Rubella virus vaccine associated arthropathy in postpartum immunized women: Influence of preimmunization serologic status on development of joint manifestations
La. Mitchell et al., Rubella virus vaccine associated arthropathy in postpartum immunized women: Influence of preimmunization serologic status on development of joint manifestations, J RHEUMATOL, 27(2), 2000, pp. 418-423
Objective. To measure preimmunization rubella virus (RV)-specific IgG level
s and to relate these to the development of acute and chronic (persistent o
r recurrent) joint manifestations following rubella vaccination.
Methods. Specific IgG was determined by whole RV enzyme immunoassays (EIA)
(Abbott Rubazyme and M33, an in-house method), immunoblot, neutralization d
omain peptide (BCH-178c) EIA, and neutralization bioassay in prevaccine sam
ples of 268 RV seronegative women (Abbott absorbance < 0.999 units) who had
received monovalent live attenuated RA27/3 strain RV vaccine in a clinical
trial that recorded joint manifestations.
Results. Of rubella vaccinated women tested for prevaccine antibodies, 21.7
% were actually positive (greater than or equal to 10 IU/ml) by M33 EIA, 33
.2% had Abbott values greater than or equal to 0.250 units, and 47.6% had R
V protein-specific antibody (immunoblot), while only 17.6% were positive (g
reater than or equal to 10 IU/ml) by neutralization domain peptide EIA and
12.7% had neutralization titers greater than or equal to 1:8, Seropositivit
y by the various methods was compared to recorded occurrence of acute and c
hronic arthropathy (arthralgia and/or arthritis) after RV vaccination. Rela
tive to women who had no joint manifestations, prevaccine seropositivity ra
tes for subjects with acute arthropathy were significantly (p < 0.05) lower
in the Abbott test (< 0.250 units), BCH-178c peptide EIA, and neutralizati
on bioassay, while those who also developed chronic arthropathy had signifi
cantly lower prevaccine seropositivity rates for the Abbott (< 0.250 units)
and M33 EIA and neutralization bioassay,
Conclusion. Results suggest that risk for arthropathy following RA27/3 rube
lla vaccination may be higher in women who have very low prevaccine levels
of antibody, particularly in assays measuring functional (neutralizing) ant
ibodies.