Lotz M, Tsoukas C D, Curd J G, Carson D A, Vaughan J H
J Rheumatol. 1987 Feb;14(1):42-5.
We evaluated the effects of all 3 classes of recombinant human interferon (IFN) on Epstein-Barr virus (EBV) infection of purified B lymphocytes from patients with rheumatoid arthritis (RA). After EBV infection, RA B cells secreted more IgM and significantly more IgM rheumatoid factor (RF) than normals. Spontaneous (no EBV) proliferation, IgM, and IgM RF were also higher in RA. All 3 types of IFN inhibited dose dependently EBV induced B cell activation. In RA, however, higher doses of each class of IFN were necessary to obtain 50% inhibition. IFN gamma was most potent in normals and RA. Four IgM RF production IFN gamma was significantly more potent than IFN alpha and IFN beta in reducing the spontaneous activation of RA B cells, and a similar trend was seen in B cell proliferation. These findings are discussed in the context of ongoing clinical trials with IFN gamma in RA.
我们评估了3类重组人干扰素(IFN)对类风湿关节炎(RA)患者纯化B淋巴细胞感染爱泼斯坦-巴尔病毒(EBV)的影响。EBV感染后,RA B细胞分泌的IgM以及IgM类风湿因子(RF)显著多于正常人。RA患者的自发(无EBV)增殖、IgM和IgM RF水平也更高。所有3种类型的IFN均剂量依赖性地抑制EBV诱导的B细胞活化。然而,在RA患者中,每类IFN都需要更高剂量才能达到50%的抑制效果。IFN-γ对正常人和RA患者的作用最为显著。在降低RA B细胞的自发活化方面,IFN-γ抑制IgM RF产生的效力显著高于IFN-α和IFN-β,在B细胞增殖方面也观察到类似趋势。我们结合目前正在进行的IFN-γ治疗RA的临床试验对这些发现进行了讨论。