CD4+CD25+ Regulatory Lymphocytes Induce Regression of Intestinal Tumors in ApcMin/+ Mice

SE Erdman, JJ Sohn, VP Rao, PR Nambiar, Z Ge… - Cancer research, 2005 - AACR
SE Erdman, JJ Sohn, VP Rao, PR Nambiar, Z Ge, JG Fox, DB Schauer
Cancer research, 2005AACR
Colorectal cancer in humans results from sequential genetic changes in intestinal epithelia
commencing with inactivation of the APC tumor suppressor gene. Roles for host immunity in
epithelial tumorigenesis are poorly understood. It has been previously shown that CD4+
CD25+ lymphocytes inhibit colitis-associated epithelial tumors in Rag-deficient mice. Here
we show that addition of CD4+ CD25+ lymphocytes in Apc Min/+ mice reduces multiplicity of
epithelial adenomas. Interleukin-10 was required in regulatory cells for therapeutic effect …
Abstract
Colorectal cancer in humans results from sequential genetic changes in intestinal epithelia commencing with inactivation of the APC tumor suppressor gene. Roles for host immunity in epithelial tumorigenesis are poorly understood. It has been previously shown that CD4+CD25+ lymphocytes inhibit colitis-associated epithelial tumors in Rag-deficient mice. Here we show that addition of CD4+CD25+ lymphocytes in ApcMin/+ mice reduces multiplicity of epithelial adenomas. Interleukin-10 was required in regulatory cells for therapeutic effect. Recipients of regulatory cells showed increased apoptosis and down-regulation of cyclooxygenase-2 within tumors coincident with tumor regression. These data suggest a role for regulatory lymphocytes in epithelial homeostasis in the ApcMin/+ mouse model of intestinal polyposis. Similarities with cancer of the breast, prostate, lung, and other sites raise the possibility of broader roles for regulatory lymphocytes in prevention and treatment of epithelial cancers in humans.
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