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Eradication of Spontaneous Metastases and Activation of Alveolar Macrophages by Intravenous Injection of Liposomes Containing Muramyl Dipeptide

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Specialty Science
Date 1981 Mar 1
PMID 6940181
Citations 89
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Abstract

The multiple systemic administration of multilamellar liposomes composed of phosphatidylserine and phosphatidylcholine (molar ratio 3:7) that contained water-soluble muramyl dipeptide (MDP) activated alveolar macrophages to become tumoricidal and eradicated established spontaneous pulmonary and lymph node metastases. Spontaneously metastasizing melanoma cells were injected into the footpads of mice. After 4-5 weeks, the tumors were resected by a midfemoral amputation; 3 days later, twice-weekly injections of liposomes were initiated and continued for 4 weeks. In some experiments the mice were killed 2 weeks after the final treatment. Seventy-four percent of animals injected with liposomes containing MDP were free of visible metastases. In a separate life-span experiment, 60% of mice treated with liposome-encapsulated MDP were tumor-free 120 days after the last liposome treatment or 110 days after all control mice treated with free MDP or control liposome preparations had died of disseminated cancer. These data suggest that the systemic administration of liposomes containing MDP, or similar compounds that produce macrophage activation, may provide an additional useful approach to the therapeutic regimens currently used to eradicate cancer metastases.

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References
1.
Griswold Jr D . Consideration of the subcutaneously implanted B16 melanoma as a screening model for potential anticancer agents. Cancer Chemother Rep 2. 1972; 3(1):315-24. View

2.
Sone S, Poste G, Fidler I . Rat alveolar macrophages are susceptible to activation by free and liposome-encapsulated lymphokines. J Immunol. 1980; 124(5):2197-202. View

3.
Ellouz F, Adam A, Ciorbaru R, Lederer E . Minimal structural requirements for adjuvant activity of bacterial peptidoglycan derivatives. Biochem Biophys Res Commun. 1974; 59(4):1317-25. DOI: 10.1016/0006-291x(74)90458-6. View

4.
Fidler I . Activation in vitro of mouse macrophages by syngeneic, allogeneic, or xenogeneic lymphocyte supernatants. J Natl Cancer Inst. 1975; 55(5):1159-63. DOI: 10.1093/jnci/55.5.1159. View

5.
Audibert F, CHEDID L, Lefrancier P, CHOAY J . Distinctive adjuvanticity of synthetic analogs of mycobacterial water-soluble components. Cell Immunol. 1976; 21(2):243-9. DOI: 10.1016/0008-8749(76)90053-8. View