Burkholderia cepacia in cystic fibrosis children and adolescents: overall survival and immune alterations

Background: In current literature there are only scarce data on the host inflammatory response during Burkholderia cepacia complex (Bcc) persistence. The primary objective of the present research was to carry out cross-sectional analyses of biomarkers and evaluate disease progression in cystic fibrosis (CF) patients with chronic Bcc infection and pathogen-free ones. The secondary aim was to assess prospectively overall survival of the study participants during up to 8 years of follow-up. Methods: The study included 116 paediatric patients with CF; 47 CF patients were chronically infected with Bcc, and 69 individuals were Bcc free. Plasma and sputum biomarkers (neutrophil elastase, MMP-8, MMP-9, MMP-12, IL-2, IL-4, IL-6, IL-8, IL-10, IL-18, IL-22, IL-23, IL-17, IFN-γ, TGFβ1, TNF-α) were analysed using commercially available kits. Besides, inhibitory effect of dexamethasone on proliferative response of PHA-stimulated peripheral blood lymphocytes had been assessed. Results: Bcc infected patients did not differ from Bcc free ones in demographic and clinical parameters, but demonstrated an increased rate of glucose metabolism disturbances and survival disadvantage during prolong follow-up period. Biomarkers analyses revealed elevated TNF-α and reduced IL-17F levels in sputum samples of Bcc infected patients. These patients also demonstrated improvement of peripheral blood lymphocyte sensitivity to steroid treatment and reduction in plasma pro-inflammatory (IL-17F and IL-18) and anti-inflammatory (TGFβ1 and IL-10) cytokine concentrations. Conclusions: Reduction in IL-17F levels may have several important consequences including increase in steroid sensitivity and glycemic control disturbances. Further investigations are needed to clarify the role of IL-17 cytokines in CF complication development. Low plasma TGFβ1 and IL-10 levels in Bcc infected group may be a sign of subverted activity of regulatory T cells. Such immune alterations may be one of the factors contributing to the development of the cepacia syndrome. Copyright © 2024 Shmarina, Pukhalskaya, Shmarin, Semykin, Avakyan, Krasovsky, Goryainova, Kostyuk, Zinchenko and Kashirskaya.

Авторы
Shmarina G. , Pukhalskaya D. , Shmarin V. , Semykin S. , Avakyan L. , Krasovsky S. , Goryainova A. , Kostyuk S. , Zinchenko R. , Kashirskaya N.
Издательство
Frontiers Media SA
Язык
English
Статус
Published
Номер
1374318
Том
14
Год
2024
Организации
  • 1 Research Centre for Medical Genetics, Moscow, Russian Federation
  • 2 Peoples’ Friendship University of Russia (RUDN University), Moscow, Russian Federation
  • 3 First Moscow State Medical University, Moscow, Russian Federation
  • 4 Russian Clinical Children’s Hospital, a separate structural unit of the Russian National Research Medical University, Moscow, Russian Federation
  • 5 Pulmonary Research Institute, Moscow, Russian Federation
Ключевые слова
Burkholderia cepacia complex; cystic fibrosis; glucose metabolism disturbances; IL-17F; inflammation; lymphocyte sensitivity to steroid suppression; MMP; TNFα
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