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CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls

BACKGROUND: The mechanisms driving the transition from inflammation to fibrosis in sarcoidosis patients are poorly understood; prognostic features are lacking. Immune cell profiling may provide insights into pathogenesis and prognostic factors of the disease. This study aimed to establish associatio...

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Autores principales: Aleksonienė, Regina, Besusparis, Justinas, Gruslys, Vygantas, Jurgauskienė, Laimutė, Laurinavičienė, Aida, Laurinavičius, Arvydas, Malickaitė, Radvilė, Norkūnienė, Jolita, Zablockis, Rolandas, Žurauskas, Edvardas, Danila, Edvardas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107533/
https://www.ncbi.nlm.nih.gov/pubmed/34012580
http://dx.doi.org/10.21037/jtd-20-2396
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author Aleksonienė, Regina
Besusparis, Justinas
Gruslys, Vygantas
Jurgauskienė, Laimutė
Laurinavičienė, Aida
Laurinavičius, Arvydas
Malickaitė, Radvilė
Norkūnienė, Jolita
Zablockis, Rolandas
Žurauskas, Edvardas
Danila, Edvardas
author_facet Aleksonienė, Regina
Besusparis, Justinas
Gruslys, Vygantas
Jurgauskienė, Laimutė
Laurinavičienė, Aida
Laurinavičius, Arvydas
Malickaitė, Radvilė
Norkūnienė, Jolita
Zablockis, Rolandas
Žurauskas, Edvardas
Danila, Edvardas
author_sort Aleksonienė, Regina
collection PubMed
description BACKGROUND: The mechanisms driving the transition from inflammation to fibrosis in sarcoidosis patients are poorly understood; prognostic features are lacking. Immune cell profiling may provide insights into pathogenesis and prognostic factors of the disease. This study aimed to establish associations in simultaneous of lymphocyte subset profiles in the blood, bronchoalveolar lavage fluid (BALF), and lung biopsy tissue in the patients with newly diagnosed sarcoidosis. METHODS: A total of 71 sarcoid patients (SPs) and 20 healthy controls (HCs) were enrolled into the study. CD31, CD38, CD44, CD103 positive T lymphocytes in blood and BALF were analysed. Additionally, the densities of CD4, CD8, CD38, CD44, CD103 positive cells in lung tissue biopsies were estimated by digital image analysis. RESULTS: Main findings: (I) increase of percentage of CD3(+)CD4(+)CD38(+) in BALF and blood, and increase of percentage of CD3(+)CD4(+)CD44(+) in BALF in Löfgren syndrome patients comparing with patients without Löfgren syndrome, (II) increase of percentage of CD3(+)CD4(+)103(+) in BALF and in blood in patients without Löfgren syndrome (comparing with Löfgren syndrome patients) and increase of percentage of CD3(+)CD4(+)103(+) in BALF and in blood in more advanced sarcoidosis stage. (III) Increasing percentage of BALF CD3(+)CD4(+)CD31(+) in sarcoidosis patients when comparing with controls independently of presence of Löfgren syndrome, smoking status or stage of sarcoidosis. Several significant correlations were found. CONCLUSIONS: Lymphocyte subpopulations in blood, BALF, and lung tissue were substantially different in SPs at the time of diagnosis compared to HCs. CD3(+)CD4(+)CD31(+) in BALF might be a potential supporting marker for the diagnosis of sarcoidosis. CD3(+)CD4(+)CD38(+) in BALF and blood and CD3(+)CD4(+)CD44(+) in BALF may be markers of the acute immune response in sarcoidosis patients. CD4(+)CD103(+) T-cells in BALF and in blood are markers of the persistent immune response in sarcoidosis patients and are potential prognostic features of the chronic course of this disease.
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spelling pubmed-81075332021-05-18 CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls Aleksonienė, Regina Besusparis, Justinas Gruslys, Vygantas Jurgauskienė, Laimutė Laurinavičienė, Aida Laurinavičius, Arvydas Malickaitė, Radvilė Norkūnienė, Jolita Zablockis, Rolandas Žurauskas, Edvardas Danila, Edvardas J Thorac Dis Original Article BACKGROUND: The mechanisms driving the transition from inflammation to fibrosis in sarcoidosis patients are poorly understood; prognostic features are lacking. Immune cell profiling may provide insights into pathogenesis and prognostic factors of the disease. This study aimed to establish associations in simultaneous of lymphocyte subset profiles in the blood, bronchoalveolar lavage fluid (BALF), and lung biopsy tissue in the patients with newly diagnosed sarcoidosis. METHODS: A total of 71 sarcoid patients (SPs) and 20 healthy controls (HCs) were enrolled into the study. CD31, CD38, CD44, CD103 positive T lymphocytes in blood and BALF were analysed. Additionally, the densities of CD4, CD8, CD38, CD44, CD103 positive cells in lung tissue biopsies were estimated by digital image analysis. RESULTS: Main findings: (I) increase of percentage of CD3(+)CD4(+)CD38(+) in BALF and blood, and increase of percentage of CD3(+)CD4(+)CD44(+) in BALF in Löfgren syndrome patients comparing with patients without Löfgren syndrome, (II) increase of percentage of CD3(+)CD4(+)103(+) in BALF and in blood in patients without Löfgren syndrome (comparing with Löfgren syndrome patients) and increase of percentage of CD3(+)CD4(+)103(+) in BALF and in blood in more advanced sarcoidosis stage. (III) Increasing percentage of BALF CD3(+)CD4(+)CD31(+) in sarcoidosis patients when comparing with controls independently of presence of Löfgren syndrome, smoking status or stage of sarcoidosis. Several significant correlations were found. CONCLUSIONS: Lymphocyte subpopulations in blood, BALF, and lung tissue were substantially different in SPs at the time of diagnosis compared to HCs. CD3(+)CD4(+)CD31(+) in BALF might be a potential supporting marker for the diagnosis of sarcoidosis. CD3(+)CD4(+)CD38(+) in BALF and blood and CD3(+)CD4(+)CD44(+) in BALF may be markers of the acute immune response in sarcoidosis patients. CD4(+)CD103(+) T-cells in BALF and in blood are markers of the persistent immune response in sarcoidosis patients and are potential prognostic features of the chronic course of this disease. AME Publishing Company 2021-04 /pmc/articles/PMC8107533/ /pubmed/34012580 http://dx.doi.org/10.21037/jtd-20-2396 Text en 2021 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Aleksonienė, Regina
Besusparis, Justinas
Gruslys, Vygantas
Jurgauskienė, Laimutė
Laurinavičienė, Aida
Laurinavičius, Arvydas
Malickaitė, Radvilė
Norkūnienė, Jolita
Zablockis, Rolandas
Žurauskas, Edvardas
Danila, Edvardas
CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title_full CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title_fullStr CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title_full_unstemmed CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title_short CD31(+), CD38(+), CD44(+), and CD103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
title_sort cd31(+), cd38(+), cd44(+), and cd103(+) lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107533/
https://www.ncbi.nlm.nih.gov/pubmed/34012580
http://dx.doi.org/10.21037/jtd-20-2396
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