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Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma

BACKGROUND: The incidence of Hodgkin lymphoma (HL) has increased since introduction of combined antiretroviral therapy (cART). While HIV-related HL is highly associated with EBV, the causes underlying the rising incidence remain unclear. The aim of this study was to evaluate the effect of immune rec...

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Autores principales: Kowalkowski, Marc A., Mims, Martha P., Amiran, E. Susan, Lulla, Premal, Chiao, Elizabeth Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788758/
https://www.ncbi.nlm.nih.gov/pubmed/24098586
http://dx.doi.org/10.1371/journal.pone.0077409
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author Kowalkowski, Marc A.
Mims, Martha P.
Amiran, E. Susan
Lulla, Premal
Chiao, Elizabeth Y.
author_facet Kowalkowski, Marc A.
Mims, Martha P.
Amiran, E. Susan
Lulla, Premal
Chiao, Elizabeth Y.
author_sort Kowalkowski, Marc A.
collection PubMed
description BACKGROUND: The incidence of Hodgkin lymphoma (HL) has increased since introduction of combined antiretroviral therapy (cART). While HIV-related HL is highly associated with EBV, the causes underlying the rising incidence remain unclear. The aim of this study was to evaluate the effect of immune reconstitution on HL incidence among a cohort of HIV-infected male veterans ever receiving cART. METHODS: We performed a retrospective cohort study utilizing data from the Veterans Affairs HIV Clinical Case Registry from 1985-2010. HL cases were identified using ICD-9 codes (201.4-9). Poisson regression was conducted to evaluate relationships between cART-related immunologic measures (e.g., nadir CD4 before cART, time-updated CD4, % time undetectable HIV RNA) and HL incidence. Additionally, we examined CD4 change after cART initiation. RESULTS: 31,056 cART users contributed 287,256 person-years and 196 HL cases (IR=6.8/10,000 person-years). Rate of CD4 increase after cART was worse among HL cases than non-cases (p<0.05). In multivariate regression, HL risk was elevated among veterans with recent CD4 200-350 cells/µL (IRR=1.67, 95%CI=1.16-2.40) and <200 cells/µL (IRR=1.61, 95%CI=1.09-2.39), compared to >350 cells/µL. HL risk was lower among veterans with >80% time undetectable HIV RNA (IRR=0.57, 95%CI=0.35-0.92) and 40-80% undetectable (IRR=0.68, 95%CI=0.47-0.99), compared to <40% undetectable. HL risk was higher in the first 12 months (IRR=2.02, 95%CI=1.32-3.10) and 12-24 months (IRR=1.75, 95%CI=1.16-2.64) after cART initiation, compared to >36 months. CONCLUSION: These data highlight immunosuppression and poor viral control may increase HL risk, specifically during immune reconstitution in the interval post cART initiation. Findings suggest an immune reconstitution type mechanism in HIV-related HL development.
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spelling pubmed-37887582013-10-04 Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma Kowalkowski, Marc A. Mims, Martha P. Amiran, E. Susan Lulla, Premal Chiao, Elizabeth Y. PLoS One Research Article BACKGROUND: The incidence of Hodgkin lymphoma (HL) has increased since introduction of combined antiretroviral therapy (cART). While HIV-related HL is highly associated with EBV, the causes underlying the rising incidence remain unclear. The aim of this study was to evaluate the effect of immune reconstitution on HL incidence among a cohort of HIV-infected male veterans ever receiving cART. METHODS: We performed a retrospective cohort study utilizing data from the Veterans Affairs HIV Clinical Case Registry from 1985-2010. HL cases were identified using ICD-9 codes (201.4-9). Poisson regression was conducted to evaluate relationships between cART-related immunologic measures (e.g., nadir CD4 before cART, time-updated CD4, % time undetectable HIV RNA) and HL incidence. Additionally, we examined CD4 change after cART initiation. RESULTS: 31,056 cART users contributed 287,256 person-years and 196 HL cases (IR=6.8/10,000 person-years). Rate of CD4 increase after cART was worse among HL cases than non-cases (p<0.05). In multivariate regression, HL risk was elevated among veterans with recent CD4 200-350 cells/µL (IRR=1.67, 95%CI=1.16-2.40) and <200 cells/µL (IRR=1.61, 95%CI=1.09-2.39), compared to >350 cells/µL. HL risk was lower among veterans with >80% time undetectable HIV RNA (IRR=0.57, 95%CI=0.35-0.92) and 40-80% undetectable (IRR=0.68, 95%CI=0.47-0.99), compared to <40% undetectable. HL risk was higher in the first 12 months (IRR=2.02, 95%CI=1.32-3.10) and 12-24 months (IRR=1.75, 95%CI=1.16-2.64) after cART initiation, compared to >36 months. CONCLUSION: These data highlight immunosuppression and poor viral control may increase HL risk, specifically during immune reconstitution in the interval post cART initiation. Findings suggest an immune reconstitution type mechanism in HIV-related HL development. Public Library of Science 2013-10-02 /pmc/articles/PMC3788758/ /pubmed/24098586 http://dx.doi.org/10.1371/journal.pone.0077409 Text en © 2013 Kowalkowski et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kowalkowski, Marc A.
Mims, Martha P.
Amiran, E. Susan
Lulla, Premal
Chiao, Elizabeth Y.
Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title_full Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title_fullStr Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title_full_unstemmed Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title_short Effect of Immune Reconstitution on the Incidence of HIV-Related Hodgkin Lymphoma
title_sort effect of immune reconstitution on the incidence of hiv-related hodgkin lymphoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788758/
https://www.ncbi.nlm.nih.gov/pubmed/24098586
http://dx.doi.org/10.1371/journal.pone.0077409
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