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[Serum cytokine profiles in stable survivors with clinical liver transplantation].

Authors :
Wan YL
Zheng SS
Wei JF
Jia CK
Hu ZR
Source :
Zhonghua wai ke za zhi [Chinese journal of surgery] [Zhonghua Wai Ke Za Zhi] 2004 Feb 22; Vol. 42 (4), pp. 207-9.
Publication Year :
2004

Abstract

Objective: To elucidate the profile of serum cytokines and adhesion molecules in stable survivors with clinical liver transplantation.<br />Methods: Flow cytometric analysis was used to analyse the phenotype of T cell subsets in peripheral blood mononuclear cells (PBMCs) from group of liver transplantation (LTx) (n = 22), primary liver carcinoma (PLC) (n = 13) and healthy control (n = 12). Enzyme-linked immunoabsorbent assay (ELISA) was used to determine the serum cytokines and adhesion molecules profiles in stable survivors with clinical liver transplantation.<br />Results: Percentage of CD3(+) T cell and CD8(+) T cell, as well as ratio of CD4(+) to CD8(+) revealed no difference among three groups. The percentage of CD3(+)CD25(+) T cells in LTx group was found higher than that in healthy group (P = 0.022). Th1 cytokines (IL-2, IFN-gamma) and Th2 cytokines (IL-4, IL-10), as well as TNF-alpha displayed no significant difference among three groups. The levels of IL-6, ICAM-1 and P-selectin in serum were not found any difference between LTx group and PLC group, while the levels of IL-6, ICAM-1 and P-selectin in serum shown significant difference between LTx and healthy groups (P = 0.048, 0.000 and 0.025, respectively).<br />Conclusions: Our data demonstrates that effector T-cells can also be activated and exert immunoresponse to grafts permanently under the treatment of immunosuppressant. Adhesion molecules (ICAM-1, P-Selectin) and pro-inflammatory cytokines (IL-6, TNF-alpha) might be involved in the process of chronic graft damage induced by allo-immunoresponse.

Details

Language :
Chinese
ISSN :
0529-5815
Volume :
42
Issue :
4
Database :
MEDLINE
Journal :
Zhonghua wai ke za zhi [Chinese journal of surgery]
Publication Type :
Academic Journal
Accession number :
15062036