Correlation of interferon-induced expression of MxA mRNA in peripheral blood mononuclear cells with the response of patients with chronic active hepatitis C to IFN-alpha therapy.
Correlation of interferon-induced expression of MxA mRNA in peripheral blood mononuclear cells with the response of patients with chronic active hepatitis C to IFN-alpha therapy.
复制标题
干扰素诱导的外周血单核细胞中 MxA mRNA 表达与慢性活动性丙型肝炎患者对 IFN-α 治疗的反应的相关性。
DOI:
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发表时间:
1999
影响因子:
2.3
通讯作者:
Ferdinando Dianzani
中科院分区:
文献类型:
--
作者:
Guido Antonelli;E. Simeoni;O. Turriziani;R. Tesoro;Alessandro Redaelli;L. Roffi;L. Antonelli;Mauro Pistello;Ferdinando Dianzani
MxA, a protein with selective activity against certain viruses, is an accepted specific indicator of type I interferon (IFN) activity. We have developed an internally controlled quantitative-competitive PCR to measure the amounts of MxA mRNA expressed in peripheral blood mononuclear cells (PBMC). This assay is more sensitive, quantitative, and easily applied to serial clinical samples than previously described methods. We have applied this assay retrospectively to 27 patients with chronic active hepatitis C given IFN-alpha2. Most such patients gain no sustained benefit but nevertheless suffer from the side effects, expense, and inconvenience of the treatment. Fourteen of the 27 had been classified on clinical grounds as responders and 13 as nonresponders at the end of a 6 month treatment period. We measured MxA mRNA in PBMC obtained before and after 8 weeks of IFN-alpha2 treatment. All the patients expressed some level of mRNA before treatment began, and after 8 weeks of treatment, the level rose in 19. This increase was significant (p < 0.001) only in patients classified as responders. This strongly suggests that hepatitis C virus (HCV) patients who express increased amounts of MxA mRNA in their PBMC during IFN-alpha treatment are most likely to obtain long-term benefit. If this finding is confirmed in future prospective studies, it will provide an extremely important predictive marker for managing IFN-alpha therapy in patients with HCV.
DOI:
10.1172/jci119836
发表时间:
1997
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Li,Y;Youssoufian,H
通讯作者:
Youssoufian,H
DOI:
10.1006/viro.1996.0321
发表时间:
1996
期刊:
Virology.
影响因子:
--
作者:
Zhao,H;De,BP;Das,T;Banerjee,AK
通讯作者:
Banerjee,AK