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幼龄无胸腺大鼠的持续性大鼠病毒感染及其免疫血清的调节作用

Persistent rat virus infection in juvenile athymic rats and its modulation by immune serum.

作者信息

Gaertner D J, Jacoby R O, Johnson E A, Paturzo F X, Smith A L

机构信息

Section of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520-8016, USA.

出版信息

Lab Anim Sci. 1995 Jun;45(3):249-53.

PMID:7650893
Abstract

In contrast to euthymic juvenile rats, which develop acute, self-limiting infection with rat virus (RV), RV infection of juvenile athymic rats was persistent for up to 12 weeks as demonstrated by recovery of infective virus, transmission to cagemates, and detection of viral DNA in the lungs. Administration of RV antiserum at the time of virus inoculation prevented persistent infection in five of six rats. Among rats given RV antiserum 1 week after virus, the interval at which euthymic rats begin to seroconvert, RV was not detected 1 week later but was recovered from four of six rats 3 weeks later. Results of these studies confirm that T-cell deficiency facilitates persistent RV infection and indicate that antibody provides significant protection from persistent infection only if it is present at the time of virus inoculation. The results support the concept that factors which prevent persistent infection in euthymic rats act early after virus inoculation and may include cellular immunity.

摘要

与患胸腺正常的幼年大鼠不同,后者感染大鼠病毒(RV)后会发生急性、自限性感染,而幼年无胸腺大鼠的RV感染会持续长达12周,这可通过感染性病毒的恢复、向同笼伙伴的传播以及在肺中检测到病毒DNA来证明。在接种病毒时给予RV抗血清可防止六只大鼠中的五只发生持续性感染。在病毒感染1周后给予RV抗血清的大鼠中,即患胸腺正常的大鼠开始血清转化的间隔时间,1周后未检测到RV,但3周后从六只大鼠中的四只中分离出了RV。这些研究结果证实,T细胞缺陷促进了RV的持续性感染,并表明只有在接种病毒时存在抗体,抗体才能提供对持续性感染的显著保护。这些结果支持这样一种概念,即防止患胸腺正常的大鼠发生持续性感染的因素在接种病毒后早期起作用,并且可能包括细胞免疫。

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