Chen Y, Nakane A, Minagawa T
Department of Microbiology, Hokkaido University School of Medicine, Sapporo, Japan.
Infect Immun. 1989 Aug;57(8):2345-9. doi: 10.1128/iai.57.8.2345-2349.1989.
Neonatal mice within 24 h of birth were highly susceptible to intraperitoneal infection with Listeria monocytogenes. The 50% lethal dose of bacterial cells was 6.3 X 10(1) CFU for neonates and 3.2 X 10(6) CFU for adult mice. A single injection of recombinant murine gamma interferon (rMuIFN-gamma) protected neonatal mice from simultaneous challenge with a lethal dose of L. monocytogenes cells. The rMuIFN-gamma effect was dose dependent: protection was consistently observed in mice treated with rMuIFN-gamma at doses of more than 4 X 10(2) U (0.1 microgram of protein) per mouse. Bacterial growth in the spleens and livers of rMuIFN-gamma-treated neonates was significantly suppressed in comparison with that in the nontreated controls. The infected neonatal mice showed acquired antilisterial resistance against secondary intravenous infection after 4 weeks of age, and this resistance was significantly augmented in mice that had been treated with rMuIFN-gamma.
出生24小时内的新生小鼠对单核细胞增生李斯特菌的腹腔感染高度易感。细菌细胞对新生小鼠的半数致死剂量为6.3×10¹CFU,对成年小鼠为3.2×10⁶CFU。单次注射重组鼠γ干扰素(rMuIFN-γ)可保护新生小鼠免受致死剂量的单核细胞增生李斯特菌细胞的同时攻击。rMuIFN-γ的作用呈剂量依赖性:在每只小鼠接受剂量超过4×10²U(0.1微克蛋白质)的rMuIFN-γ治疗的小鼠中,始终观察到保护作用。与未治疗的对照组相比,rMuIFN-γ治疗的新生小鼠脾脏和肝脏中的细菌生长受到显著抑制。受感染的新生小鼠在4周龄后对继发性静脉感染表现出获得性抗李斯特菌抗性,并且在用rMuIFN-γ治疗的小鼠中这种抗性显著增强。