Natural regulatory T cells and de novo-induced regulatory T cells contribute independently to tumor-specific tolerance

Gang Zhou, Hyam I. Levitsky

Research output: Contribution to journalArticle

159 Citations (Scopus)

Abstract

Thymus-derived, naturally occurring CD4+CD25 +Foxp3+ regulatory T cells (nTregs) and Tregs induced in the periphery (iTregs) have both been implicated in regulating immune responses. However, the relationship between these populations in the same host, and their relative contribution to the overall Treg pool, has not been examined. Using a tumor-induced T cell tolerance model, we find that expansion of nTregs and de novo generation of iTregs both contribute to tumor-specific T cell tolerance. In this system in which the number of tumor-specific nTregs can be controlled, the efficiency of nTreg expansion significantly exceeds that of the induction of Tregs from uncommitted progenitors in the tumor-bearing host. However, pre-existing nTregs are neither required for the induction of Tregs nor measurably impact on the extent of their accumulation. Instead, induction of Ag-specific regulatory cells from naive cells is intrinsically influenced by the tumor microenvironment and the presence of tumor Ag.

Original languageEnglish (US)
Pages (from-to)2155-2162
Number of pages8
JournalJournal of Immunology
Volume178
Issue number4
DOIs
StatePublished - Feb 15 2007
Externally publishedYes

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Regulatory T-Lymphocytes
Neoplasms
T-Lymphocytes
Tumor Microenvironment
Thymus Gland
Population

ASJC Scopus subject areas

  • Immunology

Cite this

Natural regulatory T cells and de novo-induced regulatory T cells contribute independently to tumor-specific tolerance. / Zhou, Gang; Levitsky, Hyam I.

In: Journal of Immunology, Vol. 178, No. 4, 15.02.2007, p. 2155-2162.

Research output: Contribution to journalArticle

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