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免疫个体中的疟疾特异性抗体亚类:疫苗设计的关键信息来源。

Malaria-specific antibody subclasses in immune individuals: a key source of information for vaccine design.

作者信息

Garraud Olivier, Mahanty Siddhartha, Perraut Ronald

机构信息

Groupe Immunité des Muqueuses et Agents Pathogènes-Equipe d'Accueil (GIMAP-EA) 3064, Université Jean Monnet, Faculté de Médecine, 15 rue Ambroise Paré, 42023 Saint-Etienne Cédex, France.

出版信息

Trends Immunol. 2003 Jan;24(1):30-5. doi: 10.1016/s1471-4906(02)00012-1.

Abstract

Immunity against the blood stage of Plasmodium falciparum malaria is associated with protective-type antibodies of certain classes and subclasses. Field studies have demonstrated the differential regulation of various IgG subclasses depending on the dynamics of parasite transmission and on the immune status of the individuals tested. The intrinsic properties of each IgG subclass has a crucial role in protection, both because immunoglobulin levels are dependent on their production and clearance from blood and because antibodies are actively used for parasite clearance. In vitro models using B cells obtained from P. falciparum-immune adults have enabled study of the production of various antibody subclasses depending on the individual and on the antigens used. Ex vivo and in vitro observations from immune donors have helped to extend our understanding of the development and regulation of the antibody response and to design more effective vaccine strategies.

摘要

针对恶性疟原虫疟疾血液阶段的免疫与某些类别和亚类的保护性抗体相关。现场研究表明,各种IgG亚类的调节存在差异,这取决于寄生虫传播的动态以及所测试个体的免疫状态。每个IgG亚类的内在特性在保护中起着关键作用,这既是因为免疫球蛋白水平取决于它们在血液中的产生和清除,也是因为抗体被积极用于清除寄生虫。使用从感染恶性疟原虫的成年人中获得的B细胞的体外模型,能够研究取决于个体和所用抗原的各种抗体亚类的产生。来自免疫供体的体外和体内观察结果有助于扩展我们对抗体反应的发展和调节的理解,并设计更有效的疫苗策略。

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