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Journal of Virology, February 2007, p. 2078-2082, Vol. 81, No. 4
0022-538X/07/$08.00+0 doi:10.1128/JVI.02525-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Section of Microbial Pathogenesis,1 Department of Pathology, Yale University School of Medicine, New Haven, Connecticut 065102
Received 15 November 2006/ Accepted 16 November 2006
Live-attenuated vesicular stomatitis virus (VSV) vectors expressing foreign antigens induce potent immune responses and protect against viral diseases in animal models. Highly attenuated (VSV-CT1) or single-cycle VSV (VSV
G) vectors induce immune responses lower than those generated by attenuated wild-type VSV vectors when given intranasally. We show here that reduced spread of the more highly attenuated or single-cycle vectors to other organs, including lymph nodes, correlates with the reduction in the immune responses. A reverse transcription, real-time PCR assay for VSV genomic RNA (gRNA) sequences showed long-term persistence of gRNA from replicating vectors in lymph nodes, long after viral clearance. Such persistence may be important for induction of potent immune responses by VSV vectors.
Published ahead of print on 6 December 2006.
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