Bloom B R
Cell Immunol. 1986 Apr 15;99(1):61-72. doi: 10.1016/0008-8749(86)90216-9.
Despite enormous advances made in recent years, there remain fundamental and fascinating unanswered questions in immunology. They would include the mechanism of tolerance, the biological significance of the major histocompatibility complex (MHC) restriction, generation of diversity in T cells, control of V region and isotype selection in B cells, how immune response genes work and how important their function is in man, among others. With the advent of monoclonal antibodies and recombinant DNA technologies, together with greater understanding of immunological interactions within the network and of the intracellular networks between membrane-associated receptors and cell function, a variety of immunological strategies are available for modulating immune responses in man. Some nonspecific strategies include immunomodulatory lymphokines, receptor modulation, and development of agonists and antagonists for important receptors. In addition, there is great potential for immunologically specific strategies for intervention, including the use of idiotypes and anti-idiotypes and genetic engineering of antibodies. Ultimately, there is the possibility of predicting antigenic epitopes likely to engage the cellular and humoral arms of the immune response on the basis of protein or DNA sequences. The potential of exploring these developments for new diagnostic tests and vaccines is emphasized here, as is the unpredictable importance of seemingly nonrelevant fundamental science in producing many of the tools for intervention, now and in the future.
尽管近年来取得了巨大进展,但免疫学中仍存在一些基本且引人入胜的未解决问题。这些问题包括耐受性机制、主要组织相容性复合体(MHC)限制的生物学意义、T细胞多样性的产生、B细胞中V区和同种型选择的控制、免疫反应基因如何发挥作用以及它们在人类中的功能有多重要等等。随着单克隆抗体和重组DNA技术的出现,以及对网络内免疫相互作用和膜相关受体与细胞功能之间细胞内网络的更深入理解,现在有多种免疫策略可用于调节人类的免疫反应。一些非特异性策略包括免疫调节性淋巴因子、受体调节以及开发重要受体的激动剂和拮抗剂。此外,免疫特异性干预策略具有很大潜力,包括使用独特型和抗独特型以及抗体的基因工程。最终,有可能根据蛋白质或DNA序列预测可能引发免疫反应的细胞和体液分支的抗原表位。这里强调了探索这些进展用于新诊断测试和疫苗的潜力,以及看似不相关的基础科学在产生许多当前和未来干预工具方面不可预测的重要性。