Journal article

Blimp-1 Transcription Factor Is Required for the Differentiation of Effector CD8 T Cells and Memory Responses

A Kallies, A Xin, GT Belz, SL Nutt

Immunity | Published : 2009

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 id..

View full abstract

University of Melbourne Researchers

Grants

Funding Acknowledgements

We are grateful to N. Bernard, M. Camilleri, K. Elder, F. Masson, D. Tarlinton, and E. Cretney for technical assistance and discussions. This work was supported by grants from the National Health and Medical Research Council of Australia (NHMRC), the Leukemia & Lymphoma Society (A.K.), the Wellcome Trust Foundation, the Howard Hughes Medical Institute, the Viertel Foundation (G.T.B.), and the Pfizer Australia Research Fellowship (S.L.N.).