Schmutzler W
Allergol Immunopathol (Madr). 1978 Jul-Aug;6(4):345-60.
"Immunopharmacology" evolved as a field of research in its own right when it was appreciated that pharmacological methods can contribute to the understanding of immune mechanisms on the one hand or can be used to influence or even control immune reactions at all stages and levels. The best studied subjects of immunopharmacology are release and effects of the chemical mediator substances which are responsible for the reactions of effector cells thus causing the clinical symptoms in allergic or inflammatory diseases. In the type I allergic (anaphylactic) reactions the primary target cells are tissue mast cells or basophil granulocytes which discharge their granular contents upon interaction of immunoglobulin E fixed to their surface with the specific antigen or--in the anaphylactoid reaction--upon stimulation with an appropriate chemical substance (so-called histamine-liberator). In both cases the stimulus leads to an influx or intracellular shift from one compartment to another of calcium ions, which in turn trigger membrane fusion and degranulation. This process can vary from a physiological secretion (in the case of IgE-antigen-interaction) to a pathological cytolysis (in the case of high concentrations of activated complement components or other chemical histamine releasers). As long as it is secretory it is subject to vegetative and hormonal modulation and regulation, mainly by catecholamines and other substances which increase cellular cAMP levels or inhibit calcium fluxes. Although cholinergic stimuli under certain circumstances induce mast cell degranulation and histamine release no definite role has yet been established for cholinergic mechanisms in type I allergies. Type II (Cytotoxic) and type III (immune complex mediated) allergies share the complement requirement. As far as mast cells and basophils are involved in such reactions their sensitivity towards pharmacological modulators is comparable to reactions induced by chemical histamine releasers. Otherwise these types of allergic reactions are dominated by phenomena of general inflammation. In those mainly cytotoxic effects of lipases and hydrolases are involved. cAMP active agents have, therefore, only limited modulating effects and steroid hormones are more effective in inhibiting the acute lesions in type II and III allergies. Only during the last decade the involvement of chemical mediators in type IV (cellular immunity) allergic reactions has been appreciated. 26 different factors called lymphokines have been discovered and classified as mediators of cellular immune reactions. However, rather little is yet known about their chemical nature and about the influence of drugs on their production or action.
“免疫药理学”作为一个独立的研究领域发展起来,是因为人们认识到药理学方法一方面有助于理解免疫机制,另一方面可用于在各个阶段和水平影响甚至控制免疫反应。免疫药理学研究得最多的对象是化学介质物质的释放及其作用,这些介质负责效应细胞的反应,从而在过敏性或炎症性疾病中引发临床症状。在I型过敏(过敏反应)中,主要靶细胞是组织肥大细胞或嗜碱性粒细胞,当固定在其表面的免疫球蛋白E与特异性抗原相互作用时,或者在类过敏反应中,当受到适当化学物质(所谓的组胺释放剂)刺激时,它们会释放其颗粒内容物。在这两种情况下,刺激都会导致钙离子流入或从一个区室向另一个区室的细胞内转移,进而引发膜融合和脱颗粒。这个过程可以从生理分泌(在IgE - 抗原相互作用的情况下)到病理细胞溶解(在高浓度活化补体成分或其他化学组胺释放剂的情况下)有所不同。只要它是分泌性的,就会受到自主神经和激素的调节,主要是通过儿茶酚胺和其他增加细胞cAMP水平或抑制钙通量的物质。虽然在某些情况下胆碱能刺激会诱导肥大细胞脱颗粒和组胺释放,但胆碱能机制在I型过敏中的明确作用尚未确立。II型(细胞毒性)和III型(免疫复合物介导)过敏都需要补体。就肥大细胞和嗜碱性粒细胞参与此类反应而言,它们对药理调节剂的敏感性与化学组胺释放剂诱导的反应相当。否则,这些类型的过敏反应以一般炎症现象为主。在这些反应中,主要涉及脂肪酶和水解酶的细胞毒性作用。因此,cAMP活性剂的调节作用有限,而类固醇激素在抑制II型和III型过敏的急性病变方面更有效。直到最近十年,化学介质在IV型(细胞免疫)过敏反应中的作用才被认识到。已经发现并分类了26种不同的称为淋巴因子的因子,作为细胞免疫反应的介质。然而,关于它们的化学性质以及药物对其产生或作用的影响,人们所知甚少。