Antiparanodal antibodies and IgG subclasses in acute autoimmune neuropathy.
Luise AppeltshauserAnna-Michelle BrunderAnnika HeiniusPeter KörtvélyessyKlaus-Peter WandingerRalf JunkerCarmen VillmannClaudia SommerChristian SchmidtKathrin DopplerPublished in: Neurology(R) neuroimmunology & neuroinflammation (2020)
Our data (1) confirm and extend previous observations that antiparanodal IgG2/3 but not IgG4 antibodies can occur in acute-onset neuropathies manifesting as monophasic GBS, (2) suggest association of IgG3 to a favorable response to IVIg, and (3) lend support to the hypothesis that in some patients, an IgG subclass switch from IgG3 to IgG4 may be the correlate of a secondary progressive or relapsing course following a GBS-like onset.