Arrowood M J, Mead J R, Mahrt J L, Sterling C R
Department of Veterinary Science, University of Arizona, Tucson 85721.
Infect Immun. 1989 Aug;57(8):2283-8. doi: 10.1128/iai.57.8.2283-2288.1989.
A neonatal BALB/c mouse model of cryptosporidiosis was used to examine the potential passive transfer of immunity via immune colostrum and oral treatment with anticryptosporidial monoclonal antibodies. Neonates suckled by dams that recovered from Cryptosporidium parvum infections were equally susceptible to infection as their control counterparts suckled by naive dams. Parasite loads among the control and immune colostrum-fed mice were indistinguishable. Neonates receiving orally administered antisporozoite monoclonal antibodies were equally susceptible to infections compared with the control and immune colostrum-fed mice. Parasite loads among the mice receiving daily oral treatment with monoclonal antibody mixtures exhibited significantly lower parasite loads compared with the control mice (P less than 0.05).
采用新生BALB/c小鼠隐孢子虫病模型,研究通过免疫初乳进行免疫被动转移的可能性以及用抗隐孢子虫单克隆抗体进行口服治疗的效果。由感染微小隐孢子虫后康复的母鼠哺育的新生小鼠,与由未感染的母鼠哺育的对照新生小鼠一样,对感染同样易感。对照小鼠和喂食免疫初乳的小鼠体内的寄生虫载量没有差异。与对照小鼠和喂食免疫初乳的小鼠相比,口服抗子孢子单克隆抗体的新生小鼠对感染同样易感。与对照小鼠相比,每天口服单克隆抗体混合物进行治疗的小鼠体内的寄生虫载量显著降低(P小于0.05)。