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Nat Commun ; 9(1): 2561, 2018 07 02.
Article in English | MEDLINE | ID: mdl-29967450

ABSTRACT

Dysfunction of CD8+ T cells can lead to the development of chronic viral infection. Identifying mechanisms responsible for such T cell dysfunction is therefore of great importance to understand how to prevent persistent viral infection. Here we show using lymphocytic choriomeningitis virus (LCMV) infection that carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) is fundamental for recruiting lymphocyte-specific protein kinase (Lck) into the T cell receptor complex to form an efficient immunological synapse. CEACAM1 is essential for activation of CD8+ T cells, and the absence of CEACAM1 on virus-specific CD8+ T cells limits the antiviral CD8+ T cell response. Treatment with anti-CEACAM1 antibody stabilizes Lck in the immunological synapse, prevents CD8+ T cell exhaustion, and improves control of virus infection in vivo. Treatment of human virus-specific CD8+ T cells with anti-CEACAM1 antibody similarly enhances their proliferation. We conclude that CEACAM1 is an important regulator of virus-specific CD8+ T cell functions in mice and humans and represents a promising therapeutic target for modulating CD8+ T cells.


Subject(s)
Antigens, CD/metabolism , CD8-Positive T-Lymphocytes/immunology , Carcinoembryonic Antigen/metabolism , Cell Adhesion Molecules/metabolism , Lymphocytic Choriomeningitis/immunology , Lymphocytic choriomeningitis virus/immunology , Adoptive Transfer , Animals , Bone Marrow Transplantation , CD8-Positive T-Lymphocytes/metabolism , Carcinoembryonic Antigen/genetics , Chimera , Chronic Disease , Female , Humans , Lymphocyte Specific Protein Tyrosine Kinase p56(lck)/metabolism , Lymphocytic Choriomeningitis/virology , Lymphocytic choriomeningitis virus/pathogenicity , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic
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