Concentration of fecal β-defensin-2 in children with cystic fibrosis: how the inneral intestinal immune response?

Cystic fibrosis is a disease caused by mutations in a gene encoding CFTR-protein (Cystic Fibrosis Transmembrane conductance Regulator), located in the apical membrane of epithelial cells of the respiratory tract, intestines and pancreas. Defensins serve as important components of the innate human im...

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Bibliographic Details
Main Authors: A. T. Kamilova, D. I. Akhmedova, Z. E. Umarnazarova, D. A. Abdullaeva, S. I. Geller
Format: Article
Language:Russian
Published: Ltd. “The National Academy of Pediatric Science and Innovation” 2022-01-01
Series:Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:
Online Access:https://www.ped-perinatology.ru/jour/article/view/1532