Author: Steinman, Lawrence
Title: A sugarâ€coated strategy to treat a rare neurologic disease provides a blueprint for a decoy glycan therapeutic and a potential vaccine for CoViDâ€19: An Editorial Highlight for “Selective inhibition of antiâ€MAG IgM autoantibody binding to myelin by an antigen specific glycopolymerâ€on https://doi.org/10.1111/jnc.15021 Cord-id: yy2p4wmg Document date: 2020_6_23
ID: yy2p4wmg
Snippet: In a rare neurologic disease known as IgM monoclonal gammopathy the immune system targets a sulfated trisaccharide known as the Human Natural Killerâ€1 (HNKâ€1) epitope that comprises a constituent of the myelin sheath known as MAG (myelinâ€associated glycoprotein). This Editorial highlights a study by Aliu and colleagues in the current issue of the Journal of Neurochemistry, in which the investigators constructed a biodegradable polyâ€lâ€lysine backbone with multiple copies of this sulfate
Document: In a rare neurologic disease known as IgM monoclonal gammopathy the immune system targets a sulfated trisaccharide known as the Human Natural Killerâ€1 (HNKâ€1) epitope that comprises a constituent of the myelin sheath known as MAG (myelinâ€associated glycoprotein). This Editorial highlights a study by Aliu and colleagues in the current issue of the Journal of Neurochemistry, in which the investigators constructed a biodegradable polyâ€lâ€lysine backbone with multiple copies of this sulfated HNKâ€1 trisaccharide. This decoy, poly(phenyl disodium 3â€Oâ€sulfoâ€Î²â€dâ€glucopyranuronate)â€(1→3)â€Î²â€dâ€galactopyranoside, known as PPSGG, removed antiâ€MAG IgM autoantibodies from the blood, while not activating the immune system. These findings provide a path for the selective removal of a pathogenic set of antibodies that target the myelin sheath resulting in neuropathy. These findings are applicable to a parallel strategy for the generation of polysaccharides similar to those present in the receptorâ€binding domain of CoViDâ€19, which might inhibit viral adhesion to its receptor, the angiotensinâ€converting enzymeâ€2 (ACE2) protein, thereby impairing cellular uptake of the virus itself. The deployment of complex polysaccharides that mimic actual COVID19 polysaccharides on the spike protein may also provide a feasible structural basis for a vaccine. Carbohydrate mimics, if conjugated to a carrier or backbone, might provoke an immune response to the spike protein. A vaccine that targets critical carbohydrates on COVID19, and then neutralizes the virus would recapitulate a successful strategy employed in other microbial vaccines, like the pneumococcal vaccines and the meningococcal vaccines. These vaccines direct an immune response to complex carbohydrates and successfully prevent lifeâ€threatening disease. This paper provides lessons from a rare neurologic disease that may teach us strategies applicable to a global pandemic. [Image: see text]
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