BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1

  • Nat Immunol. 2003 Jul;4(7):670-9. doi: 10.1038/ni944.
Norihiko Watanabe  1 ,  Maya Gavrieli ,  John R Sedy ,  Jianfei Yang ,  Francesca Fallarino ,  Susan K Loftin ,  Michelle A Hurchla ,  Natalie Zimmerman ,  Julia Sim ,  Xingxing Zang ,  Theresa L Murphy ,  John H Russell ,  James P Allison ,  Kenneth M Murphy
Affiliations
  • 1. Department of Pathology & Immunology, Howard Hughes Medical Institute, Washington University School of Medicine, Box 8118, 660 South Euclid Avenue, St. Louis, Missouri 63110, USA.
PMID: 12796776 DOI: 10.1038/ni944
Abstract

During activation, T cells express receptors for receiving positive and negative costimulatory signals. Here we identify the B and T lymphocyte attenuator (BTLA), an immunoglobulin domain-containing glycoprotein with two immunoreceptor tyrosine-based inhibitory motifs. BTLA is not expressed by naive T cells, but it is induced during activation and remains expressed on T helper type 1 (T(H)1) but not T(H)2 cells. Crosslinking BTLA with antigen receptors induces its tyrosine phosphorylation and association with the Src homology domain 2 (SH2)-containing Protein tyrosine phosphatases SHP-1 and SHP-2, and attenuates production of interleukin 2 (IL-2). BTLA-deficient T cells show increased proliferation, and BTLA-deficient mice have increased specific antibody responses and enhanced sensitivity to Experimental Autoimmune Encephalomyelitis. B7x, a peripheral homolog of B7, is a ligand of BTLA. Thus, BTLA is a third inhibitory receptor on T lymphocytes with similarities to cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and programmed death 1 (PD-1).