Cytokine gene polymorphisms across tuberculosis clinical spectrum in Pakistani patients

• Published in: PloS one 2009-03, Vol.4 (3), p.e4778-e4778
• Main Authors: Ansari, Ambreen, Talat, Najeeha, Jamil, Bushra, Hasan, Zahra, Razzaki, Tashmeem, Dawood, Ghaffar, Hussain, Rabia
• Format: Article
• Language: English
• Subjects: Aging; Antigens; Binding sites; Case-Control Studies; Cytokines; Cytokines - genetics; Disease control; Disease susceptibility; Gene Frequency; Genes; Genetic aspects; Genetic polymorphisms; Genetic Predisposition to Disease; Genotype; Genotypes; Growth factors; Humans; Immunology; Immunology/Genetics of the Immune System; Infectious Diseases; Interferon-gamma - blood; Interferon-gamma - genetics; Interleukin 1; Interleukin 10; Interleukin-10 - blood; Interleukin-10 - genetics; Lung diseases; Mutation; Pakistan; Pathology; Patients; Polymorphism, Genetic; Rankings; Severity of Illness Index; Tuberculosis; Tuberculosis - epidemiology; Tuberculosis - genetics; Tumor necrosis factor-TNF; γ-Interferon
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0004778

Pakistan ranks 7(th) globally in terms of tuberculosis (TB) disease burden (incidence 181/100000 pop./yr; prevalence of 329/pop./yr). Reports from different populations show variable associations of TB susceptibility and severity with cytokine gene polymorphisms. Tuberculosis clinical severity is multi-factorial and cytokines play a pivotal role in the modulation of disease severity. We have recently reported that the ratio of two key cytokines (IFNgamma and IL10) show significant correlation with the severity spectrum of tuberculosis. The objective of the current study was to analyze the frequency of cytokine gene polymorphisms linked to high and low responder phenotypes (IFNgamma +874 T(hi)-->A(lo) and IL10 -1082 G(lo)-->A(hi)) in tuberculosis patients. STUDY GROUPS WERE STRATIFIED ACCORDING TO DISEASE SITE AS WELL AS DISEASE SEVERITY: Pulmonary N = 111 (Minimal, PMN = 19; Moderate, PMD = 63; Advance, PAD = 29); Extra-pulmonary N = 67 (Disseminated DTB = 20, Localized LTB = 47) and compared with healthy controls (TBNA = 188). Genotype analyses were carried out using amplification refractory mutation system-PCR (ARMS-PCR) and stimulated whole blood (WB) culture assay was used for assessing cytokine profiles. Our results suggest that the IFNgamma +874 TT genotype and T allele was overrepresented in PMN (p = 0.01) and PMD (p = 0.02). IFNgamma +874 TT in combination with IL10 GG(lo) genotypes showed the highest association (chi(2) = 6.66, OR = 6.06, 95% CI = 1.31-28.07, p = 0.01). IFNgamma AA(lo) on the other hand in combination with IL10 GG(lo) increased the risk of PAD (OR = 5.26; p = 0.005) and DTB (OR = 3.59; p = 0.045). These findings are consistent with the role of IL10 in reducing collateral tissue damage and the protective role of IFNgamma in limiting disease in the lung.