PLASMID DNA AND PROTEIN VACCINATION OF MICE TO THE OUTER SURFACE PROTEIN-A OF BORRELIA-BURGDORFERI LEADS TO INDUCTION OF T-HELPER CELLS WITH SPECIFICITY FOR A MAJOR EPITOPE AND AUGMENTATION OF PROTECTIVE IGG ANTIBODIES IN-VIVO

Citation
Wm. Zhong et al., PLASMID DNA AND PROTEIN VACCINATION OF MICE TO THE OUTER SURFACE PROTEIN-A OF BORRELIA-BURGDORFERI LEADS TO INDUCTION OF T-HELPER CELLS WITH SPECIFICITY FOR A MAJOR EPITOPE AND AUGMENTATION OF PROTECTIVE IGG ANTIBODIES IN-VIVO, European Journal of Immunology, 26(11), 1996, pp. 2749-2757
Citations number
57
Categorie Soggetti
Immunology
ISSN journal
00142980
Volume
26
Issue
11
Year of publication
1996
Pages
2749 - 2757
Database
ISI
SICI code
0014-2980(1996)26:11<2749:PDAPVO>2.0.ZU;2-O
Abstract
Plasmid DNA-based vaccination is an efficient way to evoke various for ms of protective immunity in laboratory animals. Our previous experime nts have shown that mice immunized with either plasmid DNA encoding th e outer surface lipoprotein A (pOspA) of Borrelia burgdorferi or the r espective lipoprotein (Lip-OspA) produce protective antibodies against subsequent challenge with virulent spirochetes. In the present study, we compared the specificity and function of T cells generated in AKR/ N mice previously immunized to either pOspA or Lip-OspA. T cell popula tions derived by either of the two protocols consistently responded by proliferation in vitro to one (residues 186-203; B4) out of a panel o f 27 overlapping 20-mer peptides spanning the entire OspA molecule of strain ZS7. B4 was shown to express allele-specific ligand motifs for I-E(k). Most of the other peptides produced variable and much less pro nounced or marginal proliferative T cell responses. T cells reactive t o B4 as well as to some minor epitopes were CD4(+)CD8(-) T cells which produced IFN-gamma but no detectable IL-4 upon antigen stimulation in vitro. Priming of AKR/N mice with B4 but not with inactive peptides o f OspA led to an enhanced production of IgG antibodies, mainly of the IgG1 isotype, including those to a prominent protective epitope (LA-2) upon subsequent challenge with Lip-OspA or intact spirochetes. The da ta demonstrate that both plasmid DNA and protein immunization with Osp A results in T cell responses with specificity for a dominant OspA epi tope and suggest priming of mice with immunodominant peptides accelera tes the appearance of protective antibodies in vivo. The identificatio n of T helper cell epitopes relevant for the induction of protective a ntibodies will also facilitate the design of more potent vaccines agai nst Lyme disease.