Pregled bibliografske jedinice broj: 443140
Dendritic cells at the maternal fetal interface
Dendritic cells at the maternal fetal interface // Final Program and Abstract Book / Georgieva, Rayna (ur.).
Sofija: Institute of Biology and Immunology of Reproduction, Acad. Kiril Bratanov, Bulgarian Academy of Sciences, 2009. str. 44-44 (plenarno, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 443140 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Dendritic cells at the maternal fetal interface
Autori
Laškarin, Gordana ; Redžović, Arnela ; Vlastelić, Ivan ; Haller, Herman ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Final Program and Abstract Book
/ Georgieva, Rayna - Sofija : Institute of Biology and Immunology of Reproduction, Acad. Kiril Bratanov, Bulgarian Academy of Sciences, 2009, 44-44
Skup
12th International Symposium for Immunology of Reproduction
Mjesto i datum
Varna, Bugarska, 25.06.2009. - 27.06.2009
Vrsta sudjelovanja
Plenarno
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Dendritic cells; TAG-72; early pregnancy
Sažetak
Dendritic cells (DCs) are able to balance between inflammation and tolerance and therefore could be involved in the implantation processes and regulation of trophoblast invasion. There is no unique concept about the characteristics of distinct DCs subsets which differentially bias NK and T cell response. Beside foreign antigens, it is considered that local microenvironment, are potent modulators of DCc function. Epithelial cells product, Tumor Associated Glycoprotein-72 (TAG-72) is physiologically presented in secretory phase human endometrium, but negative immunostaining of TAG-72 was seen in uterine deciduas of normal first trimester pregnancies. The importance of TAG-72 removal in early pregnancy and its possible immunological role still remain obscure. In vitro experiments showed that decidual CD1a+ cells are able to bind and internalize TAG-72 by carbohydrate recognition domain of CD206 and CD209 endocytic receptors. TAG-72 decreased CD83 and IFN- expressions in CD1a+ cells disabling them to settle decidual T cells toward pro-inflammatory orientation. Down-regulation of IL-15 and IL-18 cytokines expression in TAG-72 treated CD1a+ cells hampered the NK cell proliferation in a close contact with TAG-72 treated CD1a+ cells. In ectopic pregnancy TAG-72 was found by immunohistology in tubal mucosa close to the implantation site and away from the implantation site, but not in the uterine decidua. The percentage of IL-15+ cells and NK cells were drastically reduced at the mucosal sites characterized with the appearance of TAG- 72. All these results suggest that TAG-72, if present at the implantation site could hamper physiological mild pro-inflammatory response and NK cells proliferation, which could lead to inadequate trophoblast growth control. Acknowledgement: The experiments were financed by the Grants of Croatian Ministry of Science, Education and Sports No. 0620402-0376, No. 062- 620402-0377 and No. 0620402-0379.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
062-0620402-0376 - Citokini i citolitički mehanizmi tijekom rane trudnoće (Rukavina, Daniel, MZOS ) ( CroRIS)
062-0620402-0377 - Imunoregulacijske funkcije antigen predočnih stanica tijekom rane trudnoće (Laškarin, Gordana, MZOS ) ( CroRIS)
062-0620402-0379 - Imunološki mehanizmi u žena s patološkim trudnoćama (Haller, Herman, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka
Profili:
Herman Haller
(autor)
Ivan Vlastelić
(autor)
Daniel Rukavina
(autor)
Arnela Redžović
(autor)
Gordana Laškarin
(autor)