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CGRP-Mediated Prolactin Upregulation: a Possible Pathomechanism in IgG4-Related Disease.

Qicai LiuYunfeng LinSheng ZhangMin ChenQingquan ChenHongbin RuiFang WangXiaoting LvFeng Gao
Published in: Inflammation (2020)
Similar to other immune-mediated diseases, IgG4-related disease (IgG4-RD) is the disease that develops in genetically susceptible individuals exposed to external or endogenous antigens. In the present study, it was confirmed that MAG (myelin-associated glycoprotein) antibodies (IgG, IgG4, and IgM) were detected by immunofluorescence (IFA) in serum of the patients with IgG4-RD. In vivo, the levels of prolactin and Th2 cytokines in CGRP+/- rats were higher than those in wild-type. Our findings indicate that the presence of CGRP-deficiency-mediated MAG antibodies is a probable molecular basis for the initial events which were triggered in IgG4-RD immune responses via prolactin upregulation.
Keyphrases
  • immune response
  • wild type
  • cell proliferation
  • poor prognosis
  • signaling pathway
  • dendritic cells
  • toll like receptor
  • growth hormone
  • white matter
  • replacement therapy