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http://dx.doi.org/10.4014/jmb.1210.10010

Lactobacillus plantarum HY7712 Ameliorates Cyclophosphamide-Induced Immunosuppression in Mice  

Jang, Se-Eun (Department of Food and Nutrition, Kyung Hee University)
Joh, Eun-Ha (Department of Life and Nanopharmaceutical Sciences, Kyung Hee University)
Lee, Ho-Yong (R&B D Center, Korea Yakult Co., Ltd.)
Ahn, Young-Tae (R&B D Center, Korea Yakult Co., Ltd.)
Lee, Jung-Hee (R&B D Center, Korea Yakult Co., Ltd.)
Huh, Chul-Sung (R&B D Center, Korea Yakult Co., Ltd.)
Han, Myung Joo (Department of Food and Nutrition, Kyung Hee University)
Kim, Dong-Hyun (Department of Life and Nanopharmaceutical Sciences, Kyung Hee University)
Publication Information
Journal of Microbiology and Biotechnology / v.23, no.3, 2013 , pp. 414-421 More about this Journal
Abstract
Lactic acid bacteria (LAB) in fermented foods have attracted considerable attention recently as treatment options for immune diseases, the incidence of which has been increasing worldwide. The ability of 500 strains of LAB, isolated from kimchi, to induce TNF-${\alpha}$ production in peritoneal macrophages was investigated. Lactobacillus plantarum HY7712 most strongly induced TNF-${\alpha}$ production as well as NF-${\kappa}B$ activation. However, HY7712 inhibited NF-${\kappa}B$ activation in LPS-stimulated peritoneal macrophages. When HY7712 was orally treated in cyclophosphamide (CP)-immunosuppressed mice for 5 or 15 days, it reversed the body and spleen weights, blood RBC and WBC levels, and splenocyte and bone marrow cells that were reduced by CP. Orally administered HY7712 increased concanavalin A-induced T cell proliferation to 84.5% of the normal group on day 15, although treatment with CP alone markedly reduced it to 53.7% of the normal group. Furthermore, orally administered HY7712 significantly induced the expressions of IL-2 and IFN-${\gamma}$ in ConA-induced splenic cytotoxic T cells of CP-treated mice. Orally administered HY7712 restored the CP-impaired phagocytosis of macrophages in mice. Orally administered HY7712 also restored the cytotoxicity of NK and cytotoxic T cells derived from spleen and bone marrow against YAC-1 in CP-immunosuppressed mice. Based on these findings, orally administered HY7712 may accelerate the recovery of cyclophosphamide-caused immunosuppression, without evident side effects, by immunopotentiating NK and Tc cells, and may provide a mechanistic basis for using HY7712 as an alternative means in lessening chemotherapyinduced immunosuppression in cancer patients.
Keywords
Lactic acid bacteria; Lactobacillus plantarum HY7712; immunopotentiation; cyclophosphamide;
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1 Joh, E. H., I. A. Lee, I. H. Jung, and D. H. Kim. 2011. Ginsenoside Rb1 and its metabolite compound K inhibit IRAK-1 activation - the key step of inflammation. Biochem. Pharmacol. 82: 278-286.   DOI   ScienceOn
2 Lee, I. A., E. A. Bae, J. H. Lee, H. Lee, Y. T. Ahn, C. S. Huh, and D. H. Kim. Bifidobacterium longum HY8004 attenuates TNBS-induced colitis by inhibiting lipid peroxidation in mice. Inflamm. Res. 59: 359-368.
3 Joh, E. H., W. Gu, and D. H. Kim. 2012. Echinocystic acid ameliorates lung inflammation in mice and alveolar macrophages by inhibiting the binding of LPS to TLR4 in NF-$\kappa$B and MAPK pathways. Biochem. Pharmacol. 84: 331-340.   DOI   ScienceOn
4 Joly, C., M. Palisse, D. Ribbe, O. De Calmes, and P. Genevey. 1988. Acute levamisole poisoning. Presse Med. 27: 717.
5 Kato, I., T. Yokokura, and M. Mutai. 1983. Macrophage activation by Lactobacillus casei in mice. Microbiol. Immunol. 41: 611-618.
6 Masood, M. I., M. I. Qadir, J. H. Shirazi, and I. U. Khan. 2011. Beneficial effects of lactic acid bacteria on human beings. Crit. Rev. Microbiol. 37: 91-98.   DOI   ScienceOn
7 Bagga, A. and P. Hari. 2000. Levamisole-induced vasculitis. Ped. Nephrol. 14: 1057-1058.
8 Ballas, Z. K. 1986. Lymphokine-activated killer (LAK) cells. I. Differential recovery of LAK, natural killer cells, and cytotoxic T lymphocytes after a sublethal dose of cyclophosphamide. J. Immunol. 137: 2380-2384.
9 Bear, H. D. 1986. Tumor-specific suppressor T-cells which inhibit the in vitro generation of cytolytic T-cells from immune and early tumor-bearing host spleens. Cancer Res. 46: 1805-1812.
10 Bujalance, C., E. Moreno, M. Jimenez-Valera, and A. Ruiz- Bravo. 2007. A probiotic strain of Lactobacillus plantarum stimulates lymphocyte responses in immunologically intact and immunocompromised mice. Int. J. Food Microbiol. 113: 28-34.   DOI   ScienceOn
11 Palcoux, J. B., P. Niaudet, and P. Goumy. 1994. Side effects of levamisole in children with nephrosis. Ped. Nephrol. 8: 263-264.
12 Elmadfa, I., P. Klein, and A. L. Meyer. 2010. Immune-stimulating effects of lactic acid bacteria in vivo and in vitro. Proc. Nutr. Soc. 69: 416-420.   DOI   ScienceOn
13 Carvalho, C., R. X. Santos, S. Cardoso, S. Correia, P. J. Oliveira, M. S. Santos, and P. I. Moreira. 2009. Doxorubicin: The good, the bad and the ugly effect. Curr. Med. Chem. 16: 3267-3285.   DOI   ScienceOn
14 Cho, J., D. Lee, C. Yang, J. Jeon, J. Kim, and H. Han. 2006. Microbial population dynamics of kimchi, a fermented cabbage product. FEMS Microbiol. Lett. 257: 262-267.   DOI   ScienceOn
15 Collins, M. P. and G. R. Gibson. 1999. Probiotics, prebiotics, and synbiotics: Approaches for modulating the microbial ecology of the gut. Am. J. Clin. Nutr. 69: s1052-s1057.
16 De Simone, C., R. Vesely, B. Bianchi Salvadori, and E. Jirillo. 1993. The role of probiotics in modulation of the immune system in man and in animals. Int. J. Immunother. 27: 23-28.
17 Foligne, B., S. M. Deutsch, J. Breton, F. J. Cousin, J. Dewulf, M. Samson, et al. 2010. Promising immunomodulatory effects of selected strains of dairy propionibacteria as evidenced in vitro and in vivo. Appl. Environ. Microbiol. 76: 8259-8264.   DOI   ScienceOn
18 Gazit, Z. and E. Kedar. 1994. Chemotherapy-induced modulation of natural killer and lymphokine-activated killer cell activity in euthymic and athymic mice. Cancer Immunol. Immunother. 38: 243-252.
19 Hoover, S. K., S. K. Barrett, T. M. Turk, T. C. Lee, and H. D. Bear. 1990. Cyclophosphamide and abrogation of tumor-induced suppressor T cell activity. Cancer Immunol. Immunother. 31: 121-127.   DOI
20 Huang, G. C., L. S. Wu, L. G. Chen, L. L. Yang, and C. C. Wang. 2007. Immuno-enhancement effects of Huang Qi Liu Yi Tang in a murine model of cyclophosphamide-induced leucopenia. J. Ethnopharmacol. 109: 229-235.   DOI   ScienceOn
21 Pass, J., D. Carrie, N. Boylan, S. Lorimore, E. Wright, B. Houston, et al. 2005. Role of hepatic cytochrome P450s in the pharmacokinetics and toxicity of cyclophosphamide: Studies with the hepatic cytochrome P450 reductase null mouse. Cancer Res. 65: 4211-4217.   DOI   ScienceOn
22 Campieri, M. and P. Gionchetti. 1999. Probiotics in inflammatory bowel disease: New insight to pathogenesis or a possible therapeutic alternative. Gastroenterology 116: 1246-1260.   DOI   ScienceOn
23 Mace, E. M., S. J. Monkley, D. R. Critchley, and F. Takei. 2009. A dual role for talin in NK cell cytotoxicity: Activation of LFA-1-mediated cell adhesion and polarization of NK cells. J. Immunol. 182: 948-956.
24 O'Connell, M. J. 2001. North Central Cancer Treatment Group - Mayo Clinic trials in colon cancer. Semin. Oncol. 28 (Suppl 1): 4-8.
25 Simon, G. L. and S. L. Gorbach. 1984. Intestinal flora in health and disease. Gastroenterology 86: 174-193.
26 Singh, K. P., R. K. Gupta, H. Shau, and P. K. Ray. 1993. Effect of ASTA-Z 7575 (INN maphosphamide) on human lymphokineactivated killer cell induction. Immunopharmacol. Immunotoxicol. 15: 525-538.
27 Wang, J., X. Tong, P. Li, H. Cao, and W. Su. 2012. Immunoenhancement effects of Shenqi Fuzheng Injection on cyclophosphamide-induced immunosuppression in Balb/c mice. J. Ethnopharmacol. 139: 788-795.   DOI   ScienceOn
28 Weeks, B. A., A. S. Keisler, Q. N. Myrvik, and J. E. Warinner. 1987. Differential uptake of neutral red by macrophages from three species of estuarine fish. Dev. Comp. Immunol. 11: 117-124.   DOI   ScienceOn
29 Won, T. J., B. Kim, E. S. Oh, J. S. Bang, Y. J. Lee, J. S. Yoo, et al. 2011. Immunomodulatory activity of Lactobacillus strains isolated from fermented vegetables and infant stool. Can. J. Physiol. Pharmacol. 89: 429-434.   DOI   ScienceOn
30 Zhu, X. L., A. F. Chen, and Z. B. Lin. 2007. Ganoderma lucidum polysaccharides enhance the function of immunological effector cells in immunosuppressed mice. J. Ethnopharmacol. 111: 219-226.   DOI   ScienceOn