Although natural mumps virus infection is believed to induce lifelong
immunity, our laboratory was confronted with 82 patients who developed
mumps-evoking lesions but exhibited serological evidence of a booster
immune response, namely a rise or a high titer of virus-specific IgG,
without IgM. In order to provide arguments favoring the existence of
recurrent mumps attacks, the age, symptomatology, and humoral response
of these patients (group 1) were compared to that of 82 randomly sele
cted true primary infected patients (group 2), 10 parainfluenza virus-
infected patients (group 3), and 20 noninfected mumps-immune subjects
(group 4). Enzyme-linked immunosorbent assay (ELISA) procedures with d
ifferent viral antigenic preparations were used for determination of s
pecific IgM, IgA, IgG, IgG subclasses, and IgG avidity. The patients o
f group 1, older than those of group 2 (28 vs. 10 years, P < 0.0001),
presented a significantly less severe and less typical symptomatology.
Against the whole virus they exhibited IgG of higher avidity (P < 0.0
01), a lower prevalence and titer of IgA (10 vs. 68%, P < 0.0001 and 2
78 vs. 5,009, P < 0.001, respectively). Values obtained for IgG 1, 2,
and 3 were significantly different between the two groups. Prevalence
and absorbance of nucleocapsid-directed IgG 3 were significantly lower
in group 1 (27 vs. 46%, P < 0.01 and 0.444 vs. 0.869, P < 0.01, respe
ctively). A significant discrepancy also allowed patients from group 1
to be distinguished from those of groups 3 and 4. So the presumed mum
ps-reinfected patients were different from primary infected ones and p
resented features reminiscent of a secondary immune response, suggesti
ng the not uncommon occurrence of symptomatic reinfections by the mump
s virus. This concept is of importance in medical practice. (C) 1995 W
iley-Liss, Inc.