http://www.cnr.it/ontology/cnr/individuo/prodotto/ID322941
Impact of human leukocyte antigen polymorphisms in human immunodeficiency virus progression in a paediatric cohort infected with a mono-phyletic human immunodeficiency virus-1 strain (Articolo in rivista)
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- Impact of human leukocyte antigen polymorphisms in human immunodeficiency virus progression in a paediatric cohort infected with a mono-phyletic human immunodeficiency virus-1 strain (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.4172/2155-6113.1000282 (literal)
- Alternative label
Montesano, Carla; Bonanno, Cesira Tiziana; Grifoni, Alba; Di Sano, Caterina; Palma, Paolo Dalla; Castelli Gattinara, Guido; Mattei, Maurizio; Mancino, Giorgio; Salerno, Alfredo; Colizzi, Vittorio C.; Amicosante, Massimo (2014)
Impact of human leukocyte antigen polymorphisms in human immunodeficiency virus progression in a paediatric cohort infected with a mono-phyletic human immunodeficiency virus-1 strain
in Journal of AIDS and Clinical Research
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Montesano, Carla; Bonanno, Cesira Tiziana; Grifoni, Alba; Di Sano, Caterina; Palma, Paolo Dalla; Castelli Gattinara, Guido; Mattei, Maurizio; Mancino, Giorgio; Salerno, Alfredo; Colizzi, Vittorio C.; Amicosante, Massimo (literal)
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- Department of Biology, University of Rome Tor Vergata, Rome, Italy
Department of Biopathology and Biomedical Methodologies, University of Palermo, Palermo, Italy
Institute of Biomedicine and Molecular Immunology, National Research Council, Palermo, Italy
Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy
Department of Immunology and Infectious Diseases, Bambino Gesù, Children's Hospital, Rome, Italy
Animal Technology Station, University of Rome Tor Vergata, Rome, Italy
San Pietro Fatebenefratelli Hospital, Rome, Italy
ProxAgen Ltd, Sofia, Bulgaria (literal)
- Titolo
- Impact of human leukocyte antigen polymorphisms in human immunodeficiency virus progression in a paediatric cohort infected with a mono-phyletic human immunodeficiency virus-1 strain (literal)
- Abstract
- Objective: HLA polymorphisms within the peptide binding pocket have been associated with rapid and slowprogression to AIDS, suggesting that the capability to present efficiently HIV-1 epitopes is crucial for the infection control. To minimize the effects of genetic background due to population coming from different geographic area and viral strain variability in the cohort, an analysis of all the polymorphisms associated with the HLA-A, -B and -DR alleles has been performed in a cohort of children with a monophyletic HIV-1 infection (CRF02_AG) during an outbreak in Libya. Methods: High-resolution HLA-typing has been performed in 58 children infected with a monophyletic strain of HIV-1: 26 Long-Term Non-Progressors (LTNP), 9 Slow-Progressors (SP) and 23 Fast-Progressors (FP). HLA amino acid polymorphism frequency has been compared in the in FP respect to LTNP. Results: HLA-B resulted the most interesting locus of the study; 10 positions located in B- and F-pocket for peptidebinding have been found significant after Bonferroni's correction: 11S (LTNP=7.69% FP=34.78% OR=0.156 P<0.05), 74D (LTNP=15.38%, FP=52.17%, OR=0.167; p<0.015) and 94T (LTNP=15.38%, FP=52.17%, OR=0.045; p<0.001), resulted associated with AIDS progression; 66N (LTNP=42.31% FP=8.7% OR=7.7; p<0.02), 80I (LTNP=80.77%, FP=34.78%, OR=7.86; p<0.036), 81A (LTNP=84.61%, FP=47.83%, OR=6; p<0.015), 82L (LTNP=88.46%, FP=47.83%, OR=7.86; p<0.006) and 83R (LTNP=88.46%, FP=47.83%, OR=7.86; p<0.006), has been associated with non-progression. Further, carrying Bw4-epitope resulted associated with LTNP (phenotype-frequency: LTNP=88.46%, FP=47.83%, OR=8.36; p<0.006), with homozygosis for Bw4 (LTNP=30.8%, FP=8.7%, p<0.05) associated with delayed progression and homozygosis for Bw6 (LTNP=11.5%, FP=52.1%, p<0.05) associated with fast progression to AIDS. Conclusion: The progression to AIDS might be in part determined by the binding capability of B-pocket and F-pocket of HLA-B and in part by the interaction of NK's inhibitory receptor with HLA-B Bw4-epitope which regulate innate immune response and might have important implications for a better disease control. © 2014 Montesano C, et al. (literal)
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