Harvard Institute of Proteomics, Harvard Medical School, Cambridge, MA, USA.
Proteomics Clin Appl. 2008 Oct;2(10-11):1518-27. doi: 10.1002/prca.200800034. Epub 2008 Sep 10.
The humoral immune response is a highly specific and adaptive sensor for changes in the body's protein milieu, which responds to novel structures of both foreign and self antigens. Although Igs represent a major component of human serum and are vital to survival, little is known about the response specificity and determinants that govern the human immunome. Historically, antigen-specific humoral immunity has been investigated using individually produced and purified target proteins, a labor-intensive process that has limited the number of antigens that have been studied. Here, we present the development of methods for applying self-assembling protein microarrays and a related method for producing 96-well formatted macroarrays for monitoring the humoral response at the proteome scale. Using plasmids encoding full-length cDNAs for over 850 human proteins and 1700 pathogen proteins, we demonstrate that these microarrays are highly sensitive, specific, reproducible, and can simultaneously measure immunity to thousands of proteins without a priori protein purification. Using this approach, we demonstrate the detection of humoral immunity to known and novel self-antigens, cancer antigens, autoimmune antigens, as well as pathogen-derived antigens. This represents a powerful and versatile tool for monitoring the immunome in health and disease.
体液免疫反应是一种高度特异和适应性的传感器,可以检测到体内蛋白质环境的变化,对来自外源和内源抗原的新结构都有反应。虽然 Igs 是人体血清的主要成分,对生存至关重要,但对于控制人类免疫组的反应特异性和决定因素知之甚少。从历史上看,使用单独产生和纯化的靶蛋白来研究抗原特异性体液免疫,这是一个劳动密集型的过程,限制了研究的抗原数量。在这里,我们介绍了应用自组装蛋白质微阵列的方法的发展,以及用于监测蛋白质组规模体液反应的相关 96 孔格式宏阵列的生产方法。使用编码超过 850 个人类蛋白和 1700 种病原体蛋白全长 cDNA 的质粒,我们证明这些微阵列具有高度的灵敏度、特异性、重现性,并且可以在无需事先进行蛋白纯化的情况下同时测量对数千种蛋白的免疫反应。使用这种方法,我们证明了对已知和新型自身抗原、癌症抗原、自身免疫抗原以及病原体衍生抗原的体液免疫的检测。这代表了一种监测健康和疾病中免疫组的强大而通用的工具。