Corbillet V, Celerier P, Lebon P, Litoux P, Dreno B
Clinique Dermatologique, CHU, Nantes.
Ann Med Interne (Paris). 1995;146(6):399-403.
In this study, we determined the frequency of interferon antibodies in patients with skin diseases treated with low doses of recombinant interferon alpha 2a (1.5 - 18 x 10(6) IU). We assayed serum specimens from 181 patients with malignant melanoma or cutaneous T cell lymphomas (78 patients treated with recombinant interferon alpha 2a and 103 patients in control group) for interferon antibodies before treatment and every 6 months for at least 18 months. Neutralizing interferon alpha 2a antibodies were detected in 27 of 77 treated patients (35%), but none in control group (p < 10(-6)): 38.2% in melanoma and 12.5% in T cell lymphomas. However antibody formation was not correlated with nonresponse or with frequency of interferon antibodies in patients receiving the combined therapy: interleukin-2 and interferon alpha 2a.
在本研究中,我们测定了接受低剂量重组干扰素α2a(1.5 - 18×10⁶IU)治疗的皮肤病患者中干扰素抗体的出现频率。我们检测了181例恶性黑色素瘤或皮肤T细胞淋巴瘤患者(78例接受重组干扰素α2a治疗,103例为对照组)治疗前及之后至少18个月内每6个月的血清标本中的干扰素抗体。在77例接受治疗的患者中有27例(35%)检测到中和性干扰素α2a抗体,而对照组未检测到(p < 10⁻⁶):黑色素瘤患者中为38.2%,T细胞淋巴瘤患者中为12.5%。然而,抗体形成与联合治疗(白细胞介素-2和干扰素α2a)患者的无反应情况或干扰素抗体频率无关。