明确的细胞因子中,白细胞介素-3和结缔组织激活肽III(或其降解产物,中性粒细胞激活肽2)可增强分泌反应,而白细胞介素-8则特异性抑制对细胞因子的反应。目前正在研究其他因素。初步研究表明,这些组胺释放因子在特应性疾病以及其他无法证明存在IgE依赖性机制的病症中起重要作用。此外,这些细胞因子可能在生理条件下(如组织修复和宿主防御)调节嗜碱性粒细胞和肥大细胞的反应。