Induction of Colony-Stimulating Factor(s) After Administration of A Traditional Chinese Medicine, Xiao-Chai-Hu-Tang (Japanese Name: Shosaiko-To)

References

• Kawakita T., Yamada A., Kumazawa Y., Nomoto K. Functional maturation of immature B cells accumulated in the periphery by an intraperitoneal administration of a traditional Chinese medicine, xiao-chai-hu-tang (Japanese name: shosaiko-to). Immunopharmacol. Immunotoxicol. 1987; 9: 299
   PubMed Web of Science ®Google Scholar
• Kawakita T., Yamada A., Mitsuyama M., Kumazawa Y., Nomoto K. Protective effect of a traditional Chinese medicine, xiao-chai-hu-tang (Japanese name: shosaiko-to), on Pseudomonas aeruginosa infection in mice, Immunopharmacol. Immunotoxicol. 1987; 9: 523
   PubMed Web of Science ®Google Scholar
• Kumazawa Y., Takimoto H., Miura S., Nishimura C., Yamada A., Kawakita T., Nomoto K. Activation of murine peritoneal macrophages by intraperineal administration of a traditional Chinese medicine, xiao-chi-hu-tang (Japanese name: shosaiko-to). Int. J. Immunopharmacol. 1988; 10: 395
   PubMed Web of Science ®Google Scholar
• Kawakita T., Nakai S., Kumazawa Y., Miura O., Yumioka E., Nomoto K. Induction of interferon after administration of a traditional Chinese medicine, xiao-chai-hu-tang (Japanese name: shosaiko-to). Int. J. Immunopharamacol. 1990, in press
   Google Scholar
• Kawakita T., Yamada A., Mitsuyama M., Kumazawa Y., Nomoto K. Protective effect of a traditional Chinese medicine, xiao-chai-hu-tang (Japanese name: shosaiko-to), on Listeria monocytogenes infection in mice. Immunopharmacol. Immunotoxicol. 1988; 10: 345
   PubMed Web of Science ®Google Scholar
• Kawakita T., Mitsuyama M., Kumazawa Y., Miura O., Yumioka E., Nomoto K. Contribution of cytokines to time-dependent augmentation of resistance against Listeria monocytogenes after administration of a traditional Chinese medicine, xiao-chi-hu-tang (Japanese name: shosaiko-to). Immunopharmacol. Immunotoxicol. 1989; 11: 233
   PubMed Web of Science ®Google Scholar
• Bradley T. R., Metcalf D. The growth of mouse bone marrow cells in vitro. Aust. J. Exp. Biol. Med. Sci. 1966; 44: 287
   PubMedGoogle Scholar
• Pluznik D. H., Sachs L. The cloning of normal “Mast” cells in tissue culture. J. Cell. Comp. Physiol. 1965; 66: 319
   Google Scholar
• Gasson J. C., Weisbart R. H., Kaufman S. E., Clark S. C., Hewick R. M., Wong G. G., Golde D. W. Purified human granulocyte-macrophage colony-stimulating factor:direct action on neutrophils. Science 1984; 226: 1339
   PubMed Web of Science ®Google Scholar
• Grabstein K. H., Urdal D. L., Tushinski R. J, Mochizuki D. Y., Price' V. L., Cantrell M. A., Gillis S., Conlon P. J. Induction of macrophage tumoricidal activity by granulocyte-macrophage colony-stimulating factor. Science 1986; 232: 506
   PubMed Web of Science ®Google Scholar
• Weibart R. H., Golde D. W., Clark S. C., Wong G. G., Gasson J. C. Human granulocyte-macrophage colony-stimulating factor is a neutrophil activator. Nature 1985; 314: 361
   PubMedGoogle Scholar
• Wing E. J., Ampel N. M., Waheed A., Shadduck R. K. macrophage colony-stimulating factor (M-CSF) enhances the capacity of murine macrophages to secrete oxygen reduction products. J. Immunol. 1985; 135: 2052
   PubMedGoogle Scholar
• Wing E. J., Waheen A., Shadduck R. K., Nagle L. S., Stephenson K. Effect of colony stimulating factor on murine macrophages. Induction of antitumor activity. J. Clin. Invest. 1982; 69: 270
   PubMed Web of Science ®Google Scholar
• Metcalf D., Foster R. Bone marrow colony-stimulating activity of serum from mice with viral-induced leukemia. J. Natl. Cancer Inst. 1967; 39: 1235
   PubMed Web of Science ®Google Scholar
• Rickard K. A., Morley A., Howard D., et al. The in vitro colony forming cell and the response to neutropenia. Blood 1971; 37: 6
   PubMed Web of Science ®Google Scholar
• Iscove N. N., Senn J. S., Till J. E., McCulloch E. A. Colony formation by normal and leukemic human marrow cells in culture: Effect of conditioned medium from human Leukocytes. Blood 1971; 37: 1
   PubMed Web of Science ®Google Scholar
• Horwitz D. A., Allison A. C., Ward P, Kight N. Identification of human mononuclear leukocyte populations by esterase staining. Clin. exp. Immunol. 1977; 30: 289
   PubMed Web of Science ®Google Scholar
• Leder L. D. Diagnostic experiences with the naphthol AS-D chloroacetate reaction. Blut 1969; 21: 1
   Google Scholar
• Watson J., Riblet R. Genetic control of response to bacterial lipopolysaccharides in mice I. Evidence for a single gene that influences mitogenic and immunogenic responses to lipopolysaccharides. J. Exp. Med. 1974; 140: 1147
   PubMedGoogle Scholar
• Staber F. G., Burgess A. W. Serum of lipopolysaccharide treated mice contains two types of colony stimulating factor, separable by affinity chromatography. J. Cell. Physiol. 1980; 102: 1
   PubMedGoogle Scholar
• Miura S., Kawamura I., Yamada A., Kawakita T., Kumazawa Y., Himeno K., Nomoto K. Effect of a traditional Chinese herbal medicine, ren-shen-yang-rong-tang (Japanese name: ninjin-yoei-to) on hematopoietic stem cells in mice. Int. J. Immunopharmacol. 1989; 11: 771
   PubMed Web of Science ®Google Scholar
• Magee D. M., Wing E. J. Secretion of colony-stimulating factors by T cell clones role in adoptive protection against Listeria monocytogenes. J. Immunol. 1989; 143: 2336
   PubMed Web of Science ®Google Scholar
• Buchmeier N. A., Schreiber R. D. Requirement of endogenous interferon-γ production for resolution of Listeria monocytogenes infection. Proc. Natl. Acad. Sci. USA 1985; 82: 7404
   PubMed Web of Science ®Google Scholar
• Kiderlen A. F., Kaufmann S. H.E., Lohmann-Mathes M. Protection of mice against the intracellular bacterium Listeria monocytogenes by recombinant immune interferon, Eur. J. Immunol. 1984; 14: 964
   Google Scholar
• Havell E. A. Evidence that tumor necrosis factor has an important role in antibacterial resistance. J. Immunol. 1989; 143: 2894
   PubMed Web of Science ®Google Scholar
• Desiderio J. V., Kiener P. A., Lin P., Warr G. A. Protection of mice against Listeria monocytogenes infection by recombinant human tumor necrosis factor alpha, Infect. Immun. 1989; 57: 1615
   Google Scholar
• Czuprynski C. J., Brown J. F., Young K. M., Cooley A. J., Kurtz R. Effect of murine recombinant Interleukin-1 on the host resistance to bacterial infection. J. Immunol. 1988; 140: 962
   PubMed Web of Science ®Google Scholar
• Czuprynski C. J., Brown J. F. Recombinant murine Interleukin-1 Q enhancement of nonspecific antibacterial resistance. Infection and Immunity 1987; 55: 2061
   PubMed Web of Science ®Google Scholar
• Quesenberry P., Morley A., Stohlman F., Jr., Rickarad K., Howard D., Smith M. Effect of endotoxin on granulopoiesis and colony-stimulating factor. New. Eng. J. Med. 1972; 286: 227
   PubMed Web of Science ®Google Scholar
• Mosmann T. R., Cherwinski H., Bond M. W., Giedlin M. A., Coffman R. L. Two types of murine helper T cell clone I. Definition according to profiles of lymphokine activities and secreted proteins. J. Immunol. 1986; 136: 2348
   PubMed Web of Science ®Google Scholar
• Zucali J. R., Dinarello C. A., Oblon D. J., Gross M. A., Anderson L., Weiner R. S. Interleukin 1 stimulate fibroblasts to produce granulocyte-macrophage colony-stimulating activity and prostaglandin E2. J. Clin. Invest. 1986; 77: 1857
   PubMed Web of Science ®Google Scholar
• Broudy V. C., Kaushansky K., Harlan J. M., Adamson J. W. Interleukin 1 stimulates human endothelial cells to produce granulocyte-macrophage colony-stimulating factor and granulocyte colony-stimulating factor. J. Immunol. 1987; 139: 464
   PubMed Web of Science ®Google Scholar
• Metcalf D. The molecular biology and functions of the granulocyte-macrophage colony-stimulating factors. Blood 1986; 67: 257
   PubMed Web of Science ®Google Scholar
• Cheers C., Haigh A. M., Kelso A., Metcalf D., Stanley E. R. Production of colony-stimulating factors (CSFs) during infection: separate determinating of macrophage-, granulocyte, granulocyte-macrophage-, and multi-CSFs. Infect. Immun. 1988; 56: 247, 35
   PubMed Web of Science ®Google Scholar
• Myers M. J., Witsell A. L., Schook L. B. Induction of serum colony-stimulating activity (CSA) following dimethylnitrosamine (DMN) exposure: effects on macrophage differentiation. Immunopharmacology 1989; 18: 125
   PubMedGoogle Scholar
• Nagatsu Y., Inoue M., Ogihara Y. Modification of macrophage functions by shosaikoto (Kampo medicine) leads to enhancement of immune response. Chem. Pharm. Bull. 1989; 37: 1540
   PubMed Web of Science ®Google Scholar