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Immunological adjuvants promote activated T cell survival via induction of Bcl-3

  • Thomas C. Mitchell
  • , David Hildeman
  • , Ross M. Kedl
  • , T. Kent Teague
  • , Brian C. Schaefer
  • , Janice White
  • , Yanan Zhu
  • , John Kappler
  • , Philippa Marrack*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

203 Scopus citations

Abstract

Injection of soluble protein antigen into animals causes abortive proliferation of the responding T cells. Immunological adjuvants boost T cell responses at least in part by increasing the survival of activated T cells during and after the initial proliferative phase of their clonal expansion. To understand how adjuvants promote T cell survival, we used gene microarrays to analyze gene expression in T cells activated either with antigen alone or in the presence of two different adjuvants. Among the genes whose expression was increased by both adjuvants was the IκB family member Bcl-3. Retroviral infection experiments showed that expression of Bcl-3 increased survival of activated T cells in vitro and in vivo. Adjuvants may therefore improve survival of activated T cells via induction of Bcl-3.

Original languageEnglish
Pages (from-to)397-402
Number of pages6
JournalNature Immunology
Volume2
Issue number5
DOIs
StatePublished - May 2001
Externally publishedYes

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