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We read with interest the paper by Wallace ZS, plasmablasts as a biomarker for IgG4-related disease (IgG4-RD), independent of serum IgG4 concentrations.1 Evidently, the study showed that patients with active, untreated IgG4-RD have elevations in their circulating plasmablast counts. We strongly approve their results and propose new insights into plasmablast subsets in …
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