Pickel K, Müller M A, ter Meulen V
Infect Immun. 1981 Dec;34(3):648-54. doi: 10.1128/iai.34.3.648-654.1981.
Resistance to intraperitoneal murine coronavirus JHM infection in mice develops with age. C3H mice were found to be fully susceptible up to the age of 20 days and resistant after 23 days of age. Protection of susceptible animals from death due to infection could be achieved by maternal antibodies or by transfer of spleen cells from immunized, but not from nonimmunized, donor mice. Lack of protection by transfer of unprimed adult spleen cells was not related to immunosuppression by the host. Moreover, resistance of adult mice could not be abrogated by application of lymphocytes from suckling mice, although immune suppression by other means did affect the resistance of adult animals. On the other hand, spleen cells from nonimmunized mice could be primed with inactivated JHM virus in suckling mice and protected these mice from death due to a subsequent virus infection. Thus, the outcome of infection with JHM virus in suckling and adult mice can be influenced by immunological events, but is not exclusively due to the different stages of immune competence.
小鼠对腹腔内感染鼠冠状病毒JHM的抵抗力随年龄增长而发展。发现C3H小鼠在20日龄前对该病毒完全易感,而在23日龄后具有抗性。通过母源抗体或从免疫供体小鼠而非未免疫供体小鼠转移脾细胞,可以保护易感动物免于因感染而死亡。未致敏的成年脾细胞转移后缺乏保护作用与宿主的免疫抑制无关。此外,尽管其他方式的免疫抑制确实会影响成年动物的抵抗力,但哺乳小鼠的淋巴细胞应用并不能消除成年小鼠的抗性。另一方面,未免疫小鼠的脾细胞可以在哺乳小鼠中用灭活的JHM病毒进行致敏,并保护这些小鼠免于因随后的病毒感染而死亡。因此,JHM病毒在哺乳小鼠和成年小鼠中的感染结果可受免疫事件影响,但并非完全取决于免疫能力的不同阶段。