Am J Transl Res. 2016 Dec 15;8(12):5628-5636. eCollection 2016.
Bone marrow-derived mesenchymal stem cells reduce immune reaction in a mouse model of allergic rhinitis.
American journal of translational research
Ning Zhao, Yanjuan Liu, Hongfeng Liang, Xuejun Jiang
Affiliations
Affiliations
- Department of E. N. T., The First Hospital Affiliated of China Medical University 155 Nanjing Bei Street, Shenyang 110001, China.
- Department of E. N. T., The First Hospital Affiliated of Dalian Medical University 222 Zhongshan Road, Dalian 116013, China.
PMID: 28078033
PMCID: PMC5209513
Abstract
OBJECT: To determine the potential of bone marrow-derived mesenchymal stem cells (BMSCs) for immunomodulatory mechanism in mice model of allergic rhinitis (AR).
METHODS: BMSCs were isolated and the surface markers and stemness were analyzed. The effect of BMSCs was evaluated in BALB/c mice that were randomly divided into three groups (control group, ovalbumin (OVA) group, OVA+BMSCs group). BMSCs were administered intravenously to OVA sensitized mice on days 1, 7, 14 and 21, and subsequent OVA challenge was conducted daily from days 22 to 35. Several parameters of allergic inflammation were assessed.
RESULTS: Mesenchymal stem cells can be successfully isolated from bone marrow of mice. Intravenous injection of BMSCs significantly reduced allergic symptoms, eosinophil infiltration, OVA-specific immunoglobulin E (IgE), T-helper 2 (Th2) cytokine profile (interleukin (IL)-4, IL-5 and IL-13) and regulatory cytokines (IL-10). In addition, level of Th1 (IFN-γ) was significantly increased.
CONCLUSION: Administration of BMSCs effectively reduced allergic symptoms and inflammatory parameters in the mice model of AR. BMSCs treatment is potentially an alternative therapeutic modality in AR.
Keywords: Cell therapy; allergic rhinitis; cytokines; immunosuppression; mesenchymal stem cell
References
- Methods Mol Med. 2007;140:67-81 - PubMed
- Transfus Med Hemother. 2008;35(4):272-277 - PubMed
- J Immunol. 2002 Mar 15;168(6):3017-23 - PubMed
- Allergy Asthma Proc. 2001 Jul-Aug;22(4):185-9 - PubMed
- J Allergy Clin Immunol. 2012 Apr;129(4):1094-101 - PubMed
- Altern Med Rev. 2003 Aug;8(3):223-46 - PubMed
- Stem Cells. 2009 Jan;27(1):259-65 - PubMed
- Clin Vaccine Immunol. 2006 Sep;13(9):981-90 - PubMed
- Lancet. 2004 May 1;363(9419):1439-41 - PubMed
- Mediators Inflamm. 2014;2014:436476 - PubMed
- Front Immunol. 2012 Nov 27;3:345 - PubMed
- Nature. 2008 Jul 24;454(7203):445-54 - PubMed
- Stem Cells. 2008 Jan;26(1):212-22 - PubMed
- Panminerva Med. 2009 Mar;51(1):5-16 - PubMed
- Stem Cells. 2011 Jul;29(7):1137-48 - PubMed
- Stem Cells. 2007 Mar;25(3):750-60 - PubMed
- Blood. 2001 Nov 1;98(9):2615-25 - PubMed
- Eur J Immunol. 2006 Oct;36(10):2566-73 - PubMed
- J Cell Physiol. 2007 Nov;213(2):341-7 - PubMed
- Otolaryngol Head Neck Surg. 2005 Sep;133(3):429-35 - PubMed
- Dev Growth Differ. 2006 Aug;48(6):361-70 - PubMed
- Allergy. 2012 Oct;67(10):1215-22 - PubMed
- Immunology. 2004 Sep;113(1):106-13 - PubMed
- Arthritis Res Ther. 2003;5(1):32-45 - PubMed
- Ann Allergy Asthma Immunol. 2011 Feb;106(2 Suppl):S12-6 - PubMed
- Blood. 2008 Feb 1;111(3):1327-33 - PubMed
- J Immunol. 2009 May 15;182(10):5994-6002 - PubMed
- Stem Cells. 2012 Dec;30(12):2692-9 - PubMed
- Immunol Lett. 2008 Jan 15;115(1):50-8 - PubMed
- Clin Transl Immunology. 2013 Oct 18;2(10):e7 - PubMed
- Science. 1999 Apr 2;284(5411):143-7 - PubMed
- Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3071-6 - PubMed
- Stem Cells. 2006 Nov;24(11):2466-77 - PubMed
- Surgery. 1997 Aug;122(2):146-52 - PubMed
Publication Types