Relationship of the Content of Systemic and Endobronchial Soluble Molecules of CD25, CD38, CD8, and HLA-I-CD8 and Lung Function Parameters in COPD Patients

Author:

Kubysheva Nailya1ORCID,Postnikova Larisa2,Soodaeva Svetlana34,Novikov Viкtor5ORCID,Eliseeva Tatyana2ORCID,Batyrshin Ildar6ORCID,Li Timur7,Klimanov Igor3,Chuchalin Alexander3

Affiliation:

1. Kazan Federal University, Kremlyovskaya St, 18, Kazan 420000, Russia

2. Nizhny Novgorod State Medical Academy, Minin and Pozharsky Square 10/1, Nizhny Novgorod 603005, Russia

3. Pulmonology Research Institute, 11-Parkovaya 32, Moscow 105077, Russia

4. I.M. Sechenov First Moscow State Medical University, Trubetskaya, 8- 2, Moscow, Russia

5. Lobachevsky State University of Nizhny Novgorod, Gagarina Avenue 23, Nizhny Novgorod 603950, Russia

6. Centro de Investigación en Computación, Instituto Politécnico Nacional (CIC-IPN), Av. Juan de Dios Bátiz, Esq. Miguel Othón de Mendizábal S/N, Gustavo A. Madero, 07738 Mexico City, Mexico

7. Central Clinical Hospital of RAS, Litovskiy Blvd. 1A, Moscow 117593, Russia

Abstract

The definition of new markers of local and systemic inflammation of chronic obstructive pulmonary disease (COPD) is one of the priority directions in the study of pathogenesis and diagnostic methods improvement for this disease. We investigated 91 patients with COPD and 21 healthy nonsmokers. The levels of soluble CD25, CD38, CD8, and HLA-I-CD8 molecules in the blood serum and exhaled breath condensate (EBC) in moderate-to-severe COPD patients during exacerbation and stable phase were studied. An unidirectional change in the content of sCD25, sCD38, and sCD8 molecules with increasing severity of COPD was detected. The correlations between the parameters of lung function and sCD8, sCD25, and sHLA-I-CD8 levels in the blood serum and EBC were discovered in patients with severe COPD. The findings suggest a pathogenetic role of the investigated soluble molecules of the COPD development and allow considering the content of sCD8, sCD25, and sHLA-I-CD8 molecules as additional novel systemic and endobronchial markers of the progression of chronic inflammation of this disease.

Funder

Russian Government Program of Competitive Growth of Kazan Federal University

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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