Hooper D C, Pierard I, Modelska A, Otvos L, Fu Z F, Koprowski H, Dietzschold B
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107-6799.
Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10908-12. doi: 10.1073/pnas.91.23.10908.
The administration of rabies ribonucleocapsid (RNP) by oral as well as parenteral routes was found to prime specific T cells and elicit N-protein-specific antibodies. per os and intramuscular immunization led to the production of antibodies of the IgA and IgG isotypes, respectively. Mice primed orally with RNP produced significantly enhanced amounts of virus-neutralizing antibody, compared with non-immune controls, upon subsequent parenteral booster immunization with inactivated rabies virus. Thus oral immunization with rabies RNP primed cells capable of mediating a secondary systemic response to rabies virus. The results of experiments in which peptide and protein antigens were administered either physically coupled to or mixed with RNP indicate that RNP has an inherent capacity to enhance immune responses.
通过口服和非肠道途径给予狂犬病核糖核蛋白(RNP)可启动特异性T细胞并引发N蛋白特异性抗体。经口免疫和肌肉注射免疫分别导致产生IgA和IgG同种型抗体。与非免疫对照相比,用RNP经口启动的小鼠在随后用灭活狂犬病病毒进行非肠道加强免疫后产生了显著增加量的病毒中和抗体。因此,用狂犬病RNP进行口服免疫可启动能够介导对狂犬病病毒的二次全身反应的细胞。将肽和蛋白质抗原与RNP物理偶联或混合给药的实验结果表明,RNP具有增强免疫反应的内在能力。