Abstract |
A transplantable hepatocarcinoma of strain 2 guinea pigs was used as an experimental model for immunotherapy of cancer. 6,6'-Dideoxy-6,6'-bis-mycoloylamino-alpha,alpha- trehalose (TDNM) was found to be more effective in producing regression of transplantable line-10 tumours than 6,6'-di-O-mycoloyl-alpha,alpha-trehalose (TDM) when combined with 6-O-stearoyl muramyldipeptide (L18-MDP). TDNM showed potent antitumour activity in combination with synthetic lipid A of Escherichia coli (compound 506), but not with the lipid A analogues (GLA-59 and 60). As with the combination of MDP derivative and lipid A analogue, MDP derivatives conjugated with GLA-60 (GMD compounds) showed no tumour regression activity of line-10 cells in guinea-pigs.
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Authors | H Ishida, I Saiki, S Saito, A Hasegawa, M Kiso, I Azuma |
Journal | Vaccine
(Vaccine)
Vol. 6
Issue 5
Pg. 440-4
(Oct 1988)
ISSN: 0264-410X [Print] Netherlands |
PMID | 3195200
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adjuvants, Immunologic
- Cord Factors
- Lipid A
- GLA 60
- Acetylmuramyl-Alanyl-Isoglutamine
- romurtide
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Topics |
- Acetylmuramyl-Alanyl-Isoglutamine
(administration & dosage, analogs & derivatives)
- Adjuvants, Immunologic
(administration & dosage)
- Animals
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage)
- Cord Factors
(administration & dosage)
- Guinea Pigs
- Lipid A
(administration & dosage, analogs & derivatives)
- Liver Neoplasms
(pathology, therapy)
- Liver Neoplasms, Experimental
(pathology, therapy)
- Remission Induction
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