HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

High doses of thymosin alpha 1 enhance the anti-tumor efficacy of combination chemo-immunotherapy for murine B16 melanoma.

AbstractBACKGROUND:
We have reported previously that combined chemo-immunotherapy with cyclophosphamide (CY), thymosin alpha 1 (T alpha 1) and low dose interferon alpha,beta (IFN alpha beta) has significant anti-tumour effects. Here, using mouse B16 melanoma as a model, we tested whether increasing the dose of T alpha 1 could increase the anti-tumour activity of triple combination chemo-immunotherapy.
MATERIALS AND METHODS:
C57BL/6 mice were challenged subcutaneously with B16 melanoma cells and injected intraperitoneally with saline, CY (200 mg/kg, day 7), or CY with T alpha 1 (200, 600 or 6000 micrograms/kg/day, days 10-13) and IFN alpha beta (30,000 I.U., day 13).
RESULTS:
Chemo-immunotherapy with high dose (HD)-T alpha 1 caused complete tumour regression for 27.5 days after tumour cell injection (3.9 times longer than untreated controls) and delayed tumour relapse compared to all other groups. Moreover, it significantly increased the median survival time of treated mice, and cured an average of 23% of animals, while none was cured in any other group. Splenocytes from HD-T alpha 1-treated mice showed markedly increased cytotoxic activities against both YAC-l and autologous B16 tumour cells. HD-T alpha 1 treatment reversed the tumour-induced reduction in percentages of CD3 and CD4-positive splenocytes to non-tumour levels, and it increased percentages of CD8, B220 and IL-2R beta-positive cells to well beyond non-tumour controls.
CONCLUSIONS:
High doses of T alpha 1 improve anti-tumour efficacy of tnple chemo-immunotherapy against B16 melanoma. These effects appear to be mediated by stimulation of the host immune response.
AuthorsF Pica, M Fraschetti, C Matteucci, C Tuthill, G Rasi
JournalAnticancer research (Anticancer Res) 1998 Sep-Oct Vol. 18 Issue 5A Pg. 3571-8 ISSN: 0250-7005 [Print] Greece
PMID9858941 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adjuvants, Immunologic
  • Interferon-alpha
  • Thymosin
  • Interferon-beta
  • Cyclophosphamide
  • Thymalfasin
Topics
  • Adjuvants, Immunologic (therapeutic use)
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Cyclophosphamide (administration & dosage)
  • Immunotherapy
  • Interferon-alpha (administration & dosage)
  • Interferon-beta (administration & dosage)
  • Killer Cells, Lymphokine-Activated (drug effects, immunology)
  • Lymphocyte Subsets (immunology)
  • Male
  • Melanoma, Experimental (drug therapy, immunology, therapy)
  • Mice
  • Mice, Inbred C57BL
  • Spleen (cytology, immunology)
  • Thymalfasin
  • Thymosin (analogs & derivatives, therapeutic use)

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: