Göcke Kerstin, Baumann Ulrich, Hagemann Hartmut, Gabelsberger Josef, Hahn Heinz, Freihorst Joachim, von Specht Bernd Ulrich
Paediatric Pulmonology and Neonatology, Hanover Medical School, 30623, Hanover, Germany.
FEMS Immunol Med Microbiol. 2003 Jul 15;37(2-3):167-71. doi: 10.1016/S0928-8244(03)00094-4.
We compared the immunogenicity of two vaccination schedules with either a systemic or a mucosal booster, both following a mucosal primary vaccination with a recombinant outer membrane fusion protein of Pseudomonas aeruginosa (OprF-I) in 12 healthy volunteers. The systemic booster induced higher levels of OprF-I-specific serum antibodies of IgG isotype, with a mean+/-S.E.M. of 32.6+/-7.8x10(7) enzyme-linked immunosorbent assay (ELISA) units (EU) as compared to the nasal booster with 14.6+/-2.1x10(7) EU (P=0.05). Specific serum IgA antibodies and antibodies in saliva did not differ between the two vaccination groups. We conclude that a combined mucosal/systemic vaccination with the OprF-I vaccine may offer an enhanced systemic immunogenicity. Further studies on the long-term immunogenicity and induction of antibodies on the respiratory airway surface are warranted.
我们在12名健康志愿者中,比较了两种接种方案的免疫原性,这两种方案分别采用全身加强或黏膜加强,均在以铜绿假单胞菌重组外膜融合蛋白(OprF-I)进行黏膜初次接种之后。全身加强诱导产生了更高水平的IgG同种型OprF-I特异性血清抗体,酶联免疫吸附测定(ELISA)单位的平均值±标准误为32.6±7.8×10⁷,而鼻腔加强组为14.6±2.1×10⁷ EU(P = 0.05)。两组接种组之间的特异性血清IgA抗体和唾液中的抗体没有差异。我们得出结论,OprF-I疫苗的黏膜/全身联合接种可能会增强全身免疫原性。有必要对长期免疫原性以及呼吸道表面抗体的诱导进行进一步研究。