Abstract:
:Development of an effective vaccine for severe acute respiratory syndrome (SARS) remains to be a priority to prevent possible re-emergence of SARS coronavirus (SARS-CoV). We previously demonstrated that the receptor-binding domain (RBD) of SARS-CoV S protein is a major target of neutralizing antibodies. This suggests that the RBD may serve as an ideal vaccine candidate. Recombinant adeno-associated virus (rAAV) has been proven to be an effective system for gene delivery and vaccine development. In this study, a novel vaccine against SARS-CoV was developed based on the rAAV delivery system. The gene encoding RBD was cloned into a pAAV-IRES-hrGFP plasmid. The immunogenicity induced by the resulting recombinant RBD-rAAV was evaluated in BALB/c mice. The results demonstrated that (1) a single dose of RBD-rAAV vaccination could induce sufficient neutralizing antibody against SARS-CoV infection; (2) two more repeated doses of the vaccination boosted the neutralizing antibody to about 5 times of the level achieved by a single dose of the immunization and (3) the level of the antibody continued to increase for the entire duration of the experiment of 5.5 months. These results suggested that RBD-rAAV is a promising SARS candidate vaccine.
journal_name
Virologyjournal_title
Virologyauthors
Du L,He Y,Wang Y,Zhang H,Ma S,Wong CK,Wu SH,Ng F,Huang JD,Yuen KY,Jiang S,Zhou Y,Zheng BJdoi
10.1016/j.virol.2006.03.049subject
Has Abstractpub_date
2006-09-15 00:00:00pages
6-16issue
1eissn
0042-6822issn
1096-0341pii
S0042-6822(06)00235-2journal_volume
353pub_type
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