Human Vaccines & Immunotherapeutics · 2015 · 31 citations · 34 references
Veterinary MedicineImmunologyInfectious DiseasesImmunology Of Infectious DiseasesInnate ImmunityMolecular ImmunologyCellular Immunity In InfectionImmune Responses To InfectionImmunological Disease ModelsImmunopathology Of Infectious DiseasesMammalian ImmunologyRickettsial DiseasesCd8 Positive T CellsCd8 T Cell ActivationCytokine Secretion RegulationImmunopathological MechanismsInflammatory Cytokine SecretionOuter Membrane ProteinsRickettsia Rickettsii InfectionRocky Mountain Spotted Fever
Rickettsia rickettsii is the etiological agent of Rocky Mountain spotted fever (RMSF). YbgF and TolC are outer membrane-associated proteins of R. rickettsii that play important roles in its interaction with host cells. We investigated the immunogenicity of YbgF and TolC for protection against RMSF. We immunized C3H/HeN mice with recombinant R. rickettsii YbgF (rYbgF) or TolC (rTolC). Rickettsial burden and impairment in the lungs, spleens, and livers of rYbgF-immunized mice were significantly lower than in rTolC-immunized mice. The ratio of IgG2a to IgG1 in rYbgF-immunized mice continued to increase over the course of our experiments, while that in rTolC-immunized mice was reduced. The proliferation and cytokine secretion of CD4(+) and CD8(+) T cells isolated from R. rickettsii-infected mice were analyzed following antigen stimulation. The results indicated that proliferation and interferon (IFN)-γ secretion of CD4(+) or CD8(+) T cells in R. rickettsii-infected mice were significantly greater than in uninfected mice after stimulation with rYbgF. YbgF is a novel protective antigen of R. rickettsii. Protection conferred by YbgF is dependent upon IFN-γ-producing CD4(+) and CD8(+) T cells and IgG2a, which act in synergy to control R. rickettsii infection.
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