Interleukin-8 and hIRH (SDF1-alpha/PBSF) mRNA expression and histological activity index in patients with chronic hepatitis C.
Interleukin-8 and hIRH (SDF1-alpha/PBSF) mRNA expression and histological activity index in patients with chronic hepatitis C.
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慢性丙型肝炎患者白细胞介素8和hIRH (SDF1-α/PBSF) mRNA表达量及组织学活性指数
DOI:
10.1002/hep.510280116
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发表时间:
1998
期刊:
影响因子:
--
通讯作者:
Barnard,GF
中科院分区:
文献类型:
--
作者:
Shimoda,K;Begum,NA;Shibuta,K;Mori,M;Bonkovsky,HL;Banner,BF;Barnard,GF
Recombinant human intercrine reduced in hepatomas (hIRH)/stromal cell-derived factor 1 (SDF1-α)/pre-B-cell growth-stimulating factor (PBSF), a new chemokine, exhibits an in vitro chemotaxis to neutrophils and a mixed in vivo chemotactic activity to neutrophils, lymphocytes, and monocytes in a rat intradermal injection model. We have investigated the messenger RNA (mRNA) expression of interleukin-8 (IL-8) and hIRH, in chronic hepatitis C of differing severity. Levels of expression of IL-8 and hIRH mRNA obtained from 37 human liver biopsy samples were measured by reverse-transcription and semiquantitative polymerase chain reaction (RT-PCR) amplification. We examined the correlation between mRNA expression and components of the histological activity index (HAI). Patients with HAI≥ 8 had a significantly higher corrected IL-8 mRNA expression ratio (0.24±0.13 [mean±SD]; n= 20) than those with HAI≤ 7 (0.05±0.03; n= 17; P<. 0001). Additionally, IL-8 mRNA expression was strongly associated with the severity of portal inflammation (PI)(high PI vs. low PI, 0.22±0.14 vs. 0.05±0.04; P<. 0001) and with the presence of bile duct lesions (0.29±0.15 vs. 0.11±0.1; P<. 01). In contrast, hIRH mRNA expression was not associated with the total HAI, any components of the HAI, or bile duct inflammation or injury. These results suggest that hIRH, although having the-CXC-, alpha chemokine motif, and exhibiting in vivo and in vitro inflammatory activity as does IL-8, plays a different role from IL-8 in hepatic inflammation and injury. IL-8 expression is directly associated with inflammation in patients with chronic hepatitis C, while hIRH expression does not correlate with histopathological severity of inflammation.