Abstract |
The growth of MethA tumor was significantly inhibited by oral administration of the alpha- glucan SPR-901 in BALB/c (+/+) mice but not in nude mice. Mice treated orally with SPR-901 exhibited an augmentation of antigen-specific resistance against rechallenge with the tumor cells. The tumor-neutralizing activity of regional lymph node cells from MethA-bearing mice against the tumor was augmented by oral administration of SPR-901. The tumor-neutralizing activity of lymph node cells from SPR-901-treated mice mainly appeared in Lyt2+ cells. Furthermore, lymphokine-activated killer activity of these cells was enhanced by administration of SPR-901. The antitumor effect of SPR-901 was abrogated in mice depleted of either L3T4+ or Lyt2+ cells, and in cyclosporin-A-treated mice. These results suggest that Lyt2+ cells are important effector cells in MethA-bearing mice orally administered SPR-901 and that functional exertion of both Lyt2+ and L3T4+ T cells is necessary for the antitumor effect of orally administered SPR-901 in vivo.
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Authors | Y Takeda, M Tanaka, H Miyazaki, S Takeo, K Nomoto, Y Yoshikai |
Journal | Cancer immunology, immunotherapy : CII
(Cancer Immunol Immunother)
Vol. 38
Issue 3
Pg. 143-8
(Mar 1994)
ISSN: 0340-7004 [Print] Germany |
PMID | 7907272
(Publication Type: Journal Article)
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Chemical References |
- Adjuvants, Immunologic
- Antigens, Ly
- Antineoplastic Agents
- Glucans
- rice bran saccharide
- Cyclosporine
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Topics |
- Adjuvants, Immunologic
- Administration, Oral
- Animals
- Antigens, Ly
(immunology)
- Antineoplastic Agents
- CD4-Positive T-Lymphocytes
(immunology)
- Cyclosporine
(pharmacology)
- Female
- Glucans
(administration & dosage)
- Immunotherapy
- Killer Cells, Lymphokine-Activated
(immunology)
- Lymph Nodes
(cytology)
- Lymphocyte Depletion
- Mice
- Mice, Inbred BALB C
- Sarcoma, Experimental
(therapy)
- T-Lymphocyte Subsets
(immunology)
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