Serum cytokine profiles in stable survivors with clinical liver transplantation.
- Author:
Yun-le WAN
1
;
Shu-sen ZHENG
;
Jian-feng WEI
;
Chang-ku JIA
;
Zhong-rong HU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Cytokines; blood; Enzyme-Linked Immunosorbent Assay; Female; Flow Cytometry; Humans; Intercellular Adhesion Molecule-1; blood; Interleukin-10; blood; Interleukin-2; blood; Interleukin-4; blood; Interleukin-6; blood; Liver Neoplasms; blood; therapy; Liver Transplantation; Male; Middle Aged; P-Selectin; blood; Survivors; T-Lymphocytes; classification; cytology; Tumor Necrosis Factor-alpha; analysis
- From: Chinese Journal of Surgery 2004;42(4):207-209
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo elucidate the profile of serum cytokines and adhesion molecules in stable survivors with clinical liver transplantation.
METHODSFlow 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.
RESULTSPercentage 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).
CONCLUSIONSOur 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.