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Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment
Vaginal proinflammatory cytokine expression during herpes virus reactivation was examined in human immunodeficiency virus-infected women before and after initiation of antiretroviral therapy (ART). Vaginal swabs were screened for levels of cytokines interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-8, IL-10...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867667/ https://www.ncbi.nlm.nih.gov/pubmed/27191006 http://dx.doi.org/10.1093/ofid/ofw073 |
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author | Nason, Martha C. Patel, Eshan U. Kirkpatrick, Allison R. Prodger, Jessica L. Shahabi, Kamnoosh Tobian, Aaron A. R. Gianella, Sara Kalibbala, Sarah Ssebbowa, Paschal Kaul, Rupert Gray, Ronald H. Quinn, Thomas C. Serwadda, David Reynolds, Steven J. Redd, Andrew D. |
author_facet | Nason, Martha C. Patel, Eshan U. Kirkpatrick, Allison R. Prodger, Jessica L. Shahabi, Kamnoosh Tobian, Aaron A. R. Gianella, Sara Kalibbala, Sarah Ssebbowa, Paschal Kaul, Rupert Gray, Ronald H. Quinn, Thomas C. Serwadda, David Reynolds, Steven J. Redd, Andrew D. |
author_sort | Nason, Martha C. |
collection | PubMed |
description | Vaginal proinflammatory cytokine expression during herpes virus reactivation was examined in human immunodeficiency virus-infected women before and after initiation of antiretroviral therapy (ART). Vaginal swabs were screened for levels of cytokines interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, tumor necrosis factor (TNF)-α, and interferon-γ. The relative risk (RR) of herpes simplex virus-2 or cytomegalovirus (CMV) shedding being associated with cytokine levels above the median were estimated. Herpes simplex virus-2 shedding was significantly associated with higher levels of IL-6 (RR = 1.4, P = .003) and TNF-α (RR = 1.3, P = .010), whereas CMV shedding was associated with higher IL-6 (RR = 1.3, P = .006) and IL-2 (RR = 1.4, P = .01). The association of viral shedding with higher IL-6 levels suggests that herpes virus reactivation may be playing a role in immune activation after ART initiation. |
format | Online Article Text |
id | pubmed-4867667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48676672016-05-17 Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment Nason, Martha C. Patel, Eshan U. Kirkpatrick, Allison R. Prodger, Jessica L. Shahabi, Kamnoosh Tobian, Aaron A. R. Gianella, Sara Kalibbala, Sarah Ssebbowa, Paschal Kaul, Rupert Gray, Ronald H. Quinn, Thomas C. Serwadda, David Reynolds, Steven J. Redd, Andrew D. Open Forum Infect Dis Brief Reports Vaginal proinflammatory cytokine expression during herpes virus reactivation was examined in human immunodeficiency virus-infected women before and after initiation of antiretroviral therapy (ART). Vaginal swabs were screened for levels of cytokines interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, tumor necrosis factor (TNF)-α, and interferon-γ. The relative risk (RR) of herpes simplex virus-2 or cytomegalovirus (CMV) shedding being associated with cytokine levels above the median were estimated. Herpes simplex virus-2 shedding was significantly associated with higher levels of IL-6 (RR = 1.4, P = .003) and TNF-α (RR = 1.3, P = .010), whereas CMV shedding was associated with higher IL-6 (RR = 1.3, P = .006) and IL-2 (RR = 1.4, P = .01). The association of viral shedding with higher IL-6 levels suggests that herpes virus reactivation may be playing a role in immune activation after ART initiation. Oxford University Press 2016-04-06 /pmc/articles/PMC4867667/ /pubmed/27191006 http://dx.doi.org/10.1093/ofid/ofw073 Text en Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2016. This work is written by (a) US Government employee(s) and is in the public domain in the US. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | Brief Reports Nason, Martha C. Patel, Eshan U. Kirkpatrick, Allison R. Prodger, Jessica L. Shahabi, Kamnoosh Tobian, Aaron A. R. Gianella, Sara Kalibbala, Sarah Ssebbowa, Paschal Kaul, Rupert Gray, Ronald H. Quinn, Thomas C. Serwadda, David Reynolds, Steven J. Redd, Andrew D. Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title | Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title_full | Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title_fullStr | Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title_full_unstemmed | Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title_short | Immunological Signaling During Herpes Simplex Virus-2 and Cytomegalovirus Vaginal Shedding After Initiation of Antiretroviral Treatment |
title_sort | immunological signaling during herpes simplex virus-2 and cytomegalovirus vaginal shedding after initiation of antiretroviral treatment |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867667/ https://www.ncbi.nlm.nih.gov/pubmed/27191006 http://dx.doi.org/10.1093/ofid/ofw073 |
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