A 6-amino acid insertion/deletion polymorphism in the mucin domain of TIM-1 confers protections against HIV-1 infection

ABSTRAC: We investigated whether a 6-amino acid insertion/deletion polymorphism in the mucin domain of TIM-1 (T-cell immunoglobulin and mucin domain 1), modulates susceptibility to HIV-1 infection. The polymorphism was genotyped in three case/control cohorts of HIV-1 exposed seronegative individuals...

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Autores:
Aguilar Jimenez, Wbeimar
Sironi, Manuela
Saulle, Irma
Pontremoli, Chiara
Garziano, Micaela
Cagliani, Rachael
Trabattoni, Daria
Lo Caputo, Sergio
Vichi, Francesca
Mazzotta, Francesco
Forni, Diego
Riva, Stefania
Cedeño, Samandhy
Sánchez, Jorge
Brander, Christian
Zapata Builes, Wildeman
Rugeles López, María Teresa
Clerici, Mario
Biasin, Mara
Tipo de recurso:
Article of journal
Fecha de publicación:
2017
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/36567
Acceso en línea:
https://hdl.handle.net/10495/36567
Palabra clave:
Infecciones por VIH
HIV Infections
Polimorfismo Genético
Polymorphism, Genetic
Mucina-1
Mucin-1
Aminoácidos
Amino Acids
Estudios de Casos y Controles
Case-Control Studies
Replicación Viral
Virus Replication
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Description
Summary:ABSTRAC: We investigated whether a 6-amino acid insertion/deletion polymorphism in the mucin domain of TIM-1 (T-cell immunoglobulin and mucin domain 1), modulates susceptibility to HIV-1 infection. The polymorphism was genotyped in three case/control cohorts of HIV-1 exposed seronegative individuals (HESN) and HIV-1 infected subjects from Italy, Peru, and Colombia; data from a Thai population were retrieved from the literature. Across all cohorts, homozygosity for the short TIM-1 allele was more common in HESNs than in HIV-1 infected subjects. A meta analysis of the four association analyses yielded a p value of 0.005. In vitro infection assays of CD4þ T lymphocytes indicated that homo zygosity for the short allele is associated with lower rate of HIV-1 replication. These results suggest that the deletion allele protects from HIV-1 infection with a recessive effect.