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
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
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.