Blimp-1 transcription factor is required for the differentiation of effector CD8(+) T cells and memory responses

Immunity. 2009 Aug 21;31(2):283-95. doi: 10.1016/j.immuni.2009.06.021. Epub 2009 Aug 6.

Abstract

In response to viral infection, naive CD8(+) T cells proliferate and differentiate into cytotoxic and cytokine-producing effector cells. Here we showed that the transcription factor Blimp-1, a crucial regulator of plasma cell differentiation, was required for CD8(+) T cells to differentiate into functional killer T cells in response to influenza virus. Blimp-1 was not essential for the generation of memory T cells but was crucial for their efficient recall response upon reinfection. Antigen-specific Blimp-1-deficient CD8(+) T cells failed to appropriately regulate the transcriptional program essential for killer T cell responses and showed impaired migration to the site of infection. This study identifies Blimp-1 as a master regulator of the terminal differentiation of CD8(+) effector T cells and uncovers a conservation of the pathways that regulate the terminal differentiation of T and B cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / virology
  • Cell Differentiation / immunology*
  • Cell Movement / immunology
  • Cytotoxicity, Immunologic / immunology
  • Immunologic Memory / genetics
  • Immunologic Memory / immunology*
  • Lung / immunology
  • Lung / pathology
  • Lung / virology
  • Mice
  • Mice, Inbred C57BL
  • Orthomyxoviridae / immunology
  • Orthomyxoviridae Infections / immunology*
  • Orthomyxoviridae Infections / virology
  • Positive Regulatory Domain I-Binding Factor 1
  • Transcription Factors / genetics
  • Transcription Factors / immunology*
  • Transcription Factors / metabolism

Substances

  • Prdm1 protein, mouse
  • Transcription Factors
  • Positive Regulatory Domain I-Binding Factor 1