A 6-amino acid insertion/deletion polymorphism in the mucin domain of TIM-1 confers protections against HIV-1 infection
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) a...
- Autores:
-
Biasin M.
Sironi M.
Saulle I.
Pontremoli C.
Garziano M.
Cagliani R.
Trabattoni D.
Lo Caputo S.
Vichi F.
Mazzotta F.
Forni D.
Riva S.
Aguilar-Jimenez W.
Cedeño S.
Sanchez J.
Brander C.
Zapata Builes, Wildeman
Rugeles M.T.
Clerici M.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2023
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/49545
- Acceso en línea:
- https://doi.org/10.1016/j.micinf.2016.09.005
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994430954&doi=10.1016%2fj.micinf.2016.09.005&partnerID=40&md5=b619dd5c65ced0aa67f42a0b7959afc2
https://hdl.handle.net/20.500.12494/49545
- Palabra clave:
- HESN
HIV
POLYMORPHISM
RESISTANCE TO INFECTION
TIM-1
- Rights
- openAccess
- License
- http://purl.org/coar/access_right/c_abf2
Summary: | 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 CD4+ T lymphocytes indicated that homozygosity 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. © 2016 Institut Pasteur |
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