HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Inhibition of spontaneous pulmonary metastases of Lewis lung carcinoma by oral treatment with Respivax and Broncho-Vaxom.

Abstract
The antimetastatic activity of orally administered polybacterial vaccines, Broncho-Vaxom (BV) and Respivax (RV) was examined in C57BL/6 mice, bearing implants of Lewis lung carcinoma (3LL) in the footpad. The oral administration of BV or RV for 10 consecutive days before or after surgery caused significant reduction of the number and volume of lung metastases. In addition, the therapeutic potential of BV and RV was examined in combination with chemotherapy to determine if there is additive activity. In animals bearing pulmonary micrometastases, treatment with a combination of cyclophosphamide at 50-150 mg/kg with BV or RV was found to be more effective than each of these treatments alone. In immune function studies it was established that the oral administration of BV and RV induced an increase in the number of cells, recovered by broncho-alveolar lavage, and alveolar macrophages were dominant in these cell populations. Furthermore, oral treatment of mice with these vaccines rendered their alveolar macrophages tumoricidal for syngeneic metastatic 3LL cells in vitro. These results show that pulmonary macrophages induced by oral administration of BV and RV played a key role in the inhibition of metastasis in 3LL-bearing mice.
AuthorsK T Kassabov, J N Stoychkov
JournalCancer immunology, immunotherapy : CII (Cancer Immunol Immunother) Vol. 33 Issue 5 Pg. 307-13 ( 1991) ISSN: 0340-7004 [Print] Germany
PMID1868489 (Publication Type: Journal Article)
Chemical References
  • Adjuvants, Immunologic
  • Bacterial Vaccines
  • Broncho-Vaxom
  • Cell Extracts
  • respivax
  • Cyclophosphamide
Topics
  • Adjuvants, Immunologic (therapeutic use)
  • Administration, Oral
  • Animals
  • Bacteria
  • Bacterial Vaccines (therapeutic use)
  • Cell Extracts
  • Combined Modality Therapy
  • Cyclophosphamide (therapeutic use)
  • Female
  • Immunotherapy
  • Lung (cytology, immunology)
  • Lung Neoplasms (drug therapy, secondary, therapy)
  • Macrophage Activation (immunology)
  • Macrophages (immunology)
  • Mice
  • Mice, Inbred C57BL
  • Pulmonary Alveoli (cytology, immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: