Mathur A, Rawat S, Chaturvedi U C
Immunology. 1984 Jul;52(3):395-402.
The delayed-type hypersensitivity (DTH) to Japanese encephalitis virus (JEV) and the suppressor cells controlling it and the antibody-forming cells in inbred Swiss mice have been studied. JEV induces DTH, with a peak response at day 7 following infection which persists at low levels at least up to 119 days. Suppressor activity appeared on day 18. It was transferable by immune spleen cells. Treatment of spleen cells with anti-Thy-1.2 antisera and complement abrogated the suppressor activity. The homogenate of the spleen was equally effective in mediating suppression of DTH and the humoral response as measured by direct antibody plaque-forming cell (IgM-PFC) assay. The suppressor activity was antigen-specific both on DTH and T helper for antibody response as the immune responses against SRBC or Coxsackie B4 virus were not suppressed. The suppressor cells were sensitive to cyclophosphamide treatment when the drug was given 48 hr before their appearance. It is, therefore, concluded that in JEV infection of mice, antigen-specific suppressor T cells are generated, both for DTH and IgM antibody, which are cyclophosphamide-sensitive and mediate suppression through soluble product(s).
对近交系瑞士小鼠的日本脑炎病毒(JEV)迟发型超敏反应(DTH)及其调控抑制细胞和抗体形成细胞进行了研究。JEV诱导DTH,感染后第7天出现反应高峰,至少持续到119天,反应水平较低。抑制活性在第18天出现。它可由免疫脾细胞转移。用抗Thy-1.2抗血清和补体处理脾细胞可消除抑制活性。脾匀浆在介导DTH抑制和体液反应方面同样有效,通过直接抗体空斑形成细胞(IgM-PFC)测定法进行测量。抑制活性在DTH和抗体反应的T辅助细胞上均具有抗原特异性,因为对绵羊红细胞(SRBC)或柯萨奇B4病毒的免疫反应未受到抑制。当在抑制细胞出现前48小时给予环磷酰胺时,抑制细胞对该药物敏感。因此,得出结论,在小鼠JEV感染中,针对DTH和IgM抗体产生了抗原特异性抑制性T细胞,它们对环磷酰胺敏感,并通过可溶性产物介导抑制作用。