Lasfar Ahmed, Abushahba Walid, Balan Murugabaskar, Cohen-Solal Karine A
Department of Biochemistry and Molecular Biology, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, University Hospital Cancer Center, Newark, NJ 07103, USA.
Clin Dev Immunol. 2011;2011:349575. doi: 10.1155/2011/349575. Epub 2011 Dec 6.
The discovery of the interferon-lambda (IFN-λ) family has considerably contributed to our understanding of the role of interferon not only in viral infections but also in cancer. IFN-λ proteins belong to the new type III IFN group. Type III IFN is structurally similar to type II IFN (IFN-γ) but functionally identical to type I IFN (IFN-α/β). However, in contrast to type I or type II IFNs, the response to type III IFN is highly cell-type specific. Only epithelial-like cells and to a lesser extent some immune cells respond to IFN-λ. This particular pattern of response is controlled by the differential expression of the IFN-λ receptor, which, in contrast to IFN-α, should result in limited side effects in patients. Recently, we and other groups have shown in several animal models a potent antitumor role of IFN-λ that will open a new challenging era for the current IFN therapy.
干扰素-λ(IFN-λ)家族的发现极大地促进了我们对干扰素作用的理解,其不仅在病毒感染中发挥作用,在癌症方面也有重要意义。IFN-λ蛋白属于新型III型干扰素组。III型干扰素在结构上与II型干扰素(IFN-γ)相似,但在功能上与I型干扰素(IFN-α/β)相同。然而,与I型或II型干扰素不同,对III型干扰素的反应具有高度的细胞类型特异性。只有上皮样细胞以及在较小程度上的一些免疫细胞对IFN-λ有反应。这种特殊的反应模式由IFN-λ受体的差异表达控制,与IFN-α相比,这应该会使患者的副作用有限。最近,我们和其他研究小组在多个动物模型中证明了IFN-λ具有强大的抗肿瘤作用,这将为当前的干扰素治疗开启一个新的具有挑战性的时代。