Browse > Article
http://dx.doi.org/10.4014/jmb.1709.09024

Immune-Enhancing Effect of Nanometric Lactobacillus plantarum nF1 (nLp-nF1) in a Mouse Model of Cyclophosphamide-Induced Immunosuppression  

Choi, Dae-Woon (Food Biotechnology Program, Korea University of Science and Technology)
Jung, Sun Young (Food Biotechnology Program, Korea University of Science and Technology)
Kang, Jisu (Food Biotechnology Program, Korea University of Science and Technology)
Nam, Young-Do (Food Biotechnology Program, Korea University of Science and Technology)
Lim, Seong-Il (Division of Strategic Food Research, Korea Food Research Institute)
Kim, Ki Tae (Biogenics Korea Co. Ltd.)
Shin, Hee Soon (Food Biotechnology Program, Korea University of Science and Technology)
Publication Information
Journal of Microbiology and Biotechnology / v.28, no.2, 2018 , pp. 218-226 More about this Journal
Abstract
Nanometric Lactobacillus plantarum nF1 (nLp-nF1) is a biogenics consisting of dead L. plantarum cells pretreated with heat and a nanodispersion process. In this study, we investigated the immune-enhancing effects of nLp-nF1 in vivo and in vitro. To evaluate the immunostimulatory effects of nLp-nF1, mice immunosuppressed by cyclophosphamide (CPP) treatment were administered with nLp-nF1. As expected, CPP restricted the immune response of mice, whereas oral administration of nLp-nF1 significantly increased the total IgG in the serum, and cytokine production (interleukin-12 (IL-12) and tumor necrosis factor alpha (TNF-${\alpha}$)) in bone marrow cells. Furthermore, nLp-nF1 enhanced the production of splenic cytokines such as IL-12, TNF-${\alpha}$, and interferon gamma (IFN-${\gamma}$). In vitro, nLp-nF1 stimulated the immune response by enhancing the production of cytokines such as IL-12, TNF-${\alpha}$, and IFN-${\gamma}$. Moreover, nLp-nF1 given a food additive enhanced the immune responses when combined with various food materials in vitro. These results suggest that nLp-nF1 could be used to strengthen the immune system and recover normal immunity in people with a weak immune system, such as children, the elderly, and patients.
Keywords
Nanometric Lactobacillus plantarum nF1; immune enhancement; interleukin-12; macrophage; immunoglobulin G; cyclophosphamide;
Citations & Related Records
Times Cited By KSCI : 4  (Citation Analysis)
연도 인용수 순위
1 Schiavoni G, D'Amato G, Afferni C. 2017. The dangerous liaison between pollens and pollution in respiratory allergy. Ann. Allergy Asthma Immunol. 118: 269-275.   DOI
2 LaKind JS, Overpeck J, Breysse PN, Backer L, Richardson SD, Sobus J, et al. 2016. Exposure science in an age of rapidly changing climate: challenges and opportunities. J. Expo. Sci. Environ. Epidemiol. 26: 529-538.
3 Cesarone MR, Belcaro G, Di Renzo A, Dugall M, Cacchio M, Ruffini I, et al. 2007. Prevention of influenza episodes with colostrum compared with vaccination in healthy and high-risk cardiovascular subjects: the epidemiologic study in San Valentino. Clin. Appl. Thromb. Hemost. 13: 130-136.
4 Xu ML, Kim HJ, Chang DY, Kim HJ. 2013. The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection. J. Microbiol. 51: 389-393.   DOI
5 Park HY, Lee SH, Lee KS, Yoon HK, Yoo YC, Lee J, et al. 2015. Ginsenoside Rg1 and 20(S)-Rg3 induce IgA production by mouse B cells. Immune Netw. 15: 331-336.   DOI
6 Du XF, Jiang CZ, Wu CF, Won EK, Choung SY. 2008. Synergistic immunostimulatory effect of pidotimod and red ginseng acidic polysaccharide on humoral immunity of immunosuppressed mice. Pharmazie 63: 904-908.
7 Byeon SE, Lee J, Kim JH, Yang WS, Kwak YS, Kim SY, et al. 2012. Molecular mechanism of macrophage activation by red ginseng acidic polysaccharide from Korean red ginseng. Mediators Inflamm. 2012: 732860.
8 Choi S, Chung M-H. 2003. A review on the relationship between aloe vera components and their biologic effects. Semin. Integr. Med. 1: 53-62.
9 Isidro RA, Lopez A, Cruz ML, Gonzalez Torres MI, Chompre G, Isidro AA, et al. 2017. The probiotic VSL#3 modulates colonic macrophages, inflammation, and microflora in acute trinitrobenzene sulfonic acid colitis. J. Histochem. Cytochem. 65: 445-461.   DOI
10 Adams CA. 2010. The probiotic paradox: live and dead cells are biological response modifiers. Nutr. Res. Rev. 23: 37-46.
11 De Vries MC, Vaughan EE, Kleerebezem M, De Vos WM. 2006. Lactobacillus plantarum survival, functional and potential probiotic properties in the human intestinal tract. Int. Dairy J. 16: 1018-1028.
12 Mitsuoka T. 2000. Significance of dietary modulation of intestinal flora and intestinal environment. Biosci. Microflora 19: 15-25.   DOI
13 Ohshima T, Kojima Y, Seneviratne CJ, Maeda N. 2016. Therapeutic application of synbiotics, a fusion of probiotics and prebiotics, and biogenics as a new concept for oral Candida infections: a mini review. Front. Microbiol. 7: 10.
14 Terada A, Bukawa W, Kan T, Mitsuoka T. 2004. Effects of the consumption of heat-killed Enterococcus faecalis EC-12 preparation on microbiota and metabolic activity of the faeces in healthy adults. Microbial Ecol. Health Dis. 16: 188-194.   DOI
15 Sawada D, Sugawara T, Ishida Y, Aihara K, Aoki Y, Takehara I, et al. 2016. Effect of continuous ingestion of a beverage prepared with Lactobacillus gasseri CP2305 inactivated by heat treatment on the regulation of intestinal function. Food Res. Int. 79: 33-39.
16 Hasegawa H, Kan T. 2008. Immunity for longevity and lactic acid bacteria: the effect of nanometric particles of lactic acid bacteria on Th1 cell induction. New Food Ind. 50: 1-8.
17 Kan T, Ohwaki M. 2014. Lactobacillus having ability to induce IL-12 production, and method for culturing same. WO Patent, 2014/ 088183.
18 Lee HA, Kim H, Lee KW, Park KY. 2016. Dead Lactobacillus plantarum stimulates and skews immune responses toward T helper 1 and 17 polarizations in RAW 264.7 cells and mouse splenocytes. J. Microbiol. Biotechnol. 26: 469-476.   DOI
19 Lee HA, Kim H, Lee KW, Park KY. 2015. Dead nano-sized Lactobacillus plantarum inhibits azoxymethane/dextran sulfate sodium-induced colon cancer in Balb/c mice. J. Med. Food 18: 1400-1405.   DOI
20 Lee HA, Bong YJ, Kim H, Jeong JK, Kim HY, Lee KW, et al. 2015. Effect of nanometric Lactobacillus plantarum in kimchi on dextran sulfate sodium-induced colitis in mice. J. Med. Food. 18: 1073-1080.   DOI
21 Woof J, Burton D. 2004. Human antibody-Fc receptor interactions illuminated by crystal structures. Nat. Rev. Immunol. 4: 89-99.   DOI
22 Pier GB, Lyczak JB, Wetzler LM. 2004. Imunology, Infection, and Immunity. ASM Press, Washington, D.C.
23 Mallery DL, McEwan WA, Bidgood SR, Towers GJ, Johnson CM, James LC. 2010. Antibodies mediate intracellular immunity through tripartite motif-containing 21 (TRIM21). Proc. Natl. Acad. Sci. USA 107: 19985-19990.   DOI
24 Jin R, Wan LL, Mitsuishi T, Sato S, Akuzawa Y, Kodama K, et al. 1994. Effect of shi-ka-ron and Chinese herbs on cytokine production of macrophage in immunocompromised mice. Am. J. Chin. Med. 22: 255-266.   DOI
25 Zuluaga AF, Salazar BE, Rodriguez CA, Zapata AX, Agudelo M, Vesga O. 2006. Neutropenia induced in outbred mice by a simplified low-dose cyclophosphamide regimen: characterization and applicability to diverse experimental models of infectious diseases. BMC Infect. Dis. 6: 1-10.   DOI
26 Yasunami R, Bach JF. 1988. Anti-suppressor effect of cyclophosphamide on the development of spontaneous diabetes in NOD mice. Eur. J. Immunol. 18: 481-484.   DOI
27 Swirski FK, Nahrendorf M, Etzrodt M, Wildgruber M, Cortez-Retamozo V, Panizzi P, et al. 2009. Identification of splenic reservoir monocytes and their deployment to inflammatory sites. Science 325: 612-616.
28 Jia T, Pamer EG. 2009. Immunology. Dispensable but not irrelevant. Science 325: 549-550.   DOI
29 Smith KM, Pottage L, Thomas ER, Leishman AJ, Doig TN, Xu D, et al. 2000. Th1 and Th2 $CD4^+$ T cells provide help for B cell clonal expansion and antibody synthesis in a similar manner in vivo. J. Immunol. 165: 3136-3144.   DOI
30 Birbrair A, Frenette PS. 2016. Niche heterogeneity in the bone marrow. Ann. NY Acad. Sci. 1370: 82-96.   DOI
31 Vunjak-Novakovic G, Tandon N, Godier A, Maidhof R, Marsano A, Martens TP, et al. 2010. Challenges in cardiac tissue engineering. Tissue Eng. Part B Rev. 16: 169-187.
32 Kaushik RS, Uzonna JE, Zhang Y, Gordon JR, Tabel H. 2000. Innate resistance to experimental African trypanosomiasis: differences in cytokine (TNF-alpha, IL-6, IL-10 and IL-12) production by bone marrow-derived macrophages from resistant and susceptible mice. Cytokine 12: 1024-1034.   DOI
33 Wang C, Yu X, Cao Q, Wang Y, Zheng G, Tan TK, et al. 2013. Characterization of murine macrophages from bone marrow, spleen and peritoneum. BMC Immunol. 14: 6.   DOI
34 Zhao E, Xu H, Wang L, Kryczek I, Wu K, Hu Y, et al. 2012. Bone marrow and the control of immunity. Cell. Mol. Immunol. 9: 11-19.   DOI
35 Springer TA. 1980. Cell-surface differentiation in the mouse, pp. 185-217. In Kennett RH, McKearn TJ, Bechtol KB (eds.), Monoclonal Antibodies. Springer, Boston, MA.
36 Ma X, Yan W, Zheng H, Du Q, Zhang L, Ban Y, et al. 2015. Regulation of IL-10 and IL-12 production and function in macrophages and dendritic cells. F1000Res 4: 1465.   DOI
37 Kruglov AA, Lampropoulou V, Fillatreau S, Nedospasov SA. 2011. Pathogenic and protective functions of TNF in neuroinflammation are defined by its expression in Tlymphocytes and myeloid cells. J. Immunol. 187: 5660-5670.   DOI
38 Sforcin JM. 2007. Propolis and the immune system: a review. J. Ethnopharmacol. 113: 1-14.   DOI
39 Orsolic N, Sver L, Terzic S, Basic I. 2005. Peroral application of water-soluble derivative of propolis (WSDP) and its related polyphenolic compounds and their influence on immunological and antitumor activity. Vet. Res. Commun. 29: 575-593.
40 Lane ER, Zisman TL, Suskind DL. 2017. The microbiota in inflammatory bowel disease: current and therapeutic insights. J. Inflamm. Res. 10: 63-73.   DOI
41 D’Angelo C, Reale M, Costantini E. 2017. Microbiota and probiotics in health and HIV infection. Nutrients 9: 1-15.
42 McKenzie C, Tan J, Macia L, Mackay CR. 2017. The nutritiongut microbiome-physiology axis and allergic diseases. Immunol. Rev. 278: 277-295
43 Aitoro R, Paparo L, Amoroso A, Di Costanzo M, Cosenza L, Granata V, et al. 2017. Gut microbiota as a target for preventive and therapeutic intervention against food allergy. Nutrients 9: 1-12.
44 Manuzak JA, Hensley-McBain T, Zevin AS, Miller C, Cubas R, Agricola B, et al. 2016. Enhancement of microbiota in healthy macaques results in beneficial modulation of mucosal and systemic immune function. J. Immunol. 196: 2401-2409.   DOI
45 Schiavi E, Barletta B, Butteroni C, Corinti S, Boirivant M, Di Felice G. 2011. Oral therapeutic administration of a probiotic mixture suppresses established Th2 responses and systemic anaphylaxis in a murine model of food allergy. Allergy 66: 499-508.   DOI
46 Christaki EV, Florou-Paneri PC. 2010. Aloe vera: a plant for many uses. J. Food Agric. Environ. 8: 245-249.
47 Distrutti E, Cipriani S, Mencarelli A, Renga B, Fiorucci S. 2013. Probiotics VSL#3 protect against development of visceral pain in murine model of irritable bowel syndrome. PLoS One 8: e63893.