4.8 Article

Pathogenicity of IgG in patients with IgG4-related disease

期刊

GUT
卷 65, 期 8, 页码 1322-1332

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2015-310336

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资金

  1. JSPS [21229009, 24229005, 24659363]
  2. research programme of the Project for Development of Innovative Research on Cancer Therapeutics (P-Direct) from the Ministry of Education, Culture, Sports, Science and Technology of Japan
  3. Health and Labour Sciences Research Grants for Research on Intractable Diseases from the Ministry of Health, Labour and Welfare, Japan
  4. Practical Research Project for Rare/Intractable Diseases Grant in Japan Agency for Medical Research and Development (AMED)
  5. Grants-in-Aid for Scientific Research [15K15290, 24659363, 21229009, 26893123, 26293173, 16K19339, 16K15427] Funding Source: KAKEN

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Objective IgG4-related disease (IgG4-RD) is a systemic disease characterised by elevated serum IgG4 and IgG4-positive lymphoplasmacytic infiltration in the affected tissues. The pathogenic role of IgGs, including IgG4, in patients with IgG4-RD, however, is unknown. Design We examined the pathogenic activity of circulating IgGs in patients with IgG4-RD by injecting their IgGs into neonatal male Balb/c mice. Binding of patient IgGs to pancreatic tissue was also analysed in an ex vivo mouse organ culture model and in tissue samples from patients with autoimmune pancreatitis (AIP). Results Subcutaneous injection of patient IgG, but not control IgG, resulted in pancreatic and salivary gland injuries. Pancreatic injury was also induced by injecting patient IgG1 or IgG4, with more destructive changes induced by IgG1 than by IgG4. The potent pathogenic activity of patient IgG1 was significantly inhibited by simultaneous injection of patient IgG4. Binding of patient IgG, especially IgG1 and IgG4, to pancreatic tissue was confirmed in both the mouse model and AIP tissue samples. Conclusions IgG1 and IgG4 from patients with IgG4-RD have pathogenic activities through binding affected tissues in neonatal mice.

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