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KVÄLLSSYMPOSIUM 2008 Vaccinering av hund och katt

KVÄLLSSYMPOSIUM 2008 Vaccinering av hund och katt

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272 S.M. Moore et al. / Biologicals 33 (2005) 269e276<br />

Fig. 2. Amino acid alignment of the rabies glycoprotein from Flury, CVS and PM strains (courtesy of Dr Iris Stalkamp, Institut fu¨r Virologie,<br />

Giessen, Germany). There are fewer amino acid sequence changes from CVS to PM (filled arrows) than CVS to Flury (open arrows). The changes are<br />

not in areas of the mapped antigenic sites of the rabies glycoprotein (shaded triangles). The transmembrane sequence is indicated by the boxed area.<br />

eliminate the need to calculate international units using<br />

titer results obtained from an international rabies<br />

reference serum that originated from subjects only<br />

vaccinated with a rabies vaccine produced from a PM<br />

seed strain of rabies virus.<br />

2.5. Statistical analyses<br />

After all serum samples were tested separately with<br />

both the CVS-11 and the Flury-LEP rabies challenge<br />

virus strains, the identification of the two vaccination<br />

groups (PVRV and PCECV) was unblinded and the<br />

RVNA titers were statistically analyzed to determine the<br />

effect of serological testing by means of a homologous<br />

vs. heterologous test. To determine whether any straindependent<br />

difference in neutralizing antibody was<br />

magnified at higher titers, the titer results (both day 14<br />

and day 90) were sorted into response groups, the<br />

geometric mean titer (GMT) of the groups was<br />

calculated, and the GMT by challenge virus was<br />

compared. Additionally, to determine whether maturation<br />

of the antibody response amplified the differences in<br />

GMT, the titer responses by day of serum drawn were<br />

sorted and the GMT of the groups was calculated and<br />

compared by challenge virus.<br />

3. Results<br />

The virus titer of CVS-11 and Flury-LEP, used as the<br />

challenge virus in each of the five serological testing<br />

groups, remained consistently equivalent throughout the<br />

testing period (Table 1). There was a similar wide range<br />

of RVNA titers obtained for each vaccination group,<br />

independent of whether CVS-11 or Flury-LEP was used<br />

as the challenge virus strain (Table 2). There were two<br />

outlier reciprocal titer values in the PVRV vaccination<br />

group, 9500 and 19 700, exhibited by the same subject

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