|Year : 2013 | Volume
| Issue : 4 | Page : 523-530
Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
Ho Yun Lee1, Ji Hyun Chung1, Sun Kyu Lee1, Jae Yong Byun1, Young Il Kim2, Seung Geun Yeo1
1 Department of Otolaryngology-Head & Neck Surgery, School of Medicine, Kyung Hee University, Seoul, Korea
2 Medical Science Research Institute, Kyung Hee University Medical Center, Seoul, Korea
|Date of Submission||13-May-2012|
|Date of Web Publication||19-Nov-2013|
Seung Geun Yeo
#1 Hoegi-dong, dongdaemun-gu, Seoul 130-702
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background & objectives : Microbial infections in the normally sterile environment of the middle ear cavity in patients with otitis media trigger expression of Toll-like receptors (TLRs), cytokines, and nitric oxide. We evaluated the expression levels of TLR-1, -2, -4, -5, -6, and -9, interleukin (IL)-6, -8, -10, and -12, interferon-γ (IFN-γ), tumour necrosis factor-α (TNF-α), and nitric oxide (NO), in paediatric patients with otitis media with effusion (OME).
Methods: The levels of TLR, cytokine, and nitric oxide synthase (NOS) mRNAs in middle ear effusion were assessed by real-time polymerase chain reaction in 96 children with OME, 24 prone and 72 not prone to otitis. The level of expression of each mRNA was compared in the otitis-prone and non-otitis-prone groups, in patients with and without bacteria, and by frequency of ventilation tube insertion.
Results: The expression of TLR-1, -2, -4, -5, -6, and -9; IL-6, -8, -10, and -12; IFN-γ; TNF-α; and NOS mRNAs in the effusion fluid of both the otitis-prone and non-otitis-prone groups were measured. The expression levels of TLR-2, -4, -6, and -9 mRNA were significantly lower in the otitis-prone than in the non-otitis-prone group (P<0.05). Although higher levels of TLR, cytokine, and NOS mRNAs were generally observed in culture positive than in culture negative patients, none of these differences was statistically significant. No differences were observed in the expressions relative to the frequencies of ventilation tube insertion.
Interpretation & conclusions: TLRs, cytokines, and NOS, which act cooperatively in the innate immune response, were closely associated with OME. Decreased expression of TLRs may be associated with increased susceptibility to OME.
Keywords: Cytokine - nitric oxide synthase - otitis media with effusion - Toll-like receptors
|How to cite this article:|
Lee HY, Chung JH, Lee SK, Byun JY, Kim YI, Yeo SG. Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion. Indian J Med Res 2013;138:523-30
|How to cite this URL:|
Lee HY, Chung JH, Lee SK, Byun JY, Kim YI, Yeo SG. Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion. Indian J Med Res [serial online] 2013 [cited 2021 May 8];138:523-30. Available from: https://www.ijmr.org.in/text.asp?2013/138/4/523/121500
Otitis media with effusion (OME) is a disease in which secreted fluid accumulates in the middle ear cavity and is a major cause of hearing loss in children  . Although most patients spontaneously recover, some patients show frequent recurrence of otitis media. About 5 per cent of children are otitis-prone, defined as experiencing more than three recurrences of otitis media within six months or more than four per year  . Inflammatory reactions induced by pathogens are regarded as important in understanding the mechanisms of immune response in the middle ear and in treating these patients , .
The first step in the activation of the human defense mechanism against microbes is the recognition of pathogens by macrophages. Macrophages recognize pathogen-associated molecular patterns (PAMPs), generating intracellular signals and producing cytokines and chemokines, leading to the activation of the acquired immune system  . The recognition and reaction of PAMPs is controlled by pattern-recognition receptors (PRRs), including Toll-like receptors (TLRs), which bind to infecting microbes and directly induce innate host defense responses  . The pathogenesis of OME also involves the inflammatory mediator nitric oxide, which mediates the development of OME by increasing vascular extravasation, neutrophil migration, and mucin hypersecretion , . The cytokines, a group of glycoproteins that participate in modulating inflammatory and immune reactions in many diseases, were found to be involved in OME in humans and experimental animals  .
Although the immunologic aetiology and mechanisms of recurrent otitis media have been thoroughly investigated, but the TLRs, cytokines, and NO were evaluated separately. Little is known about how the innate immune system first reacts with pathogens invading the middle ear cavity, or about the combined expression of TLRs, cytokines, and NO during OME. We therefore, studied the expression levels of TLRs, cytokines, and NO and their relationship in patients with OME.
| Material & Methods|| |
Study subjects: Effusion fluid samples were obtained from 96 paediatric patients who visited the Department of Otorhinolaryngology, School of Medicine, Kyung Hee University, Seoul, Korea, and who underwent ventilation tube (v-tube) insertion to treat chronic OME between September 2009 and August 2011. Children were enrolled after approval of the study protocol was obtained from the Medical Ethics Committee of Kyung Hee University Hospital; all parents or guardians provided written informed consent.
The subject group consisted of 96 paediatric patients (62 males, 32 females) ranging in age from 2-10 yr (mean ± SD age, 4.4 ± 2.2 yr); 72 non-otitis-prone children (49 males, 23 females) ranging in age from 2-9 yr (mean ± SD age, 5.3 ± 4.5 yr); and 24 otitis-prone children (15 males, 9 females) ranging in age from 2-10 yr (mean ± SD age, 4.9 ± 3.9 yr). On evaluating the characteristics of middle ear effusion (MEE), 16 had serous, 29 had mucoid and 27 had purulent MEE in non-otitis-prone children. For otitis-prone group, six had serous, 11 had mucoid and seven had purulent MEE [Table 1].
At the first visit, each patient underwent a detailed medical history and physical examinations, including anterior rhinoscopy, otoscopy, impedance audiometry, pure tone audiometry and speech audiometry. OME was diagnosed by the presence of an amber-coloured tympanic membrane on otoscopic examination and by the presence of B- or C-type tympanograms on impedance audiometry. Of these 96 children, 24 had been treated more than four times within the previous year, or more than three times within the previous six months, and were categorized as the otitis-prone group, whereas the other 72 children constituted the non-otitis-prone group. Surgery was performed on patients with chronic OME who did not show improvement after two wk of antibiotic treatment and after a 2-3 month follow up, in patients who showed progressive retraction of the eardrum or progression of hearing loss as shown by continuous increase in pure tone threshold.
Middle ear effusion fluid: When surgery was required, the external acoustic meatus was washed with a potadine solution and a radial incision was made in the anterior inferior quadrant of the tympanic membrane. Effusion fluid was aseptically collected with the aid of Juhn Tym-Tap collectors (Medtronic Xomed; Jacksonville, FL, USA); care was taken to avoid bleeding. Fluid samples were transferred to Eppendorf tubes and stored at -80°C.
Effusion fluid samples, in the original collectors, were sampled using sterile cotton swabs (Xomed Trace Products, Jacksonville, FL, USA); the swabs were submerged in Stuart transport medium. Such samples were used to inoculate solid blood agar and liquid thioglycollate medium (Hangang, Kun-po, Korea). Cultures were incubated for 24 h at 35 o C, and bacteria that formed colonies were identified by Gram staining and biochemical testing  .
Amplification: Total RNA was extracted from effusion fluid using RNA-Bee solution kits (Tel-Test, Friendswood, TX, USA), according to the manufacturer's protocol. First-strand cDNA was synthesized by reverse transcription in a total volume of 20 μl reaction mixture containing 1 μg of RNA, 1x reaction buffer, 1 mM dNTP, 5 μM random primers, 20 units RNase inhibitor, and 20 units AMV reverse transcriptase (Promega, Madison, WI, USA). The reaction mixture was incubated at 42°C for 1 h, the reaction was terminated by heating at 95°C for 5 min. Primers specific for Toll-like receptors (TLRs) -1, 2, -4, -5, 6, and -9, interleukins (IL)-6, -8, -10, and -12, interferon (IFN)-γ, tumour necrosis factor (TNF)-α, and NOS are shown in [Table 2] ,,,, . Real-time polymerase chain reactions (PCR) were performed using a Chromo4 Detector real-time system (Bio-Rad, Hercules, CA, USA) and the SsoFast EvaGreen supermix (Bio-Rad). Each PCR reaction included 2 μl of cDNA in a 20-μl reaction mixture containing 10 μl SsoFast EvaGreen supermix, 2 μl of each primer and 6 μl PCR grade water. The amplification protocols consisted of an initial denaturation at 95°C for 30 sec, followed by 45 cycles of denaturation at 95°C for 5 sec and annealing and extension at 55 to 64°C for 12 sec. The point at which expression of each of the above cDNAs crossed with that for β-actin was applied to the formula, 2 -(target gene- β actin) , and the relative amounts were quantitated  .
The level of expression of each mRNA was compared in the otitis-prone and non-otitis-prone groups, in patients with and without bacteria, and by frequency of ventilation tube insertion.
Statistical analysis: The data were analyzed by Mann-Whitney U test using SPSS version 13 (Chicago, IL, USA), with a P value less than 0.05 was considered significant. Pearson's correlation analysis was used to study correlations between the expression levels of TLRs, IL, IFN- γ, TNF- α and N os0 mRNA.
| Results|| |
Of the 96 effusion fluid samples examined, 67 (69.8 %) were apparently sterile, whereas bacteria grew from the remaining 29 samples (30.2%). The bacteria detected included coagulase-negative Staphylococcus (CNS), Haemophilus influenzae, Streptococcus pneumoniae, multhicillin-resistant Staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Streptococcus viridans, Staphylococcus aureus, Acinetobacter lwoffii, Micrococcus sp., Corynebacterium sp., and Bacillus sp. [Table 3].
The expression of TLR-1, -2, -4, -5, -6, and -9; IL-6, -8, -10, and -12; IFN-γ; TNF-α; and NOS mRNAs in the effusion fluid of both the otitis-prone and non-otitis-prone groups was measured. The expression levels of TLR-2, -4, -6, and -9 mRNA were significantly lower in the otitis-prone than in the non-otitis-prone group (P<0.05) [Figure 1] and [Figure 2].
|Figur 1: TLR mRNA expression in the effusion fluid of the otitis-prone and non-otitis-prone groups. ΔCt, threshold cycle; *=P<0.5.|
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|Figure 2: Cytokine and NOS mRNA expression in the effusion fluid of the otitis-prone and non-otitis-prone groups.|
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Although higher levels of TLR, cytokine, and NOS mRNAs were generally observed in culture positive than in culture negative patients, none of these differences was statistically significant. No differences were observed in the expressions relative to the frequencies of v-tube insertion [Table 4]. The expression levels of these mRNAs were correlated [Table 5].
|Table 4: Relative levels of expression of TLRs, cytokines, and NOS mRNA according to the presence of bacteria and the frequency of ventilation tube (v-tube) insertion|
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|Table 5: Correlations between TLRs, cytokine, and NOS mRNAs in effusion fluid|
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| Discussion|| |
Otitis-prone children showed significantly lower expression levels of mRNAs encoding TLR-2, -4, -6, and -9 than did those who were not otitis-prone, indicating that reduced TLR expression in the middle-ear cavity may increase susceptibility to recurrent OME.
Of the various relevant factors, TLR2 and TLR4, in particular, are known to play important roles in molecular pathogenesis and in the development of host defenses to otitis media ,, . An experimental study suggested that decreased production of proinflammatory cytokines by virtue of defective TLR2 functionality in those with acute otitis media might hinder bacterial clearance from the middle ear  . We previously reported that the expression level of TLR9 was significantly lower in an otitis-media-prone group; a similar trend was evident in the present study  . It has also been reported that the otitis-prone condition is associated with certain genetic polymorphisms, especially in genes involved in the innate immune response. Such alleles include TNFA-863A, TNFA-376G, TNFA-238G, IL10-1082A, and IL6-174G; the variant alleles differ in the promoter regions  .
Bacteria are potent triggers of monocyte/ macrophage cytokine secretion as well as TLR expression. Gram-positive bacteria induce the secretion of IL-12, TNF, and IFN-γ, whereas Gram-negative bacteria induce the secretion of IL-6 and IL-10  . TNF-α is central for extravasation of polymorphonuclear leukocytes into infected tissue. IL-12, IFN-γ, and TNF-α are key cytokines in cell mediated immune reactions  . In addition, TNF-α plays a role in prostaglandin and cytokine release, as well as in the activation of neutrophils, eosinophils, and macrophages. TNF-α has many of the same functions as IL-1, with the two having a synergistic effect  . IL-6 activates B and T cells, resulting in the production of antibodies, and the induction of fever and bone resorption. IL-6 expression is significantly correlated with OME and degree of hearing loss  . IL-10 downregulates the inflammatory properties of IL-1, IL-6, and TNF-α and is thought to contribute to the eradication of middle ear inflammation as well as providing a negative feedback mechanism related to TNF-α in patients with otitis media , . IL-12 is the major cytokine responsible for the differentiation of T H 1 cells, which produce IFN-γ. IFN-γ activates macrophages and NK cells, and potentiates the proliferation of activated T cells  .
In our study, the levels of expression of all the cytokines tested, IL-6, -8, -10, and -12; IFN-γ; and TNF-α did not differ significantly between otitis-prone and non-otitis-prone groups. Effusion in the middle ear is a chronic state, with inflammation occurring for at least three months. Thus, effusion fluid, in contrast to middle ear mucosa, could not fully reflect inflammatory reactions in this organ.
Nitric oxide is responsible for vasodilation, increased vascular permeability, and production of mucoid effusion in patients with otitis media  . Incubation of middle ear epithelial cells with IL-1 ί or TNF-α induced NO, both in vivo and in vitro, suggesting that NO may be a secondary mediator of inflammation produced by middle ear epithelium in response to primary proinflammatory cytokines  .
This study had several limitations. We did not include any children with early stage OME. In addition, all patients had been treated with antibiotics for two week for early stage symptoms. Third, 69.8 per cent of the middle ear samples were negative for bacterial growth despite bacterial infection, which could have been due to treatment with antibiotics before surgery, creating a bacteriostatic condition and delaying the proliferation and growth of pathogens. Fourth, the exudates used in this study were collected during surgery 2-3 months after the initial onset of otitis media. Thus, our findings may not fully reflect the initial immune response in the middle ear cavity. Moreover, though our study group included patients with OME, all patients had normal immunity, and both otitis-prone and non-otitis prone patients had chronic effusions in the middle ear cavity without improvement. Furthermore, for ethical reasons, we could not harvest the middle ear mucosa from the patients in this study and performed experiments on exudates. These exudates contained only a few partially exfoliated mucosal epithelial cells and inflammatory cells; therefore, these would not fully reflect the immune cells present in the middle ear mucosa during infection. Finally, we could not determine the expression levels of TLR, cytokine, and NOS mRNAs at the initial time of otitis media, but only in fluid secreted after inflammatory reactions. Therefore, our results may reflect more complex anti-infective mechanisms occurring in the middle ear cavity. Therefore, our results eflect the situation obtained when complex anti-infective mechanisms are triggered in the middle-ear cavity, and thus need to be interpreted with caution.
In conclusion, our findings showed that TLRs, cytokines, and NOS worked cooperatively in innate immune responses and were closely associated with OME. However, all exudates of OME patients showed some level of TLR expression related to the immune response, regardless of the presence of the bacteria in exudates, or the frequency of ventilation tube insertion. Thus different levels of expression of TLRs may be important indicators of immune responses in patients with OME, and decreased expression of TLRs may be associated with increased susceptibility to OME.
| Acknowledgment|| |
This research was supported by the Kyung Hee University Research Fund, Korea, in 2011(KHU-2011-0899).
| References|| |
|1.||Scholz F, Köhn A, Rissmann A, Arens C, Vorwerk W, Vorwerk U. Otitis media with effusion: Frequency, diagnosis and therapy in early childhood. HNO 2013; 61 : 859-65. |
|2.||Kitajiri M, Sando I, Takahara T. Postnatal development of the Eustachian tube and its surrounding structure. Ann Otol Rhinol Laryngol 1987; 96 : 191-8. |
|3.||Yeo SG, Park DC, Lee SK, Cha CI. Relationship between effusion bacteria and concentrations of immunoglobulin in serum and effusion fluid in otitis media with effusion patients. Int J Pediatr Otorhinolaryngol 2008; 72 : 337-42. |
|4.||Ilia S, Goulielmos GN, Samonis G, Galanakis E. Host's response in otitis media: understanding genetic susceptibility. Pediatr Infect Dis J 2008; 27 : 929-33. |
|5.||Cook DN, Pisesky DS, Schwarts DA. Toll-like receptors in the pathogenesis of human disease. Nat Immunol 2004; 5 : 975-9. |
|6.||Kim MG, Park DC, Shim JS, Jung H, Park MS, Kim YI, et al. TLR-9, NOD-1, NOD-2, RIG-I and immunoglobulins in recurrent otitis media with effusion. Int J Pediatr Otorhinolaryngol 2010; 74 : 1425-9. |
|7.||Yang RB, Mark MR, Gurney AL, Godowski PJ. Signaling events induced by lipopolysaccharide-activated toll-like receptor 2. J Immunol 1999; 163 : 639-43. |
|8.||Aliprantis AO, Yang RB, Mark MR. Cell activation and apoptosis by bacterial lipoproteins through toll-like receptor-2. Science 1999; 285 : 736-9. |
|9.||Skotnicka B, Hassmann E. Cytokines in children with otitis media with effusion. Eur Arch Otorhinolaryngol 2000; 257 : 323-6. |
|10.||Shin IH, Shin OY, Cha SH, Kim YI, Lee JW, Yeo SG. IgA and differentiation-associated transcription factors in chronic otitis media with effusion. Clin Exp Otorhinolaryngol 2009; 2 : 131-5. |
|11.||Homma T. Corticosteroid and cytokines synergistically enhance Toll-like receptor 2 expression in respiratory epithelial cells. Am J Respir Cell Mol Biol 2004; 31 : 463-9. |
|12.||Bellone G, Smirne C, Mauri FA, Tonel E, Carbone A, Buffolino A, et al. Cytokine expression profile in human pancreatic carcinoma cells and in surgical specimens: implications for survival. Cancer Immunol Immunother 2005; 55 : 684-98. |
|13.||Törnblom SA, Maul H, Klimaviciute A, Garfield RE, Byström B, Malmström A, et al. mRNA expression and localization of bNOS, eNOS and iNOS in human cervix at preterm and term labour. Reprod Biol Endocrinol 2005; 3 : 33. |
|14.||Uehara A, Fujimoto Y, Fukase K, Takada H. Various human epithelial cells express functional Toll-like receptors, NOD1 and NOD2 to produce anti-microbial peptides, but not proinflammatory cytokines. Mol Immunol 2007; 44 : 3100-11. |
|15.||Song JJ, Kwon SK, Cho CG, Park SW, Chae SW. Guggulsterone suppresses LPS induced inflammation of human middle ear epithelial cells (HMEEC). Int J Pediatr Otorhinolaryngol 2010; 74: 1384-7. |
|16.||Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta delta C(T)) method. Methods 2001; 25 : 402-8. |
|17.||Lee YC, Kim C, Shim JS, Byun JY, Park MS, Cha CI, et al. Toll-like receptors 2 and 4 and their mutations in patients with otitis media and middle ear effusion. Clin Exp Otorhinolaryngol 2008; 1 : 189-95. |
|18.||Song JJ, Cho JG, Woo JS, Lee HM, Hwang SJ, Chae SW. Differential expression of toll-like receptors 2 and 4 in rat middle ear. Int J Pediatr Otorhinolaryngol 2009; 73 : 821-4. |
|19.||Leichtle A, Lai Y, Wollenberg B, Wasserman SI, Ryan AF. Innate signaling in otitis media: pathogenesis and recovery. Curr Allergy Asthma Rep 2011; 11 : 78-84. |
|20.||Li SL, Zhang MY, Li BY, Zheng QY, Zhu HL. Toll-like receptor 2 and Toll-like receptor 4 participates in mediation of acute otitis media and mortality in pneumococcal infections in mice. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 2011; 46 : 1009-18. |
|21.||Emonts M, Veenhoven RH, Wiertsema SP, Houwing-Duistermaat JJ, Walraven V, de Groot R, et al. Genetic polymorphisms in immunoresponse genes TNFA, IL6, IL10, and TLR4 are associated with recurrent acute otitis media. Pediatrics 2007; 120 : 814-23. |
|22.||Skovbjerg S, Martner A, Hynsjö L, Hessle C, Olsen I, Dewhirst FE, et al. Gram-positive and Gram-negative bacteria induce different patterns of cytokine production in human mononuclear cells irrespective of taxonomic relatedness. J Interferon Cytokine Res 2010; 30 : 23-32. |
|23.||Kim SJ, Choi JY, Son EJ, Namkung W, Lee MG, Yoon JH. Interleukin-1beta upregulates Na+-K+-2Cl- cotransporter in human middle ear epithelia. J Cell Biochem 2007; 101 : 576-86. |
|24.||Ikejima T, Okusawa S, Ghezzi P, van der Meer JW, Dinarello CA. Interleukin-1 induces tumor necrosis factor (TNF) in human peripheral blood mononuclear cells in vitro and a circulating TNF-like activity in rabbits. J Infect Dis 1990; 162 : 215-23. |
|25.||Kerschner JE, Meyer TK, Yang C, Burrows A. Middle ear epithelial mucin production in response to interleukin-6 exposure in vitro. Cytokine 2004; 26 : 30-6. |
|26.||Smirnova MG, Birchall JP, Pearson JP. Evidence of T-helper cell 2 cytokine regulation of chronic otitis media with effusion. Acta Otolaryngol 2005; 125 : 1043-50. |
|27.||Hebda PA, Piltcher OB, Swarts JD, Alper CM, Zeevi A, Doyle WJ. Cytokine profiles in a rat model of otitis media with effusion caused by eustachian tube obstruction with and without Streptococcus pneumoniae infection. Laryngoscope 2002; 112 : 1657-62. |
|28.||Juhn SK, Jung MK, Hoffman MD, Drew BR, Preciado DA, Sausen NJ, et al. The role of inflammatory mediators in the pathogenesis of otitis media and sequelae. Clin Exp Otorhinolaryngol 2008; 1 : 117-38. |
|29.||Pudrith C, Martin D, Kim YH, Jahng P, Kim B, Wall M, et al. Glucocorticoids reduce nitric oxide concentration in middle ear effusion from lipopolysaccharide induced otitis media. Int J Pediatr Otorhinolaryngol 2010; 74 : 384-6. |
|30.||Li W, Lin J, Adams GL, Juhn SK. Expression of inducible nitric oxide synthase (iNOS) in middle ear epithelial cells by IL-1beta and TNF-alpha. Int J Pediatr Otorhinolaryngol 2000; 55 : 91-8. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]