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两种小鼠辅助性T细胞克隆。III. 通过RNA杂交、功能单特异性生物测定法和单克隆抗体揭示的Th1和Th2克隆在淋巴因子合成方面的进一步差异。

Two types of mouse helper T cell clone. III. Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies.

作者信息

Cherwinski H M, Schumacher J H, Brown K D, Mosmann T R

机构信息

Department of Immunology, DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, California 94304.

出版信息

J Exp Med. 1987 Nov 1;166(5):1229-44. doi: 10.1084/jem.166.5.1229.

Abstract

Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the two types have now been extended to six induced products. With minor exceptions, only Th1 clones synthesized mRNA for IL-2, IFN-gamma, and lymphotoxin, and only Th2 clones synthesized mRNA for IL-4, IL-5, and another induced gene, P600. Four more induced products were expressed preferentially but not uniquely by one or another type of clone: mRNAs for GM-CSF, TNF, and another induced, secreted product (TY5) were produced in larger amounts by Th1 clones, whereas preproenkephalin was preferentially expressed by Th2 clones. IL-3 was produced in similar amounts by both types of clone. mAbs were used to establish three bioassays that were functionally monospecific for IL-2, IL-3, and IL-4, and a new anti-IFN gamma mAb, XMG1.2, was used to establish an ELISA for IFN-gamma. These four assays were used to show that secreted protein and mRNA levels correlated well for all cell lines. The implications of these findings for normal T cells are discussed.

摘要

利用mRNA杂交方法检测了19个T细胞克隆对11种由刀豆蛋白A诱导产生的不同mRNA的淋巴因子合成模式。通过该方法可清楚区分先前描述的两种CD4+ Th细胞克隆,且这两种类型之间的差异现已扩展至六种诱导产物。除少数例外情况,仅Th1克隆能合成IL-2、IFN-γ和淋巴毒素的mRNA,仅Th2克隆能合成IL-4、IL-5和另一种诱导基因P600的mRNA。另外四种诱导产物在一种或另一种类型的克隆中优先表达,但并非唯一:GM-CSF、TNF和另一种诱导分泌产物(TY5)的mRNA由Th1克隆大量产生,而前脑啡肽原优先由Th2克隆表达。两种类型的克隆产生IL-3的量相似。利用单克隆抗体建立了三种分别对IL-2、IL-3和IL-4功能单一特异性的生物测定法,并且使用一种新的抗IFNγ单克隆抗体XMG1.2建立了IFN-γ的ELISA法。这四种测定法用于表明所有细胞系中分泌蛋白和mRNA水平具有良好的相关性。讨论了这些发现对正常T细胞的意义。

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