New England Journal of Medicine · 2005 · 342 citations · 26 references
MedicinePharmacologyPharmacotherapyImmunopharmacologyImmunotherapyInnate ImmunityCrohn Disease PharmacotherapyGastrointestinal ImmunologyGastrointestinal InflammationImmunomodulatory Drug TherapyImmunomodulatory DrugsInflammatory Bowel DiseaseComparative Disease SeverityDisease Activity MeasurementDisease Severity IndexGranulocyte Colony-stimulating Factor AdministrationInflammatory Bowel Disease TherapyInnate Immune FunctionPlacebo Comparators
BACKGROUND: Sargramostim, granulocyte-macrophage colony-stimulating factor, a hematopoietic growth factor, stimulates cells of the intestinal innate immune system. Preliminary studies suggest sargramostim may have activity in Crohn's disease. To evaluate this novel therapeutic approach, we conducted a randomized, placebo-controlled trial. METHODS: Using a 2:1 ratio, we randomly assigned 124 patients with moderate-to-severe active Crohn's disease to receive 6 mug of sargramostim per kilogram per day or placebo subcutaneously for 56 days. Antibiotics and aminosalicylates were allowed; immunosuppressants and glucocorticoids were prohibited. The primary end point was a clinical response, defined by a decrease from baseline of at least 70 points in the Crohn's Disease Activity Index (CDAI) at the end of treatment (day 57). Other end points included changes in disease severity and the health-related quality of life and adverse events. RESULTS: There was no significant difference in the rate of the primary end point of a clinical response defined by a decrease of at least 70 points in the CDAI score on day 57 between the sargramostim and placebo groups (54 percent vs. 44 percent, P=0.28). However, significantly more patients in the sargramostim group than in the placebo group reached the secondary end points of a clinical response defined by a decrease from baseline of at least 100 points in the CDAI score on day 57 (48 percent vs. 26 percent, P=0.01) and of remission, defined by a CDAI score of 150 points or less on day 57 (40 percent vs. 19 percent, P=0.01). The rates of either type of clinical response and of remission were significantly higher in the sargramostim group than in the placebo group on day 29 of treatment and 30 days after treatment. The sargramostim group also had significant improvements in the quality of life. Mild-to-moderate injection-site reactions and bone pain were more common in the sargramostim group, and three patients in this group had serious adverse events possibly or probably related to treatment. CONCLUSIONS: This study was negative for the primary end point, but findings for the secondary end points suggest that sargramostim therapy decreased disease severity and improved the quality of life in patients with active Crohn's disease.
26
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Jean‐Pierre Hugot, Mathias Chamaillard, Habib Zouali et al. · Nature · 2001 · 5.6K citations
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Yasunori Ogura, Denise K. Bonen, Naohiro Inohara et al. · Nature · 2001 · 5K citations · Full text
Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2
Naohiro Inohara, Yasunori Ogura, Ana Fontalba et al. · Journal of Biological Chemistry · 2003 · 1.7K citations · Full text
J Y Mary, R Modigliani · Gut · 1989 · 881 citations · Full text