Abstract
RHINOVIRUSES belong to the picornavirus family and cause about 50% of common colds1. Most rhinoviruses and some cox-sackie viruses share a common receptor on human cells. The glycoprotein intercellular adhesion molecule-1 (ICAM-1) has recently been identified as the cellular receptor for the subgroup of rhinoviruses known as the major groups2–4. ICAM-1 is a member of the immunoglobulin supergene family and is a ligand for lymphocyte function-associated antigen-1 (LFA-1)5–7; these ICAM-1/LFA-1 interactions are critical to many cell adhesion processes involved in the immunological response8–11. Because anti-ICAM-1 antibodies can block binding of major-group rhinoviruses to cells, we considered that antagonism of virus-receptor interaction might be a way of preventing rhinovirus infection. We have constructed and purified a soluble form of the ICAM-1 molecule, which is normally membrane-bound, and demonstrated that it is a potent and specific inhibitor of rhinovirus infection.
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Marlin, S., Staunton, D., Springer, T. et al. A soluble form of intercellular adhesion molecule-1 inhibits rhinovirus infection. Nature 344, 70–72 (1990). https://doi.org/10.1038/344070a0
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DOI: https://doi.org/10.1038/344070a0
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