Detection of soluble TRAIL in HBV infected patients and its clinical implications

被引:42
作者
Han, LH
Sun, WS [1 ]
Ma, CH
Zhang, LN
Liu, SX
Zhang, Q
Gao, LF
Chen, YH
机构
[1] Shandong Univ, Coll Med, Inst Immunol, Jinan 250012, Shandong Prov, Peoples R China
[2] Univ Penn, Inst Human Gene Therapy, Philadelphia, PA 19104 USA
关键词
D O I
10.3748/wjg.v8.i6.1077
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To detect the expression of soluble TRAIL (TNF-related apoptosis inducing ligand, TRAIL) in the peripheral blood of HBV infected patients and try to elucidate whether the expression level of sTRAIL have any correlativity with the clinical staging, the expression level of HBV markers and the degree of liver damage. METHODS: 52 cases of HBV infect patients were investigated, including 8 HBV carriers, 30 chronic hepatitis B, 11 cirrhotics and 3 HBV infection related hepatocellular carcinoma. Expression of soluble TRAIL and markers of the hepatitis B were mearsured by enzyme-linked immunosorbent assay. RESULTS: The expression level of sTRAIL in the peripheral blood of the HBV infected patients was significantly higher than that of healthy controls (1378.35+/-540.23 mug/ml vs 613.75+/-175.80 mug/ml, P<0.001). In the group of chronic hepatitis, the expression level of sTRAIL was coincident with the status of the disease and was significantly correlated with the level of ALT. In the group of cirrhosis and liver cancer, its expression level was significantly higher than that of the healthy persons and HBV carriers, but lower than that of the hepatitis B patients; meanwhile, the expression of sTRAIL did not have any correlativity with the functional indexes of the liver. CONCLUSION: The soluble TRAIL in the HBV infected people may participate in the liver damage. Our results indicated that the expression level of soluble TRAIL may reflect the ravage of liver caused by host immune reaction to a certain degree.
引用
收藏
页码:1077 / 1080
页数:4
相关论文
共 22 条
[1]   Safety and antitumor activity of recombinant soluble Apo2 ligand [J].
Ashkenazi, A ;
Pai, RC ;
Fong, S ;
Leung, S ;
Lawrence, DA ;
Masters, SA ;
Blackie, C ;
Chang, L ;
McMurtrey, AE ;
Hebert, A ;
DeForge, L ;
Koumenis, IL ;
Lewis, D ;
Harris, L ;
Bussiere, J ;
Koeppen, H ;
Shahrokh, Z ;
Schwall, RH .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (02) :155-162
[2]  
Ehrmann Jiri Jr., 2000, Pathology and Oncolgy Research, V6, P130
[3]   Osteoprotegerin is a receptor for the cytotoxic ligand TRAIL [J].
Emery, JG ;
McDonnell, P ;
Burke, MB ;
Deen, KC ;
Lyn, S ;
Silverman, C ;
Dul, E ;
Appelbaum, ER ;
Eichman, C ;
DiPrinzio, R ;
Dodds, RA ;
James, IE ;
Rosenberg, M ;
Lee, JC ;
Young, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14363-14367
[4]   Involvement of Fas system-mediated apoptosis in pathogenesis of viral hepatitis [J].
Hayashi, N ;
Mita, E .
JOURNAL OF VIRAL HEPATITIS, 1999, 6 (05) :357-365
[5]  
HAYASHI N, 1997, J GASTROEN HEPATOL, V12, P223
[6]   Analysis of FasL and TRAIL induced apoptosis pathways in glioma cells [J].
Knight, MJ ;
Riffkin, CD ;
Muscat, AM ;
Ashley, DM ;
Hawkins, CJ .
ONCOGENE, 2001, 20 (41) :5789-5798
[7]   ROLE OF T-CELL TOLERANCE IN THE PERSISTENCE OF HEPATITIS-B VIRUS-INFECTION [J].
MILICH, DR ;
JONES, J ;
HUGHES, J ;
MARUYAMA, T .
JOURNAL OF IMMUNOTHERAPY, 1993, 14 (03) :226-233
[8]   IS A FUNCTION OF THE SECRETED HEPATITIS-BE ANTIGEN TO INDUCE IMMUNOLOGICAL-TOLERANCE INUTERO [J].
MILICH, DR ;
JONES, JE ;
HUGHES, JL ;
PRICE, J ;
RANEY, AK ;
MCLACHLAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6599-6603
[9]   Fas antigen expression in liver tissues of patients with chronic hepatitis B [J].
Mochizuki, K ;
Hayashi, N ;
Hiramatsu, N ;
Katayama, K ;
Kawanishi, Y ;
Kasahara, A ;
Fusamoto, H ;
Kamada, T .
JOURNAL OF HEPATOLOGY, 1996, 24 (01) :1-7
[10]   An antagonist decoy receptor and a death domain-containing receptor for TRAIL [J].
Pan, GH ;
Ni, J ;
Wei, YF ;
Yu, GL ;
Gentz, R ;
Dixit, VM .
SCIENCE, 1997, 277 (5327) :815-818