J 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.

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