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脂质体模型膜在小鼠脾细胞培养中的原发性体外免疫原性

Primary in vitro immunogenicity of liposomal model membranes in mouse spleen cell cultures.

作者信息

Yasuda T, Tadakuma T, Pierce C W, Kinsky S C

出版信息

J Immunol. 1979 Oct;123(4):1535-9.

PMID:314464
Abstract

Neither 2,4-dinitrophenyl-6-N-aminocaproylphosphatidylethanolamine (DNP-Cap-PE) nor fluoresceinthiocarbamylphosphatidylethanolamine (F1-PE) induces hapten-specific plaque-forming cells (PFC) when incubated with suspensions of spleen cells from unimmunized C57BL/6J mice. However, PFC are produced after incorporation of these synthetic lipid antigens into liposomal model membranes. The in vitro response is characterized by the following: a) it is time and dose dependent; b) the frequency of IgM PFC exceeds IgG PFC; c) both nonadherent and adherent cells are required (2-mercaptoethanol can replace the requirement for adherent cells in some experiments); d) depletion of thymus-derived cells by treatment with anti-theta antiserum plus complement does not diminish the response; e) spleen cells from nude BALB/c mice also produce PFC. Thus, the essential features of the in vivo immunogenicity of DNP-Cap-PE and F1-PE sensitized liposomes, which have been previously described, can be replicated in an in vitro cell culture system.

摘要

当用未免疫的C57BL/6J小鼠的脾细胞悬液孵育时,2,4-二硝基苯基-6-N-氨基己酰磷脂酰乙醇胺(DNP-Cap-PE)和异硫氰酸荧光素磷脂酰乙醇胺(F1-PE)均不能诱导半抗原特异性空斑形成细胞(PFC)。然而,将这些合成脂质抗原掺入脂质体模型膜后会产生PFC。体外反应具有以下特征:a)它具有时间和剂量依赖性;b)IgM PFC的频率超过IgG PFC;c)非黏附细胞和黏附细胞均是必需的(在某些实验中2-巯基乙醇可替代对黏附细胞的需求);d)用抗θ抗血清加补体处理耗尽胸腺来源的细胞不会减弱反应;e)来自裸BALB/c小鼠的脾细胞也能产生PFC。因此,先前已描述的DNP-Cap-PE和F1-PE致敏脂质体的体内免疫原性的基本特征可在体外细胞培养系统中重现。

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