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Role of T lymphocytes in recovery from murine cytomegalovirus infection.

机译:T淋巴细胞在从小鼠巨细胞病毒感染中恢复中的作用。

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摘要

Congenitally athymic nude (Nu/Nu) mice inoculated intraperitoneally with murine cytomegalovirus (MCMV), in doses as low as 1.3 X 10(1) plaque-forming units succumbed to the infection. In contrast, the mean lethal dose for heteroxygous euthymic (Nu/+) littermates was 4 X 10(3) plaque-forming units. Though histopathological changes consistent with MCMV infection were found in the spleen, lungs, and adrenals of nude mice, there were only small focal areas of involvement in the liver. In contrast, Nu/+ mice dying from infection had pathological evidence of severe hepatitis. Spleen cells from immune and control BALB/c mice were injected intravenously into syngeneic mice that had been inoculated previously with lethal doses of MCMV intraperitoneally. Mice receiving 1 X 10(7) or more immune spleen cells were protected against the infection, whereas mice receiving 1 X 10(8) control spleen cells or immune serum were not. Treatment of immune spleen cells with anti-theta serum and complement significantly reduced their protective effect. Immune mechanisms associated with T lymphocytes appear to be critical for recovery from MCMV infection.
机译:先天性无胸腺裸鼠(Nu / Nu)腹腔内接种鼠巨细胞病毒(MCMV),其剂量低至感染后的1.3 X 10(1)噬菌斑形成单位。相比之下,杂合性常乐(Nu / +)同窝仔的平均致死剂量为4 X 10(3)噬菌斑形成单位。尽管在裸鼠的脾脏,肺脏和肾上腺中发现了与MCMV感染相一致的组织病理学变化,但肝脏中只有很小的病灶区域。相反,死于感染的Nu / +小鼠具有严重肝炎的病理学证据。将来自免疫和对照BALB / c小鼠的脾细胞静脉内注射到同种小鼠中,该同种小鼠先前已在腹膜内接种了致死剂量的MCMV。接受1 X 10(7)或更多免疫脾细胞的小鼠可以预防感染,而接受1 X 10(8)的对照脾细胞或免疫血清的小鼠则不能。用抗θ血清和补体治疗免疫脾细胞会大大降低其保护作用。与T淋巴细胞相关的免疫机制对于从MCMV感染中恢复至关重要。

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