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白细胞介素4和γ干扰素在人类IgE合成调节中的作用:特应性患者可能存在的改变。

Role of interleukin 4 and gamma interferon in the regulation of human IgE synthesis: possible alterations in atopic patients.

作者信息

Romagnani S, Maggi E, Del Prete G F, Parronchi P, Macchia D, Tiri A, Ricci M

机构信息

Department of Internal Medicine and Clinical Immunology, University of Florence, Italy.

出版信息

Int Arch Allergy Appl Immunol. 1989;88(1-2):111-3. doi: 10.1159/000234758.

Abstract

The IgE helper function of human T cell clones or their phytohemagglutinin-induced supernatants was positively correlated with their ability to produce or their content in interleukin 4 (IL-4), whereas it was inversely correlated with production of or content in gamma interferon. The addition to B cell cultures of anti-IL-4 antibody abolished not only the IgE synthesis induced by recombinant human IL-4, but also that induced by IL-4-producing T cell clones or their phytohemagglutinin-induced supernatants. A clonal analysis in nonatopic donors and patients with common atopy showed that atopics possess in their peripheral blood significantly higher numbers of T cells able to secrete IL-4 and to provide helper function for IgE.

摘要

人T细胞克隆或其经植物血凝素诱导的上清液的IgE辅助功能与其产生白细胞介素4(IL-4)的能力或IL-4含量呈正相关,而与γ干扰素的产生或含量呈负相关。向B细胞培养物中添加抗IL-4抗体不仅消除了重组人IL-4诱导的IgE合成,也消除了产生IL-4的T细胞克隆或其经植物血凝素诱导的上清液诱导的IgE合成。对非特应性供体和常见特应性患者的克隆分析表明,特应性个体外周血中能够分泌IL-4并为IgE提供辅助功能的T细胞数量明显更多。

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