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A novel molecular interaction for the adhesion of follicular CD4 T cells to follicular DC
Authors:Kent S. Boles  William Vermi  Fabio Facchetti  Anja Fuchs  Timothy J. Wilson  Thomas G. Diacovo  Marina Cella  Marco Colonna
Affiliation:1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA;2. Department of Pathology, University of Brescia, Brescia, Italy;3. Department of Pediatrics, Irving Cancer Research Center, Columbia University Medical Center, NY, USA;4. Department of Pathology, Irving Cancer Research Center, Columbia University Medical Center, NY, USA
Abstract:Nectins and Nectin‐like molecules (Necl) play a critical role in cell polarity within epithelia and in the nervous and reproductive systems. Recently, immune receptors specific for Nectins/Necl have been described. Since the expression and distribution of Nectins/Necl is often subverted during tumorigenesis, it has been suggested that the immune system may use these receptors to recognize and eliminate tumors. Here we describe a novel immunoreceptor, Washington University Cell Adhesion Molecule, which is expressed on human follicular B helper T cells (TFH) and binds a Nectin/Necl family member, the poliovirus receptor (PVR), under both static and flow conditions. Furthermore, we demonstrate that PVR is abundantly expressed by follicular DC (FDC) within the germinal center. These results reveal a novel molecular interaction that mediates adhesion of TFH to FDC and provide the first evidence that immune receptors for Nectins/Necl may be involved the generation of T cell‐dependent antibody responses.
Keywords:Follicular B helper T cells  Follicular DC  Human  Nectins
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