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The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma

Although HIV-positive patients are at higher risk for developing a variety of infection-related cancers, the prevalence of infections with the seven known cancer-associated viruses has not been studied. Luciferase immunoprecipitation systems were used to evaluate antiviral antibodies in four 23-pers...

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Autores principales: Burbelo, Peter D., Kovacs, Joseph A., Wagner, Jason, Bayat, Ahmad, Rhodes, Craig S., De Souza, Yvonne, Greenspan, John S., Iadarola, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423820/
https://www.ncbi.nlm.nih.gov/pubmed/22924124
http://dx.doi.org/10.1155/2012/634523
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author Burbelo, Peter D.
Kovacs, Joseph A.
Wagner, Jason
Bayat, Ahmad
Rhodes, Craig S.
De Souza, Yvonne
Greenspan, John S.
Iadarola, Michael J.
author_facet Burbelo, Peter D.
Kovacs, Joseph A.
Wagner, Jason
Bayat, Ahmad
Rhodes, Craig S.
De Souza, Yvonne
Greenspan, John S.
Iadarola, Michael J.
author_sort Burbelo, Peter D.
collection PubMed
description Although HIV-positive patients are at higher risk for developing a variety of infection-related cancers, the prevalence of infections with the seven known cancer-associated viruses has not been studied. Luciferase immunoprecipitation systems were used to evaluate antiviral antibodies in four 23-person groups: healthy blood donors and HIV-infected patients with oral hairy leukoplakia (OLP), Kaposi's sarcoma (KS), or non-Hodgkin lymphoma (NHL). Antibody profiling revealed that all HIV-positive individuals were strongly seropositive for anti-gp41 and antireverse transcriptase antibodies. However, anti-p24 HIV antibody levels were highly variable and some OLP and KS patients demonstrated weak or negative responses. Profiling two EBV antigens revealed no statistical difference in antibody levels among the three HIV-infected groups. A high frequency of KSHV infection was detected in HIV patients including 100% of KS, 78% of OLP, and 57% of NHL patients. Most HIV-infected subjects (84%) showed anti-HBV core antibodies, but only a few showed antibodies against HCV. MCV seropositivity was also common (94%) in the HIV-infected individuals and KS patients showed statistically higher antibody levels compared to the OLP and NHL patients. Overall, 68% of the HIV-infected patients showed seropositivity with at least four cancer-associated viruses. Antibody profiles against these and other infectious agents could be useful for enhancing the clinical management of HIV patients.
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spelling pubmed-34238202012-08-24 The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma Burbelo, Peter D. Kovacs, Joseph A. Wagner, Jason Bayat, Ahmad Rhodes, Craig S. De Souza, Yvonne Greenspan, John S. Iadarola, Michael J. AIDS Res Treat Research Article Although HIV-positive patients are at higher risk for developing a variety of infection-related cancers, the prevalence of infections with the seven known cancer-associated viruses has not been studied. Luciferase immunoprecipitation systems were used to evaluate antiviral antibodies in four 23-person groups: healthy blood donors and HIV-infected patients with oral hairy leukoplakia (OLP), Kaposi's sarcoma (KS), or non-Hodgkin lymphoma (NHL). Antibody profiling revealed that all HIV-positive individuals were strongly seropositive for anti-gp41 and antireverse transcriptase antibodies. However, anti-p24 HIV antibody levels were highly variable and some OLP and KS patients demonstrated weak or negative responses. Profiling two EBV antigens revealed no statistical difference in antibody levels among the three HIV-infected groups. A high frequency of KSHV infection was detected in HIV patients including 100% of KS, 78% of OLP, and 57% of NHL patients. Most HIV-infected subjects (84%) showed anti-HBV core antibodies, but only a few showed antibodies against HCV. MCV seropositivity was also common (94%) in the HIV-infected individuals and KS patients showed statistically higher antibody levels compared to the OLP and NHL patients. Overall, 68% of the HIV-infected patients showed seropositivity with at least four cancer-associated viruses. Antibody profiles against these and other infectious agents could be useful for enhancing the clinical management of HIV patients. Hindawi Publishing Corporation 2012 2012-08-08 /pmc/articles/PMC3423820/ /pubmed/22924124 http://dx.doi.org/10.1155/2012/634523 Text en Copyright © 2012 Peter D. Burbelo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Burbelo, Peter D.
Kovacs, Joseph A.
Wagner, Jason
Bayat, Ahmad
Rhodes, Craig S.
De Souza, Yvonne
Greenspan, John S.
Iadarola, Michael J.
The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title_full The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title_fullStr The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title_full_unstemmed The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title_short The Cancer-Associated Virus Landscape in HIV Patients with Oral Hairy Leukoplakia, Kaposi's Sarcoma, and Non-Hodgkin Lymphoma
title_sort cancer-associated virus landscape in hiv patients with oral hairy leukoplakia, kaposi's sarcoma, and non-hodgkin lymphoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423820/
https://www.ncbi.nlm.nih.gov/pubmed/22924124
http://dx.doi.org/10.1155/2012/634523
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