Li Y, Stefura W P, Simons F E, Jay F T, HayGlass K T
Department of Immunology, University of Manitoba, Winnipeg, Canada.
J Immunol Methods. 1994 Oct 14;175(2):169-79. doi: 10.1016/0022-1759(94)90360-3.
Limiting dilution analysis (LDA) of fresh human mononuclear cell populations has previously been used to estimate the frequency of specific B cells, CTL, proliferative T cells, or cells capable of IL-2 production in various clinical situations. Such approaches evaluate the intensity of the response but provide little information concerning the balance between Th1- vs. Th2-like patterns of cytokine gene expression. Here, we describe development of an LDA method to obtain quantitative estimates of the frequency of antigen-specific IFN-gamma or IL-4 producing cells in human peripheral blood. The approach utilizes 3-4 day antigen-mediated restimulation of mononuclear cell populations freshly derived from grass pollen sensitive allergic rhinitis subjects. IFN-gamma and IL-4 production in culture supernatants are determined by ELISA and CT.h4S bioassay. Cytokine production elicited in this assay is CD4 dependent and antigen specific. As such, it provides a useful non-invasive approach for rapid evaluation of low frequency, antigen-induced cytokine production in the circulating repertoire. This method can readily be extended to analysis of other cytokines in other immunologic disorders or in infectious disease states, allowing longitudinal analysis of individuals and facilitating efforts to establish clear correlations between in vivo patterns of cytokine gene expression and disease exacerbation and remission.
新鲜人单核细胞群体的有限稀释分析(LDA)此前已被用于估计各种临床情况下特定B细胞、细胞毒性T淋巴细胞(CTL)、增殖性T细胞或能够产生白细胞介素-2(IL-2)的细胞的频率。此类方法评估了反应强度,但关于细胞因子基因表达的Th1样与Th2样模式之间的平衡提供的信息很少。在此,我们描述了一种LDA方法的开发,以获得人外周血中抗原特异性产生干扰素-γ(IFN-γ)或白细胞介素-4(IL-4)的细胞频率的定量估计。该方法利用从草花粉敏感型过敏性鼻炎受试者新鲜分离的单核细胞群体进行3 - 4天的抗原介导再刺激。培养上清液中的IFN-γ和IL-4产生通过酶联免疫吸附测定(ELISA)和CT.h4S生物测定法确定。该测定中引发的细胞因子产生依赖于CD4且具有抗原特异性。因此,它为快速评估循环库中低频、抗原诱导的细胞因子产生提供了一种有用的非侵入性方法。该方法可以很容易地扩展到分析其他免疫疾病或感染性疾病状态下的其他细胞因子,允许对个体进行纵向分析,并有助于建立细胞因子基因表达的体内模式与疾病加重和缓解之间的明确相关性。