Přehled o publikaci
2024
Phenotype and oxidative burst of low-density neutrophil subpopulations are altered in common variable immunodeficiency patients
SLANINA, Peter, Julie ŠTÍCHOVÁ, Veronika BOSÁKOVÁ, Iva STANICZKOVÁ ZAMBO, Marcela HORTOVÁ KOHOUTKOVÁ et. al.Basic information
Original name
Phenotype and oxidative burst of low-density neutrophil subpopulations are altered in common variable immunodeficiency patients
Name in Czech
Fenotyp a oxidační vzplanutí subpopulací neutrofilů s nízkou hustotou jsou změněny u pacientů s běžnou variabilní imunodeficiencí
Authors
SLANINA, Peter, Julie ŠTÍCHOVÁ, Veronika BOSÁKOVÁ, Iva STANICZKOVÁ ZAMBO, Marcela HORTOVÁ KOHOUTKOVÁ, Petra LÁZNIČKOVÁ, Zita CHOVANCOVÁ, Jiří LITZMAN, Terezie STEJSKALOVÁ, Jan FRIČ and Marcela VLKOVÁ
Edition
CYTOMETRY PART B-CLINICAL CYTOMETRY, UNITED STATES, WILEY, 2024, 1552-4949
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
United States of America
Confidentiality degree
is not subject to a state or trade secret
References:
Organization
Lékařská fakulta – Repository – Repository
UT WoS
001109148500001
EID Scopus
2-s2.0-85177603270
Keywords in English
common variable immunodeficiency; intravenous immunoglobulins; low-density neutrophils; oxidative burst; suppression.
Links
LX22NPO5107, research and development project. MUNI/A/1098/2022, interní kód Repo. MUNI/A/1244/2021, interní kód Repo. MUNI/A/1393/2022, interní kód Repo. NU21-06-00408, research and development project.
Changed: 13/7/2024 05:10, RNDr. Daniel Jakubík
Abstract
V originále
Common variable immunodeficiency disorder (CVID) is the most common form of primary antibody immunodeficiency. Due to low antibody levels, CVID patients receive intravenous or subcutaneous immunoglobulin replacement therapy as treatment. CVID is associated with the chronic activation of granulocytes, including an increased percentage of low-density neutrophils (LDNs). In this study, we examined changes in the percentage of LDNs and the expression of their surface markers in 25 patients with CVID and 27 healthy donors (HD) after in vitro stimulation of whole blood using IVIg. An oxidative burst assay was used to assess the functionality of LDNs. CVID patients had increased both relative and absolute LDN counts with a higher proportion of mLDNs compared to iLDNs, distinguished based on the expression of CD10 and CD16. Immature LDNs in the CVID and HD groups had significantly reduced oxidative burst capacity compared to mature LDNs. Interestingly we observed reduced oxidative burst capacity, reduced expression of CD10 after stimulation of WB, and higher expression of PD-L1 in mature LDNs in CVID patients compared to HD cells. Our data indicate that that the functional characteristics of LDNs are closely linked to their developmental stage. The observed reduction in oxidative burst capacity in mLDNs in CVID patients could contribute to an increased susceptibility to recurrent bacterial infections among CVID patients.