HLA-G 14bp polymorphism on HIV-1 perinatal transmission (P3041)
Background/aims: HLA-G is expressed at maternal-fetal interface and is strongly involved on maternal-fetal tolerance. The 3' untranslated region of HLA-G gene presents an insertion (INS) and/or deletion (DEL) of a 14bp fragment, which is associated with stability and expression levels of HLA-G...
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Published in: | The Journal of immunology (1950) Vol. 190; no. 1_Supplement; pp. 55 - 55.21 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-05-2013
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Online Access: | Get full text |
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Summary: | Background/aims: HLA-G is expressed at maternal-fetal interface and is strongly involved on maternal-fetal tolerance. The 3' untranslated region of HLA-G gene presents an insertion (INS) and/or deletion (DEL) of a 14bp fragment, which is associated with stability and expression levels of HLA-G mRNA. The aim of this study was to analyze the hypothesis that the 14bp polymorphism can influence the HIV vertical transmission. Methods: Blood samples were obtained from 49 mother-child pairs (26 pairs with and 23 without vertical transmission). All children were born from HIV-positive mothers who did not receive antiretroviral therapy during pregnancy. The 14 pp polymorphism was detected by PCR-amplified DNA using specific primers. Statistical analyses were made by Fisher's exact test. This study was approved by the local ethics committee. Results: We did not detect significant differences in allele and genotype frequencies between HIV-infected and HIV-uninfected child; however, the presence of the D/D homozygous genotype was more frequent among mothers with HIV-infected child (p=0.05). In addition, the 14pb similarity among mother and child pairs was more frequent on vertical transmission (69%) than on its absence. Conclusion: The presence of the genotype (DEL/DEL), associated with high production of HLA-G, and the similarities of the 14bp DEL/INS genotypes between mother and child may favor HIV mother to child transmission. |
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ISSN: | 0022-1767 1550-6606 |
DOI: | 10.4049/jimmunol.190.Supp.55.21 |