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1 Intestinal Disease Research Program and 2 Department of Pathology, McMaster University, Hamilton, Ontario, Canada L8N 3Z5
Immune responses elicited by nematode
parasite infections are characterized by T helper 2 (Th2) cell
induction. The immunologic basis for changes in intestinal physiology
accompanying nematode infection is poorly understood. This study
examined whether worm expulsion and associated goblet cell hyperplasia
and muscle contractility share a similar immune basis by shifting the
response from Th2 to Th1 using interleukin-12 (IL-12) overexpression.
We used a single administration of recombinant adenovirus vector
expressing IL-12 (Ad5IL-12) in Trichinella spiralis-infected
mice. Ad5IL-12 administered 1 day after infection prolonged worm
survival and inhibited infection-induced muscle hypercontractility and
goblet cell hyperplasia. This was correlated with upregulated
interferon-
(IFN-
) expression and downregulated IL-13 expression
in the muscularis externa layer. We also observed increased IFN-
production and decreased IL-4 and IL-13 production from in vitro
stimulated spleen and mesenteric lymph node cells of infected
Ad5IL-12-treated mice. These results indicate that transfer and
overexpression of the IL-12 gene during Th2-based nematode infection
shifts the immune response toward Th1 and delays worm expulsion.
Moreover, the immune response shift abrogated the physiological
responses to infection, attenuating both muscle hypercontractility and
goblet cell hyperplasia. These findings strongly indicate that worm
expulsion, muscle hypercontractility, and goblet cell hyperplasia share
a common immunologic basis and may be causally linked.
adenovirus; interleukin-12; Trichinella spiralis; smooth muscle; goblet cells
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