The incidence and clinical significance of antibodies to interferon-a in patients with solid tumors.

K Oberg, G Alm
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引用次数: 29

Abstract

It is well known that natural and recombinant proteins can cause antibody formation in the host. We have studied the incidence of binding and neutralizing antibodies in carcinoid patients (n = 327). All together 204 patients received interferon-alpha 2b (Intron-A), median does 15 MU range 9-35 MU/week subcutaneously and 51% of the patients developed binding antibodies by immunoassay and 17% showed positive neutralization assay but high titer antibodies (> 800 NU/ml) were only found in 4% of the patients. The median time until the development of binding antibodies was 26 months and neutralizing antibodies 25 months. Twenty-nine patients received interferon-alpha 2a (Roferon), median does 18 MU/week subcutaneously and 45% developed binding antibodies, 38% had positive neutralization assay and 28% presented high titer antibodies. Binding and neutralizing antibodies occurred at the same time after median six months of treatment. Patients treated with Wellferon (n = 45) and leukocyte interferon (n = 48), median dose of 15 MU/week subcutaneously did not develop any neutralizing antibodies. The majority of the interferon-alpha 2 antibodies were of the IgG isotype. The clinical relevance of the development of high titer neutralizing antibodies was evaluated in the patients. All together 17 patients developed high titer neutralizing antibodies and of these 12 patients showed loss of antitumor response measured as increased level of tumor markers and of tumor progression. In nine of these patients a switch to human leukocyte interferon reinstituted an antitumor response. Neutralizing antibodies against recombinant interferon-alpha 2a and 2b might occur in patients with carcinoid tumors. The incidence of high titer neutralizing antibodies is significantly higher in patients treated with interferon-alpha 2a compared to interferon-alpha 2b. A significant number of patients lost the antitumor effect during development of neutralizing antibodies at high titers, but human leukocyte interferon can be used as rescue treatment.

实体瘤患者干扰素-a抗体的发生率及临床意义。
众所周知,天然蛋白和重组蛋白可在宿主体内引起抗体的形成。我们研究了类癌患者中结合抗体和中和抗体的发生率(n = 327)。204例患者接受了干扰素- α 2b(内含素-a)治疗,皮下注射的中位剂量为15 MU,范围为9-35 MU/周,51%的患者免疫测定产生结合抗体,17%的患者中和试验呈阳性,但高效价抗体(> 800 NU/ml)仅在4%的患者中发现。产生结合抗体的平均时间为26个月,产生中和抗体的平均时间为25个月。29例患者接受干扰素- α 2a (Roferon)皮下注射,平均剂量为18 MU/周,45%的患者产生结合抗体,38%的患者中和试验呈阳性,28%的患者出现高滴度抗体。中位治疗6个月后,结合抗体和中和抗体同时出现。接受威铁龙(n = 45)和白细胞干扰素(n = 48)治疗的患者,中位剂量为15 μ MU/周皮下注射,未产生任何中和抗体。大多数干扰素- α 2抗体为IgG同型。在患者中评估高滴度中和抗体发展的临床相关性。总共有17名患者产生了高滴度中和抗体,其中12名患者表现出抗肿瘤反应的丧失,这是通过肿瘤标志物水平的增加和肿瘤进展来衡量的。其中9名患者改用人白细胞干扰素后,重新产生了抗肿瘤反应。类癌患者可能出现抗重组干扰素- α 2a和2b的中和抗体。与干扰素- α 2b相比,使用干扰素- α 2a治疗的患者出现高滴度中和抗体的几率明显更高。在高滴度中和抗体的发展过程中,大量患者失去了抗肿瘤作用,但人白细胞干扰素可以作为抢救治疗。
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