Browse > Article
http://dx.doi.org/10.5851/kosfa.2022.e44

Monitoring Cellular Immune Responses after Consumption of Selected Probiotics in Immunocompromised Mice  

Kang, Seok-Jin (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Yang, Jun (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Lee, Na-Young (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Lee, Chang-Hee (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Park, In-Byung (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Park, Si-Won (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Lee, Hyeon Jeong (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Park, Hae-Won (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Yun, Hyun Sun (CJ CheilJedang Corporation)
Chun, Taehoon (Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University)
Publication Information
Food Science of Animal Resources / v.42, no.5, 2022 , pp. 903-914 More about this Journal
Abstract
Probiotics are currently considered as one of tools to modulate immune responses under specific clinical conditions. The purpose of this study was to evaluate whether oral administration of three different probiotics (Lactiplantibacillus plantarum CJLP243, CJW55-10, and CJLP475) could evoke a cell-mediated immunity in immunodeficient mice. Before conducting in vivo experiments, we examined the in vitro potency of these probiotics for macrophage activation. After co-culture with these probiotics, bone marrow derived macrophages (BMDMs) produced significant amounts of proinflammatory cytokines including interleukin-6 (IL-6), IL-12, and tumor necrosis factor-α (TNF-α). Levels of inducible nitric oxide synthase (inos) and co-stimulatory molecules (CD80 and CD86) were also upregulated in BMDMs after treatment with some of these probiotics. To establish an immunocompromised animal model, we intraperitoneally injected mice with cyclophosphamide on day 0 and again on day 2. Starting day 3, we orally administered probiotics every day for the last 15 d. After sacrificing experimental mice on day 18, splenocytes were isolated and co-cultured with these probiotics for 3 d to measure levels of several cytokines and immune cell proliferation. Results clearly indicated that the consumption of all three probiotic strains promoted secretion of interferon-γ (IFN-γ), IL-1β, IL-6, IL-12, and TNF-α. NK cell cytotoxicity and proliferation of immune cells were also increased. Taken together, our data strongly suggest that consumption of some probiotics might induce cell-mediated immune responses in immunocompromised mice.
Keywords
animal model; immune response; probiotics;
Citations & Related Records
Times Cited By KSCI : 3  (Citation Analysis)
연도 인용수 순위
1 Li D, Wu M. 2021. Pattern recognition receptors in health and diseases. Signal Transduct Target Ther 6:291.
2 Nguyen KG, Vrabel MR, Mantooth SM, Hopkins JJ, Wagner ES, Gabaldon TA, Zaharoff DA. 2020. Localized interleukin-12 for cancer immunotherapy. Front Immunol 11:575597.
3 Salva S, Marranzino G, Villena J, Aguero G, Alvarez S. 2014. Probiotic Lactobacillus strains protect against myelosuppression and immunosuppression in cyclophosphamide-treated mice. Int Immunopharmacol 22:209-221.   DOI
4 Bui VT, Tseng HC, Kozlowska A, Maung PO, Kaur K, Topchyan P, Jewett A. 2015. Augmented IFN-γ and TNF-α induced by probiotic bacteria in NK cells mediate differentiation of stem-like tumors leading to inhibition of tumor growth and reduction in inflammatory cytokine release; regulation by IL-10. Front Immunol 6:576.
5 Bujalance C, Moreno E, Jimenez-Valera M, Ruiz-Bravo A. 2007. A probiotic strain of Lactobacillus plantarum stimulates lymphocyte responses in immunologically intact and immunocompromised mice. Int J Food Microbiol 113:28-34.   DOI
6 de Melo Pereira GV, de Oliveira Coelho B, Magalhaes Junior AI, Thomaz-Soccol V, Soccol CR. 2018. How to select a probiotic? A review and update of methods and criteria. Biotechnol Adv 36:2060-2076.   DOI
7 Gutierrez-Merino J, Isla B, Combes T, Martinez-Estrada F, Maluquer De Motes C. 2020. Beneficial bacteria activate type-I interferon production via the intracellular cytosolic sensors STING and MAVS. Gut Microbes 11:771-788.   DOI
8 Kambayashi T, Laufer TM. 2014. Atypical MHC class II-expressing antigen-presenting cells: Can anything replace a dendritic cell? Nat Rev Immunol 14:719-730.   DOI
9 Mohsen S, Dickinson JA, Somayaji R. 2020. Update on the adverse effects of antimicrobial therapies in community practice. Can Fam Physician 66:651-659.
10 Shida K, Kiyoshima-Shibata J, Nagaoka M, Watanabe K, Nanno M. 2006. Induction of interleukin-12 by Lactobacillus strains having a rigid cell wall resistant to intracellular digestion. J Dairy Sci 89:3306-3317.   DOI
11 Jang SE, Joh EH, Lee HY, Ahn YT, Lee JH, Huh CS, Han MJ, Kim DH. 2013. Lactobacillus plantarum HY7712 ameliorates cyclophosphamide-induced immunosuppression in mice. J Microbiol Biotechnol 23:414-421.   DOI
12 Vincenzi A, Goettert MI, Volken de Souza CF. 2021. An evaluation of the effects of probiotics on tumoral necrosis factor (TNF-α) signaling and gene expression. Cytokine Growth Factor Rev 57:27-38.   DOI
13 Sukhithasri V, Nisha N, Biswas L, Anil Kumar V, Biswas R. 2013. Innate immune recognition of microbial cell wall components and microbial strategies to evade such recognitions. Microbiol Res 168:396-406.   DOI
14 Ulisse S, Gionchetti P, D'Alo S, Russo FP, Pesce I, Ricci G, Rizzello F, Helwig U, Cifone MG, Campieri M, De Simone C. 2001. Expression of cytokines, inducible nitric oxide synthase, and matrix metalloproteinases in pouchitis: Effects of probiotic treatment. Am J Gastroenterol 96:2691-2699.   DOI
15 Weischenfeldt J, Porse B. 2008. Bone marrow-derived macrophages (BMM): Isolation and applications. Cold Spring Harb Protoc 2008:pdb.prot5080.
16 Won TJ, Kim B, Oh ES, Bang JS, Lee YJ, Yoo JS, Yu H, Yoon J, Hyung KE, Park SY, Hwang KW. 2011. Immunomodulatory activity of Lactobacillus strains isolated from fermented vegetables and infant stool. Can J Physiol Pharmacol 89:429-434.   DOI
17 Choi DW, Jung SY, Kang J, Nam YD, Lim SI, Kim KT, Shin HS. 2018. Immune-enhancing effect of nanometric Lactobacillus plantarum nF1 (nLp-nF1) in a mouse model of cyclophosphamide-induced immunosuppression. J Microbiol Biotechnol 28:218-226.   DOI
18 Crump GM, Zhou J, Mashayekh S, Grimes CL. 2020. Revisiting peptidoglycan sensing: Interactions with host immunity and beyond. Chem Commun 56:13313-13322.   DOI
19 Geha RS, Notarangelo LD, Casanova JL, Chapel H, Conley ME, Fischer A, Hammarstrom L, Nonoyama S, Ochs HD, Puck JM, Roifman C, Seger R, Wedgwood J. 2007. Primary immunodeficiency diseases: An update from the international union of immunological societies primary immunodeficiency diseases classification committee. J Allergy Clin Immunol 120:776-794.   DOI
20 Gramajo Lopez A, Gutierrez F, Saavedra L, Hebert EM, Alvarez S, Salva S. 2021. Improvement of myelopoiesis in cyclophosphamide-immunosuppressed mice by oral administration of viable or non-viable Lactobacillus strains. Front Immunol 12:647049.
21 Jimenez-Valera M, Moreno E, Amat MA, Ruiz-Bravo A. 2003. Modification of mitogen-driven lymphoproliferation by ceftriaxone in normal and immunocompromised mice. Int J Antimicrob Agents 22:607-612.   DOI
22 Lee J, Yun HS, Cho KW, Oh S, Kim SH, Chun T, Kim B, Whang KY. 2011. Evaluation of probiotic characteristics of newly isolated Lactobacillus spp.: Immune modulation and longevity. Int J Food Microbiol 148:80-86.   DOI