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Infection and Immunity, December 2005, p. 8425-8428, Vol. 73, No. 12
0019-9567/05/$08.00+0 doi:10.1128/IAI.73.12.8425-8428.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Division of Geographic Medicine and Infectious Diseases, Tufts-New England Medical Center, Boston, Massachusetts,1 Division of Gastroenterology, Brigham and Women's Hospital, Boston, Massachusetts2
Received 18 February 2005/ Returned for modification 29 March 2005/ Accepted 2 September 2005
Resistance to and control of Cryptosporidium parvum infection in mice in the absence of adaptive immunity appears to be gamma interferon (IFN-
) dependent. Using an IFN-
-neutralizing antibody in a murine model, we demonstrated increased susceptibility to infection within 24 h. We correlated this early resistance and control with increased mucosal expression of IFN-
and demonstrate that CD8+ T-cell receptor
ß intestinal intraepithelial lymphocytes express and secrete this cytokine shortly after infection. The rapid kinetics of IFN-
expression and secretion by naive CD8+ T cells in response to a protozoan pathogen have not previously been demonstrated.
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