- Poster presentation
- Open Access
Absence of association of IFNL3/IL28B rs 12979860 and IFNL4 ss 469415590 polymorphisms with the neurological status of HTLV-1 Afro-Caribbean subjects in Martinique.
© Jeannin et al. 2015
- Published: 28 August 2015
- Linkage Disequilibrium
- Neurological Status
- Asymptomatic Individual
The polymorphism of Interferon-lambda3/Interleukine28B (IFNL3/IL28B) rs 12979860 has been described as important in the development of HTLV-1-associated myelopathy/spastic paraparesis (HAM/TSP). Recently, the dinucleotide polymorphism, IFNL4 ss469415590 has been discovered and is in high linkage disequilibrium with rs12979860. In a transversal study, we aimed to examine the polymorphisms of these two nucleotides in our HTLV-1 Afro-Caribbean population.
The frequencies of the CC, CT and TT genotypes of the single nucleotide rs12979860 and the frequencies of ΔG/ΔG, ΔG/TT and TT/TT genotypes of the dinucleotide ss469415590 are reported in the entire HTLV-1 group and compared between asymptomatic individuals and HAM/TSP patients.
In our 94 HTLV-1 subjects, frequencies of rs1299860 were CC, 13.3%; CT, 44.7%; TT, 42% and frequencies of ss469415590 genotypes were ΔG/ΔG, 45.7%; ΔG/TT, 42.6%; TT/TT, 11.7%. We found no significant difference in allele distribution in both studied nucleotide polymorphism between 53 asymptomatic carriers (60.7 years and 72% females) and 41 HAM/TSP patients (70 years and 80% females).
In our population, the polymorphisms of IFNL3/IL28B rs12979860 and IFNL4 ss469415590 are not associated with HTLV-1 neurological phenotype status. Different genotypes target should be considered.
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