期刊论文详细信息
BMC Infectious Diseases
Expression of M. tuberculosis-induced suppressor of cytokine signaling (SOCS) 1, SOCS3, FoxP3 and secretion of IL-6 associates with differing clinical severity of tuberculosis
Zahra Hasan2  Rabia Hussain2  Muniba Islam2  Berit Carow4  Nisar Rao1  Muhammad Irfan2  Naseem Salahuddin3  Martin E Rottenberg4  Kiran I Masood2 
[1] OJHA Institute of Chest Diseases, DOW University of Health Sciences, Karachi, Pakistan;Department of Pathology and Microbiology, Aga Khan University, P.O. Box 3500, Stadium Road, Karachi, 74800, Pakistan;Indus Hospital, Karachi, Pakistan;Department of Microbiology and Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden
关键词: Tuberculosis;    Cytokine regulation;    SOCS molecules;   
Others  :  1158597
DOI  :  10.1186/1471-2334-13-13
 received in 2012-06-16, accepted in 2013-01-10,  发布年份 2013
PDF
【 摘 要 】

Background

Appropriate immune activation of T cells and macrophages is central for the control of Mycobacterium tuberculosis infections. IFN-γ stimulated responses are lowered in tuberculosis (TB), while expression of Suppressor of Cytokine Signaling (SOCS) molecules – 1 and 3 and CD4+CD25+FoxP3+T regulatory cells is increased. Here we investigated the association of these molecules in regard to clinical severity of TB.

Methods

Peripheral blood mononuclear cells (PBMCs) were isolated from patients with pulmonary TB (PTB, n = 33), extra-pulmonary TB (ETB, n = 33) and healthy endemic controls (EC, n = 15). Cases were classified as moderately advanced or far advanced PTB, and less severe or severe disseminated ETB. M. tuberculosis -stimulated IFN-γ, SOCS1, SOCS3 and FoxP3 gene expression and secretion of Th1 and Th2 cytokines was measured. Statistical analysis was performed using Mann–Whitney U, Wilcoxon Rank and Kruskal Wallis non-parametric tests.

Results

In un-stimulated PBMCs, IL-6 (p = 0.018) and IL-10 (p = 0.013) secretion levels were increased in PTB while IL-10 was also increased in ETB (p = 0.003), all in comparison with EC. M. tuberculosis-stimulated IL-6 (p = 0.003) was lowered in ETB as compared with EC. SOCS1 mRNA expression in M. tuberculosis stimulated PBMCs levels in moderately advanced PTB (p = 0.022), far advanced (p = 0.014) PTB, and severe ETB (p = 0.009) were raised as compared with EC. On the other hand, SOCS1 mRNA titers were reduced in less severe ETB, in comparison with severe ETB (p = 0.027) and far advanced PTB (p = 0.016). SOCS3 mRNA accumulation was reduced in far advanced PTB (p = 0.007) and FoxP3 mRNA expression was increased in less severe ETB as compared with EC (p = 0.017).

Conclusions

The lowered SOCS1 mRNA levels in patients with less severe extra-pulmonary TB as compared to those with more severe ETB and PTB may lead to elevated IFN-γ pathway gene expression in the latter group. As localized ETB has shown to be associated with more effective Th1 immunity and adaptive responses, this suggests a role for SOCS1 in determining disease outcome in extra-pulmonary TB.

【 授权许可】

   
2013 Masood et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150408022349305.pdf 549KB PDF download
Figure 2. 78KB Image download
Figure 1. 87KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]WHO: Tuberculosis Factsheet. Geneva: World Health Organisation; 2011.
  • [2]WHO: Global Tuberculosis Control. Geneva: World Health Organisation; 2011.
  • [3]Stenger S, Modlin RL: T cell mediated immunity to Mycobacterium tuberculosis. Curr Opin Microbiol 1999, 2(1):89-93.
  • [4]Dalton DK, Pitts-Meek S, Keshav S, Figari IS, Bradley A, Stewart TA: Multiple defects of immune cell function in mice with disrupted Interferon-gamma genes. Science 1993, 259(5102):1739-1742.
  • [5]Kaufmann SH: Protection against tuberculosis: cytokines, T cells, and macrophages. Ann Rheum Dis 2002, 61(Suppl 2):ii54-ii58.
  • [6]Qiu L, Huang D, Chen CY, Wang R, Shen L, Shen Y, Hunt R, Estep J, Haynes BF, Jacobs WR Jr, et al.: Severe tuberculosis induces unbalanced up-regulation of gene networks and overexpression of IL-22, MIP-1alpha, CCL27, IP-10, CCR4, CCR5, CXCR3, PD1, PDL2, IL-3, IFN-beta, TIM1, and TLR2 but low antigen-specific cellular responses. J Infect Dis 2008, 198(10):1514-1519.
  • [7]Flynn JL, Chan J: Immunology of tuberculosis. Annu Rev Immunol 2001, 19:93-129.
  • [8]Hirsch CS, Toossi Z, Othieno C, Johnson JL, Schwander SK, Robertson S, Wallis RS, Edmonds K, Okwera A, Mugerwa R, et al.: Depressed T-cell Interferon-gamma responses in pulmonary tuberculosis: analysis of underlying mechanisms and modulation with therapy. J Infect Dis 1999, 180(6):2069-2073.
  • [9]Sharma SK, Mitra DK, Balamurugan A, Pandey RM, Mehra NK: Cytokine polarization in miliary and pleural tuberculosis. J Clin Immunol 2002, 22(6):345-352.
  • [10]Sahiratmadja E, Alisjahbana B, de Boer T, Adnan I, Maya A, Danusantoso H, Nelwan RH, Marzuki S, van der Meer JW, van Crevel R, et al.: Dynamic changes in pro- and anti-inflammatory cytokine profiles and gamma interferon receptor signaling integrity correlate with tuberculosis disease activity and response to curative treatment. Infect Immun 2007, 75(2):820-829.
  • [11]Jamil B, Shahid F, Hasan Z, Nasir N, Razzaki T, Dawood G, Hussain R: Interferon gamma/IL-10 ratio defines the disease severity in pulmonary and extra pulmonary tuberculosis. Tuberculosis (Edinb) 2007, 87(4):279-287.
  • [12]Gazzola L, Tincati C, Gori A, Saresella M, Marventano I, Zanini F: FoxP3 mRNA expression in regulatory T cells from patients with tuberculosis. Am J Respir Crit Care Med 2006, 174(3):356. author reply 357
  • [13]Shevach EM: Mechanisms of FoxP3+ T regulatory cell-mediated suppression. Immunity 2009, 30(5):636-645.
  • [14]Guyot-Revol V, Innes JA, Hackforth S, Hinks T, Lalvani A: Regulatory T cells are expanded in blood and disease sites in patients with tuberculosis. Am J Respir Crit Care Med 2006, 173(7):803-810.
  • [15]Lesho E, Forestiero FJ, Hirata MH, Hirata RD, Cecon L, Melo FF, Paik SH, Murata Y, Ferguson EW, Wang Z, et al.: Transcriptional responses of host peripheral blood cells to tuberculosis infection. Tuberculosis (Edinb) 2011, 91(5):390-399.
  • [16]Berry MP, Graham CM, McNab FW, Xu Z, Bloch SA, Oni T, Wilkinson KA, Banchereau R, Skinner J, Wilkinson RJ, et al.: An Interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis. Nature 2010, 466(7309):973-977.
  • [17]Almeida AS, Lago PM, Boechat N, Huard RC, Lazzarini LC, Santos AR, Nociari M, Zhu H, Perez-Sweeney BM, Bang H, et al.: Tuberculosis is associated with a down-modulatory lung immune response that impairs Th1-type immunity. J Immunol 2009, 183(1):718-731.
  • [18]Wormald S, Zhang JG, Krebs DL, Mielke LA, Silver J, Alexander WS, Speed TP, Nicola NA, Hilton DJ: The comparative roles of Suppressor of Cytokine Signaling-1 and −3 in the inhibition and desensitization of cytokine signaling. J Biol Chem 2006, 281(16):11135-11143.
  • [19]Croker BA, Krebs DL, Zhang JG, Wormald S, Willson TA, Stanley EG, Robb L, Greenhalgh CJ, Forster I, Clausen BE, et al.: SOCS3 negatively regulates IL-6 signaling in vivo. Nat Immunol 2003, 4(6):540-545.
  • [20]Niemand C, Nimmesgern A, Haan S, Fischer P, Schaper F, Rossaint R, Heinrich PC, Muller-Newen G: Activation of STAT3 by IL-6 and IL-10 in primary human macrophages is differentially modulated by Suppressor of Cytokine Signaling 3. J Immunol 2003, 170(6):3263-3272.
  • [21]Somoskovi A, Zissel G, Zipfel PF, Ziegenhagen MW, Klaucke J, Haas H, Schlaak M, Muller-Quernheim J: Different cytokine patterns correlate with the extension of disease in pulmonary tuberculosis. Eur Cytokine Netw 1999, 10(2):135-142.
  • [22]Hasan Z, Jamil B, Ashraf M, Islam M, Yusuf MS, Khan JA, Hussain R: ESAT6-induced IFNgamma and CXCL9 can differentiate severity of tuberculosis. PLoS One 2009, 4(4):e5158.
  • [23]Kellar KL, Gehrke J, Weis SE, Mahmutovic-Mayhew A, Davila B, Zajdowicz MJ, Scarborough R, LoBue PA, Lardizabal AA, Daley CL, et al.: Multiple cytokines are released when blood from patients with tuberculosis is stimulated with Mycobacterium tuberculosis antigens. PLoS One 2011, 6(11):e26545.
  • [24]WHO: Treatment of Tuberculosis: Guidelines for National Programmes. 3rd edition. Geneva: World Health Organisation; 2003. WHO/CDS/TB/2003.313. 2003
  • [25]Crofton J: Clinical features of tuberculosis. Crofton and Douglas’s respiratory diseases. 4th edition. London: Wiley-Blackwell scientific; 1991.
  • [26]Hasan Z, Jamil B, Ashraf M, Islam M, Dojki M, Irfan M, Hussain R: Differential live Mycobacterium tuberculosis-, M. bovis BCG-, recombinant ESAT6-, and Culture filtrate protein 10-induced immunity in tuberculosis. Clin Vaccine Immunol 2009, 16(7):991-998.
  • [27]Hasan Z, Cliff JM, Dockrell HM, Jamil B, Irfan M, Ashraf M, Hussain R: CCL2 Responses to Mycobacterium tuberculosis are associated with disease severity in tuberculosis. PLoS One 2009, 4(12):e8459.
  • [28]Masood KI, Rottenberg ME, Carow B, Rao N, Ashraf M, Hussain R, Hasan Z: SOCS1 Gene expression is increased in severe pulmonary tuberculosis. Scand J Immunol 2012, 76(4):398-404.
  • [29]Dheda K, Huggett JF, Bustin SA, Johnson MA, Rook G, Zumla A: Validation of housekeeping genes for normalizing RNA expression in real-time PCR. Biotechniques 2004, 37(1):112-114. 116, 118–119
  • [30]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(4):402-408.
  • [31]Talat N, Shahid F, Perry S, Dawood G, Hussain R: Th1/Th2 cytometric bead array can discriminate cytokine secretion from endogenously activated cells in pulmonary disease, recent and remote infection in tuberculosis. Cytokine 2011, 54(2):136-143.
  • [32]Shiratsuchi H, Johnson JL, Ellner JJ: Bidirectional effects of cytokines on the growth of Mycobacterium avium within human monocytes. J Immunol 1991, 146(9):3165-3170.
  • [33]Gong JH, Zhang M, Modlin RL, Linsley PS, Iyer D, Lin Y, Barnes PF: Interleukin-10 downregulates Mycobacterium tuberculosis-induced Th1 responses and CTLA-4 expression. Infect Immun 1996, 64(3):913-918.
  • [34]Beamer GL, Flaherty DK, Assogba BD, Stromberg P, Gonzalez-Juarrero M, de Waal Malefyt R, Vesosky B, Turner J: Interleukin-10 promotes Mycobacterium tuberculosis disease progression in CBA/J mice. J Immunol 2008, 181(8):5545-5550.
  • [35]Verbon A, Juffermans N, Van Deventer SJ, Speelman P, Van Deutekom H, Van Der Poll T: Serum concentrations of cytokines in patients with active tuberculosis (TB) and after treatment. Clin Exp Immunol 1999, 115(1):110-113.
  • [36]Kursar M, Koch M, Mittrucker HW, Nouailles G, Bonhagen K, Kamradt T, Kaufmann SH: Cutting edge: regulatory T cells prevent efficient clearance of Mycobacterium tuberculosis. J Immunol 2007, 178(5):2661-2665.
  • [37]Boussiotis VA, Tsai EY, Yunis EJ, Thim S, Delgado JC, Dascher CC, Berezovskaya A, Rousset D, Reynes JM, Goldfeld AE: IL-10-producing T cells suppress immune responses in anergic tuberculosis patients. J Clin Invest 2000, 105(9):1317-1325.
  • [38]Hasan Z, Mahmood A, Zafar S, Khan AA, Hussain R: Leprosy patients with lepromatous disease have an up-regulated IL-8 response that is unlinked to TNF-alpha responses. Int J Lepr Other Mycobact Dis 2004, 72(1):35-44.
  • [39]Antas PR, Sales JS, Pereira KC, Oliveira EB, Cunha KS, Sarno EN, Sampaio EP: Patterns of intracellular cytokines in CD4 and CD8 T cells from patients with mycobacterial infections. Braz J Med Biol Res 2004, 37(8):1119-1129.
  • [40]Ferrand RA, Bothamley GH, Whelan A, Dockrell HM: Interferon-gamma responses to ESAT-6 in tuberculosis patients early into and after anti-tuberculosis treatment. Int J Tuberc Lung Dis 2005, 9(9):1034-1039.
  • [41]Egwuagu CE, Yu CR, Zhang M, Mahdi RM, Kim SJ, Gery I: Suppressors of cytokine signaling proteins are differentially expressed in Th1 and Th2 cells: implications for Th cell lineage commitment and maintenance. J Immunol 2002, 168(7):3181-3187.
  • [42]Whyte CS, Bishop ET, Ruckerl D, Gaspar-Pereira S, Barker RN, Allen JE, Rees AJ, Wilson HM: Suppressor of Cytokine Signaling (SOCS)1 is a key determinant of differential macrophage activation and function. J Leukoc Biol 2011, 90(5):845-854.
  • [43]Hasan Z, Rao N, Salahuddin N, Islam M, Ashraf M, Rottenberg ME, Hussain R: M. tuberculosis sonicate induced IFN gamma, CXCL10 and IL-10 can differentiate severity in tuberculosis. Scand J Immunol 2012, 74(2):220-226.
  • [44]Krebs DL, Hilton DJ: SOCS proteins: negative regulators of cytokine signaling. Stem Cells 2001, 19(5):378-387.
  • [45]Liu Y, Stewart KN, Bishop E, Marek CJ, Kluth DC, Rees AJ, Wilson HM: Unique expression of Suppressor of Cytokine Signaling 3 is essential for classical macrophage activation in rodents in vitro and in vivo. J Immunol 2008, 180(9):6270-6278.
  文献评价指标  
  下载次数:6次 浏览次数:0次