Suppr超能文献

白介素-4依赖型、过敏型以及白介素-4非依赖型、非过敏型IgG1抗体的诱导受到佐剂的调节。

Induction of IL-4-dependent, anaphylactic-type and IL-4-independent, non-anaphylactic-type IgG1 antibodies is modulated by adjuvants.

作者信息

Faquim-Mauro E L, Macedo M S

机构信息

Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, Avenue Professor Lineu Prestes 1730, 05508-900 São Paulo, Brazil.

出版信息

Int Immunol. 2000 Dec;12(12):1733-40. doi: 10.1093/intimm/12.12.1733.

Abstract

Adjuvants can modulate the levels of anaphylactic- and non-anaphylactic-type IgG1 antibodies produced in response to a particular antigen. Mice immunized with ovalbumin (OVA) in Al(OH)(3) gel (alum) produced mostly the anaphylactic type, irrespective of the s.c. or i.p. route used, and this antibody was not detectable in IL-4(-/-) mice. In contrast, when OVA was injected in complete Freund's adjuvant (CFA), it induced substantial amounts of non-anaphylactic-type IgG1 in both IL-4(+/+) and IL-4(-/-) mice, and some anaphylactic IgG1 antibody in IL-4(+/+) mice only. When IFN-gamma was neutralized by specific mAb in wild-type mice immunized with OVA in CFA, the anaphylactic-type IgG1 antibody increased reaching the same levels as in alum-injected mice. This result indicates that the induction of IFN-gamma by the immunization with CFA down-regulates the production of IL-4-dependent, anaphylactic-type IgG1. Despite their different effects on IgG1 antibody production, both adjuvants dramatically increased the production of IgG2a in IL-4-deprived mice and did not induce any detectable IgE in these mice.

摘要

佐剂可以调节针对特定抗原产生的过敏性和非过敏性IgG1抗体的水平。用卵清蛋白(OVA)在氢氧化铝(Al(OH)(3))凝胶(明矾)中免疫的小鼠,无论采用皮下还是腹腔注射途径,大多产生过敏性抗体,而在IL-4基因敲除小鼠中检测不到这种抗体。相反,当OVA注射到完全弗氏佐剂(CFA)中时,它在IL-4基因敲除小鼠和野生型小鼠中均诱导产生大量非过敏性IgG1,而仅在野生型小鼠中诱导产生一些过敏性IgG1抗体。在用CFA免疫OVA的野生型小鼠中,当用特异性单克隆抗体中和IFN-γ时,过敏性IgG1抗体增加,达到与注射明矾的小鼠相同的水平。这一结果表明,用CFA免疫诱导的IFN-γ下调了IL-4依赖的过敏性IgG1的产生。尽管这两种佐剂对IgG1抗体产生的影响不同,但它们都显著增加了IL-4缺陷小鼠中IgG2a的产生,并且在这些小鼠中未诱导出任何可检测到的IgE。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验