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接受变应原特异性免疫治疗患者中IgG抗体反应的亚类性质及临床意义。

The subclass nature and clinical significance of the IgG antibody response in patients undergoing allergen-specific immunotherapy.

作者信息

Djurup R

出版信息

Allergy. 1985 Oct;40(7):469-86. doi: 10.1111/j.1398-9995.1985.tb00253.x.

Abstract

The purpose of this paper is to discuss the methodological difficulties in quantitation of human IgG subclass antibodies to allergens, to describe the subclass nature of the IgG antibody response in patients undergoing allergen-specific immunotherapy, and to discuss the possible immunological functions and clinical significance of allergen-specific IgG antibodies of different subclasses. Based on results obtained by use of assays with documented specificity it is concluded that the IgG antibody response during allergen-specific immunotherapy is IgG1 and IgG4 restricted, although low levels of IgG2 and IgG3 antibodies to some allergens may occur. In most patients the early IgG antibody response is IgG1 dominated and the late IgG4 dominated. A too early or too pronounced IgG4 dominated antibody response seems to indicate a poor clinical outcome of immunotherapy with inhalant allergens, whereas a pronounced early IgG1 antibody production has been found to be associated with a decrease in synthesis of IgE antibodies to an insect venom. It is therefore proposed that an early IgG1 dominated response is necessary to induce suppression of the ongoing IgE antibody production, which in its turn may be a prerequisite for long-lasting clinical effect. The possibility of induction of an early IgG1 dominated response in every patient by use of alternative immunotherapy procedures is discussed.

摘要

本文旨在探讨定量检测人抗变应原IgG亚类抗体的方法学难点,描述接受变应原特异性免疫治疗患者中IgG抗体应答的亚类特性,并讨论不同亚类变应原特异性IgG抗体可能的免疫功能及临床意义。基于使用具有明确特异性的检测方法所获得的结果,得出结论:变应原特异性免疫治疗期间的IgG抗体应答受IgG1和IgG4限制,尽管对某些变应原可能会出现低水平的IgG2和IgG3抗体。在大多数患者中,早期IgG抗体应答以IgG1为主,晚期以IgG4为主。过早或过于明显的IgG4主导的抗体应答似乎表明吸入性变应原免疫治疗的临床效果不佳,而明显的早期IgG1抗体产生已被发现与针对昆虫毒液的IgE抗体合成减少有关。因此,有人提出早期以IgG1为主的应答对于诱导抑制正在进行的IgE抗体产生是必要的,而这反过来可能是获得持久临床效果的先决条件。本文还讨论了通过使用替代免疫治疗程序在每位患者中诱导早期以IgG1为主的应答的可能性。

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