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The impact of KIR2DS4 gene on clinical outcome after hematopoietic stem cell transplantation (CROSBI ID 235575)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Burek Kamenarić, Marija ; Štingl Janković, Katarina ; Grubić, Zorana ; Serventi Seiwerth, Ranka ; Maskalan, Marija ; Nemet, Damir ; Mikulić, Mirta ; Žunec, Renata The impact of KIR2DS4 gene on clinical outcome after hematopoietic stem cell transplantation // Human immunology, 78 (2016), 2; 95-102. doi: 10.1016/j.humimm.2016.11.010

Podaci o odgovornosti

Burek Kamenarić, Marija ; Štingl Janković, Katarina ; Grubić, Zorana ; Serventi Seiwerth, Ranka ; Maskalan, Marija ; Nemet, Damir ; Mikulić, Mirta ; Žunec, Renata

engleski

The impact of KIR2DS4 gene on clinical outcome after hematopoietic stem cell transplantation

Killer cell immunoglobulin-like receptors (KIR) are a family of inhibitory/activating receptors expressed on NK cells. Interactions of KIR receptors with KIR ligands have been shown to modify hematopoietic stem cell transplantation (HSCT) outcome. The aim of this research was to determine the KIR2DS4 allele variants distribution among 111 patients with different hematological malignancy who underwent HSCT and their donors, and to evaluate KIR2DS4 alleles’ impact on HSCT outcome. The KIR gene frequency analysis showed a significantly higher incidence of full-length KIR2DS4 alleles among patients. The impact of KIR2DS4 alleles on transplantation outcomes revealed that donors’ full-length KIR2DS4 alleles is associated with lower overall survival rates, higher risk of GVHD and higher relapse incidence. The expression of full-length KIR2DS4 allele variants may contribute to a worse clinical outcome after HSCT. KIR typing for KIR2DS4 could be used as an additional criterion for selecting suitable donors in cases when more than one HLA identical donor is identified for a specific patient.

killer cell immunoglobuline-like receptors (KIR), KIR2DS4 alleles, hematopoietic stem cell transplantation (HSCT), Croatian population

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Podaci o izdanju

78 (2)

2016.

95-102

objavljeno

0198-8859

10.1016/j.humimm.2016.11.010

Povezanost rada

Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti

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