TY - JOUR
T1 - Impaired Th2 development and increased mortality during Schistosoma mansoni infection in the absence of CD40/CD154 interaction
AU - MacDonald, Andrew S.
AU - Patton, Elisabeth A.
AU - La Flamme, Anne C.
AU - Araujo, Maria I.
AU - Huxtable, Clive R.
AU - Bauman, Beverley
AU - Pearce, Edward J.
PY - 2002/5/1
Y1 - 2002/5/1
N2 - The role of CD40/CD154 interaction during infection has primarily focused on pathogens that drive inflammatory Th1 responses. In this study, we show that CD40/CD154 interaction is a fundamental requirement for Th2 response development to the parasitic helminth Schistosoma mansoni. Compared with infected wild-type mice, greatly reduced levels of Th2-associated cytokines were measured both in vitro and in vivo, and no IgE or IgG1 was detected in infected CD154-/- mice. In the absence of an overt Th2 response, no exaggerated Th1 response was mounted by CD154-/- mice. Infected CD154-/- mice suffered severe morbidity and mortality, even though parasitemias in wild-type and CD154-/- mice did not differ significantly. These data indicate that CD40/CD154 interaction is required to allow development of a Th2-dominated immune response to S. mansoni and support the view that failure to develop such a response can have fatal consequences.
AB - The role of CD40/CD154 interaction during infection has primarily focused on pathogens that drive inflammatory Th1 responses. In this study, we show that CD40/CD154 interaction is a fundamental requirement for Th2 response development to the parasitic helminth Schistosoma mansoni. Compared with infected wild-type mice, greatly reduced levels of Th2-associated cytokines were measured both in vitro and in vivo, and no IgE or IgG1 was detected in infected CD154-/- mice. In the absence of an overt Th2 response, no exaggerated Th1 response was mounted by CD154-/- mice. Infected CD154-/- mice suffered severe morbidity and mortality, even though parasitemias in wild-type and CD154-/- mice did not differ significantly. These data indicate that CD40/CD154 interaction is required to allow development of a Th2-dominated immune response to S. mansoni and support the view that failure to develop such a response can have fatal consequences.
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U2 - 10.4049/jimmunol.168.9.4643
DO - 10.4049/jimmunol.168.9.4643
M3 - Article
C2 - 11971013
AN - SCOPUS:0036569444
SN - 0022-1767
VL - 168
SP - 4643
EP - 4649
JO - Journal of Immunology
JF - Journal of Immunology
IS - 9
ER -