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弓形虫感染小鼠中主要抗体反应的非特异性抑制及塑料贴壁抑制细胞的存在

Nonspecific suppression of primary antibody responses and presence of plastic-adherent suppressor cells in Toxoplasma gondii-infected mice.

作者信息

Suzuki Y, Watanabe N, Kobayashi A

出版信息

Infect Immun. 1981 Oct;34(1):30-5. doi: 10.1128/iai.34.1.30-35.1981.

Abstract

The effect of Toxoplasma infection on primary antibody responses to both T-dependent and T-independent antigens was examined in mice. Drastic suppression of primary responses to sheep erythrocytes (SRBC) occurred when mice were immunized 7 days after infection. The suppression was observed in both 2-mercaptoethanol-sensitive and -resistant hemagglutinin responses. Anti-dinitrophenol (DNP) immunoglobulin E and G1 responses to DNP-conjugated keyhole limpet hemocyanin were also suppressed by infection. It was suggested that the suppressive effect is nonspecific for the antigens and immunoglobulin classes produced. Anti-DNP responses to DNP-Ficoll, a T-independent antigen, were suppressed by infection, but the suppressive effect was weaker than that on the responses to SRBC. This suggests that both T and B cells are suppressed by infection. In vitro responses of infected mouse spleen cells to SRBC and DNP-Ficoll confirmed the results of in vivo experiments. In addition, the presence of plastic-adherent suppressor cells was demonstrated in the spleen cells of infected mice, which suppressed the ability of normal mouse spleen cells to mount an SRBC-specific plaque-forming cell response. These plastic-adherent suppressor cells appeared to be a major cause of nonspecific suppression of primary antibody responses in Toxoplasma-infected mice.

摘要

在小鼠中研究了弓形虫感染对针对T细胞依赖性和T细胞非依赖性抗原的初次抗体反应的影响。当小鼠在感染后7天进行免疫时,对绵羊红细胞(SRBC)的初次反应受到显著抑制。在对2-巯基乙醇敏感和抗性的血凝素反应中均观察到了这种抑制作用。感染也抑制了对二硝基苯酚(DNP)偶联的钥孔戚血蓝蛋白的抗DNP免疫球蛋白E和G1反应。提示这种抑制作用对抗原和产生的免疫球蛋白类别是非特异性的。感染抑制了对T细胞非依赖性抗原DNP-Ficoll的抗DNP反应,但抑制作用比对SRBC反应的抑制作用弱。这表明T细胞和B细胞均受到感染的抑制。感染小鼠脾细胞对SRBC和DNP-Ficoll的体外反应证实了体内实验的结果。此外,在感染小鼠的脾细胞中证实存在塑料贴壁抑制细胞,其抑制了正常小鼠脾细胞产生SRBC特异性空斑形成细胞反应的能力。这些塑料贴壁抑制细胞似乎是弓形虫感染小鼠中初次抗体反应非特异性抑制的主要原因。

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