Langford M P, Weigent D A, Chan T S, Johnson H M, Stanton G J
J Interferon Res. 1987 Feb;7(1):95-101. doi: 10.1089/jir.1987.7.95.
Antibodies to a synthetic carboxy-terminal peptide (Cys-Ser-Leu-Arg-Lys-Arg-Lys-Arg-Ser-Arg-Abu) (gamma-C-TP) of mouse interferon-gamma (MuIFN-gamma) were produced in rabbits. They neutralized the antiviral activity of MuIFN-gamma but not that of MuIFN-alpha/beta or human (Hu) IFN-alpha/beta or -gamma. They also inhibited the IFN-dependent enhancement of natural cytotoxic cells (NCC) and the in vivo plaque-forming cell (PFC) response to sheep red blood cells (SRBC). Thus, our results indicate that polyclonal antibodies specific for the nine carboxy-terminal amino acids of MuIFN-gamma can specifically inhibit the antiviral and immunoregulatory activities of this IFN in vitro. In addition, our findings indicate that endogenous production of MuIFN-gamma in vivo plays a role in development of the full antibody response to SRBC surface antigens.
在兔体内产生了针对小鼠干扰素-γ(MuIFN-γ)合成羧基末端肽(半胱氨酸-丝氨酸-亮氨酸-精氨酸-赖氨酸-精氨酸-赖氨酸-精氨酸-丝氨酸-精氨酸-氨基丁酸)(γ-C-TP)的抗体。它们中和了MuIFN-γ的抗病毒活性,但未中和MuIFN-α/β或人(Hu)IFN-α/β或-γ的抗病毒活性。它们还抑制了天然细胞毒性细胞(NCC)的IFN依赖性增强以及体内对绵羊红细胞(SRBC)的空斑形成细胞(PFC)反应。因此,我们的结果表明,对MuIFN-γ的九个羧基末端氨基酸具有特异性的多克隆抗体可在体外特异性抑制该IFN的抗病毒和免疫调节活性。此外,我们的研究结果表明,体内MuIFN-γ的内源性产生在对SRBC表面抗原的完全抗体反应的发展中起作用。