2019
Neutrophil and Granulocytic Myeloid-Derived Suppressor Cell-Mediated T Cell Suppression Significantly Contributes to Immune Dysregulation in Common Variable Immunodeficiency Disorders
VLKOVÁ, Marcela, Zita CHOVANCOVÁ, Jana NECHVÁTALOVÁ, Ashley Nicole CONNELLY, Marcus Darrell DAVIS et. al.Základní údaje
Originální název
Neutrophil and Granulocytic Myeloid-Derived Suppressor Cell-Mediated T Cell Suppression Significantly Contributes to Immune Dysregulation in Common Variable Immunodeficiency Disorders
Autoři
VLKOVÁ, Marcela (203 Česká republika, garant, domácí), Zita CHOVANCOVÁ (203 Česká republika, domácí), Jana NECHVÁTALOVÁ (203 Česká republika, domácí), Ashley Nicole CONNELLY (840 Spojené státy), Marcus Darrell DAVIS (840 Spojené státy), Peter SLANINA (703 Slovensko, domácí), Lucie KUČEROVÁ (203 Česká republika, domácí), Marek LITZMAN (203 Česká republika), Tereza GRYMOVÁ (203 Česká republika, domácí), Přemysl SOUČEK (203 Česká republika, domácí), Tomáš FREIBERGER (203 Česká republika, domácí), Jiří LITZMAN (203 Česká republika, domácí) a Zdenek HEL (203 Česká republika)
Vydání
Journal of immunology, Bethesda, American association of immunologists, 2019, 0022-1767
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30102 Immunology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.886
Kód RIV
RIV/00216224:14110/19:00108489
Organizační jednotka
Lékařská fakulta
UT WoS
000454422600011
Klíčová slova anglicky
Common variable immunodeficiency disorders
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 3. 2020 09:28, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Common variable immunodeficiency disorders (CVID) represent a group of primary immunodeficiency diseases characterized by hypogammaglobulinemia and impaired specific Ab response, resulting in recurrent infections due to dysfunctional immune response. The specific mechanisms mediating immune deficiency in CVID remain to be determined. Previous studies indicated that immune dysregulation in CVID patients is associated with chronic microbial translocation, systemic immune activation, and altered homeostasis of lymphocytic and myeloid lineages. A detailed phenotypic, functional characterization of plasma markers and immune cell populations was performed in 46 CVID patients and 44 healthy donors. CVID patients displayed significantly elevated plasma levels of a marker of neutrophil activation neutrophil gelatinase-associated lipocalin. Neutrophils from CVID patients exhibited elevated surface levels of CD11b and PD-L1 and decreased levels of CD62L, CD16, and CD80, consistent with a phenotype of activated neutrophils with suppressive properties. Neutrophils from CVID patients actively suppressed T cell activation and release of IFN-gamma via the production of reactive oxygen species. Furthermore, CVID was associated with an increased frequency of low-density neutrophils (LDNs)/granulocytic myeloid-derived suppressor cells. LDN/granulocytic myeloid-derived suppressor cell frequency in CVID patients correlated with reduced T cell responsiveness. Exogenous stimulation of whole blood with bacterial LPS emulated some but not all of the phenotypic changes observed on neutrophils from CVID patients and induced neutrophil population with LDN phenotype. The presented data demonstrate that neutrophils in the blood of CVID patients acquire an activated phenotype and exert potent T cell suppressive activity. Specific targeting of myeloid cell-derived suppressor activity represents a novel potential therapeutic strategy for CVID.
Návaznosti
NV15-28732A, projekt VaV |
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