Lymphocyte Subsets and Pulmonary Nodules to Predict the Progression of Sarcoidosis

Author:

Danila Edvardas12,Aleksonienė Regina2,Besusparis Justinas34,Gruslys Vygantas12,Jurgauskienė Laimutė56,Laurinavičienė Aida34,Laurinavičius Arvydas34,Mainelis Antanas7,Zablockis Rolandas12,Zeleckienė Ingrida8,Žurauskas Edvardas3,Malickaitė Radvilė56

Affiliation:

1. Clinic of Chest Diseases, Immunology and Allergology, Faculty of Medicine, Vilnius University, 03101 Vilnius, Lithuania

2. Center of Pulmonology and Allergology, Vilnius University Hospital Santaros Klinikos, 08661 Vilnius, Lithuania

3. National Center of Pathology, Vilnius University Hospital Santaros Klinikos, 08406 Vilnius, Lithuania

4. Faculty of Medicine, Vilnius University, 03101 Vilnius, Lithuania

5. Clinic of Cardiac and Vascular Diseases, Faculty of Medicine, Vilnius University, 03101 Vilnius, Lithuania

6. Center of Laboratory Medicine, Vilnius University Hospital Santaros Klinikos, 08661 Vilnius, Lithuania

7. Faculty of Mathematics and Informatics, Vilnius University, 03225 Vilnius, Lithuania

8. Center of Radiology and Nuclear Medicine, Vilnius University Hospital Santaros Klinikos, 08661 Vilnius, Lithuania

Abstract

The search for biological markers, which allow a relatively accurate assessment of the individual course of pulmonary sarcoidosis at the time of diagnosis, remains one of the research priorities in this field of pulmonary medicine. The aim of our study was to investigate possible prognostic factors for pulmonary sarcoidosis with a special focus on cellular immune inflammation markers. A 2-year follow-up of the study population after the initial prospective and simultaneous analysis of lymphocyte activation markers expression in the blood, as well as bronchoalveolar lavage fluid (BALF) and lung biopsy tissue of patients with newly diagnosed pulmonary sarcoidosis, was performed. We found that some blood and BAL fluid immunological markers and lung computed tomography (CT) patterns have been associated with a different course of sarcoidosis. We revealed five markers that had a significant negative association with the course of sarcoidosis (worsening pulmonary function tests and/or the chest CT changes)—blood CD4+CD31+ and CD4+CD44+ T lymphocytes, BALF CD8+CD31+ and CD8+CD103+ T lymphocytes and a number of lung nodules on chest CT at the time of the diagnosis. Cut-off values, sensitivity, specificity and odds ratio for predictors of sarcoidosis progression were calculated. These markers may be reasonable predictors of sarcoidosis progression.

Funder

European Union

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference64 articles.

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