Leishmania infantum-specific IgG, IgG1 and IgG2 antibody responses in healthy and ill dogs from endemic areas - Evolution in the course of infection and after treatment
L. Solano-gallego et al., Leishmania infantum-specific IgG, IgG1 and IgG2 antibody responses in healthy and ill dogs from endemic areas - Evolution in the course of infection and after treatment, VET PARASIT, 96(4), 2001, pp. 265-276
The expression of IgG, IgG1 and IgG2 specific antibodies for Leishmania inf
antum was studied in five groups of dogs in Catalonia (Spain): I, 99 asympt
omatic dogs (infected and uninfected) from a highly endemic area for leishm
aniosis; II, 139 untreated dogs with clinically patent leishmaniosis; LII,
11 naturally infected asymptomatic dogs monitored for up to 5 years since t
hey were found seropositive to Leishmania antigen and without treatment; IV
, 25 naturally infected dogs with clinically patent leishmaniosis and treat
ed with either meglumine antimoniate and allopurinol or allopurinol alone a
nd V, six experimentally infected dogs, treated with meglumine antimoniate
and controlled for 5 years. The levels (ELISA units) of IgG, IgG1 and IgG2
in asymptomatic dogs (group I) were very variable (24 +/- 33, 32 +/- 31 and
26 +/- 31, respectively), and, as expected, lower than in ill dogs (group
II) (168 +/- 34, 84 +/- 71 and 172 +/- 31, respectively). In both groups, t
he correlation between IgG and IgG2 levels (r = 0.95, P < 0.001 in group I
and r = 0.63, P < 0.001 in group II) was higher than between IgG and IgG1 l
evels (I = 0.01, P > 0.05 in group I and r = 0.31, P < 0.001 in group II).
In group III, IgG and IgG2 expression increased during infection, while IgG
1 expression remained the same. In dogs of group IV, IgG levels after 1 yea
r of treatment decreased more in responsive (mean values, 163 +/- 42 before
treatment (b.t.) and 100 +/- 36 after treatment (a.t.)) than in unresponsi
ve dogs (158 +/- 29 b.t. and 124 +/- 51 a.t.), especially for IgG1 (94 +/-
89 b.t, and 20 +/- 21 a.t. in responsive dogs and 35 +/- 25 b.t. and 22 +/-
13 a.t. in unresponsive dogs) rather than for IgG2 (156 +/- 16 b.t, and 11
4 +/- 45 a.t. in responsive and 151 +/- 11 b.t. and 125 +/- 36 a.t. in unre
sponsive dogs). Similar results were observed in the evolution of experimen
tally infected animals after consecutive and specific treatments. Overall r
esults show the great variation in Leishmania-specific IgG1 expression in a
symptomatic and symptomatic dogs, their lack of correlation with that of Ig
G2 and chemotherapy is more effective in dogs with initially high expressio
n of IgG1. (C) 2001 Elsevier Science B.V. All rights reserved.