M. Moretto et al., Lack of CD4(+) T cells does not affect induction of CD8(+) T-cell immunityagainst Encephalitozoon cuniculi infection, INFEC IMMUN, 68(11), 2000, pp. 6223-6232
Cell-mediated immunity has been reported to play an important role in defen
se against Encephalitozoon cuniculi infection. Previous studies from our la
boratory have underlined the importance of cytotoxic CD8(+) T lymphocytes (
CTL) in survival of mice infected with E, cuniculi. In the present study, i
mmune response against E. cuniculi infection in CD4(+) T-cell-deficient mic
e was evaluated. Similar to resistant wild-type animals, CD4(-/-) mice were
able to resolve E. cuniculi infection even at a very high challenge dose (
5 x 10(7) spores/ mouse). Tissues from infected CD4(-/-) mice did not exhib
it higher parasite loads in comparison to the parental wild-type mice. Conv
ersely, at day 21 postinfection, susceptible CD8(-/-) mice had 10(14) times
more parasites in the liver compared to control wild-type mice. Induction
of the CD8(+) T-cell response in CD4(-/-) mice against E. cuniculi infectio
n was studied. Interestingly, a normal antigen-specific CD8(+) T-cell respo
nse to E. cuniculi infection was observed in CD4(-/-) mice (precursor proli
feration frequency, 1/2.5 x 10(4) versus 1/10(4) in wild-type controls), La
ck of CD4(+) T cells did not alter the magnitude of the antigen-specific CT
L response (precursor CTL frequency; 1/1.4 x 10(4) in CD4(-/-) mice versus
1/3 x 10(4) in control mice). Adoptive transfer of immune CD8(+) T cells fr
om both CD4(-/-) and wild-type animals prevented the mortality in CD8(-/-)
mice. E. cuniculi infection thus offers an example of an intracellular para
sitic infection where CD8(+) T-cell immunity can be induced in the absence
of CD4(+) T cells.