Phorbol ester-induced enhancement in lytic activity of CD8+ splenic T cells from low-dose melphalan-treated MOPC-315-tumor bearers

Author:

Weiskirch Larry M.,Baumgartel Barbara A.,Barker Edward,Mokyr Margalit B.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology,Immunology,Immunology and Allergy

Reference30 articles.

1. Awwad M, North JR (1989) Cyclophosphamide-induced immunologically mediated regression of a cyclophosphamide-resistant murine tumor: a consequence of eliminating precursor L3T4+ suppressor T cells. Cancer Res 49: 1649

2. Ben-Efraim S, Bocian RC, Mokyr MB, Dray S (1983) Increase in the effectiveness of melphalan therapy with progression of MOPC-315 plasmacytoma tumor growth. Cancer Immunol Immunother 15: 101

3. Berrebi G, Takayama H, Sitkovsky MV (1987) Antigen receptor interaction requirement for conjugate formation and lethal-hit triggering by cytotoxic T lymphocytes can be bypassed by protein kinase C activation and Ca2+ ionophores. Proc Natl Acad Sci USA 84: 1364

4. Bocian RC, Ben-Efraim S, Dray S, Mokyr MB (1984) Melphalanmediated potentiation of antitumor immune responsiveness of immunosuppressed spleen cells from mice bearing a large MOPC-315 tumor. Cancer Immunol Immunother 18: 41

5. Dialynas DP, Quan ZS, Wall KA, Pierres A, Quintans J, Loken MR, Pierres M, Fitch FW (1983) Characterization of the murine T cell surface molecule, designated L3T4 identified by monoclonal antibody GK 1.5: Similarity of L3T4 to the human Leu-3/T4 molecule. J Immunol 131: 2445

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