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Du-Moxibustion in a Mouse Model of Ankylosing Spondylitis
Published on: October 27, 2023
Treatment of ankylosing spondylitis with moxifloxacin
1Division of Rheumatology, Nazilli State Hospital, Turkey. porphyromonas@superonline.com
Abstract:
Ankylosing spondylitis (AS) is a human leukocyte antigen (HLA)-B27-associated chronic inflammatory disease of unknown etiology. There are few effective treatments for ankylosing spondylitis, which causes substantial morbidity. The relationship between AS and enterobacteria, especially Klebsiella pneumoniae, has been reported from several groups in several countries. We performed an open-label trial of moxifloxacin, a fluoroquinolone antibiotic, in patients with ankylosing spondylitis. Treatment with moxifloxacin resulted in significant and sustained improvement. At 12 weeks, patients treated with moxifloxacin had significantly greater improvement in primary outcome measures (P < 0.001). The moxifloxacin group also had significantly greater improvement in many of the secondary outcome measures (P < 0.001). In this twelve-week trial, moxifloxacin was safe, well tolerated, and associated with improvement in the inflammatory symptoms of AS.
Insights
Moxifloxacin, an antibiotic, significantly improved symptoms in patients with ankylosing spondylitis (AS) over 12 weeks. This trial suggests a potential new treatment for this chronic inflammatory disease.
Area of Science:
- Rheumatology
- Infectious Diseases
- Microbiology
Background:
- Ankylosing spondylitis (AS) is a chronic inflammatory disease linked to HLA-B27, with limited effective treatments.
- A potential connection between AS and enterobacteria, particularly Klebsiella pneumoniae, has been observed globally.
- The underlying etiology of AS remains largely unknown, contributing to treatment challenges.
Purpose of the Study:
- To evaluate the efficacy and safety of moxifloxacin, a fluoroquinolone antibiotic, in treating patients with ankylosing spondylitis.
- To assess the impact of moxifloxacin on primary and secondary outcome measures of AS inflammatory symptoms.
Main Methods:
- An open-label trial was conducted involving patients diagnosed with ankylosing spondylitis.
- Participants received treatment with moxifloxacin for a duration of twelve weeks.
- Clinical outcomes, including primary and secondary measures of inflammation, were monitored.
Main Results:
- Moxifloxacin treatment led to significant and sustained improvements in patients with AS at the 12-week mark.
- Primary outcome measures showed statistically significant improvement (P < 0.001) in the moxifloxacin group.
- Significant improvements were also observed in numerous secondary outcome measures (P < 0.001).
Conclusions:
- Moxifloxacin demonstrated safety and good tolerability in the twelve-week trial.
- The antibiotic was associated with marked improvement in the inflammatory symptoms characteristic of ankylosing spondylitis.
- These findings suggest moxifloxacin as a promising therapeutic option for managing AS.
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