Abstract |
Culturing of mouse spleen cells with aloctin A (Alo A), a lectin having anti- tumor activity, resulted in the induction of cells cytotoxic to syngeneic and allogenic tumor cells in vitro. Alo A-induced killer cells could be generated from spleen cells of natural killer cell-deficient beige mice but not from those of T cell-deficient nude mice. The results of cytotoxicity assay after treatment with antisera plus complement indicated that the killer cells mainly consisted of Thy 1+, Lyt 1-2+, asialo GM1(1)-T cells. Their cytotoxic activity was markedly augmented by the presence of Alo A during the assay for cytotoxicity. The assay of IL2 in the culture fluid from Alo A-treated spleen cells and the effect of dexamethasone (DEX) on IL2 production from Alo A-stimulated spleen cells and on generation of killer cells suggested that generation of Alo A-induced killer cells was closely associated with the amount of IL2 released from the spleen cells in culture.
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Authors | K Imanishi, I Suzuki |
Journal | International journal of immunopharmacology
(Int J Immunopharmacol)
Vol. 8
Issue 7
Pg. 781-7
( 1986)
ISSN: 0192-0561 [Print] England |
PMID | 3491058
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- Interleukin-1
- Lectins
- Mitogens
- Plant Lectins
- aloctin A
- Complement System Proteins
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Topics |
- Animals
- Antibodies, Monoclonal
(immunology)
- Cell Line
- Complement System Proteins
(immunology)
- Cytotoxicity, Immunologic
(drug effects)
- Immunity, Cellular
(drug effects)
- Interleukin-1
(biosynthesis)
- Lectins
(pharmacology)
- Mice
- Mice, Inbred Strains
- Mitogens
- Neoplasms, Experimental
(immunology)
- Plant Lectins
- Spleen
(cytology, immunology)
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