Monteiro J M, Harvey C, Trinchieri G
Wistar Institute of Anatomy and Biology, Philadelphia, Pennsylvania 19104, USA.
J Virol. 1998 Jun;72(6):4825-31. doi: 10.1128/JVI.72.6.4825-4831.1998.
The effect of endogenous interleukin-12 (IL-12) on the influenza virus immune response in BALB/c mice was evaluated. Following primary influenza virus infection, IL-12 mRNA and protein are detected in the lung, with live virus being required for cytokine induction. Endogenous IL-12 contributes to early NK cell-dependent gamma interferon (IFN-gamma) production (days 3 and 5) but not late T-cell-dependent IFN-gamma secretion (day 7). IL-12 contributes to the inhibition of early virus replication but is not required for virus clearance. IL-12 also modestly contributes to the activation of cytotoxic T lymphocytes. Thus, in this model of experimental influenza virus infection, endogenous IL-12 contributes primarily to the early development and activation of the innate immune response.
评估内源性白细胞介素-12(IL-12)对BALB/c小鼠流感病毒免疫反应的影响。初次感染流感病毒后,在肺中可检测到IL-12 mRNA和蛋白质,细胞因子诱导需要活病毒。内源性IL-12有助于早期自然杀伤细胞(NK细胞)依赖性γ干扰素(IFN-γ)的产生(第3天和第5天),但对晚期T细胞依赖性IFN-γ分泌(第7天)没有作用。IL-12有助于抑制早期病毒复制,但病毒清除并不需要它。IL-12也适度促进细胞毒性T淋巴细胞的激活。因此,在这个实验性流感病毒感染模型中,内源性IL-12主要有助于先天性免疫反应的早期发展和激活。