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口服抗原后免疫增强和抑制的剂量依赖性诱导。

Dose-dependent induction of immunologic enhancement and suppression after oral administration of antigen.

作者信息

Yasui H, Ohwaki M

出版信息

Microbiol Immunol. 1983;27(12):1107-16. doi: 10.1111/j.1348-0421.1983.tb02931.x.

Abstract

The effects of feeding various quantities of a particulate antigen, sheep red blood cells (SRBC), on plaque-forming cells (PFC) in the spleen were determined. Mice were given various numbers of SRBC orally daily for 14 days, then injected with SRBC intravenously. Splenic IgA PFC responses to SRBC were enhanced in the mice fed 5 X 10(8) SRBC and splenic IgG PFC responses to SRBC were depressed in the mice fed 5 X 10(9) SRBC. Adoptive transfer experiments showed that enhancement of splenic IgA PFC responses and suppression of splenic IgG PFC responses were induced by the T-cell rich fraction from Peyer's patches (PP) and the spleen in 5 X 10(8) SRBC- and 5 X 10(9) SRBC-fed mice, respectively. Kinetic studies revealed that IgA helper cells or IgG suppressor cells appeared in PP 2 days after oral administration and 4 days after it in the spleen.

摘要

测定了给小鼠喂食不同数量的颗粒性抗原——绵羊红细胞(SRBC)对脾脏中形成斑块细胞(PFC)的影响。小鼠每天经口给予不同数量的SRBC,持续14天,然后静脉注射SRBC。喂食5×10⁸个SRBC的小鼠脾脏对SRBC的IgA PFC反应增强,而喂食5×10⁹个SRBC的小鼠脾脏对SRBC的IgG PFC反应受到抑制。过继转移实验表明,喂食5×10⁸个SRBC和5×10⁹个SRBC的小鼠,其脾脏IgA PFC反应增强和IgG PFC反应抑制分别是由派尔集合淋巴结(PP)和脾脏中富含T细胞的部分诱导的。动力学研究显示,IgA辅助细胞或IgG抑制细胞在口服给药后2天出现在PP中,在脾脏中则在4天后出现。

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