Sarawar S R, Cardin R D, Brooks J W, Mehrpooya M, Tripp R A, Doherty P C
St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
J Virol. 1996 May;70(5):3264-8. doi: 10.1128/JVI.70.5.3264-3268.1996.
Cytokine profiles were determined following intranasal infection of C57BL/6J mice with murine gammaherpesvirus 68 (MHV-68). Spleen, mediastinal, and cervical lymph node cells from infected mice produced high levels of interleukin 6 (IL-6) and gamma interferon (IFN-gamma) and lower levels of IL-2 and IL-10 following in vitro restimulation. Little or no IL-4 or IL-5 was detected. Cytokine production was generally maximal at 10 days after infection, correlating with viral clearance from the lung, although significant levels were seen as early as 3 days after administration of the virus. In vitro infection of naive splenocytes induced B-cell- dependent secretion of IL-6 and IL-10, whereas IFN-gamma and IL-2 were produced only by cells that had been primed in vivo. Depletion of B lymphocytes from primed splenocyte populations did not, however, abrogate IL-6 and IL-10 production. Highly purified immune T cells made IL-6, IL-10. and IFN-gamma following in vitro restimulation with MHV-68. Thus, IL-6 and IL-10 are components of both the acquired and the innate host response. These cytokines have potential roles in the establishment and maintenance of persistent infection.
在用鼠γ疱疹病毒68(MHV-68)经鼻感染C57BL/6J小鼠后,测定细胞因子谱。来自感染小鼠的脾脏、纵隔和颈部淋巴结细胞在体外再刺激后产生高水平的白细胞介素6(IL-6)和γ干扰素(IFN-γ),而IL-2和IL-10水平较低。几乎未检测到IL-4或IL-5。细胞因子的产生通常在感染后10天达到最大值,这与病毒从肺部清除相关,尽管在接种病毒后3天就可检测到显著水平。体外感染未接触过抗原的脾细胞诱导依赖B细胞分泌IL-6和IL-10,而IFN-γ和IL-2仅由体内已致敏的细胞产生。然而,从致敏脾细胞群体中去除B淋巴细胞并没有消除IL-6和IL-10的产生。用MHV-68体外再刺激高度纯化的免疫T细胞可产生IL-6、IL-10和IFN-γ。因此,IL-6和IL-10是获得性宿主反应和先天性宿主反应的组成部分。这些细胞因子在持续性感染的建立和维持中具有潜在作用。