B. Bauder et al., Experimental investigations on the B and T cell immune response in pulmonary alveolar echinococcosis, PARASITE IM, 21(8), 1999, pp. 409-421
Susceptibility/resistance of the intermediate host to alveolar echinococcos
is (AE) seems to be based on hitherto unknown immunological mechanisms, pos
sibly involving the activation of different CD4(+) T cell immune responses
(Th1/Th2). Mice of two strains previously characterized as 'susceptible' (C
57BL/6 J) and 'resistant' (C57BL/10 J) to secondary AE were orally infected
with eggs of Echinococcus multilocularis and the course of infection was a
nalysed by macroscopical, pathohistological and immunohistochemical examina
tions of the lymphocytes and cytokines participating in the peri-parasitic
granulomas and by serological examinations of cytokines and E. multilocular
is-specific antibodies. Although differences in the extent of parasitic gro
wth were seen between the two groups, the composition of the granulomas was
quite similar with CD4(+) cells being the dominant lymphocyte subpopulatio
n, succeeded by B cells and CD8(+) cells. Interferon (IFN)-gamma-, interleu
kin (IL)-2- and IL-4-expressing cells could not be detected in the lesions
of the early phase of the infection, possibly indicating the host's immunos
uppression, but were present at the end IL-10 was the most prominent cytoki
ne throughout the course of the disease. Serological analyses of the cytoki
ne concentrations revealed small amounts at the beginning and high levels a
t the end of the infection. The pattern of cytokine response was similar fo
r IL-4 in both strains but different for IL-2 and IL-10 in the late phase,
when the C57BL/10 J strain developed higher levels than the C57BL/6 J strai
n. Correspondingly only small amounts of immunoglobulin (Ig)M, IgG1, IgG2a
and IgG3 could be detected at the beginning of disease, followed by higher
levels at the end. The courses of antibody titres were similar in both grou
ps except IgG3, which was more pronounced in the (C57BL/10 J strain. Parasi
te-specific IgG2b could neither be detected in the C57BL/6 J nor in the C57
BL/10 J strain by the test system used. The results of the study suggest bo
th subsets of CD4(+) T cells (Th1 and Th2) being involved in murine primary
alveolar echinococcosis. A strict differentiation of mice in susceptible a
nd resistant animals based on the activation of different CD4(+) T cell imm
une responses (Th1 'resistant' and Th2 'susceptible') should be avoided.