The IFNG rs1861494 Single Nucleotide Polymorphism Is Associated with Protection against Tuberculosis Disease in Argentina
Interferon gamma (IFNG) plays a key role during ( ) infection, and several polymorphisms located in its gene are associated with risk of tuberculosis in diverse populations. Nevertheless, the genetic resistance/susceptibility to tuberculosis in Argentina is unknown. The rs1861494 polymorphism (G→A)...
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Published in: | Genes Vol. 9; no. 1; p. 46 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
MDPI AG
22-01-2018
MDPI |
Subjects: | |
Online Access: | Get full text |
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Summary: | Interferon gamma (IFNG) plays a key role during
(
) infection, and several polymorphisms located in its gene are associated with risk of tuberculosis in diverse populations. Nevertheless, the genetic resistance/susceptibility to tuberculosis in Argentina is unknown. The
rs1861494 polymorphism (G→A) was reported to alter the binding of transcription factors to this region, influencing IFNG production. Using a case-control study, we found an association between the AA and AG genotypes and tuberculosis resistance (AA vs. GG: odds ratio (OR) = 0.235,
-value = 0.012; AG vs. GG: OR = 0.303,
-value = 0.044; AA vs. AG: OR = 0.776,
-value = 0.427; AA + AG vs. GG: OR = 0.270,
-value = 0.022). Moreover,
-antigen stimulated peripheral blood mononuclear cells (PBMCs) from healthy donors and AA carriers secreted the highest amounts of IFNG in culture supernatants (
-value = 0.034) and presented the greatest percentage of CD4⁺IFNG⁺ lymphocytes (
-value = 0.035), in comparison with GG carriers. No association between the polymorphism and clinical parameters of tuberculosis severity was detected. However, our findings indicate that the rs1861494 single nucleotide polymorphism (SNP) could be considered as a biomarker of tuberculosis resistance in the Argentinean population. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2073-4425 2073-4425 |
DOI: | 10.3390/genes9010046 |