Author/Authors :
KAMALI SARVESTANI, E Alborzi Clinical Microbiology Research Center - Nemazi Hospital - Shiraz University of Medical, Sciences, Shiraz , GHARESIFARD, B. Alborzi Clinical Microbiology Research Center - Nemazi Hospital - Shiraz University of Medical, Sciences, Shiraz , NATEGHIAN, A.R Alborzi Clinical Microbiology Research Center - Nemazi Hospital - Shiraz University of Medical, Sciences, Shiraz , Behzadbehbahani, A Alborzi Clinical Microbiology Research Center - Nemazi Hospital - Shiraz University of Medical, Sciences, Shiraz , ALborzi, A Alborzi Clinical Microbiology Research Center - Nemazi Hospital - Shiraz University of Medical, Sciences, Shiraz
Abstract :
Background: Tumor necrosis factor-alpha (TNF-a) is a determining factor in macrophage activation and direction of immunologic mechanisms to BCG. By regulating the rate of transcription, allelic polymorphism in the regulatory regions of TNF-a gene can affect the host's ability in BCG containment.
Objective: To study the prevalence of G to A transition polymorphism at position -308 of the TNF-a gene in Iranian BCG vaccinees with lymphadenitis.
Methods: In this study, we determined the polymorphism at position -308 relative to the transcription initiation site of TNF-a gene in 40 patients with BCG adenitis and 42 healthy age-matched infants without reactions by a method based on allele specific PCR. The results of PCR were confirmed by the SSCP method.
Results: The frequency of TNFA2 allele in the patient and the control groups were 0.013 and 0.04, respectively. Statistical analysis showed no significant association of TNF-a promoter polymorphism with susceptibility to BCG adenitis. However, there was a threefold increase in the frequency of TNFA2 allele in the control subjects.
Conclusion: We suggest that the lower frequency of TNFA2 allele in patients might have resulted in weaker immune response that allows bacterial burden and occurrence of lymphadenitis.
Keywords :
BCG , ADENITIS , TNF , POLYMORPHISM