Vacheron S, Renno T, Acha-Orbea H
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Switzerland.
J Virol. 1997 Oct;71(10):7289-94. doi: 10.1128/JVI.71.10.7289-7294.1997.
Mouse mammary tumor virus (MMTV) infection of adult mice induces a strong response to superantigen (Sag) in their draining lymph nodes, which results from the presentation of Sag by MMTV-infected B cells to Sag-reactive T cells. To date, infection with physiologically relevant doses of MMTV can be detected in vivo only after several days of Sag-mediated T-cell-dependent amplification of infected B cells. Furthermore, no efficient in vitro system of detecting MMTV infection is available. Such a model would allow the dissection of the early phase of infection, the assessment of the contributions of different cell types, and the screening of large panels of molecules for their potential roles in infection and Sag response. For these reasons, we have established an in vitro model for detecting infection which is as sensitive and reproducible as the in vivo model. We found that the viral envelope (Env) protein is crucial for target cell infection but not for presentation of Sag. Furthermore, we show that infection of purified B cells with MMTV induces entry of Sag-responsive T cells into the cell cycle, while other professional antigen-presenting cells, such as dendritic cells, are much less efficient in inducing a response.
成年小鼠感染小鼠乳腺肿瘤病毒(MMTV)会在其引流淋巴结中引发对超抗原(Sag)的强烈反应,这是由MMTV感染的B细胞将Sag呈递给Sag反应性T细胞所致。迄今为止,只有在Sag介导的感染B细胞的T细胞依赖性扩增数天后,才能在体内检测到生理相关剂量的MMTV感染。此外,目前尚无有效的体外检测MMTV感染的系统。这样一个模型将有助于剖析感染的早期阶段,评估不同细胞类型的作用,并筛选大量分子以确定它们在感染和Sag反应中的潜在作用。基于这些原因,我们建立了一个体外检测感染的模型,其敏感性和可重复性与体内模型相当。我们发现病毒包膜(Env)蛋白对于靶细胞感染至关重要,但对于Sag呈递并非如此。此外,我们表明用MMTV感染纯化的B细胞会诱导Sag反应性T细胞进入细胞周期,而其他专业抗原呈递细胞,如树突状细胞,在诱导反应方面效率要低得多。