Howard M, Nakanishi K, Paul W E
Immunol Rev. 1984 Apr;78:185-210. doi: 10.1111/j.1600-065x.1984.tb00482.x.
The role of T lymphocytes in regulation of B cell responsiveness has been recognized for over a decade. Early studies assigned part of this regulation to a soluble product, initially designated T cell-replacing factor or TRF. Recently, investigators have discovered a level of factor complexity skillfully camouflaged by this simple term. Accordingly, the concept has now matured to encompass a battery of antigen non-specific, genetically unrestricted soluble factors which govern all aspects of B cell immunity: activation, proliferation, and differentiation. Here, we review our developing knowledge of this area. While many questions remain unresolved, there seems cause for optimism and a hope that increased understanding of these factors and their mode of action will eventually reveal the basis of B cell immunoregulation.
T淋巴细胞在调节B细胞反应性方面的作用已被认识超过十年。早期研究将这种调节作用的一部分归因于一种可溶性产物,最初称为T细胞替代因子或TRF。最近,研究人员发现了这个简单术语巧妙掩盖的因子复杂性水平。因此,现在这一概念已经成熟,涵盖了一系列抗原非特异性、基因无限制的可溶性因子,这些因子支配着B细胞免疫的各个方面:激活、增殖和分化。在此,我们回顾我们在这一领域不断发展的知识。虽然许多问题仍未解决,但似乎有理由感到乐观,并希望对这些因子及其作用方式的更多了解最终将揭示B细胞免疫调节的基础。