Evaluation of cytokine expressions in patients with recurrent aphthous stomatitis: A systematic review and meta-analysis

被引:4
作者
Teng, Fangjun [1 ]
Jin, Qiuchen [1 ]
机构
[1] Huazhong Univ Sci & Technol, Cent Hosp Wuhan, Tongji Med Coll, Dept Stomatol, Wuhan, Hubei, Peoples R China
关键词
NECROSIS-FACTOR-ALPHA; SERUM INTERLEUKIN-6 LEVEL; CELLS; LEVAMISOLE; AUTOIMMUNE; MODULATE; QUALITY; DISEASE; HELPER; IL-10;
D O I
10.1371/journal.pone.0305355
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This systematic review and meta-analysis aimed to evaluate the expression levels of various T helper (Th) cell-secreted cytokines in recurrent aphthous stomatitis (RAS). Case-control studies comparing the serum or salivary levels of cytokines between RAS patients and healthy controls were searched in PubMed, EMBASE, Web of Science, and Google Scholar prior to September 30, 2023. Cytokines produced by Th1 (interleukin [IL]-1, IL-2, IL-8, IL-12, tumor necrosis factor alpha [TNF-alpha], interferon gamma [IFN-gamma]), Th2 (IL-4, IL-5, IL-6, IL-10, IL-13), and Th17 (IL-17A) cells were investigated. The standard mean difference (SMD) with 95% confidence interval (CI) was calculated to detect the difference. A total of 20 studies comprising 1070 RAS patients and 536 healthy controls were included. RAS patients had significantly higher salivary levels of IL-2 (SMD = 4.15, 95%CI 0.83-7.48), IL-5 (SMD = 0.53, 95%CI 0.05-1.00), IL-6 (SMD = 0.48, 95%CI 0.12-0.84), IL-12 (SMD = 0.94, 95%CI 0.18-1.71), and TNF-alpha (SMD = 1.31, 95%CI 0.44-2.18) compared to healthy controls. Serum levels of IL-6 (SMD = 0.48, 95%CI 0.30-0.66), TNF-alpha (SMD = 0.70, 95%CI 0.22-1.17), and IFN-gamma (SMD = 0.72, 95%CI 0.17-1.28) were significantly increased, while serum IL-10 levels (SMD = -2.25, 95%CI -3.99 to -0.52) were reduced in RAS patients. Patients diagnosed with major RAS had markedly elevated serum IL-8 levels (SMD = 0.39, 95%CI 0.07-0.71) and a trend toward higher serum IL-6 levels (SMD = 0.51, 95%CI -0.02 to 1.04) than those with minor RAS. In conclusion, Th1/Th2-related cytokines, especially IL-2, IL-6, and TNF-alpha, are involved in the pathogenesis of RAS development and progression and are potential therapeutic targets for RAS.
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页数:18
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共 46 条
[21]   GRADE:: an emerging consensus on rating quality of evidence and strength of recommendations [J].
Guyatt, Gordon H. ;
Oxman, Andrew D. ;
Vist, Gunn E. ;
Kunz, Regina ;
Falck-Ytter, Yngve ;
Alonso-Coello, Pablo ;
Schuenemann, Holger J. .
BRITISH MEDICAL JOURNAL, 2008, 336 (7650) :924-926
[22]   Evaluation of salivary tumour necrosis factor-alpha in patients with recurrent aphthous stomatitis [J].
Hegde, Shruthi ;
Ajila, Vidya ;
Babu, Subhas ;
Kumari, Suchetha ;
Ullal, Harshini ;
Madiyal, Ananya .
EUROPEAN ORAL RESEARCH, 2018, 52 (03) :157-161
[23]   Interleukin 6 in autoimmune and inflammatory diseases: a personal memoir [J].
Hirano, Toshio .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2010, 86 (07) :717-730
[24]  
Kalpana R, 2014, J Oral Maxillofac Pathol, V18, P361, DOI 10.4103/0973-029X.151313
[25]   Advances in immunology: Tolerance and autoimmunity. [J].
Kamradt, T ;
Mitchison, NA .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (09) :655-664
[26]   EPIDEMIOLOGY OF ORAL MUCOSAL LESIONS IN UNITED-STATES SCHOOLCHILDREN - 1986-87 [J].
KLEINMAN, DV ;
SWANGO, PA ;
PINDBORG, JJ .
COMMUNITY DENTISTRY AND ORAL EPIDEMIOLOGY, 1994, 22 (04) :243-253
[27]   Mucocutaneous IL-17 immunity in mice and humans: host defense vs. excessive inflammation [J].
Li, J. ;
Casanova, J-L ;
Puel, A. .
MUCOSAL IMMUNOLOGY, 2018, 11 (03) :581-589
[28]   Optimally estimating the sample mean from the sample size, median, mid-range, and/or mid-quartile range [J].
Luo, Dehui ;
Wan, Xiang ;
Liu, Jiming ;
Tong, Tiejun .
STATISTICAL METHODS IN MEDICAL RESEARCH, 2018, 27 (06) :1785-1805
[29]   Immune-expression of HSP27 and IL-10 in recurrent aphthous ulceration [J].
Miyamoto, Nelson T., Jr. ;
Borra, Ricardo Carneiro ;
Abreu, Marilda ;
Maurice Weckx, Luc Louis ;
Franco, Marcello .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2008, 37 (08) :462-467
[30]  
Moher D, 2009, PLOS MED, V6, DOI [10.1371/journal.pmed.1000097, 10.1016/j.ijsu.2010.02.007, 10.1136/bmj.b2535, 10.1136/bmj.b2700, 10.1136/bmj.i4086, 10.1016/j.ijsu.2010.07.299, 10.1186/2046-4053-4-1]