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Updated: May 13, 2026

Sublingual Immunotherapy as an Alternative to Induce Protection Against Acute Respiratory Infections
Published on: August 30, 2014
Inhaled liposomal ciprofloxacin protects against lethal tularemia in the common marmoset
Rachel E Ireland1, Alejandro Nunez2, Wendy Butcher1
1CBR Division, Defence Science and Technology Laboratory (Dstl), Salisbury, Wiltshire, United Kingdom.
Abstract:
Francisella tularensis is a gram-negative, intracellular bacterium that causes the disease tularemia. Tularemia is prevalent in North America, Europe, and Asia and is typically treated with injected and orally administered antibiotics, including streptomycin, gentamicin, doxycycline, and ciprofloxacin, administered for 10 to 21 days. New therapeutic options are required to reduce the potential of a relapse of disease. Inhaled liposomal-encapsulated ciprofloxacin has demonstrated protection in a murine model of tularemia. The efficacy was further assessed in a nonhuman primate model of tularemia. Mixed-sex common marmosets were challenged with F. tularensis by the inhalational route, and the efficacy of ciprofloxacin delivered by either the inhalational (Apulmiq liposomal formulation) or oral route was compared. Antibiotics were initiated either at 24 h post-challenge (post-exposure prophylaxis) or at the onset of fever (treatment) and continued for 7 days. All control (untreated) animals succumbed to infection by 8 days post-challenge. All animals that received antibiotics, by either route, survived the duration of the study, with bacterial clearance in all but one animal that received inhalational ciprofloxacin. Antibiotic treatment also reduced the physiological and immunological responses observed when compared to animals that received no antibiotics. Histological changes in the lungs were less frequent, although mild, resolving lesions were present in animals treated with ciprofloxacin delivered at the onset of fever by either route.
Insights
Inhaled liposomal ciprofloxacin effectively treated tularemia (caused by *Francisella tularensis*) in nonhuman primates, offering a promising new therapeutic option for this serious bacterial infection.
Area of Science:
- Infectious Diseases
- Microbiology
- Pharmacology
Background:
- Tularemia, caused by *Francisella tularensis*, is a serious bacterial infection prevalent globally.
- Current treatments for tularemia involve prolonged antibiotic courses, necessitating development of novel therapeutic strategies to prevent relapse.
Purpose of the Study:
- To evaluate the efficacy of inhaled liposomal ciprofloxacin against *Francisella tularensis* infection in a nonhuman primate model.
- To compare the effectiveness of inhalational versus oral ciprofloxacin administration for tularemia treatment.
Main Methods:
- Common marmosets were challenged with *F. tularensis* via inhalation.
- Ciprofloxacin was administered either via inhalation (liposomal formulation) or orally, starting at 24 hours post-challenge or at the onset of fever.
- Survival, bacterial clearance, physiological responses, and lung histology were assessed.
Main Results:
- All untreated control animals died within 8 days.
- All ciprofloxacin-treated animals survived, with most achieving bacterial clearance.
- Antibiotic treatment reduced adverse physiological and immunological responses compared to controls.
- Mild, resolving lung lesions were observed in animals treated at fever onset.
Conclusions:
- Inhaled liposomal ciprofloxacin is a potentially effective treatment for inhalational tularemia in primates.
- Both inhalational and oral ciprofloxacin administration improved outcomes, suggesting a viable alternative to current therapies.
- Further research into inhaled liposomal ciprofloxacin is warranted for tularemia treatment.
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