Vesicular stomatitis virus glycoprotein displaying retrovirus-like particles induce a type IIFN receptor-dependent switch to neutralizing IgG antibodies

Vesicular stomatitis virus (VSV) infection rapidly induces IFN-alpha beta that confers initial survival, whereas long-term protection is mediated by neutralizing IgG responses. Because coadministration of IFN-a,6 can enhance Ab responses against soluble Ags, we addressed whether virus-induced IFN-ap also had an impact on the induction of neutralizing Ab responses. To this end, we generated apathogenic retrovirus-like particles (VLP) displaying the VSV gp (VLP-VSV). Reminiscent of live VSV, VLP-VSV induced VSV-neutralizing IgM responses that switched to IgG in a T help-dependent manner. In type I IFN receptor-deficient (IFNAR(-/-)) mice, VLP-VSV injection elicited neutralizing IgM, whereas the IgG switch was absent. The lack of subclass switch was associated with a reduced germinal center reaction. Conditional knockout mice with a lymphocyte-specific IFNAR ablation showed normal Ab responses against VLP-VSV, as well as against live VSV. Thus, IFNAR triggering critically promoted the T help-dependent subclass switch of virus-neutralizing Ab responses against VLP-VSV. Interestingly, in the context of VLP-VSV as well as VSV immunization, IFNAR triggering of B lymphocytes did not play a critical role. The Journal of Immunology, 2007, 178: 5839-5847.