Bretscher P A, Corthay A, Anderson C C, Dembic Z, Havele C, Nagy Z A, Øynebråten I
University of Saskatchewan, Saskatchewan, Canada.
Oslo University Hospital, Oslo, Norway.
Scand J Immunol. 2017 Apr;85(4):242-250. doi: 10.1111/sji.12525.
We discussed different proposals for how the nature of the Th1/Th2 phenotype of an immune response is determined, and favoured one, the Threshold Hypothesis, as plausible and so useful as the basis for further discussions. The activation of a target CD4 T cell can be facilitated by helper CD4 T cells when the CD4 T cells interact via an antigen-presenting cell. The Threshold Hypothesis states that tentative and robust antigen-mediated CD4 T cell cooperation results in the target CD4 T cell, respectively giving rise, upon activation, to Th1 and Th2 cells. We primarily discussed four topics. We briefly discussed in the background section certain limitations of the Th1/Th2 paradigm in understanding immune class regulation, and the remarkable anti-inflammatory properties of human IgG antibody. Secondly, we assessed the role of class II MHC molecules in determining the number of mature CD4 T cells and so affecting the Th1/Th2 phenotype of immune responses. We also discussed the controversial role of CD8 T cells in affecting the Th1/Th2 phenotype of responses to MHC and other antigens, and the potential role of their relative scarcity in neonates in biasing responses towards an antibody, Th2 mode. Lastly, we examined the regulation of the Th1/Th2 phenotype of both primary and ongoing immune responses in the context of the intriguing proposal that antigen initially generates different classes/subclasses of immunity and then selects, by a feedback mechanism, the most effective class. We found this interesting idea difficult to reconcile with various observations.
我们讨论了关于免疫反应中Th1/Th2表型的性质是如何确定的不同提议,并支持其中一个,即阈值假说,认为它合理且对进一步讨论很有用。当CD4 T细胞通过抗原呈递细胞相互作用时,辅助性CD4 T细胞可促进靶CD4 T细胞的激活。阈值假说指出,试探性和强烈的抗原介导的CD4 T细胞合作分别导致靶CD4 T细胞在激活后产生Th1和Th2细胞。我们主要讨论了四个主题。在背景部分,我们简要讨论了Th1/Th2范式在理解免疫类别调节方面的某些局限性,以及人IgG抗体显著的抗炎特性。其次,我们评估了II类MHC分子在确定成熟CD4 T细胞数量从而影响免疫反应的Th1/Th2表型方面的作用。我们还讨论了CD8 T细胞在影响对MHC和其他抗原反应的Th1/Th2表型方面的争议性作用,以及它们在新生儿中相对稀缺在使反应偏向抗体、Th2模式方面的潜在作用。最后,我们在一个有趣的提议背景下研究了初次和持续免疫反应中Th1/Th2表型的调节,该提议认为抗原最初产生不同类别/亚类的免疫,然后通过反馈机制选择最有效的类别。我们发现这个有趣的想法很难与各种观察结果相协调。