Details

Autor(en) / Beteiligte

• Kamata, K.
• Watanabe, T.
• Minaga, K.
• Hara, A.
• Sekai, I.
• Otsuka, Y.
• Yoshikawa, T.
• Park, A.‐M.
• Kudo, M.

Titel

Gut microbiome alterations in type 1 autoimmune pancreatitis after induction of remission by prednisolone

Ist Teil von

• Clinical and experimental immunology, 2020-12, Vol.202 (3), p.308-320

Ort / Verlag

England: Wiley Subscription Services, Inc

Erscheinungsjahr

2020

Link zum Volltext

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• Intestinal colonization by Klebsiella pneumoniae may play an intensifying role in the development of type １ autoimmune pancreatitis. Summary Although increasing evidence demonstrates the association between intestinal dysbiosis and pancreatic diseases such as chronic pancreatitis and pancreatic cancer, it remains largely unknown whether intestinal dysbiosis is involved in the immunopathogenesis of autoimmune pancreatitis (AIP). Recently, we found that intestinal dysbiosis mediates experimental AIP via the activation of plasmacytoid dendritic cells (pDCs), which can produce interferon (IFN)‐α and interleukin (IL)‐33. However, candidate intestinal bacteria, which promote the development of AIP, have not been identified. Fecal samples were obtained from type 1 AIP patients before and after prednisolone (PSL) treatment and subjected to 16S ribosomal RNA sequencing to evaluate the composition of intestinal bacteria. Induction of remission by PSL was associated with the complete disappearance of Klebsiella species from feces in two of the three analyzed patients with type 1 AIP. To assess the pathogenicity of Klebsiella species, mild experimental AIP was induced in MRL/MpJ mice by repeated injections of 10 μg of polyinosinic–polycytidylic acid [poly(I:C)], in combination with oral administration of heat‐killed Klebsiella pneumoniae. The AIP pathology score was significantly higher in MRL/MpJ mice that received both oral administration of heat‐killed K. pneumoniae and intraperitoneal injections of poly(I:C) than in those administered either agent alone. Pancreatic accumulation of pDCs capable of producing large amounts of IFN‐α and IL‐33 was also significantly higher in mice that received both treatments. These data suggest that intestinal colonization by K. pneumoniae may play an intensifying role in the development of type 1 AIP.