PyNTTTTGT prototype oligonucleotide IMT504 is a potent adjuvant for the recombinant Hepatitis B vaccine that enhances the Th1 response

PyNTTTTGT oligodeoxinucleotides (ODNs) cause activation, proliferation and immunoglobulin secretion on B cells, and the expression of co-stimulatory molecules on plasmacytoid dendritic cells of primates. It has now been discovered that these ODNs are also active on rat cells. This fact allowed us to...

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Autor principal: Elias, F.
Otros Autores: Flo, J., Rodriguez, J.M, De Nichilo, A., Lopez, R.A, Zorzopulos, J., Nagle, C., Lahoz, M., Montaner, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier BV 2005
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Acceso en línea:Registro en Scopus
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100 1 |a Elias, F. 
245 1 0 |a PyNTTTTGT prototype oligonucleotide IMT504 is a potent adjuvant for the recombinant Hepatitis B vaccine that enhances the Th1 response 
260 |b Elsevier BV  |c 2005 
270 1 0 |m Zorzopulos, J.; Inst. de Invest. Biomédicas, Fund. Pablo Cassará, Saladillo 2452, Buenos Aires (1440), Argentina; email: zorzopul@hotmail.com 
506 |2 openaire  |e Política editorial 
504 |a Hepatitis B vaccination - United States, 1982-2002 (2002) MMWR Morb Mortal Wkly Rep, 51, pp. 549-563 
504 |a Incidence of acute hepatitis B - United States, 1990-2002 (2004) MMWR Morb Mortal Wkly Rep, 52 (51-52), pp. 1252-1254. , 2 Jan 
504 |a Kubba, A.K., Taylor, P., Graneek, B., Strobel, S., Non-responders to hepatitis B vaccination: A review (2003) Commun Dis Public Health, 6 (2), pp. 106-112 
504 |a Lewis, D.J., Eiden, J.E., Goilav, C., Langenberg, A.G., Suggett, F., Griffin, G.E., Rapid and frequent induction of protective immunity exceeding UK, recommendations for healthcare settings by MF59-adjuvated hepatitis B vaccine (2003) Commun Dis Public Health, 6 (4), pp. 320-324 
504 |a Evans, T.G., Hasan, M., Galibert, L., Caron, D., The use of Flt3 ligand as an adjuvant for hepatitis B vaccination of healthy adults (2002) Vaccine, 21 (3-4), pp. 322-329 
504 |a Jacques, P., Moens, G., Desombere, I., Dewijngaert, J., Leroux-Roels, G., Wettendorff, M., The immunogenicity and reactogenicity profile of a candidate hepatitis B, vaccine in an adult vaccine non-responder population (2002) Vaccine, 20 (31-32), pp. 3644-3649 
504 |a Davis, H.L., Weeratna, R., Waldschmidt, T.J., Tygrett, L., Schorr, J., Krieg, A.M., Weeranta, R., CpG DNA is a potent enhancer of specific immunity in mice immunized with recombinant hepatitis B surface antigen (1998) J Immunol, 160, pp. 870-876 
504 |a Halperin, S.A., Van Nest, G., Smith, B., Abtahi, S., Whiley, H., Eiden, J.J., A phase I study of the safety and immunogenicity of recombinant hepatitis B surface antigen co-administered with an immunostimulatory phosphorothioate oligonucleotide adjuvant (2003) Vaccine, 21, pp. 2461-2467 
504 |a Krieg, A.M., CpG motifs in bacterial DNA and their immune effects (2002) Annu Rev Immunol, 20, pp. 709-760 
504 |a Elías, F., Fló, J., Lopez, R.A., Zorzopulos, J., Montaner, A., Rodriguez, J.M., Strong cytosine-guanosine-independent immunostimulation in humans and other primates by synthetic oligodeoxynucleotides with PyNTTTTGT motifs (2003) J Immunol, 171, pp. 3697-3704 
504 |a Klinman, D.M., Immunotherapeutic uses of CpG oligonucleotides (2004) Nature Rev Immunol, 4, pp. 249-258 
504 |a Lipford, G.B., Bauer, M., Blank, C., Reiter, R., Wagner, H., Heeg, K., CpG-containing synthetic oligodeoxynucleotides promote B and cytotoxic T cell responses to protein antigen: A new class of vaccine adjuvants (1997) Eur J Immunol, 27, p. 2340 
504 |a Chu, R.S., Targoni, O.S., Krieg, A.M., Lehman, P.V., Harding, C.V., CpG oligodeoxynucleotides act as adjuvants that switch on T helper 1 (Th1) immunity (1997) J Exp Med, 186, p. 1623 
504 |a Moldovenu, G.J., Love-Homan, L., Huang, W.Q., Krieg, A.M., CpG DNA, a novel immune enhancer for systemic and mucosal immunization with influenza virus (1998) Vaccine, 16, p. 1216 
504 |a Weeratna, R., McCluskie, M.J., Yu, X., Davis, H.L., CpG DNA induces stronger immune responses with less toxicity than other adjuvants (2000) Vaccine, 18, p. 1755 
504 |a Rankin, R., Pontarollo, R., Ioannou, X., Krieg, A.M., Hecker, R., Babiuk, L.A., CpG motif identification for veterinary and laboratory species demonstrates that sequence recognition is highly conserved (2001) Antisense Nucleic Acid Drug Dev, 11 (5), pp. 333-340 
504 |a Saoudi, A., Kuhn, J., Huygen, K., De Kozak, Y., Velu, T., Goldman, M., TH2 activated cells prevent experimental autoimmune uveoretinitis, a TH1-dependent autoimmune disease (1993) Eur J Immunol, 23, pp. 3096-3103 
504 |a Gracie, J.A., Bradley, J.A., Interleukin-12 induces interferon-gamma-dependent switching of IgG alloantibody subclass (1996) Eur J Immunol, 26, pp. 1217-1221 
504 |a Bomford, R., Will adjuvants be needed for vaccines of the future? (1998) Dev Biol Stand, 92, pp. 13-17 
504 |a Gupta, R.K., Aluminum compounds as vaccine adjuvants (1998) Adv Drug Deliv Rev, 32, pp. 155-172 
504 |a Chisari, F.V., Hepatitis B virus immunopathogenesis (1995) Annu Rev Immunol, 13, pp. 29-60 
504 |a Bertoletti, A., D'Elios, M.M., Boni, C., De Carli, M., Zignego, A.L., Durazzo, M., Different cytokine profiles of intraphepatic T cells in chronic hepatitis B and hepatitis C virus infections (1997) Gastroenterology, 112 (1), pp. 193-199 
504 |a Guidotti, L.G., Ishikawa, T., Hobbs, M.V., Matzke, B., Schreiber, R., Chisari, F.V., Intracellular inactivation of the hepatitis B virus by cytotoxic T lymphocytes (1996) Immunity, 4 (1), pp. 25-36 
504 |a Jung, M.C., Hartmann, B., Gerlach, J.T., Diepolder, H., Gruber, R., Schraut, W., Virus-specific lymphokine production differs quantitatively but not qualitatively in acute and chronic hepatitis B infection (1999) Virology, 261 (2), pp. 165-172 
504 |a Penna, A., Del Prete, G., Cavalli, A., Bertoletti, A., D'Elios, M.M., Sorrentino, R., Predominant T-helper 1 cytokine profile of hepatitis B virus nucleocapsid-specific T cells in acute self-limited hepatitis B (1997) Hepatology, 25 (4), pp. 1022-1027 
504 |a McGeady, S.J., Immunocompetence and allergy (2004) Pediatrics, 113 (4 SUPPL.), pp. 1107-1113 
504 |a Chung, K.F., Individual cytokines contributing to asthma pathophysiology: Valid targets for asthma therapy? (2004) Curr Opin Invest Drugs, 4 (11), pp. 1320-1326 
504 |a Ronnblom, L., Eloranta, M.L., Alm, G.V., Role of natural interferon-alpha producing cells (plasmacytoid dendritic cells) in autoimmunity (2003) Autoimmunity, 36 (8), pp. 463-472 
504 |a Conrad, B., Potential mechanisms of interferon-alpha induced autoimmunity (2003) Autoimmunity, 36 (8), pp. 519-523 
520 3 |a PyNTTTTGT oligodeoxinucleotides (ODNs) cause activation, proliferation and immunoglobulin secretion on B cells, and the expression of co-stimulatory molecules on plasmacytoid dendritic cells of primates. It has now been discovered that these ODNs are also active on rat cells. This fact allowed us to investigate the adjuvant properties of PyNTTTTGT ODNs in a human Hepatitis B vaccine using this animal model. A very significant increment, as compared with the antigen alone, was observed in the antibody production induced by vaccination with the recombinant Hepatitis B surface antigen adjuvated with the PyNTTTTGT prototype IMT504 ODN. Analysis of the IgG subclass distribution in the sera of vaccinated animals indicated that, although an increase was observed in the titer of all the IgG subclasses, the increase on the Th1-associated IgG2b subclass was clearly more pronounced. Remarkably, this effect on the IgG2b titer was observed even if alum, a Th2 promoting adjuvant, was present together with IMT504 in the vaccine formulation. The increase in the Th1 response induced by IMT504 was also suggested by in vitro gamma interferon secretion assays. Monkeys of the species Cebus apella immunized with the recombinant Hepatitis B surface antigen plus alum and IMT504 also showed titers of antibodies against the antigen several times superior to the titers observed in control animals immunized with the antigen plus alum without ODN. Since rat and monkey cells are significantly less immunostimulated "in vitro" by PyNTTTTGT ODNs than human cells, the present results reasonably predict a very good performance of these ODNs as adjuvants in human vaccination. © 2005 Elsevier Ltd. All rights reserved.  |l eng 
593 |a Depto. de Quím. Biol., Fac. de Ciencias Exactas Y Naturales, Cuidad Universitaria, Buenos Aires (1428), Argentina 
593 |a Immunotech S.A, Florida 1, Buenos Aires (1440), Argentina 
593 |a Inst. de Invest. Biomédicas, Fund. Pablo Cassará, Saladillo 2452, Buenos Aires (1440), Argentina 
593 |a Ctro. Educacion Medica Invest. C., Galvan 4102, Buenos Aires (1431), Argentina 
690 1 0 |a IMMUNOSTIMULATORY OLIGONUCLEOTIDE 
690 1 0 |a TH1 ANSWER 
690 1 0 |a VACCINE ADJUVANT 
690 1 0 |a ALUMINUM POTASSIUM SULFATE 
690 1 0 |a GAMMA INTERFERON 
690 1 0 |a HEPATITIS B ANTIGEN 
690 1 0 |a IMMUNOGLOBULIN G2B 
690 1 0 |a IMMUNOLOGICAL ADJUVANT 
690 1 0 |a IMT 504 
690 1 0 |a OLIGONUCLEOTIDE 
690 1 0 |a RECOMBINANT HEPATITIS B VACCINE 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ANTIBODY PRODUCTION 
690 1 0 |a ANTIBODY TITER 
690 1 0 |a ANTIGEN ANTIBODY REACTION 
690 1 0 |a ARTICLE 
690 1 0 |a B LYMPHOCYTE 
690 1 0 |a BIOASSAY 
690 1 0 |a CELL SECRETION 
690 1 0 |a CELLULAR IMMUNITY 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CYTOKINE RELEASE 
690 1 0 |a DRUG POTENCY 
690 1 0 |a FEMALE 
690 1 0 |a HEPATITIS B VIRUS 
690 1 0 |a IMMUNE RESPONSE 
690 1 0 |a IMMUNOGLOBULIN PRODUCTION 
690 1 0 |a IMMUNOSTIMULATION 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a MONKEY 
690 1 0 |a NONHUMAN 
690 1 0 |a PHYSICAL CHEMISTRY 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RAT 
690 1 0 |a TH1 CELL 
690 1 0 |a TH2 CELL 
690 1 0 |a VACCINATION 
690 1 0 |a VACCINE PRODUCTION 
653 0 0 |a imt 504, Immunotech, Argentina 
700 1 |a Flo, J. 
700 1 |a Rodriguez, J.M. 
700 1 |a De Nichilo, A. 
700 1 |a Lopez, R.A. 
700 1 |a Zorzopulos, J. 
700 1 |a Nagle, C. 
700 1 |a Lahoz, M. 
700 1 |a Montaner, A. 
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