Long-Lasting Recall Response of CD4 and CD8 8ß T Cells, but not ?d T Cells, to Heat Shock Proteins of Francisella tularensis

References

• Hahn H, Kaufmann S. The role of cell-mediated immunity in bacterial infections. Rev Infect Dis 1981; 3: 1221–50.
   PubMedGoogle Scholar
• von Koenig C, Finger H, Hof H. Failure of killed Listeria monocytogenes vaccine to produce protective immunity. Nature 1982; 20: 233–4.
   Google Scholar
• Gotschlich E, Goldschneider I, Artenstein M. Human immunity to the meningococcus. V. The effect of immunization with meningococcal group C polysaccharide on the carrier state. J Exp Med 1969; 129: 1385–95.
   Google Scholar
• Austrian R, Douglas R, Schifman G, Coetzee A, Koornhof H, Hayden-Smith S, et al. Prevention of pneumococcal pneumonia by vaccination. Trans Assoc Am Physicians 1976; 89: 184–94.
   PubMedGoogle Scholar
• Andersen P. Host responses and antigens involved in protective immunity to Mycobacterium tuberculosis. Scand J Immunol 1997; 45: 115–31.
   PubMedGoogle Scholar
• Harty J, Bevan M. CD8 + T cells specific for a single nonamer epitope of Listeria monocytogenes are protective in vivo. J Exp Med 1992; 175: 1531–8.
   PubMed Web of Science ®Google Scholar
• Tärnvik A. Nature of protective immunity to Francisella tularensis. Rev Infect Dis 1989; 11: 440–51.
   PubMedGoogle Scholar
• Sandström G, Tärnvik A, Wolf-Watz H. Immunospecific T-lymphocyte stimulation by membrane proteins from Francisella tularensis. J Clin Microbiol 1987; 25: 641–4.
   PubMedGoogle Scholar
• Sjöstedt A, Eriksson M, Sandström G, Tärnvik A. Various membrane proteins of Francisella tularensis induce interferongamma production in both CD4+ and CD8+ T cells of primed humans. Immunology 1992; 76: 584–92.
   PubMed Web of Science ®Google Scholar
• Surcel HM, Sarvas M, Helander IM, Herva E. Membrane proteins of Francisella tularensis LVS differ in ability to induce proliferation of lymphocytes from tularemia-vaccinated individuals. Microb Pathog 1989; 7: 411–9.
   PubMedGoogle Scholar
• Surcel HM. Diversity of Francisella tularensis antigens recognized by human T lymphocytes. Infect Immun 1990; 58: 2664–8.
   PubMedGoogle Scholar
• Sjöstedt A, Sandström G, Tärnvik A, Jaurin B. Nucleotide sequence and T cell epitopes of a membrane protein of Francisella tularensis. J Immunol 1990; 145: 311–7.
   PubMedGoogle Scholar
• Sjöstedt A, Sandström G, Tärnvik A, Jaurin B. Molecular cloning and expression of a T cell stimulating membrane protein of Francisella tularensis. Microb Pathog 1989; 6: 403–14.
   PubMedGoogle Scholar
• Tärnvik A, Eriksson M, Sandström G, Sjöstedt A. Francisella tularensis—a model for studies of the immune response to intracellular bacteria in man. Immunology 1992; 76: 349–54.
   PubMedGoogle Scholar
• Golovliov I, Ericsson M, Åkerblom L, Sandström G, Tärnvik A, Sjöstedt A. Adjuvanticity of ISCOMs incorporating a T cell-reactive lipoprotein of the facultative intracellular pathogen Francisella tularensis. Vaccine 1995; 13: 261–7.
   Google Scholar
• Sjöstedt A, Sandström G, Tärnvik A. Humoral and cell-mediated immunity in mice to a 17-kilodalton lipoprotein of Francisella tularensis expressed by Salmonella typhimurium. Infect Immun 1992; 60: 2855–62.
   PubMed Web of Science ®Google Scholar
• Ericsson M, Tärnvik A, Kuoppa K, Sandström G, Sjöstedt A. Increased synthesis of DnaK, GroEL, and GroES homologs by Francisella tularensis LVS in response to heat and hydrogen peroxide. Infect Immun 1994; 62: 178–83.
   PubMed Web of Science ®Google Scholar
• Ericsson M, Golovliov I, Sandström G, Tärnvik A, Sjöstedt A. Characterization of the nucleotide sequence of the groE operon encoding heat shock proteins chaperone-60 and -10 of Francisella tularensis and determination of the T cell response to the proteins in individuals vaccinated with F. tularensis. Infect Immun 1997; 65: 1824–9.
   Google Scholar
• Fisch P, Malkovsky M, Kovats S, Sturm E, Braakmann E, Klein B, et al. Recognition by human Vγ9/Vδ2 T cells of a GroEL homolog on Daudi Burkitt’s lymphoma cells. Science 1990; 250: 1269–71.
   PubMed Web of Science ®Google Scholar
• Russo DM, Armitage RJ, Barral-Netto M, Barral A, Grabstein KH, Reed SG. Antigen-reactive gamma delta T cells in human leishmaniasis. J Immunol 1993; 151: 3712–8.
   Google Scholar
• Kaur I, Voss SD, Gupta RS, Schell K, Fisch P, Sondel PM. Human peripheral ‘‘gamma’’ ‘‘delta’’ T cells recognize hsp60 molecules on Daudi Burkitt’s lymphoma cells. J Immunol 1993; 150: 2046–55.
   PubMed Web of Science ®Google Scholar
• Zuber M, Hoover TA, Dertzbaugh MT, Court DL. Analysis of the DnaK molecular chaperone system of Francisella tularensis. Gene 1995; 164: 149–52.
   PubMedGoogle Scholar
• Chamberlain RE. Evaluation of live tularemia vaccine prepared in a chemically defined medium. Appl Microbiol 1965; 13: 232–5.
   PubMedGoogle Scholar
• Lee C, Levin A, Branton D. Copper staining: a five-minute protein stain for sodium dodecyl sulfate-polyacrylamide gels. Anal Biochem 1987; 166: 308–12.
   Google Scholar
• Ericsson M, Sandström G, Sjöstedt A, Tärnvik A. Persistence of cell-mediated immunity and decline of humoral immunity to the intracellular bacterium Francisella tularensis 25 years after natural infection. J Infect Dis 1994; 170: 110–4.
   PubMed Web of Science ®Google Scholar
• Sjöstedt A, Sandström G, Tärnvik A. Several membrane polypeptides of the live vaccine strain Francisella tularensis LVS stimulate T cells from naturally infected individuals. J Clin Microbiol 1990; 28: 43–8.
   PubMed Web of Science ®Google Scholar
• Wesch D, Marx S, Kabelitz D. Comparative analysis of αβ and γδ T cell activation by Mycobacterium tuberculosis and isopentenyl pyrophosphate. Eur J Immunol 1997; 27: 952–6.
   Google Scholar
• Haregewoin A, Soman G, Hom RC, Finberg RW. Human γδ + T cells respond to mycobacterial heat-shock protein. Nature 1989; 340: 309–12.
   PubMed Web of Science ®Google Scholar
• Sturm E, Braakman E, Fisch P, Vreugdenhil R, Sondel P, Bolhuis R. Human V gamma 9-V delta 2 T cell receptor-gamma delta lymphocytes show specificity to Daudi Burkitt’s lymphoma cells. J Immunol 1990; 145: 3202–8.
   PubMedGoogle Scholar
• Inaba K, Young J, Steinman R. Direct activation of CD8 ⁺ cytotoxic T lymphocytes by dendritic cells. J Exp Med 1987; 166: 182–94.
   Google Scholar
• Jin I, Shih W-K, Berkower I. Human T cell response to the surface antigen of hepatitis B virus (HBsAg). Endosomal and nonendosomal processing pathways are accessible to both endogenous and exogenous antigen. J Exp Med 1988; 168: 293–306.
   PubMedGoogle Scholar
• Germain N. MHC-dependent antigen processing and peptide presentation: providing ligands for T lymphocyte activation. Cell 1994; 76: 287–9.
   PubMedGoogle Scholar
• Rock K, Gamble S, Rothstein L. Presentation of exogenous antigen with class I major histocompatibility complex molecules. Science 1990; 249: 918–21.
   Google Scholar
• Born W, Hall L, Dallas A, Boymel J, Shinnick T, Young D, et al. Recognition of a peptide antigen by heat shock-reactive γδ T lymphocytes. Science 1990; 249: 67–9.
   PubMed Web of Science ®Google Scholar
• O’Brien RL, Happ MP, Dallas A, Palmer E, Kubo R, Born WK. Stimulation of a major subset of lymphocytes expressing T cell receptor δ by an antigen derived from Mycobacterium tuberculosis. Cell 1989; 57: 667–74.
   PubMed Web of Science ®Google Scholar
• Holoshitz JFK, Coligan J, DeBruyn J, Strober S. Isolation of CD4-CD8-mycobacteria-reactive T lymphocyte clones from rheumatoid arthritis synovial fluid. Nature 1989; 339: 226–9.
   PubMed Web of Science ®Google Scholar
• Kabelitz D, Bender A, Schondelmaier S, Schoel B, Kaufmann SHE. A large fraction of human peripheral blood γδ ⁺ T cells is activated by Mycobacterium tuberculosis but not by its 65-kD heat shock protein. J Exp Med 1990; 171: 667–79.
   Google Scholar
• Kim H, Nelson E, Calyberger C, Sanjanwala M, Sklar J, Krensky A. γδ T cells recognition of tumor Ig peptide. J Immunol 1989; 154: 1614–23.
   Google Scholar
• Rajagopalan S, Zordan T, Tsokos G, Datta S. Pathogenic anti-DNA antibody-producing T helper cell lines from patients with active lupus nephritis: isolation of CD4–CD8– T helper cell lines that express the gamma delta T cell antigen receptor. Proc Natl Acad Sci USA 1990; 87: 7020–4.
   PubMed Web of Science ®Google Scholar
• Laad AD, Thomas ML, Fakih AR, Chiplunkar SV. Human gamma delta T cells recognize heat shock protein-60 on oral tumor cells. Int J Cancer 1999; 80: 709–14.
   PubMed Web of Science ®Google Scholar
• Zhao X, Wei Y, Kariya Y, Teshigawara K, Uchida A. Accumulation of γδ T cells in human dysgerminoma and seminoma: role in autologous tumor killing and granuloma formation. Immunol Invest 1995; 24: 607–18.
   Google Scholar
• Wei Y, Zhao X, Kariya Y, Fukata H, Teshigawara K, Uchida A. Induction of autologous tumor killing by heat treatment of fresh human tumor cells: involvement of γδ T cells and heat shock protein 70. Cancer Res 1996; 56: 607–18.
   Google Scholar
• Poquet Y, Kroca M, Halary F, Stenmark S, Peyrat MA, Bonneville M, et al. Expansion of Vγ9/Vδ2 T cells is triggered by Francisella tularensis-derived phosphoantigens in tularemia but not after tularemia vaccination. Infect Immun 1998; 66: 2107–14.
   PubMed Web of Science ®Google Scholar
• Constant P, Davodeau F, Peyrat MA, Poquet Y, Puzo G, Bonneville M, et al. Stimulation of human γδ T cells by nonpeptidic mycobacterial ligands. Science 1994; 264: 267–70.
   PubMed Web of Science ®Google Scholar
• Kabelitz D, Wesch D, Hinz T. γδ T cells, their T cell receptor usage and role in human diseases. Springer Semin Immunopathol 1999; 21: 55–75.
   Google Scholar
• Forsman M, Sandström G, Sjöstedt A. Analysis of 16S ribosomal DNA sequences of Francisella strains and utilization for determination of the phylogeny of the genus and for identification of strains by PCR. Int J Syst Bacteriol 1994; 44: 38–46.
   PubMedGoogle Scholar
• Burke DS. Immunization against tularemia: analysis of the effectiveness of live Francisella tularensis vaccine in prevention of laboratory-acquired tularemia. J Infect Dis 1977; 135: 55–60.
   PubMed Web of Science ®Google Scholar
• Hou S, Hyland L, Ryan K, Portner A, Doherty P. Virus-specific CD8 ⁺ T cell memory determined by clonal burst size. Nature 1994; 369: 652–4.
   Google Scholar
• Lau LL, Jamieson BD, Somasundaram T, Ahmed R. Cytotoxic T-cell memory without antigen. Nature 1994; 369: 64852.
   Google Scholar
• Mullbacher A. The long-term maintenance of cytotoxic T cell memory does not require persistence of antigen. J Exp Med 1994; 179: 317–21.
   PubMed Web of Science ®Google Scholar
• Murali-Krishna K, Altman JD, Suresh M, Sourdive DJD, Zajac AJ, Miller JD, et al. Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. Immunity 1998; 8: 177–87.
   PubMed Web of Science ®Google Scholar
• Demkovicz W, Littaua R, Wang J, Ennis F. Human cytotoxic T-cell memory: long-lived responses to vaccinia virus. J Virol 1996; 70: 2627–31.
   PubMed Web of Science ®Google Scholar