4-1BB/4-1BBL signaling pathway in patients with influenza A (H1N1) virus-associated pneumonia
https://doi.org/10.23946/2500-0764-2022-7-1-64-69
Abstract
Aim. To evaluate the activity of the 4-1BB/4-1BBL signaling pathway in patients with influenza A (H1N1) virus-associated pneumonia.
Materials and Methods. Here we enrolled 85 patients (41 males and 44 females, median age 48 (36-62) years) with influenza A (H1N1) virus-associated pneumonia. Among the exclusion criteria were unstable hemodynamics, BMI > 30, diabetes mellitus, HIV, tuberculosis, and cancer. Control group consisted of 15 healthy donors. The diagnosis of influenza A / H1N1 was confirmed by a positive PCR test. Pneumonia was diagnosed according to the Federal Clinical Guidelines «Community-acquired pneumonia in adults». Severity of pneumonia was evaluated by using CURB-65 and SMART-COP scales as well as IDSA/ATS criteria. Plasma concentration of 4-1BB (CD137 or TNFRSF9, an inducible costimulatory receptor expressed on activated T cells and antigen-presenting cells) was determined by flow cytometry.
Results. Patients with moderate and severe influenza A (H1N1) virus-associated pneumonia had 1.5- and 2.4 fold-increased concentration of plasma 4-1ВВ as compared with the healthy controls.
Conclusion. The 4-1BB/4-1BBL signaling pathway, involved in multiple immune reactions, is associated with the severity of influenza A (H1N1) virus-associated pneumonia.
Keywords
About the Authors
A. V. MalyarchikovRussian Federation
Andrey V. Malyarchikov, MD, PhD, Head of Simulation Training
Department
39a, Gor’kogo Street, Chita, 672000
K. G. Shаpovаlov
Russian Federation
Konstantin G. Shapovalov, MD, DSc, Professor, Head of the
Department of Anesthesiology, Resuscitation and Critical Care Medicine
39a, Gor’kogo Street, Chita, 672000
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Review
For citations:
Malyarchikov A.V., Shаpovаlov K.G. 4-1BB/4-1BBL signaling pathway in patients with influenza A (H1N1) virus-associated pneumonia. Fundamental and Clinical Medicine. 2022;7(1):64-69. (In Russ.) https://doi.org/10.23946/2500-0764-2022-7-1-64-69