Immunomodulating activities of orally administered SMANCS, a polymer-conjugated derivative of the proteinaceous antibiotic neocarzinostatin, in an oily formulation

This publication has 12 references indexed in Scilit:

• Depletion of macrophages expressing I-J antigen results in efficient generation of alloreactive cytotoxic T lymphocytes
  Cellular Immunology, 1990
• Stimulation of non-specific resistance to tumors in the mouse using a poly(maleic-acid-styrene)-conjugated neocarzinostatin
  Cancer Immunology, Immunotherapy, 1989
• Conjugation of poly(styrene-co-maleic acid) derivatives to the antitumor protein neocarzinostatin: pronounced improvements in pharmacological properties
  Journal of Medicinal Chemistry, 1985
• Induction of Interferon and Activation of NK Cells and Macrophages in Mice by Oral Administration of Ge‐132, an Organic Germanium Compound
  Microbiology and Immunology, 1985
• Selective targeting of anti-cancer drug and simultaneous image enhancement in solid tumors by arterially administered lipid contrast medium
  Cancer, 1984
• Tailor-making of protein drugs by polymer conjugation for tumor targeting: A brief review on smancs
  Protein Journal, 1984
• Effect of arterial administration of high-molecular-weight anticancer agent SMANCS with lipid lymphographic agent on hepatoma: a preliminary report
  European Journal of Cancer and Clinical Oncology, 1983
• In vivo effect of anti-asialo GM1 antibody on natural killer activity
  Nature, 1981
• A LIPOPHILIC DERIVATIVE OF NEOCARZINOSTATIN A Polymer Conjugation of an Antitumor Protein Antibiotic*
  International Journal of Peptide and Protein Research, 1979
• Augmentation of delayed-type hypersensitivity by doses of cyclophosphamide which do not affect antibody responses.
  The Journal of Experimental Medicine, 1975