Enhanced LL-37 expression following vitamin D supplementation in patients with cirrhosis and spontaneous bacterial peritonitis

Liver Int. 2016 Jan;36(1):68-75. doi: 10.1111/liv.12888. Epub 2015 Sep 18.

Abstract

Background & aims: The morbidity and mortality of spontaneous bacterial peritonitis (SBP) are high among patients with cirrhosis; however, the mechanisms of SBP pathogenesis are poorly understood. This study aimed to determine the role of the vitamin D-LL-37 pathway in the pathogenesis and treatment in patients with cirrhosis and SBP.

Methods: Serum 25-hydroxyvitamin D concentrations of 119 patients with chronic liver diseases were tested. Vitamin D receptor (VDR) and LL-37 in peritoneal leucocytes of cirrhotic and ascitic patients with SBP were detected and compared with those without SBP. Then the peritoneal macrophages of non-infected patients were cultured and activated by lipopolysaccharide (LPS) to analyse the changes of VDR and LL-37 expressions after incubation with vitamin D.

Results: Vitamin D deficiency or insufficiency was found in all of patients with cirrhosis. LPS inhibited VDR and LL-37 expression in peritoneal macrophages [1.3-fold decrease (P = 0.003) and 20-fold decrease (P = 0.010) respectively]. However, vitamin D could reverse the inhibition of both VDR and LL-37 [1.5-fold increase (P = 0.001) and 2000-fold increase (P < 0.001) respectively]. The effect of the incubation time following vitamin D supplementation was significant for LL-37 expression, with a peak expression found at 36 h (P < 0.001).

Conclusions: When vitamin D levels were low, bacteria inhibited VDR and LL-37 responses in peritoneal macrophages as a mechanism to evade antibacterial defence. Vitamin D supplementation could up-regulate peritoneal macrophage VDR and LL-37 expressions, which resulted in an enhanced immunological defence against SBP in patients with cirrhosis and ascites.

Keywords: LL-37; peritoneal macrophages; spontaneous bacterial peritonitis; vitamin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Ascites* / metabolism
  • Ascites* / pathology
  • Ascites* / prevention & control
  • Ascitic Fluid / metabolism
  • Ascitic Fluid / pathology
  • Bacterial Infections* / etiology
  • Bacterial Infections* / metabolism
  • Bacterial Infections* / pathology
  • Bacterial Physiological Phenomena
  • Cathelicidins / metabolism*
  • Cells, Cultured
  • Female
  • Humans
  • Liver Cirrhosis* / complications
  • Liver Cirrhosis* / immunology
  • Macrophages, Peritoneal* / drug effects
  • Macrophages, Peritoneal* / metabolism
  • Macrophages, Peritoneal* / pathology
  • Male
  • Middle Aged
  • Peptide Fragments / metabolism*
  • Peritonitis* / etiology
  • Peritonitis* / metabolism
  • Peritonitis* / microbiology
  • Peritonitis* / pathology
  • Receptors, Calcitriol / metabolism
  • Vitamin D Deficiency* / complications
  • Vitamin D Deficiency* / metabolism
  • Vitamin D Deficiency* / pathology
  • Vitamin D* / metabolism
  • Vitamin D* / pharmacology
  • Vitamins / metabolism
  • Vitamins / pharmacology

Substances

  • Cathelicidins
  • Peptide Fragments
  • Receptors, Calcitriol
  • Vitamins
  • cathelicidin LL-37 (18-29), human
  • Vitamin D