BMC Gastroenterology (Feb 2009)

Transcript levels of different cytokines and chemokines correlate with clinical and endoscopic activity in ulcerative colitis

  • Hinz Ulf,
  • Braun Annika,
  • Karner Max,
  • Giese Thomas,
  • Zahn Alexandra,
  • Stremmel Wolfgang,
  • Ehehalt Robert

DOI
https://doi.org/10.1186/1471-230X-9-13
Journal volume & issue
Vol. 9, no. 1
p. 13

Abstract

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Abstract Background A definition of disease activity in ulcerative colitis (UC) is difficult. The clinical activity index (CAI) is only an indirect assessment tool of bowel inflammation and the endoscopic activity index (EAI) sometimes cannot reflect the severity of disease to the full extent. Therefore, there is a need for an objective means to quantify inflammatory activity in mucosal biopsies. In our study, we wanted to examine the correlation between transcript levels of interleukin 8 (CXCL8), interferon γ inducible protein 10 (CXCL10), myeloid-related protein 14 (calgranulin B), macrophage inflammatory protein 2 α (CXCL2) with CAI and EAI in UC. Methods Cytokine and chemokine transcripts were quantified using real-time PCR in 49 mucosal biopsies from 27 different patients with UC. Cytokine transcript levels were correlated with CAI and EAI. Results There was a statistically significant positive correlation between CXCL8 (r = 0.30; p Conclusion From our data, we conclude that real-time PCR quantification of CXCL8, CXCL10, calgranulin B and CXCL2 in colonic biopsies is a simple and objective method for grading inflammation of intestinal mucosa in UC. CXCL8, CXCL10, calgranulin B and CXCL2 might be used as biomarkers and thus as an objective tool especially in clinical trials to evaluate anti-inflammatory and immunomodulatory regimens.