Augmentation of Host Resistance to Listeria Monocytogenes Infection by A Traditional Chinese Medicine, Ren-Shen-Yang-Rong-Tang (Japanese Name: Ninjin-Youei-To)

References

• 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-youei-to) on hematopoietic stem cells in mice, Int. J. Immunopharmacol. 1989; 11: 771
   Google Scholar
• Yonekura K., Kawakita T., Mitsuyama M., Miura O., Yumioka E., Suzuki A., Nomoto K. Induction of colony-stimulating factor(s) after administration of a traditional Chinese medicine, xiao-chai-hu-tang (Japanese name: shosaiko-to). Immunopharmacol. Immunotoxicol. 1990; 12: 647
   PubMed Web of Science ®Google Scholar
• Okamura S., Shimoda K., Li X., Omori F., Haga K., Niho Y. A traditional Chinese herbal medicine, ren-shen-yang-rong-tang (Japanese name: ninjin-youei-to) augments the production of granulocyte-macrophage colony-stimulating factor from human peripheral blood mononuclear cells in vitro. Int. J. Immunopharmacol. 1991, in press
   Web of Science ®Google Scholar
• Harada N., Okamura S., Shimoda K., Omori F., Niho Y. Influence of a traditional Chinese herbal medicine, ren-shen-yang-rong-tang (Japanese name: ninjin-youei-to) on production of Interleukin-6 from peripheral blood mononuclear cells and bone marrow adherent cells. Res. Commun. Chem. Path. Pharmac 1991, in press
   Google Scholar
• Mitsuyama M., Takeya K., Nomoto K., Shimotori S. Three phases of phagocyte contribution to resistance against L. monocytogenes. J. Gen. Microbiol. 1978; 106: 165
   PubMedGoogle 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
   PubMed Web of Science ®Google Scholar
• Nakane A., Minagawa T., Kato K. Endogenous tumor necrosis factor (Cachectin) is essential to host resistance against Listeria monocytogenes infection. Infect. Immun. 1988; 56: 2563
   PubMed Web of Science ®Google Scholar
• Kiderlen A. F., Kaufmann S. H. E., Lohmann-Matthes M. Protection of mice against the intracellular bacterium Listeria monocytogenes by recombinant immune interferon. Eur. J. Immunol. 1984; 14: 964
   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
• Poston R. M., Kurlander R. J. Analysis of the time course of IFN-γ mRNA and protein production during primary murine Listeriosis: The immune phase of bacterial elimination is not temporally linked to IFN production in vivo. J. Immunol. 1991; 146: 4333
   PubMed Web of Science ®Google Scholar
• Czuprynski C. J., Brown J. F., Young K. M., Cooley A. O., Kurtz R. S. Effect of murine recombinant Interleukin-1α on the host response to bacterial infection. J. Immunol. 1988; 140: 962
   PubMed Web of Science ®Google Scholar
• Czuprynski C. J., Brown J. F. Recombinant murine Interleukin-1α enhancement of nonspecific antibacterial resistance. Infect. Immun. 1987; 55: 2061
   PubMed Web of Science ®Google Scholar
• Van der Meer J. W. M., Helle M., Aarden L. Comparison of the effects of recombinant interleukin 6 and recombinant interleukin 1 on nonspecific resistance to infection. Eur. J. Immunol. 1989; 19: 413
   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
• Cheers C., Hill M., Haigh A. M., Stanley E. R. Stimulation of macrophage Phagocytic but not bactericidal activity by colony-stimulating factor 1. Infect. Immun. 1989; 57: 1512
   PubMed Web of Science ®Google Scholar
• Wang A. M., Creasey A. A., Ladner M. B., Lin L. S., Strikler J., Van Arsdell J. N., Yamamoto R., Mark D. F. Molecular cloning of the complementary DNA for human tumor necrosis factor. Science 1985; 228: 149
   PubMed Web of Science ®Google Scholar
• Mizel S. B. Production and quantitation of lymphocyte-activating factor (interleukin-1). Manual of Macrophage Methodology 1981; 407
   Google Scholar
• Matsuda T., Hirano T., Kishimoto T. Establishment of interleukin 6 (IL-6)/B cell stimulating factor 2 (BSF2)-dependent cell line and preparation of anti-IL-6/BSF-2 monoclonal antibodies. Eur. J. Immunol. 1988; 18: 951
   PubMed Web of Science ®Google Scholar
• Monner D. A. An assay for growth of mouse bone marrow cells in microtiter liquid culture using the tetrazolium salt MTT, and its application to studies of myelopoiesis. Immunology Letters 1988; 19: 261
   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., Haward D., Stoelman F. J. 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
• 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-chai-hu-tang (Japanese name: shosaiko-to). Immunopharmacol. Immunotoxicol. 1989; 11: 233
   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
• Stevenson M. M., Kongshavn P. A. L., Skamen E. Genetic linkage of resistance to Listeria monocytogenes with macrophage inflammatory responses. J. Immunol. 1981; 127: 402
   PubMed Web of Science ®Google Scholar
• Czuprinski C. J., Canono B., Henson P. M., Campbell P. A. Genetically determined resistance to listeroisis is associated with increased accumulation of inflammatory neutrophils and macrophages which have enhanced listericidal activity. Immunology 1985; 55: 511
   PubMed Web of Science ®Google Scholar
• Gervais F., Stevenson M., Skamene E. Genetic control of resistance to Listeria monocytogenes; Regulation of leukocyte inflammatory responses by the He locus. J. Immunol. 1984; 132: 2078
   PubMed Web of Science ®Google Scholar
• Handa T., Mitsuyama M., Watanabe Y., Koga T., Nomoto K. A significant role of the macrophage accumulation induced by MCF in the protection of mice against Listeria monocytogenes in vivo. Cell. Immunol. 1987; 106: 330
   PubMed Web of Science ®Google Scholar
• Torok-Storb B. Cellular interactions. Blood 1988; 72: 373
   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
• Wong G. G., Witek-Glannotii J. S., Temple P. A., Kriz R., Ferenz C., Hewick R. M., Clark S. C., Ikebuchi K., Ogawa M. Stimulation of murine hematopoietic colony formation by human IL-6. J. Immunol. 1988; 140: 3040
   PubMed Web of Science ®Google Scholar
• Cheers C., Zhan Y. F., Egan P. J. In vivo IL-1 potentates both specific and non-specific arms of immune response to infection. Immunology 1990; 70: 411
   PubMed Web of Science ®Google Scholar
• Saito M., Ebina T., Koi M., Yamaguchi T., Kawade Y., Ishida N. Induction of interferon-γ in mice spleen cells by OK-432, a preparation of Streptococcus pyogenes. Cell. Immunol. 1982; 68: 187
   PubMed Web of Science ®Google Scholar
• Yamamoto A., Nagamuta M., Usami H., Sugawara Y., Ishida N. Release of tumor necrosis factor (TNF) into mouse peritoneal fluids by 0K-432, a streptococcal preparation. Immunopharmacology 1986; 11: 79
   PubMed Web of Science ®Google Scholar
• Fukui H., Koishihara Y., Nagamuta M., Mizutani Y., Uchida A. Production of interleukin 6 by human spleen cells stimulated with streptococcal preparation OK-432. Immunology Letters 1989; 21: 127
   PubMed Web of Science ®Google Scholar
• Ichimura O., Suzuki S., Saito M., et al. Augmentation of interleukin 1 and interleukin 2 production by OK-432. Int. J. Immunopharmacol. 1985; 7: 263
   PubMed Web of Science ®Google Scholar
• Hiraoka A., Yamaguchi M., Ohkubo T., Kawamoto T., Yoshida Y., Uchino H. Effect of a streptococcal preparation, OK-432, on hematopoietic spleen colony formation in irradiated mice. Cancer Res. 1981; 41: 2954
   PubMed Web of Science ®Google Scholar
• Kai S., Tanaka J., Nomoto K., Torisu M. Studies on the immunopotentiating effects of a streptococcal preparation, OK-432. Clin. exp. Immunol. 1979; 37: 98
   PubMed Web of Science ®Google Scholar
• Chirigos M. A., Saito T., Talmadge J. E. The immunomodulatory activity of picibanil (OK-432). Curr. Clin. Pract. Ser. 1984; 17: 20
   Google Scholar
• Kawaguchi T., Suematsu M., Koizumi H. M., Mitsui H., Suzuki S., Matsuno T., Ogawa H., Nomoto K. Activation of macrophage function by intraperitoneal administration of the streptococcal antitumor agent OK-432. Immunopharmacology 1983; 6: 177
   PubMed Web of Science ®Google Scholar