Fauci A S, Lane H C, Volkman D J
Ann Intern Med. 1983 Jul;99(1):61-75. doi: 10.7326/0003-4819-99-1-61.
A model of activation, proliferation, and differentiation of human lymphocyte responses is described, and the complex immunoregulatory modulation of this system discussed with regard to normal immune function and the aberrancies expressed in diseases characterized by abnormalities of immune function. Recent advances in technology of cloning and hybridizing human T cells as well as hybridizing human B cells have had a critical impact on the field of human immunobiology and have made available potentially unlimited amounts of purified antibodies and immunoregulatory factors. Of particular note has been the optimization of conditions for the production of B-cell hybridomas from human peripheral blood B cells secreting monoclonal antibody directed against predetermined antigenic specificities to which a subject has been immunized. Furthermore, the development of antigen-specific human T-cell clones has allowed a precise delineation of the genetic restriction in monocyte-T-cell interactions as well as the functional capability of T-cell subsets. Precise definition of these systems has allowed a greater understanding of the mechanisms of diseases characterized by aberrancies of immune function.
本文描述了人类淋巴细胞反应的激活、增殖和分化模型,并讨论了该系统在正常免疫功能以及以免疫功能异常为特征的疾病中所表现出的异常情况下的复杂免疫调节作用。人类T细胞克隆和杂交技术以及人类B细胞杂交技术的最新进展对人类免疫生物学领域产生了至关重要的影响,并使得获得潜在无限量的纯化抗体和免疫调节因子成为可能。特别值得注意的是,优化了从人外周血B细胞产生B细胞杂交瘤的条件,这些B细胞可分泌针对受试者已免疫的预定抗原特异性的单克隆抗体。此外,抗原特异性人类T细胞克隆的发展使得能够精确描绘单核细胞与T细胞相互作用中的遗传限制以及T细胞亚群的功能能力。对这些系统的精确界定有助于更深入地了解以免疫功能异常为特征的疾病的发病机制。