Abdul-Ahad A K, Galazka A R, Revel M, Biffoni M, Borden E C
Ares-Serono SA Geneva, Switzerland.
Cytokines Cell Mol Ther. 1997 Mar;3(1):27-32.
Patients receiving recombinant human interferon-beta 1a (IFN-beta 1a) produced in Chinese hamster ovary (CHO) cells were tested for the formation of neutralizing antibodies (NABs) to IFN-beta. Samples were tested in an enzyme-linked immunosorbent assay (ELISA), and if positive were then tested for neutralization of antiviral activity in an IFN-beta bioassay. A total of 793 patients with viral diseases, premalignant and malignant diseases, and multiple sclerosis received IFN-beta 1a in clinical studies. Long-term studies included 56 patients with cancer treated for 6 or 12 months and 334 patients with multiple sclerosis (MS) at the end of one year of treatment. All of the NAB-positive patients were found in the latter. Positivity in a single specimen was found in 14.4% of the MS patients. The incidence of sustained neutralizing antibody titres (i.e. positive in two tests at least 6 months apart) was 6.9% in this group. Comparison with results from other studies suggests that CHO-derived IFN-beta 1a induces less neutralizing antibody than IFN-beta 1b produced in E. coli.
对接受中国仓鼠卵巢(CHO)细胞生产的重组人干扰素β-1a(IFN-β-1a)治疗的患者进行了针对IFN-β的中和抗体(NABs)形成情况检测。样本采用酶联免疫吸附测定(ELISA)进行检测,若结果为阳性,则进一步在IFN-β生物测定中检测其抗病毒活性的中和情况。在临床研究中,共有793例患有病毒性疾病、癌前和恶性疾病以及多发性硬化症的患者接受了IFN-β-1a治疗。长期研究包括6个月或12个月治疗期的56例癌症患者以及治疗一年后的334例多发性硬化症(MS)患者。所有NAB阳性患者均出现在后者中。在MS患者中,14.4%的患者单次样本检测呈阳性。该组中持续中和抗体滴度(即至少间隔6个月的两次检测均为阳性)的发生率为6.9%。与其他研究结果相比表明,CHO来源的IFN-β-1a诱导产生的中和抗体比大肠杆菌生产的IFN-β-1b少。