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IFNG polymorphisms are associated with tuberculosis in Han Chinese pediatric female population

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Abstract

Host genetic factors play a major role in determining differential susceptibility to human tuberculosis (TB), a re-emerging infectious disease throughout the world. Genetic variations in the IFNG gene coding for interferon gamma (IFN-γ), have been identified in TB patients. To investigate the association of the IFNG polymorphisms with TB susceptibility in Chinese pediatric population. A case–control study of 189 TB patients and 164 controls was performed using single-nucleotide polymorphism (SNP) analysis. Genomic DNA was extracted from leukocytes in peripheral blood. Three SNPs of IFNG, including −1616C/T (rs2069705), +874A/T (rs2430561), and +3234C/T (rs2069718), were selected for genotyping and analysis. The +874A and +3234C alleles were more frequent among TB patients (P = 0.108 and P = 0.088), especially in females (both P = 0.029), although this difference was not significant since Bonferroni corrected significance threshold was 0.025 (two of three SNPs were found to be in linkage disequilibrium). More pronounced differences for the +874 and +3234 polymorphisms were found under the genotype comparison between TB cases and controls in the total population [P = 0.026 (borderline non-significance) and P = 0.020, respectively], and in the female subgroup (P = 0.020 and P = 0.020). The dominant model of inheritance was shown to be significant for +874A and +3234C alleles (both P = 0.019) in the female subgroup. The +874A and +3234C alleles were more frequently found in extrapulmonary TB patients than in controls (P = 0.039). Haplotype analysis carried out on these three SNPs showed the TTT haplotype to be more frequent in controls than in TB cases, and this difference showed a strong significance (P = 0.005). The +874A and +3234C alleles may be related to TB susceptibility in the female subgroup in the Chinese pediatric population of North China. The higher rate of +874A (known to correlate with lower IFN-γ expression) in the extrapulmonary TB subgroup suggests a sufficient IFN-γ expression to be not only an important factor for the onset of TB disease but also for limiting its dissemination to lungs.

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References

  1. World Health Organization (2011) Global tuberculosis control: WHO report 2011

  2. Jiang ZF, Yi ZW, Zhao SY (2006) Practical pediatric tuberculosis. People’s Medical Publishing House, Beijing, p 431

    Google Scholar 

  3. Dolin PJ, Raviglione MC, Kochi A (1994) Global tuberculosis incidence and mortality during 1990–2000. Bull World Health Organ 72:213–220

    PubMed  CAS  Google Scholar 

  4. Bellamy R (2003) Susceptibility to mycobacterial infections: the importance of host genetics. Genes Immun 4:4–11

    Article  PubMed  CAS  Google Scholar 

  5. Bellamy R (2005) Genetic susceptibility to tuberculosis. Clin Chest Med 26:233–246

    Article  PubMed  Google Scholar 

  6. Möller M, Hoal EG (2010) Current findings, challenges and novel approaches in human genetic susceptibility to tuberculosis. Tuberculosis (Edinb) 90:71–83

    Article  Google Scholar 

  7. Yim JJ, Selvaraj P (2010) Genetic susceptibility in tuberculosis. Respirology 15:241–256

    Article  PubMed  Google Scholar 

  8. Stark GR, Kerr IM, Williams BR, Silverman RH, Schreiber RD (1998) How cells respond to interferons. Annu Rev Biochem 67:227–264

    Article  PubMed  CAS  Google Scholar 

  9. Lee J, Kornfeld H (2010) Interferon-γ regulates the death of M. tuberculosis-infected macrophages. J Cell Death 3:1–11

    PubMed  CAS  Google Scholar 

  10. Rossouw M, Nel HJ, Cooke GS, van Helden PD, Hoal EG (2003) Association between tuberculosis and a polymorphic NF-kappa-B binding site in the interferon gamma gene. Lancet 361:1871–1872

    Article  PubMed  CAS  Google Scholar 

  11. Pacheco AG, Cardoso CC, Moraes MO (2008) IFNG +874T/A, IL10 -1082G/A and TNF -308G/A polymorphisms in association with tuberculosis susceptibility: a meta-analysis study. Hum Genet 123:477–484

    Article  PubMed  CAS  Google Scholar 

  12. Newton SM, Brent AJ, Anderson S, Whittaker E, Kampmann B (2008) Paediatric tuberculosis. Lancet Infect Dis 8:498–510

    Article  PubMed  Google Scholar 

  13. Rigouts L (2009) Clinical practice: diagnosis of childhood tuberculosis. Eur J Pediatr 168:1285–1290

    Article  PubMed  CAS  Google Scholar 

  14. Hu YM, Jiang ZF, Zhu FT (2002) Textbook of pediatrics, 7th edn. People’s Medical Publishing House, Beijing, pp 970–1013

    Google Scholar 

  15. Maher D, Chaulet P, Spinaci S, Harries A (1997) Treatment of tuberculosis-guidelines for national programmes. World Health Organization, Geneva, pp 1–78

    Google Scholar 

  16. Li Z, Zhang Z, He Z et al (2009) A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn). Cell Res 19:519–523

  17. Mosmann TR, Coffman RL (1989) TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol 7:145–173

    Article  PubMed  CAS  Google Scholar 

  18. Kuchroo VK, Das MP, Brown JA, Ranger AM, Zamvil SS, Sobel RA, Weiner HL, Nabavi N, Glimcher LH (1995) B7–1 and B7–2 costimulatory molecules differentially activate the TH1/TH2 developmental pathways: application to autoimmune disease therapy. Cell 80:707–716

    Article  PubMed  CAS  Google Scholar 

  19. Abbas AK, Murphy KM, Sher A (1996) Functional diversity of helper T lymphocytes. Nature 383:787–793

    Article  PubMed  CAS  Google Scholar 

  20. Manry J, Laval G, Patin E, Fornarino S, Tichit M, Bouchier C, Barreiro LB, Quintana-Murci L (2011) Evolutionary genetics evidence of an essential, nonredundant role of the IFN-c pathway in protective immunity. Hum Mutat 32:633–642

    Article  PubMed  CAS  Google Scholar 

  21. Cooke GS, Campbell SJ, Sillah J, Gustafson P, Bah B, Sirugo G, Bennett S, McAdam KPWJ, Sow O, Lienhardt C, Hill AVS (2006) Polymorphism within the interferon-gamma/receptor complex is associated with pulmonary tuberculosis. Am J Resp Crit Care Med 174:339–343

    Article  PubMed  CAS  Google Scholar 

  22. Vallinoto AC, Graça ES, Araújo MS, Azevedo VN, Cayres-Vallinoto I, Machado LF, Ishak MO, Ishak R (2010) IFNG +874T/A polymorphism and cytokine plasma levels are associated with susceptibility to Mycobacterium tuberculosis infection and clinical manifestation of tuberculosis. Hum Immunol 71:692–696

    Article  PubMed  CAS  Google Scholar 

  23. Torres OA, Calzada JE, Beraún Y, Morillo CA, González A, González CI, Martín J (2010) Role of the IFNG +874T/A polymorphism in Chagas disease in a Colombian population. Infect Genet Evol 10:682–685

    Article  PubMed  CAS  Google Scholar 

  24. dbSNP database. http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=2430561

  25. Mokrousov I, Wu XR, Vyazovaya A, Feng WX, Sun L, Xiao J, Miao Q, Jiao WW, Shen A (2011) Polymorphism of 3′UTR region of TNFR2 coding gene and its role in clinical tuberculosis in Han Chinese pediatric population. Infect Genet Evol 11:1312–1318

    Article  PubMed  CAS  Google Scholar 

  26. Jin J, Sun L, Jiao W, Zhao S, Li H, Guan X, Jiao A, Jiang Z, Shen A (2009) SLC11A1 (Formerly NRAMP1) gene polymorphisms associated with pediatric tuberculosis in China. Clin Infect Dis 48:733–738

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

We thank all of the subjects for their kind participation in this study. This study was supported by grants from the National Natural Science Foundation of China (No. 81071315) and Beijing Natural Science Foundation (No. 7121007).

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Correspondence to A-Dong Shen.

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Chen Shen and Wei-Wei Jiao contributed equally to this study.

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Shen, C., Jiao, WW., Feng, WX. et al. IFNG polymorphisms are associated with tuberculosis in Han Chinese pediatric female population. Mol Biol Rep 40, 5477–5482 (2013). https://doi.org/10.1007/s11033-013-2647-7

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