Falcone Valeria, Mihm Dagmar, Neumann-Haefelin Dieter, Costa Caterina, Nguyen Thien, Pozzi Gianni, Ricci Susanna
Department of Virology, University of Freiburg, Freiburg, Germany.
FEMS Immunol Med Microbiol. 2006 Oct;48(1):116-22. doi: 10.1111/j.1574-695X.2006.00130.x.
A conserved fragment comprising amino acid residues 130-230 of the G glycoprotein of human respiratory syncytial virus subtype A was expressed in the commensal bacterium Streptococcus gordonii. Recombinant streptococci displaying the G domain at the cell surface were used to immunize mice via both parenteral and mucosal routes. Subcutaneous immunization induced respiratory syncytial virus-specific serum immunoglobin G (IgG) capable of partially controlling virus replication in the lungs. Intranasal immunization with live bacteria stimulated the production of IgA against both the whole virus and the G domain in serum and bronchoalveolar fluid. Upon challenge, immunized animals had significantly lower virus titres in the lungs than the controls. Our results show for the first time that the G domain-expressing S. gordonii strain elicits both systemic and mucosal immunity that reduced respiratory syncytial virus replication in the lungs of mice.
包含人呼吸道合胞病毒A亚型G糖蛋白130 - 230位氨基酸残基的保守片段在共生细菌戈登链球菌中表达。在细胞表面展示G结构域的重组链球菌通过肠胃外和黏膜途径用于免疫小鼠。皮下免疫诱导产生呼吸道合胞病毒特异性血清免疫球蛋白G(IgG),其能够部分控制肺部的病毒复制。用活细菌进行鼻内免疫刺激血清和支气管肺泡液中产生针对全病毒和G结构域的IgA。在受到攻击后,免疫动物肺部的病毒滴度明显低于对照组。我们的结果首次表明,表达G结构域的戈登链球菌菌株可引发全身和黏膜免疫,从而减少小鼠肺部呼吸道合胞病毒的复制。