FAILURE OF PROTECTION INDUCED BY A BRAZILIAN VACCINE AGAINST BRAZILIAN WILD RABIES VIRUSES

Citation
Cr. Zanetti et al., FAILURE OF PROTECTION INDUCED BY A BRAZILIAN VACCINE AGAINST BRAZILIAN WILD RABIES VIRUSES, Archives of virology, 143(9), 1998, pp. 1745-1756
Citations number
29
Categorie Soggetti
Virology
Journal title
ISSN journal
03048608
Volume
143
Issue
9
Year of publication
1998
Pages
1745 - 1756
Database
ISI
SICI code
0304-8608(1998)143:9<1745:FOPIBA>2.0.ZU;2-Y
Abstract
This report shows that the SMB vaccine currently used in Brazil for hu man immunisation provides different degrees of protection in mice, dep ending on the rabies virus strain used as challenge. Using the NIH and Habel potency tests to evaluate the protective activity of rabies vac cine, we observed that vaccinated mice showed a higher resistance to a challenge with a fixed rabies virus (CVS Challenge Virus Strain). The vaccine potency using the I-label or NIH tests was respectively > 6.4 (log 10) and 1.0 (Relative Potency-RP) when the fixed rabies virus wa s used for challenge, and from 2.9 to 4.3 (log 10) or 0.13 to 0.8 (RP) when different wild rabies viruses were used for challenge. The prese nce of virus neutralising antibodies (VNA) could not explain the diffe rences of susceptibility after vaccination, since sera of vaccinated a nimals had similar VNA levels against both fixed and wild strains befo re virus challenge (respectively, 5.6 +/- 0.24 and 5.0 +/- 0.25 IU/ml of VNA against the fixed rabies virus and the 566-M strain of wild rab ies virus in sera of mice vaccinated with 0.2 units of vaccine). Only cell-mediated immunity parameters correlated with the protection induc ed by vaccination. The IFN gamma titers found in sera and brain tissue s of animals challenged with CVS strain were higher (from 36.7 +/- 5.7 to 293.3 +/- 46.2 IU/ml) than those found in mice challenged with 566 -M virus strain (from 16.7 +/- 5.8 to 36.7 +/- 5.8). The proliferation index of spleen cells obtained with CVS stimulation reached a maximal value of 15.1 +/- 0.7 while spleen cells from vaccinated mice stimula ted with 566-M virus failed to proliferate. The implications of these data in human protection by vaccination are discussed.