Askenase P W, Van Loverent H
Section of Clinical Immunology and Allergy, Department of Medicine, Yale University School of Medicine, New Haven, CT 06510, USA.
Department of Pathology, Rijksuniversiteit Utrecht, 3511 HX Utrecht, The Netherlands.
Immunol Today. 1983 Sep;4(9):259-64. doi: 10.1016/0167-5699(83)90046-4.
In delayed-type hypersensitivity reactions sensitized T cells orchestrate a cascade of cellular interactions. Initiation of these responses depends on a newly recognized event, namely the release of vasoactive mediators fiom mast cells that are activated by antigen-specific T-cell-derivedfactors. Here Philip Askenase and Henk Van Loveren discuss how this event initiates a sequence of steps that lead to T-cell recruitment of effector cells; and how this event differs from activation of mast cells by IgE antibody. They also suggest that the conventional time-based separation of immediate and delayed hypersensitivity should be replaced by a classcation based on the type of antigen-specific lymphocyte - B or T-responsible for the effects of hypersensitivity.
在迟发型超敏反应中,致敏T细胞协调一系列细胞间相互作用。这些反应的启动依赖于一个新认识到的事件,即血管活性介质从肥大细胞的释放,而肥大细胞是由抗原特异性T细胞衍生因子激活的。在此,菲利普·阿斯凯纳斯和亨克·范·洛弗伦讨论了这一事件如何启动一系列导致效应细胞被T细胞募集的步骤;以及这一事件与IgE抗体激活肥大细胞有何不同。他们还建议,基于传统时间的速发型和迟发型超敏反应分类,应被基于负责超敏反应效应的抗原特异性淋巴细胞类型(B细胞或T细胞)的分类所取代。