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1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study

BACKGROUND: Persons with active tuberculosis (TB) have increased immune activation, which declines with TB treatment. Whether residual immune activation is present after completion of TB treatment is unknown. We conducted immunophenotyping of T cells and monocytes from individuals who had completed...

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Autores principales: Huaman, Moises A, Moussa, Anissa, Orsborn, Kris I, Ticona, Eduardo, Sanchez, Jorge, Zavaleta, Milagros, Sterling, Timothy, Chougnet, Claire, Deepe, George S, Fichtenbaum, Carl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778047/
http://dx.doi.org/10.1093/ofid/ofaa439.1826
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author Huaman, Moises A
Moussa, Anissa
Orsborn, Kris I
Ticona, Eduardo
Sanchez, Jorge
Zavaleta, Milagros
Sterling, Timothy
Chougnet, Claire
Deepe, George S
Fichtenbaum, Carl
author_facet Huaman, Moises A
Moussa, Anissa
Orsborn, Kris I
Ticona, Eduardo
Sanchez, Jorge
Zavaleta, Milagros
Sterling, Timothy
Chougnet, Claire
Deepe, George S
Fichtenbaum, Carl
author_sort Huaman, Moises A
collection PubMed
description BACKGROUND: Persons with active tuberculosis (TB) have increased immune activation, which declines with TB treatment. Whether residual immune activation is present after completion of TB treatment is unknown. We conducted immunophenotyping of T cells and monocytes from individuals who had completed TB treatment, and compared them to controls without history of active TB. METHODS: Cross-sectional study of HIV-uninfected individuals 40 to 70 years old recruited in Lima, Peru. For this analysis, we included 6 individuals who had completed treatment for pulmonary TB within the past year, and 10 healthy controls without history of active TB (6 QuantiFERON®-TB positive; 4 QuantiFERON®-TB negative). Participants provided blood for T cell and monocyte immunophenotyping using multi-parameter flow cytometry, including expression of cell surface activation markers. RESULTS: There were no significant differences in age, sex, or comorbidities between patients previously treated for TB and controls without history of active TB. Median time since TB treatment completion was 4 months (range, 2 – 9) for the previously treated group. Compared to controls, persons previously treated for TB had increased CD4(+) to CD8(+) ratio (2.4 vs. 1.3; p=0.03), increased proportion of CD4(+) T cells co-expressing HLA-DR and CD38 activation markers (5.8% vs. 3.1%; p=0.02), increased CD4(+) T cell ICAM-1 expression (56.3% vs. 33.2%; p=0.03), as well as increased density of HLA-DR in monocytes (HLA-DR MFI; 7572 vs. 3917; p=0.03). CONCLUSION: In this pilot study, individuals who recovered from pulmonary TB exhibited increased CD4(+) T cell and monocyte activation phenotypes within one year of TB treatment completion. These results suggest residual immune activation after clinical TB cure. DISCLOSURES: Carl Fichtenbaum, MD, Amgen (Grant/Research Support, outside the submitted work)Clinical Care Options (Other Financial or Material Support, outside the submitted work)Cytodyn (Grant/Research Support, outside the submitted work)Gilead Sciences (Grant/Research Support, outside the submitted work)Janssen (Grant/Research Support, outside the submitted work)Merck (Grant/Research Support, outside the submitted work)ViiV Healthcare (Research Grant or Support, outside the submitted work)
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spelling pubmed-77780472021-01-07 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study Huaman, Moises A Moussa, Anissa Orsborn, Kris I Ticona, Eduardo Sanchez, Jorge Zavaleta, Milagros Sterling, Timothy Chougnet, Claire Deepe, George S Fichtenbaum, Carl Open Forum Infect Dis Poster Abstracts BACKGROUND: Persons with active tuberculosis (TB) have increased immune activation, which declines with TB treatment. Whether residual immune activation is present after completion of TB treatment is unknown. We conducted immunophenotyping of T cells and monocytes from individuals who had completed TB treatment, and compared them to controls without history of active TB. METHODS: Cross-sectional study of HIV-uninfected individuals 40 to 70 years old recruited in Lima, Peru. For this analysis, we included 6 individuals who had completed treatment for pulmonary TB within the past year, and 10 healthy controls without history of active TB (6 QuantiFERON®-TB positive; 4 QuantiFERON®-TB negative). Participants provided blood for T cell and monocyte immunophenotyping using multi-parameter flow cytometry, including expression of cell surface activation markers. RESULTS: There were no significant differences in age, sex, or comorbidities between patients previously treated for TB and controls without history of active TB. Median time since TB treatment completion was 4 months (range, 2 – 9) for the previously treated group. Compared to controls, persons previously treated for TB had increased CD4(+) to CD8(+) ratio (2.4 vs. 1.3; p=0.03), increased proportion of CD4(+) T cells co-expressing HLA-DR and CD38 activation markers (5.8% vs. 3.1%; p=0.02), increased CD4(+) T cell ICAM-1 expression (56.3% vs. 33.2%; p=0.03), as well as increased density of HLA-DR in monocytes (HLA-DR MFI; 7572 vs. 3917; p=0.03). CONCLUSION: In this pilot study, individuals who recovered from pulmonary TB exhibited increased CD4(+) T cell and monocyte activation phenotypes within one year of TB treatment completion. These results suggest residual immune activation after clinical TB cure. DISCLOSURES: Carl Fichtenbaum, MD, Amgen (Grant/Research Support, outside the submitted work)Clinical Care Options (Other Financial or Material Support, outside the submitted work)Cytodyn (Grant/Research Support, outside the submitted work)Gilead Sciences (Grant/Research Support, outside the submitted work)Janssen (Grant/Research Support, outside the submitted work)Merck (Grant/Research Support, outside the submitted work)ViiV Healthcare (Research Grant or Support, outside the submitted work) Oxford University Press 2020-12-31 /pmc/articles/PMC7778047/ http://dx.doi.org/10.1093/ofid/ofaa439.1826 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 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 Poster Abstracts
Huaman, Moises A
Moussa, Anissa
Orsborn, Kris I
Ticona, Eduardo
Sanchez, Jorge
Zavaleta, Milagros
Sterling, Timothy
Chougnet, Claire
Deepe, George S
Fichtenbaum, Carl
1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title_full 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title_fullStr 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title_full_unstemmed 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title_short 1648. CD4 T Lymphocyte and Monocyte Activation within One Year After Treatment Completion for Pulmonary Tuberculosis: A Pilot Study
title_sort 1648. cd4 t lymphocyte and monocyte activation within one year after treatment completion for pulmonary tuberculosis: a pilot study
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778047/
http://dx.doi.org/10.1093/ofid/ofaa439.1826
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