Ver registro no DEDALUS
Exportar registro bibliográfico

Metrics


Metrics:

Expression of Mycobacterium leprae HSP65 in tabacco and its effectiveness as an oral treatment in adjuvant-induced arthritis (2011)

  • Authors:
  • USP affiliated authors: SILVA, CELIO LOPES - FMRP
  • USP Schools: FMRP
  • DOI: 10.1007/s11248-010-9404-7
  • Subjects: PLANTAS TRANSGÊNICAS; ARTRITE (TRATAMENTO); MYCOBACTERIUM LEPRAE
  • Language: Inglês
  • Imprenta:
  • Source:
  • Acesso online ao documento

    DOI or search this record in
    Informações sobre o DOI: 10.1007/s11248-010-9404-7 (Fonte: oaDOI API)
    • Este periódico é de assinatura
    • Este artigo NÃO é de acesso aberto
    • Cor do Acesso Aberto: closed
    Informações sobre o Citescore
  • Título: Transgenic Research

    ISSN: 0962-8819

    Citescore - 2017: 2.2

    SJR - 2017: 0.904

    SNIP - 2017: 0.701


  • Exemplares físicos disponíveis nas Bibliotecas da USP
    BibliotecaCód. de barrasNúm. de chamada
    FMRP1997426pcd 1997426 Estantes Deslizantes
    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      RODRÍGUEZ-NARCISO, César; MECKES-FISHER, Mariana; SALGADO-GARCIGLIA, Rafael; et al. Expression of Mycobacterium leprae HSP65 in tabacco and its effectiveness as an oral treatment in adjuvant-induced arthritis. Transgenic Research, Dordrecht, v. 20, n. 2, p. 221-229, 2011. DOI: 10.1007/s11248-010-9404-7.
    • APA

      Rodríguez-Narciso, C., Meckes-Fisher, M., Salgado-Garciglia, R., Estrada-Parra, S., López-Gómez, R., Estrada-García, I., et al. (2011). Expression of Mycobacterium leprae HSP65 in tabacco and its effectiveness as an oral treatment in adjuvant-induced arthritis. Transgenic Research, 20( 2), 221-229. doi:10.1007/s11248-010-9404-7
    • NLM

      Rodríguez-Narciso C, Meckes-Fisher M, Salgado-Garciglia R, Estrada-Parra S, López-Gómez R, Estrada-García I, Silva CL, Pérez-Tapia M, Rangel-Cano RM. Expression of Mycobacterium leprae HSP65 in tabacco and its effectiveness as an oral treatment in adjuvant-induced arthritis. Transgenic Research. 2011 ; 20( 2): 221-229.
    • Vancouver

      Rodríguez-Narciso C, Meckes-Fisher M, Salgado-Garciglia R, Estrada-Parra S, López-Gómez R, Estrada-García I, Silva CL, Pérez-Tapia M, Rangel-Cano RM. Expression of Mycobacterium leprae HSP65 in tabacco and its effectiveness as an oral treatment in adjuvant-induced arthritis. Transgenic Research. 2011 ; 20( 2): 221-229.

    Referências citadas na obra
    Baumann G, Raschke E, Bevan M, Schöffl F (1987) Functional analysis of sequences required for transcriptional activation of a soybean heat shock gene in transgenic tobacco plants. EMBO J 6:1161–1166
    Billingham ME, Carney SL, Butler R, Colson MJ (1990) A mycobacterial 65-kD heat shock protein induces antigen-specific suppression of adjuvant arthritis, but is not itself arthritogenic. J Exp Med 171:339–344
    Blass S, Engel JM, Burmester GR (1999) The immunologic homunculus in rheumatoid arthritis. Arthritis Rheum 42:2499–2506
    Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Annual Biochem 72:248–254
    Brown JR, Doolittle WF (1997) Archaea and the prokaryote-to-eukaryote transition. Microbiol Mol Biol Rev 61:456–502
    Chen W, Syldath U, Bellmann K, Burkart V, Kolb H (1999) Human 60 kDa heat shock protein: a danger signal to the innate immune system. J Immunol 162:3212–3219
    Cobelens PM, Heijnen CJ, Nieuwenhuis EES, Kramer PG, van der Zee R, van Eden W, Kavelaars A (2000) Treatment of adjuvant-induced arthritis by oral administration of mycobacterial HSP65 during disease. Arthritis Rheum 43:2694–2702
    Daniell H, Singh ND, Mason H, Streatfield SJ (2009) Plant-made vaccine antigens and biopharmaceuticals. Trends Plant Sci 14(12):669–679
    Doyle JJ, Doyle JJ (1987) A rapid isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 9:11–15
    Elias D, Markovits D, Reshef T, van der Zee R, Cohen IR (1990) Induction and therapy of autoimmune diabetes in the non-obese diabetic (NOD/Lt) mouse by a 65-kDa heat shock protein. Proc Natl Acad Sci USA 87:1576–1580
    Gillis TP, Buchanan TM (1982) Production and partial characterization of monoclonal antibodies to Mycobacterium leprae. Infect Immun 37:172–178
    Haque MA, Yoshino S, Unada S, Nomaguchi H, Tokunaga O, Kohashi O (1996) Suppression of adjuvant arthritis in rats by induction of oral tolerance to Mycobacterial 65-kDa heat shock protein. Eur J Immunol 26:2650–2656
    Hoeckema A, Hirsch PR, Hooykaas PJJ, Schilperoot RA (1983) A binary plant vector strategy based on separation of Vir- and T-region of the Agrobacterium tumefaciens Ti-plasmid. Nature 303:179–180
    Jefferson RA, Kavanagh TA, Bevan MW (1987) GUS fusions: B-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6(13):3901–3907
    Jones PG, Sutton JM (1997) Plant molecular biology—essential techniques. Wiley, New York, pp 202–204
    Jones DB, Coulson AF, Duff GW (1993) Sequence homologies between Hsp60 and autoantigens. Immunol Today 14:115–118
    Kalra R, Singh SP, Pena-Philippides JC, Langley RJ, Razani-Boroujerdi S, Sopori ML (2004) Immunosuppressive and anti-inflammatory effects of nicotine administered by patch in an animal model. Clin Diagn Lab Immunol 11(3):563–568
    Kim HJ, Jang SII, Kim YJ, Chung HT, Yun YG, Kang TH, Jeong OS, Kim YC, Kim YC (2004) Scopoletin suppresses pro-inflammatory cytokines and PGE2 from LPS-stimulated cell line, RAW 264.7 cells. Fitoterapia 75(3–4):261–266
    Kingston AE, Hicks AC, Colston MJ, Billingham MEJ (1996) A 71-kD heat shock protein (hsp) from Mycobacterium tuberculosis has modulatory effects on experimental rat arthritis. Clin Exp Immunol 103:77–82
    Kohm AP, Fuller KG, Miller SD (2003) Mimicking the way to autoimmunity: an evolving theory of sequence and structural homology. Trends Microbiol 11:101–105
    Life P, Hassell A, Williams K, Young S, Bacon P, Southwood T (1993) Responses to Gram negative enteric bacterial antigens by synovial T cells from patients juvenile chronic arthritis: recognition of heat shock protein hsp60. J Rheumatol 20:1388–1396
    Lopes-Silva C, Bonato V, dos Santos-Junior R, Zérate Bladés CR, Sartori A (2009) Recent advances in DNA vaccines for autoimmune diseases. Expert Rev Vaccines 8:239–252
    López-Gómez R, Gómez-Lim MA (1992) A method for extracting intact RNA from fruits rich in polysaccharides using ripe mango masocarp. Hortic Sci 27:440–442
    Lukcas KV, Lowrie DB, Stokes RW, Colston MJ (1993) Tumor cells transfected with a bacterial heat shock gene lose tumorigenicity and induce protection against tumors. J Exp Med 178:343–348
    Lunardi C, Bason C, Navone R (2000) Systemic sclerosis inmunoglobulina G autoantibodies bind the human cytomegalovirus late protein UL94 and induce apoptosis in human endothelial cells. Nat Med 10:1183–1186
    Mattanovich D, Rüker F, Machado A, Laimer M, Regner F, Steinkeller H (1989) Efficient transformation of Agrobacterium sp. by electroporation. Nucleic Acids Res 17:6747
    Matzinger P (1994) Tolerance, danger, and the extended family. Annu Rev Immunol 12:991–1045
    McIntosh KB, Hulm JL, Young LW, Bonham-Smith PC (2004) A rapid Agrobacterium-mediated Arabidopsis thaliana transient assay system. Plant Mol Biol Rep 22:53–61
    Michaluart P, Abdallah KA, Lima FD et al (2008) Phase I trial of DNA-hsp65 immunotherapy for advanced squamous cell carcinoma of the heat and neck. Cancer Gene Ther 15:676–684
    Moctezuma JF (2002) Manifestaciones articulares de la artritis reumatoide. Revista Mexicana de Reumatología 17:211–219
    Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–497
    Nölke G, Schneider B, Fischer R, Schillberg S (2005) Immunomodulation of polyamine biosynthesis in tobacco plants has a significant impact on polyamine levels and generates a dwarf phenotype. Plant Biotechnol J 3:237–247
    Nomaguchi H, Yogi Y, Kawatsu K, Okamura H, Ozawa Y, Kasatani T (2002) Prevention of diabetes in non-obese diabetic mice by a single immunization with Mycobacterium leprae. Jpn J Leprosy 71:31–38
    Prescott S, Jackson AM, Hawkyard SJ, Alexandroff AB, James K (2000) Mechanisms of action of intravesical Bacille Calmette Guerin: local immune mechanisms. Clin Infect Dis 3:591–593
    Quintana FJ, Carmi P, Cohen IR (2003) DNA fragments of the human 60-kDa heat shock protein (HSP60) vaccinate against adjuvant arthritis: identification of a regulatory HSP60 peptide. J Immunol 17:3533–3541
    Ramessar K, Rademacher T, Sack M, Stadlmann J, Platis D, Stiegler G, Labrou N, Altmann F, Stöger JME, Capell T, Christou P (2009) Cost-effective production of a vaginal protein microbicide to prevent HIV transmission. Proc Natl Acad Sci USA 105(10):3727–3732
    Ribeiro AM, Bocca AL, Amaral AC et al (2009) DNAhsp65 vaccination induces protection in mice against Paracoccidioides brasiliensis infection. Vaccine 27:606–613
    Rosada R, de la Torre LG, Frantz FG et al (2008) Protection agaist tuberculosis by a single intranasal administration of DNA-hsp65 vaccine complexed with cationic liposomes. BMC Immunol 9:1–13
    Rudolphi U, Rzepka R, Batsford S et al (1997) The B cell repertoire of patients with rheumatoid arthritis. Increased frequencies of IgG + B cell specific for mycobacterial heat-shock protein 60 or human type II collagen in synovial fluid and tissue. Arthritis Rheum 40:1409–1419
    Santos-Júnior RR, Sartori A, Bonato VL, Coelho Castelo AA, Vilella CA, Zollner RL, Silva CL (2007) Immune modulation induced by tuberculosis DNA vaccine protects non-obese diabetic mice from diabetes progression. Clin Exp Immunol 149:570–578
    Sewell DL, Reinke EK, Hogan LH, Sandor M, Fabry Z (2002) Immunoregulation of CNS autoimmunity by helminth and mycobacterial infections. Immunol Lett 82:101–110
    Shoenfeld Y, Vilner Y, Coates ARM, Ranch J, Shanl D, Pinkhas J (1986) Monoclonal antibodies react with DNA, and monoclonal anti-DNA autoantibodies react with Mycobacterium tuberculosis. Clin Exp Immunol 66:255–261
    Souza PRM, Zárates-Bladés CR, Hori JI et al (2008) Protective efiicacy of different strategies employing Mycobaterium leprae heat-shock protein 65 against tuberculosis. Expert Opin Biol Ther 8:1255–1264
    Srivastava P (2002) Roles of heat- heat proteins in innate and adaptative immunity. Nat Rev Immunol 2:185–194
    Tacket CO, Mason HS, Losonsky G, Estes MK, Levine MM, Arntzen CJ (2000) Human immune responses to a novel Norwalk virus vaccine delivered in transgenic potatoes. J Infect Dis 182:302–305
    Thompson SJ, James NF, Siew LK, Webb GR, Jenner PJ, Colston MJ, Elson CJ (1998) An immunodominant epitope from mycobacterial 65-kDa heat shock protein protects against pristane-induced arthritis. J Immunol 160:4628–4634
    Thorns CJ, Morris JA (1985) Common epitopes between mycobateria and certain host tissue antigens. Clin Exp Immunol 61:323–328
    Ulmansky R (2002) Resistance to adjuvant arthritis is due to protective antibodies against heat shock protein surface epitopes and the induction of IL-10 secretion. J Immunol 168:6463–6469
    van Eden W (1988) Cloning of the mycobacterial epitope recognized by T lymphocytes in adjuvant arthritis. Nature 331:171–173
    van Eden Broek W (1989) Protection against streptococcal cell wall-induced arthritis by pretreatment with the 65-kDa mycobacterial heat shock protein. J Exp Med 170:449–466
    van Eden W, Haloshitz J, Nevo A, Frenkel A, Klajman A, Cohen JR (1985) Arthritis induced by a T-lymphocyte clone that responds to Mycobacterium tuberculosis and cartilage proteoglycanes. Proc Natl Acad Sci USA 82:5117–5120
    van Eden W, van der Zee R, Prakken B (2005) Heat shock proteins induce T cell regulation of chronic inflammation. Nat Rev Immunol 5:318–330
    Walmsley AM, Arntzen CJ (2000) Plants for delivery of edible vaccines. Curr Opin Biotechnol 11:126–129
    Zárate-Bladés CR, Deperon-Bonato VL, Volve de Silveira EL et al (2009) Comprehensive gene expression profiling in lungs of mice infected with Mycobacterium tuberculosis following DNAhsp65 immunotherapy. J Gene Med 11:66–78