Panitch H S, Hirsch R L, Haley A S, Johnson K P
Lancet. 1987 Apr 18;1(8538):893-5. doi: 10.1016/s0140-6736(87)92863-7.
In an open, randomised study, 18 patients with clinically definite, relapsing-remitting multiple sclerosis (MS) received 1 microgram, 30 micrograms, or 1000 micrograms doses of recombinant gamma interferon (IFN-gamma), given by intravenous infusion twice a week for four weeks. 7 patients had exacerbations during treatment. This exacerbation rate, compared retrospectively with the pretreatment rate and prospectively with the post-treatment rate, was significantly greater than expected. Exacerbations were not precipitated by fever or other dose-dependent side-effects. A concomitant increase in circulating monocytes bearing class II (HLA-DR) surface antigen suggested that the attacks induced during treatment were immunologically mediated. IFN-gamma is unsuitable for treatment of MS.
在一项开放性随机研究中,18例临床确诊的复发缓解型多发性硬化症(MS)患者接受了1微克、30微克或1000微克剂量的重组γ干扰素(IFN-γ),通过静脉输注给药,每周两次,共四周。7例患者在治疗期间病情加重。将该加重率与治疗前的发生率进行回顾性比较,并与治疗后的发生率进行前瞻性比较,结果显示该加重率显著高于预期。病情加重并非由发热或其他剂量依赖性副作用引起。同时,携带II类(HLA-DR)表面抗原的循环单核细胞增加,提示治疗期间诱发的发作是由免疫介导的。IFN-γ不适用于MS的治疗。