HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Mucosal expression of basic fibroblastic growth factor, syndecan 1 and tumour necrosis factor-α in Crohn's disease in deep remission under treatment with anti-TNFα antibodies.

AbstractBACKGROUND AND AIMS:
Both inflammation and fibrosis may be detected in Crohn's disease (CD). The molecular pattern of Basic Fibroblastic Growth Factor (bFGF) and Syndecan-1 (SD1) expression is altered in stenosing CD, but we do not know what the behaviour of this teamwork factor is in CD in deep remission under treatment with anti-TNFα antibodies. Our aim was to compare the expression of bFGF, SD1 and TNF-α in patients with CD in deep remission under treatment with Infliximab (IFX) or Adalimumab (ADA) and a control group of patients with active CD.
METHODS:
We assessed the expression of bFGF, SD1 and TNF-α in 10 patients with active CD and in 28 patients with CD in sustained deep remission for at least 6 months. All patients underwent surveillance colonoscopy with biopsies, while receiving maintenance therapy with IFX or ADA. Analysis was conducted by real-time reverse transcriptase PCR (RT-PCR) in biopsy samples.
RESULTS:
We found that bFGF, SD1 and TNF-α were significantly reduced under treatment with anti-TNFα versus controls (p=0.000). bFGF and SD1 expression were similar between IFX and ADA patients (p=0.335 and p=0.289, respectively), while TNF-α was significantly under-expressed in ADA patients (p=0.008).
CONCLUSIONS:
bFGF, SD1 and TNF-α are significantly reduced in CD patients in deep remission under treatment with anti-TNFα, likely as an expression of optimal control of inflammation. The significance of the TNF-α under-expression in patients under treatment with ADA with respect to those under treatment with IFX should be elucidated in further studies.
AuthorsAntonio Tursi, Walter Elisei, Mariabeatrice Principi, Cosimo Damiano Inchingolo, Rosanna Nenna, Marcello Picchio, Floriana Giorgio, Enzo Ierardi, Giovanni Brandimarte
JournalJournal of gastrointestinal and liver diseases : JGLD (J Gastrointestin Liver Dis) Vol. 23 Issue 3 Pg. 261-5 (Sep 2014) ISSN: 1842-1121 [Electronic] Romania
PMID25267953 (Publication Type: Journal Article, Multicenter Study, Observational Study)
Chemical References
  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Gastrointestinal Agents
  • SDC1 protein, human
  • Syndecan-1
  • Tumor Necrosis Factor-alpha
  • Fibroblast Growth Factor 2
  • Infliximab
  • Adalimumab
Topics
  • Adalimumab
  • Adult
  • Anti-Inflammatory Agents (therapeutic use)
  • Antibodies, Monoclonal (therapeutic use)
  • Antibodies, Monoclonal, Humanized (therapeutic use)
  • Biopsy
  • Colon (drug effects, immunology, metabolism, pathology)
  • Colonoscopy
  • Crohn Disease (diagnosis, drug therapy, immunology, metabolism)
  • Female
  • Fibroblast Growth Factor 2 (metabolism)
  • Gastrointestinal Agents (therapeutic use)
  • Humans
  • Infliximab
  • Intestinal Mucosa (drug effects, immunology, metabolism, pathology)
  • Italy
  • Male
  • Middle Aged
  • Remission Induction
  • Retrospective Studies
  • Syndecan-1 (metabolism)
  • Time Factors
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha (antagonists & inhibitors, metabolism)
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: