A novel molecular interaction for the adhesion of follicular CD4 T cells to follicular DC
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Boles, Kent S.
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Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
Boles, Kent S.
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Vermi, William
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Facchetti, Fabio
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Fuchs, Anja
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Wilson, Timothy J.
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Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
Wilson, Timothy J.
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Diacovo, Thomas G.
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Columbia Univ, Med Ctr, Irving Canc Res Ctr, Dept Pediat, New York, NY 10027 USA
Columbia Univ, Med Ctr, Irving Canc Res Ctr, Dept Pathol, New York, NY 10027 USAWashington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
Diacovo, Thomas G.
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Cella, Marina
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Colonna, Marco
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[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Univ Brescia, Dept Pathol, Brescia, Italy
[3] Columbia Univ, Med Ctr, Irving Canc Res Ctr, Dept Pediat, New York, NY 10027 USA
[4] Columbia Univ, Med Ctr, Irving Canc Res Ctr, Dept Pathol, New York, NY 10027 USA
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.