References
- Cross ML. 2002. Microbes versus microbes: immune signals generated by probiotic lactobacilli and their role in protection against microbial pathogens. FEMS Immunol. Med. Microbiol. 34: 245-253. https://doi.org/10.1111/j.1574-695X.2002.tb00632.x
- Madsen K, Cornish A, Soper P, McKaigney C, Jijon H, Yachimec C, et al. 2001. Probiotic bacteria enhance murine and human intestinal epithelial barrier function. Gastroenterology 121: 580-591. https://doi.org/10.1053/gast.2001.27224
- Erickson KL, Hubbard NE. 2000. Probiotic immunomodulation in health and disease. J. Nutr. 130: 403S-409S. https://doi.org/10.1093/jn/130.2.403S
- Sanders ME. 2003. Probiotics: considerations for human health. Nutr. Rev. 61: 91-99. https://doi.org/10.1301/nr.2003.marr.91-99
- Food and Agriculture Organization of the United Nations., World Health Organization. 2006. Probiotics in food : health and nutritional properties and guidelines for evaluation, pp. 2. Ed. Food and Agriculture Organization of the United Nations : World Health Organization, Rome.
- Taylor AL, Dunstan JA, Prescott SL. 2007. Probiotic supplementation for the first 6 months of life fails to reduce the risk of atopic dermatitis and increases the risk of allergen sensitization in high-risk children: a randomized controlled trial. J. Allergy Clin. Immunol. 119: 184-191. https://doi.org/10.1016/j.jaci.2006.08.036
- Matteuzzi D, Crociani F, Brigidi P. 1983. Antimicrobial susceptibility of Bifidobacterium. Ann. Microbiol (Paris). 134A: 339-349.
- Gupta PK, Mital BK, Gupta RS. 1995. Antibiotic sensitivity pattern of various Lactobacillus acidophilus strains. Indian J. Exp. Biol. 33: 620-621.
- Ishibashi N, Yamazaki S. 2001. Probiotics and safety. Am. J. Clin. Nutr. 73: 465S-470S. https://doi.org/10.1093/ajcn/73.2.465s
- Asheshov EH. 1966. Loss of antibiotic resistance in Staphylococcus aureus resulting from growth at high temperature. J. Gen. Microbiol. 42: 403-410. https://doi.org/10.1099/00221287-42-3-403
- Taverniti V, Guglielmetti S. 2011. The immunomodulatory properties of probiotic microorganisms beyond their viability (ghost probiotics: proposal of paraprobiotic concept). Genes Nutr. 6: 261-274. https://doi.org/10.1007/s12263-011-0218-x
- Chuang L, Wu KG, Pai C, Hsieh PS, Tsai JJ, Yen JH, et al. 2007. Heat-killed cells of lactobacilli skew the immune response toward T helper 1 polarization in mouse splenocytes and dendritic cell-treated T cells. J. Agric. Food Chem. 55: 11080-11086. https://doi.org/10.1021/jf071786o
- Matsuguchi T, Takagi A, Matsuzaki T, Nagaoka M, Ishikawa K, Yokokura T, et al. 2003. Lipoteichoic acids from Lactobacillus strains elicit strong tumor necrosis factor alpha-inducing activities in macrophages through Toll-like receptor 2. Clin. Diagn. Lab. Immunol. 10: 259-266. https://doi.org/10.1128/CDLI.10.2.259-266.2003
- Jeong M, Kim JH, Yang H, Kang SD, Song S, Lee D, et al. 2019. Heat-killed Lactobacillus plantarum KCTC 13314BP enhances phagocytic activity and immunomodulatory effects via activation of MAPK and STAT3 pathways. J. Microbiol. Biotechnol. 29: 1248-1254. https://doi.org/10.4014/jmb.1905.05066
- Jung YJ, Lee YT, Ngo VL, Cho YH, Ko EJ, Hong SM, et al. 2017. Heat-killed Lactobacillus casei confers broad protection against influenza A virus primary infection and develops heterosubtypic immunity against future secondary infection. Sci. Rep. 7: 17360. https://doi.org/10.1038/s41598-017-17487-8
- Laskin DL. 2009. Macrophages and inflammatory mediators in chemical toxicity: a battle of forces. Chem. Res. Toxicol. 22: 1376-1385. https://doi.org/10.1021/tx900086v
- Aderem A, Underhill DM. 1999. Mechanisms of phagocytosis in macrophages. Annu. Rev. Immunol. 17: 593-623. https://doi.org/10.1146/annurev.immunol.17.1.593
- Gordon S. 2016. Phagocytosis: An immunobiologic process. Immunity 44: 463-475. https://doi.org/10.1016/j.immuni.2016.02.026
- Wynn TA, Chawla A, Pollard JW. 2013. Macrophage biology in development, homeostasis and disease. Nature 496: 445-455. https://doi.org/10.1038/nature12034
- Wang C, Deng L, Hong M, Akkaraju GR, Inoue J, Chen ZJ. 2001. TAK1 is a ubiquitin-dependent kinase of MKK and IKK. Nature 412: 346-351. https://doi.org/10.1038/35085597
- Mihaly SR, Morioka S, Ninomiya-Tsuji J, Takaesu G. 2014. Activated macrophage survival is coordinated by TAK1 binding proteins. PLoS One 9: e94982. https://doi.org/10.1371/journal.pone.0094982
- Lloberas J, Valverde-Estrella L, Tur J, Vico T, Celada A. 2016. Mitogen-activated protein kinases and mitogen kinase phosphatase 1: a critical interplay in macrophage biology. Front. Mol. Biosci. 3: 28.
- Sanchez I, Palop L, Ballesteros C. 2000. Biochemical characterization of lactic acid bacteria isolated from spontaneous fermentation of 'Almagro' eggplants. Int. J. Food Microbiol. 59: 9-17. https://doi.org/10.1016/S0168-1605(00)00256-7
- De Vuyst L, Schrijvers V, Paramithiotis S, Hoste B, Vancanneyt M, Swings J, et al. 2002. The biodiversity of lactic acid bacteria in Greek traditional wheat sourdoughs is reflected in both composition and metabolite formation. Appl. Environ. Microbiol. 68: 6059-6069. https://doi.org/10.1128/AEM.68.12.6059-6069.2002
- Mante ES, Sakyi-Dawson E, Amoa-Awua WK. 2003. Antimicrobial interactions of microbial species involved in the fermentation of cassava dough into agbelima with particular reference to the inhibitory effect of lactic acid bacteria on enteric pathogens. Int. J. Food Microbiol. 89: 41-50. https://doi.org/10.1016/S0168-1605(03)00103-X
- Segawa S, Wakita Y, Hirata H, Watari J. 2008. Oral administration of heat-killed Lactobacillus brevis SBC8803 ameliorates alcoholic liver disease in ethanol-containing diet-fed C57BL/6N mice. Int. J. Food Microbiol. 128: 371-377. https://doi.org/10.1016/j.ijfoodmicro.2008.09.023
- Segawa S, Hayashi A, Nakakita Y, Kaneda H, Watari J, Yasui H. 2008. Oral administration of heat-killed Lactobacillus brevis SBC8803 ameliorates the development of dermatitis and inhibits immunoglobulin E production in atopic dermatitis model NC/Nga mice. Biol. Pharm. Bull. 31: 884-889. https://doi.org/10.1248/bpb.31.884
- Choi CY, Kim YH, Oh S, Lee HJ, Kim JH, Park SH, et al. 2017. Anti-inflammatory potential of a heat-killed Lactobacillus strain isolated from Kimchi on house dust mite-induced atopic dermatitis in NC/Nga mice. J. Appl. Microbiol. 123: 535-543. https://doi.org/10.1111/jam.13515
- Horii Y, Kaneda H, Fujisaki Y, Fuyuki R, Nakakita Y, Shigyo T, et al. 2014. Effect of heat-killed Lactobacillus brevis SBC8803 on cutaneous arterial sympathetic nerve activity, cutaneous blood flow and transepidermal water loss in rats. J. Appl. Microbiol. 116: 1274-1281. https://doi.org/10.1111/jam.12435
- Ogawa M, Saiki A, Matsui Y, Tsuchimoto N, Nakakita Y, Takata Y, et al. 2016. Effects of oral intake of heat-killed Lactobacillus brevis SBC8803 (SBL88) on dry skin conditions: a randomized, double-blind, placebo-controlled study. Exp. Ther. Med. 12: 3863-3872. https://doi.org/10.3892/etm.2016.3862
- Miyazaki K, Itoh N, Yamamoto S, Higo-Yamamoto S, Nakakita Y, Kaneda H, et al. 2014. Dietary heat-killed Lactobacillus brevis SBC8803 promotes voluntary wheel-running and affects sleep rhythms in mice. Life Sci. 111: 47-52. https://doi.org/10.1016/j.lfs.2014.07.009
- Higo-Yamamoto S, Yamamoto S, Miyazaki K, Nakakita Y, Kaneda H, Takata Y, et al. 2019. Dietary heat-killed Lactobacillus brevis SBC8803 attenuates chronic sleep disorders induced by psychophysiological stress in mice. J. Nutr. Sci. Vitaminol. (Tokyo) 65: 164-170. https://doi.org/10.3177/jnsv.65.164
- MacMicking J, Xie QW, Nathan C. 1997. Nitric oxide and macrophage function. Annu. Rev. Immunol. 15: 323-350. https://doi.org/10.1146/annurev.immunol.15.1.323
- Segers ME, Lebeer S. 2014. Towards a better understanding of Lactobacillus rhamnosus GG - host interactions. Microb. Cell Fact. 13 Supple 1: S7. https://doi.org/10.1186/1475-2859-13-S1-S7
- Zhou J, Fan Y, Zhong J, Huang Z, Huang T, Lin S, et al. 2018. TAK1 mediates excessive autophagy via p38 and ERK in cisplatin-induced acute kidney injury. J. Cell Mol. Med. 22: 2908-2921. https://doi.org/10.1111/jcmm.13585
- Arthur JS, Ley SC. 2013. Mitogen-activated protein kinases in innate immunity. Nat. Rev. Immunol. 13: 679-692. https://doi.org/10.1038/nri3495
- Heinzel S, Marchingo JM, Horton MB, Hodgkin PD. 2018. The regulation of lymphocyte activation and proliferation. Curr. Opin. Immunol. 51: 32-38. https://doi.org/10.1016/j.coi.2018.01.002
- Tange S, Scherer MN, Graeb C, Weiss T, Justl M, Frank E, et al. 2002. The antineoplastic drug paclitaxel has immunosuppressive properties that can effectively promote allograft survival in a rat heart transplant model. Transplantation 73: 216-223. https://doi.org/10.1097/00007890-200201270-00011
- Lahtinen SJ. 2012. Probiotic viability - does it matter? Microb. Ecol. Health Dis. 18: 23.
- Pique N, Berlanga M, Minana-Galbis D. 2019. Health benefits of heat-killed (Tyndallized) probiotics: an overview. Int. J. Mol. Sci. 20: 2534. https://doi.org/10.3390/ijms20102534
- Chen MF, Weng KF, Huang SY, Liu YC, Tseng SN, Ojcius DM, et al. 2017. Pretreatment with a heat-killed probiotic modulates monocyte chemoattractant protein-1 and reduces the pathogenicity of influenza and enterovirus 71 infections. Mucosal Immunol. 10: 215-227. https://doi.org/10.1038/mi.2016.31
- Link H, Rochat F, Saudan KY, Schiffrin E. 1995. Immunomodulation of the gnotobiotic mouse through colonization with lactic acid bacteria. Adv. Exp. Med. Biol. 371A: 465-467.
- Oakey HJ, Harty DW, Knox KW. 1995. Enzyme production by lactobacilli and the potential link with infective endocarditis. J. Appl. Bacteriol. 78: 142-148. https://doi.org/10.1111/j.1365-2672.1995.tb02834.x
- Imperial IC, Ibana JA. 2016. Addressing the antibiotic resistance problem with probiotics: Reducing the risk of its double-edged sword effect. Front. Microbiol. 7: 1983.
- Ishikawa H, Kutsukake E, Fukui T, Sato I, Shirai T, Kurihara T, et al. 2010. Oral administration of heat-killed Lactobacillus plantarum strain b240 protected mice against Salmonella enterica Serovar Typhimurium. Biosci. Biotechnol. Biochem. 74: 1338-1342. https://doi.org/10.1271/bbb.90871
- Billack B. 2006. Macrophage activation: role of toll-like receptors, nitric oxide, and nuclear factor kappa B. Am. J. Pharm. Educ. 70: 102. https://doi.org/10.5688/aj7005102
- Fong FL, Kirjavainen PV, El-Nezami H. 2016. Immunomodulation of Lactobacillus rhamnosus GG (LGG)-derived soluble factors on antigen-presenting cells of healthy blood donors. Sci. Rep. 6: 22845. https://doi.org/10.1038/srep22845
- Fong FLY, Kirjavainen P, Wong VHY, El-Nezami H. 2015. Immunomodulatory effects of Lactobacillus rhamnosus GG on dendritic cells, macrophages and monocytes from healthy donors. J. Funct. Foods 13: 71-79. https://doi.org/10.1016/j.jff.2014.12.040
- Paineau D, Carcano D, Leyer G, Darquy S, Alyanakian MA, Simoneau G, et al. 2008. Effects of seven potential probiotic strains on specific immune responses in healthy adults: a double-blind, randomized, controlled trial. FEMS Immunol. Med. Microbiol. 53: 107-113. https://doi.org/10.1111/j.1574-695X.2008.00413.x
- Ryan KA, Daly P, Li Y, Hooton C, O'Toole PW. 2008. Strain-specific inhibition of Helicobacter pylori by Lactobacillus salivarius and other lactobacilli. J. Antimicrob. Chemother. 61: 831-834. https://doi.org/10.1093/jac/dkn040
- Fukuda S, Toh H, Hase K, Oshima K, Nakanishi Y, Yoshimura K, et al. 2011. Bifidobacteria can protect from enteropathogenic infection through production of acetate. Nature 469: 543-U791. https://doi.org/10.1038/nature09646
- Song MW, Jang HJ, Kim KT, Paik HD. 2019. Probiotic and antioxidant properties of novel Lactobacillus brevis KCCM 12203P isolated from Kimchi and evaluation of immune-stimulating activities of its heat-killed cells in RAW 264.7 cells. J. Microbiol. Biotechnol. 29: 1894-1903. https://doi.org/10.4014/jmb.1907.07081
- Tejada-Simon MV, Pestka JJ. 1999. Proinflammatory cytokine and nitric oxide induction in murine macrophages by cell wall and cytoplasmic extracts of lactic acid bacteria. J. Food Prot. 62: 1435-1444. https://doi.org/10.4315/0362-028X-62.12.1435
- 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. https://doi.org/10.1126/science.1175202
- Klimp AH, de Vries EG, Scherphof GL, Daemen T. 2002. A potential role of macrophage activation in the treatment of cancer. Crit. Rev. Oncol. Hematol. 44: 143-161. https://doi.org/10.1016/S1040-8428(01)00203-7
- Zeng G, Ju Y, Shen H, Zhou N, Huang L. 2013. Immunopontentiating activities of the purified polysaccharide from evening primrose in H22 tumor-bearing mice. Int. J. Biol Macromol. 52: 280-285. https://doi.org/10.1016/j.ijbiomac.2012.10.005
- Conniot J, Silva JM, Fernandes JG, Silva LC, Gaspar R, Brocchini S, et al. 2014. Cancer immunotherapy: nanodelivery approaches for immune cell targeting and tracking. Front. Chem. 2: 105.
- Dumitru CD, Ceci JD, Tsatsanis C, Kontoyiannis D, Stamatakis K, Lin JH, et al. 2000. TNF-alpha induction by LPS is regulated posttranscriptionally via a Tpl2/ERK-dependent pathway. Cell 103: 1071-1083. https://doi.org/10.1016/S0092-8674(00)00210-5
- Geppert TD, Whitehurst CE, Thompson P, Beutler B. 1994. Lipopolysaccharide signals activation of tumor necrosis factor biosynthesis through the ras/raf-1/MEK/MAPK pathway. Mol. Med. 1: 93-103. https://doi.org/10.1007/BF03403535
- Swantek JL, Cobb MH, Geppert TD. 1997. Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) is required for lipopolysaccharide stimulation of tumor necrosis factor alpha (TNF-alpha) translation: glucocorticoids inhibit TNF-alpha translation by blocking JNK/SAPK. Mol. Cell Biol. 17: 6274-6282. https://doi.org/10.1128/MCB.17.11.6274
- Kontoyiannis D, Pasparakis M, Pizarro TT, Cominelli F, Kollias G. 1999. Impaired on/off regulation of TNF biosynthesis in mice lacking TNF AU-rich elements: implications for joint and gut-associated immunopathologies. Immunity 10: 387-398. https://doi.org/10.1016/S1074-7613(00)80038-2
- Sato S, Sanjo H, Takeda K, Ninomiya-Tsuji J, Yamamoto M, Kawai T, et al. 2005. Essential function for the kinase TAK1 in innate and adaptive immune responses. Nat. Immunol. 6: 1087-1095. https://doi.org/10.1038/ni1255
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