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The Journal of Immunology, 2004, 172: 2424-2430.
Copyright © 2004 by The American Association of Immunologists

Peripheral CD4 T Cells Rapidly Accumulate at the Host:Parasite Interface during an Inflammatory Th2 Memory Response1

Motoko Morimoto*, Masahiro Morimoto{dagger}, Jeannette Whitmire*, Shiyun Xiao*, Robert M. Anthony*, Hiroshi Mirakami{ddagger}, Robert A. Star{ddagger}, Joseph F. Urban, Jr{dagger} and William C. Gause2,*

* Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814; {dagger} Nutrient Requirements and Functions Laboratory, Beltsville Human Nutrition Research Center, U.S. Department of Agriculture, Beltsville, MD 20705; and {ddagger} Renal Diagnostics and Therapeutics Unit, National Institutes of Health, Bethesda, MD 20892

Memory peripheral Th2 immune responses to infectious pathogens are not well studied due to the lack of suitable models and the difficulty of assessing Th2 cytokine expression at sites of inflammation. We have examined the localized immune response to a nematode parasite that encysts in the small intestine. An unexpected architecture was observed on day 4 of the memory response, with granulocytes and macrophages infiltrating the cyst and CD4+, TCR-{alpha}{beta}+ T cells surrounding the cyst. Laser capture microdissection analysis showed a pronounced CD4-dependent Th2 cytokine pattern at the cyst region only during the memory response, demonstrating that the Th2 memory response is readily distinguished from the primary response by the rapid accumulation of Th2 effector cells at the host:parasite interface.




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