Huber B T
Department of Pathology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Clin Immunol. 1995 Nov;15(6 Suppl):22S-25S. doi: 10.1007/BF01540890.
Murine mammary tumor viruses are retroviruses which encode superantigens capable of stimulating T cells via superantigen-reactive T-cell receptor V beta chains. Murine mammary tumor viruses are transmitted to the suckling offspring through the milk. We have established that B cell-deficient pups which were foster-nursed by virus-secreting mice do not transfer infectious murine mammary tumor viruses to their offspring. No murine mammary tumor virus proviruses could be detected in the spleen and mammary tissue of these mic. We conclude that B cells are essential for the completion of the viral life cycle in vivo. This indicates that B cells are infected first and that viral amplification takes place only if infected B cells present the murine mammary tumor virus superantigen on their surface, which, in turn, results in activation of T cells expressing the appropriate T-cell receptor B beta chains. These activated T cells secrete factors which stimulate B cells, enabling viral replication.
鼠乳腺肿瘤病毒是逆转录病毒,其编码的超抗原能够通过超抗原反应性T细胞受体Vβ链刺激T细胞。鼠乳腺肿瘤病毒通过乳汁传播给哺乳的后代。我们已经证实,由分泌病毒的小鼠代乳的B细胞缺陷幼崽不会将感染性鼠乳腺肿瘤病毒传播给它们的后代。在这些小鼠的脾脏和乳腺组织中未检测到鼠乳腺肿瘤病毒前病毒。我们得出结论,B细胞对于病毒在体内的生命周期的完成至关重要。这表明B细胞首先被感染,并且只有当被感染的B细胞在其表面呈现鼠乳腺肿瘤病毒超抗原时才会发生病毒扩增,这反过来又导致表达适当T细胞受体Bβ链的T细胞活化。这些活化的T细胞分泌刺激B细胞的因子,从而使病毒得以复制。