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C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection()
When HIV was initially discovered as the causative agent of AIDS, many expected to find a vaccine within a few years. This has however proven to be elusive; it has been approximately 30 years since HIV was first discovered, and a suitable vaccine is still not in effect. In 2009, a paper published by...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133339/ https://www.ncbi.nlm.nih.gov/pubmed/27942440 http://dx.doi.org/10.1016/j.atg.2013.05.004 |
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author | Barmania, Fatima Pepper, Michael S. |
author_facet | Barmania, Fatima Pepper, Michael S. |
author_sort | Barmania, Fatima |
collection | PubMed |
description | When HIV was initially discovered as the causative agent of AIDS, many expected to find a vaccine within a few years. This has however proven to be elusive; it has been approximately 30 years since HIV was first discovered, and a suitable vaccine is still not in effect. In 2009, a paper published by Hutter et al. reported on a bone marrow transplant performed on an HIV positive individual using stem cells that were derived from a donor who was homozygous for a mutation in the CCR5 gene known as CCR5 delta-32 (Δ32) (Hütter et al., 2009). The HIV positive individual became HIV negative and remained free of viral detection after transplantation despite having halted anti-retroviral (ARV) treatment. This review will focus on CCR5 as a key component in HIV immunity and will discuss the role of CCR5 in the control of HIV infection. |
format | Online Article Text |
id | pubmed-5133339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-51333392016-12-09 C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() Barmania, Fatima Pepper, Michael S. Appl Transl Genom Review When HIV was initially discovered as the causative agent of AIDS, many expected to find a vaccine within a few years. This has however proven to be elusive; it has been approximately 30 years since HIV was first discovered, and a suitable vaccine is still not in effect. In 2009, a paper published by Hutter et al. reported on a bone marrow transplant performed on an HIV positive individual using stem cells that were derived from a donor who was homozygous for a mutation in the CCR5 gene known as CCR5 delta-32 (Δ32) (Hütter et al., 2009). The HIV positive individual became HIV negative and remained free of viral detection after transplantation despite having halted anti-retroviral (ARV) treatment. This review will focus on CCR5 as a key component in HIV immunity and will discuss the role of CCR5 in the control of HIV infection. Elsevier 2013-05-26 /pmc/articles/PMC5133339/ /pubmed/27942440 http://dx.doi.org/10.1016/j.atg.2013.05.004 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Review Barmania, Fatima Pepper, Michael S. C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title | C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title_full | C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title_fullStr | C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title_full_unstemmed | C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title_short | C-C chemokine receptor type five (CCR5): An emerging target for the control of HIV infection() |
title_sort | c-c chemokine receptor type five (ccr5): an emerging target for the control of hiv infection() |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133339/ https://www.ncbi.nlm.nih.gov/pubmed/27942440 http://dx.doi.org/10.1016/j.atg.2013.05.004 |
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