免疫原性
α-干扰素
阿尔法(金融)
抗体
生物
干扰素
分子生物学
T细胞
病毒学
免疫学
免疫系统
医学
结构效度
护理部
患者满意度
作者
Alicia V. Palleroni,Anthony Aglione,Mark Labow,Michael J. Brunda,S Pestka,Francesco Sinigaglia,Gianni Garotta,Jochem Alsenz,Andreas Braun
出处
期刊:PubMed
日期:1997-07-01
卷期号:17 Suppl 1: S23-7
被引量:42
摘要
A preclinical evaluation of the immunogenicity of various preparations of interferon-alpha (IFN-alpha) was performed with in vitro and in vivo animal models. The distribution of genes for IFN-alpha 2a, IFN-alpha 2b, and IFN-alpha 2c in various cell populations and the response of human T cell clones to IFN-alpha peptides were investigated. The immunogenicity of IFN-alpha in IFN-alpha 2b transgenic mice and factors that influence the immunogenicity of IFN-alpha in normal mice were also studied. The genes for IFN-alpha 2a and IFN-alpha 2b were found in KG-1 cells, whereas IFN-alpha 2b and IFN-alpha 2c genes were present in Namalwa cells. No difference in proliferation of human T cells, T cell lines, or T cell clones could be obtained with IFN-alpha peptides. In transgenic mice bearing the human IFN-alpha 2b gene, no antibody response was obtained following immunization with either IFN-alpha 2a or IFN-alpha 2b. Normal mice immunized with either IFN-alpha 2a or IFN-alpha 2b produced equivalent titers of antibodies, which cross-reacted with both IFNs. Studies evaluating the relative immunogenicity of IFN-alpha in normal mice demonstrated that a number of treatment and host variables can modulate immunogenicity of IFN-alpha preparations.
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