Arnheiter H, Zoon K C
J Virol. 1984 Oct;52(1):284-7. doi: 10.1128/JVI.52.1.284-287.1984.
Affinity-purified polyclonal antibodies directed against human lymphoblastoid interferon (IFN), Escherichia coli-derived human IFN-alpha 2, or two synthetic fragments of human IFN-alpha 1 all neutralized the antiviral activity of human alpha IFNs when added to the culture medium of MDBK cells together with IFNs. However, when these antibodies were microinjected into the cytoplasm or the nucleus of cells, subsequent treatment of the cells with IFNs induced full protection against vesicular stomatitis virus. This suggests that IFNs themselves need not act in the cytoplasmic compartment or the nucleus to induce an antiviral state.
针对人淋巴母细胞干扰素(IFN)、大肠杆菌衍生的人IFN-α2或人IFN-α1的两个合成片段的亲和纯化多克隆抗体,当与干扰素一起添加到MDBK细胞的培养基中时,均能中和人α干扰素的抗病毒活性。然而,当将这些抗体显微注射到细胞质或细胞核中时,随后用干扰素处理细胞可诱导对水疱性口炎病毒的完全保护。这表明干扰素本身不必在细胞质区室或细胞核中起作用来诱导抗病毒状态。