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[Enhanced cytotoxicity against leukemia cells of natural Killer cells from cord blood after expansion in vitro]

Authors :
Feng, Zhou
Wen-min, Han
Zhu-xia, Jia
Jian-he, Yang
Rong, Xiao
Ling-di, Ma
Xu-zhang, Lu
Source :
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 34(11)
Publication Year :
2013

Abstract

To investigate the enhanced cytotoxicity against leukemia cells of natural Killer (NK) cells from cord blood (CB) after expansion in vitro.NK cells was expanded on a layer of trophoblast cells with irradiated K562-mb15-41BBL cell line for 21 days. The levels of receptors on NK cells were detected by flow cytometry. Cytotoxicity of expanded NK cells against leukemia cells and specific ligand of immunoglobulin like(Ig- liKe)receptors were assessed using 51Cr released assay.There were no differences of inhibitory receptors expression between fresh NK cells and expanded NK cells [CD158a:(16.77±11.65)% vs(14.37±11.12)%, P0.05; CD158b: (42.48±18.11)% vs (40.92±19.02)%, P0.05; NKG2A: (70.20±18.43)% vs (78.90±13.69)%, P0.05], but higher activated receptors expression on expanded NK cells [NKp30: (54.10±13.27)% vs (4.14±2.05)%, P0.05; NKp44: (72.10±17.30)% vs (0.52±1.16)%, P0.05; NKp46: (80.63±14.01)% vs (44.19±6.19)%, P0.05; NKG2D: (97.50±2.55)% vs (72.25±14.35)%, P0.05]. Expanded NK cells showed higher cytotoxicity against leuKemia cell lines than fresh NK cells [K562: (74.3±3.6)% vs (55.3±4.2)%, P0.05; Raji: (60.6±5.0)% vs (12.0±3.6)%, P0.05]. CD158a⁻ CD158b⁻ NK cells had higher cytotoxicity on four types of target cells, but CD158a⁺CD158b⁻ CB-NK cell had lower cytotoxicity on 221-Cw4 and 221-Cw3Cw4 cells. CD158a⁻ CD158b⁺ CB- NK cells had lower cytotoxicity on 221-Cw3 and 221-Cw3Cw4, but CD158a⁺CD158b⁺ CB-NK cells had higher cytotoxicity on 721- 221 cells.Expression of activated receptors of expanded NK cells were up-regulated, but no changes of inhibitory receptors. Expanded NK cells showed high cytotoxicity against leukemia cells and kept the specificity of ligand of Ig-like receptors, which could be beneficial to cell-therapy for tumor.

Details

ISSN :
02532727
Volume :
34
Issue :
11
Database :
OpenAIRE
Journal :
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Accession number :
edsair.pmid..........94708151ad69d7333ead8635fb3132a9