Hanson S J, Gause W, Natelson B
Department of Psychology, Rutgers University, Newark, New Jersey 07102, USA.
Clin Diagn Lab Immunol. 2001 May;8(3):658-62. doi: 10.1128/CDLI.8.3.658-662.2001.
Neural-network classifiers were used to detect immunological differences in groups of chronic fatigue syndrome (CFS) patients that heretofore had not shown significant differences from controls. In the past linear methods were unable to detect differences between CFS groups and non-CFS control groups in the nonveteran population. An examination of the cluster structure for 29 immunological factors revealed a complex, nonlinear decision surface. Multilayer neural networks showed an over 16% improvement in an n-fold resampling generalization test on unseen data. A sensitivity analysis of the network found differences between groups that are consistent with the hypothesis that CFS symptoms are a consequence of immune system dysregulation. Corresponding decreases in the CD19(+) B-cell compartment and the CD34(+) hematopoietic progenitor subpopulation were also detected by the neural network, consistent with the T-cell expansion. Of significant interest was the fact that, of all the cytokines evaluated, the only one to be in the final model was interleukin-4 (IL-4). Seeing an increase in IL-4 suggests a shift to a type 2 cytokine pattern. Such a shift has been hypothesized, but until now convincing evidence to support that hypothesis has been lacking.
神经网络分类器被用于检测慢性疲劳综合征(CFS)患者组之间的免疫学差异,而此前这些差异与对照组相比并不显著。过去,线性方法无法在非退伍军人人群中检测出CFS组与非CFS对照组之间的差异。对29种免疫因子的聚类结构进行检查后发现了一个复杂的非线性决策面。多层神经网络在对未见数据的n折重采样泛化测试中显示出超过16%的改进。对该网络的敏感性分析发现了组间差异,这与CFS症状是免疫系统失调所致的假设一致。神经网络还检测到CD19(+) B细胞区室和CD34(+)造血祖细胞亚群相应减少,这与T细胞扩增一致。特别值得关注的是,在所有评估的细胞因子中,最终模型中唯一出现的是白细胞介素-4(IL-4)。IL-4的增加表明向2型细胞因子模式转变。这种转变已有假设,但直到现在仍缺乏支持该假设的令人信服的证据。