Surfactant prevention of lung complications from cancer chemotherapy
A means and method for treating pulmonary fibrosis in animals is described. The compositions include surfactant lipids in a pharmaceutically acceptable carrier. Surfactant lipids have been found to suppress the synergistic effect of bleomycin and SP-A in enhancing proinflammatory cytokine production. Surfactant lipids are also effective in the prevention and treatment of pulmonary fibrosis resulting from exposure to inflammatory agents affecting cytokine production.
1. A method of reducing pulmonary cytokine production caused by inflammatory agents and treating pulmonary fibrosis in animals comprising: administering to an animal between about 30–800 mg/kg of a composition comprising surfactant lipids; wherein the composition is administered by a method selected from the group consisting of intratracheally, orally, subcutaneously, intravenously, intranasally, rectally, sublingually, and buccally; and further providing that the surfactant lipids are administered concurrently with an agent selected from the group consisting of bleomycin, nitrofurantoin, amiodarone, cyclophosphamide, methotrexate, and mixtures thereof.
2. The method of claim 1 wherein the surfactant lipids are administered concurrently with bleomycin.
3. A composition for reducing pulmonary cytokine production caused by inflammatory agents and treating pulmonary fibrosis in animals, said composition comprising surfactant lipids and an agent selected from the group consisting of bleomycin, nitrofurantoin, amiodarone, cyclophosphamide, and methotrexate; and a pharmaceutically acceptable carrier.
4. The composition of claim 3 comprising 30–800 mg/kg surfactant lipids.
5. The composition of claim 3 whereby the agent is bleomycin.
6. A composition for reducing pulmonary cytokine production caused by inflammatory agents and treating pulmonary fibrosis in animals, said composition comprising surfactant lipids and an agent selected from the group consisting of bleomycin, nitrofurantoin, amiodarone, cyclophosphamide, methotrexate, and mixtures thereof; and a pharmaceutically acceptable carrier.