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Cell-Mediated Immunity in Virus Infections (Nobel Lecture)

机译:病毒感染中细胞介导的免疫力(诺贝尔讲座)

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摘要

Many key concepts concerning the nature of immunity have originated from the very practical need to control virus infections. This year, 1996, has been designated the "Year of the Vaccine" commemorating the 200th anniversary of Edward Jen-ner's vaccination of James Phipps with cowpox virus, and the subsequent challenge with smallpox virus. Insight into the nature of viruses, and how viruses interact with mammalian cells, has evolved since the turn of the century. Our concepts of immunity developed concurrently, beginning with Pasteur's treatment of Joseph Meissner with "aged" rabies virus. Antibody-mediated protection conferred by attenuated, live yellow-fever virus won the Nobel Prize for Max Theiler in 1951. Perhaps the most exciting area of immunology when I graduated from the University of Queensland Veterinary School in 1962 was the nature of virus neutralization, a topic that is still being resolved with the monoclonal antibody (mAb) technology originated by Georges Kohler and Cesar Milstein(Nobel Prize 1985). Crystallographic analysis of influenza virus neuraminidase-mAb complexes and variants of neuraminidase selected by mAbs led to the clear demonstration that Ig molecules normally bind to tertiary structure on proteins.
机译:有关免疫性质的许多关键概念源自控制病毒感染的非常实际的需求。 1996年被指定为“疫苗年”,以纪念Edward Jen-ner对James Phipps接种牛痘病毒200周年以及随后对天花病毒的挑战。自本世纪初以来,人们对病毒的本质以及病毒如何与哺乳动物细胞相互作用的认识不断发展。我们的免疫概念同时发展,始于巴斯德用“老龄”狂犬病病毒治疗约瑟夫·迈斯纳。减毒的活黄热病毒赋予的抗体介导的保护作用于1951年获得了诺贝尔奖的麦克斯泰勒(Max Theiler)。也许当我1962年从昆士兰大学兽医学院毕业时,免疫学中最激动人心的领域就是病毒中和的性质。乔治·科勒(Georges Kohler)和塞萨尔·米尔斯坦(Cesar Milstein)提出的单克隆抗体(mAb)技术仍在解决这个话题(1985年诺贝尔奖)。流感病毒神经氨酸酶-mAb复合物和由单克隆抗体选择的神经氨酸酶变体的晶体学分析清楚地表明,Ig分子通常与蛋白质的三级结构结合。

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