Antiphospholipid antibody-mediated NK cell cytotoxicity
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00098892%3A_____%2F23%3A10157321" target="_blank" >RIV/00098892:_____/23:10157321 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15110/23:73621441
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S0165037822003205?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0165037822003205?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jri.2022.103791" target="_blank" >10.1016/j.jri.2022.103791</a>
Alternative languages
Result language
angličtina
Original language name
Antiphospholipid antibody-mediated NK cell cytotoxicity
Original language description
Antiphospholipid syndrome (APS) is an autoimmune thrombophilia that is characterised by thrombosis and obstetric complications in the presence of antiphospholipid antibodies (aPL). Pregnancy complications remain a challenging problem for patients with APS, especially during the first trimester. Although natural killer (NK) cells constitute up to 70% of decidual lymphocytes during the first trimester, their contribution to early pregnancy loss in APS is largely unknown. We aimed to analyse whether aPL are able to recruit antibody-dependent cellular cytotoxicity (ADCC) of NK cells, with special emphasis on the differences in the effects of aPL containing anti-β2GPI domain 1 (anti-β2GPI-D1) antibodies (aPL+/D1+) and those that do not (aPL+/D1-). Our findings revealed a differential distribution of NK subsets in the presence of different aPL. Namely, aPL+/D1- IgGs increased CD56dim/CD16dim cells, while aPL+/D1+ IgGs increased the number of CD56bright/CD16dim cells. ADCC NK cell cytotoxicity was found to be higher in the presence of aPL+/D1- IgGs, as defined by an increased target cell death, degranulation and increased expression of CD11b, CD69 and NKG2D. Overall, our evidence showed that aPL are able to recruit ADCC, suggesting NK cells as candidate cells for APS-related obstetric complications.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Reproductive Immunology
ISSN
0165-0378
e-ISSN
1872-7603
Volume of the periodical
155
Issue of the periodical within the volume
February
Country of publishing house
IE - IRELAND
Number of pages
7
Pages from-to
103791
UT code for WoS article
000925739600001
EID of the result in the Scopus database
2-s2.0-85145740594