Tan Eng M, Zhang Jianying
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Immunol Rev. 2008 Apr;222:328-40. doi: 10.1111/j.1600-065X.2008.00611.x.
Although autoantibodies have been recognized as participants in pathogenesis of tissue injury, the collateral role of autoantibodies as reporters from the immune system identifying cellular participants in tumorigenesis has not been fully appreciated. The immune system appears to be capable of sensing aberrant structure, distribution, and function of certain cellular components involved in tumorigenesis and making autoantibody responses to the tumor-associated antigens (TAAs). Autoantibodies to TAAs can report malignant transformation before standard clinical studies and may be useful as early detection biomarkers. The autoantibody response also provides insights into factors related to how cellular components may be rendered immunogenic. As diagnostic biomarkers, specific TAA miniarrays for identifying autoantibody profiles could have sufficient sensitivity in differentiating between types of tumors. Such anti-TAA profiles could also be used to monitor response to therapy. The immune system of cancer patients reveals the immune interactive sites or the autoepitopes of participants in tumorigenesis, and this information should be used in the design of immunotherapy.
尽管自身抗体已被视为组织损伤发病机制的参与者,但自身抗体作为免疫系统识别肿瘤发生中细胞参与者的报告者所起的附带作用尚未得到充分认识。免疫系统似乎能够感知参与肿瘤发生的某些细胞成分的异常结构、分布和功能,并对肿瘤相关抗原(TAAs)产生自身抗体反应。针对TAAs的自身抗体可以在标准临床研究之前报告恶性转化,并且可能作为早期检测生物标志物有用。自身抗体反应还提供了关于细胞成分如何变得具有免疫原性的相关因素的见解。作为诊断生物标志物,用于识别自身抗体谱的特定TAA微阵列在区分肿瘤类型方面可能具有足够的灵敏度。这种抗TAA谱也可用于监测治疗反应。癌症患者的免疫系统揭示了肿瘤发生中参与者的免疫相互作用位点或自身表位,并且该信息应用于免疫治疗的设计。