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Published in: Drugs 10/2013

01-07-2013 | Leading Article

Vaccine Development for Tuberculosis: Current Progress

Author: Ian M. Orme

Published in: Drugs | Issue 10/2013

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Abstract

Very substantial efforts have been made over the past decade or more to develop vaccines against tuberculosis. Historically, this began with a view to replace the current vaccine, Bacillus Calmette Guérin (BCG), but more recently most candidates are either new forms of this bacillus, or are designed to boost immunity in children given BCG as infants. Good progress is being made, but very few have, as yet, progressed into clinical trials. The leading candidate has advanced to phase IIb efficacy testing, with disappointing results. This article discusses the various types of vaccines, including those designed to be used in a prophylactic setting, either alone or BCG-boosting, true therapeutic (post-exposure) vaccines, and therapeutic vaccines designed to augment chemotherapy. While there is no doubt that progress is still being made, we have a growing awareness of the limitations of our animal model screening processes, further amplified by the fact that we still do not have a clear picture of the immunological responses involved, and the precise type of long-lived immunity that effective new vaccines will need to induce.
Literature
1.
go back to reference Smith KC, Orme IM, Starke J. The BCG Vaccine. In: Plotkin S, Orenstein W, Offit P, editors. Vaccines. 6th ed. London: WB Saunders; 2012. Smith KC, Orme IM, Starke J. The BCG Vaccine. In: Plotkin S, Orenstein W, Offit P, editors. Vaccines. 6th ed. London: WB Saunders; 2012.
2.
go back to reference Andersen P, Doherty TM. The success and failure of BCG: implications for a novel tuberculosis vaccine. Nat Rev Microbiol. 2005;3:656–62.PubMedCrossRef Andersen P, Doherty TM. The success and failure of BCG: implications for a novel tuberculosis vaccine. Nat Rev Microbiol. 2005;3:656–62.PubMedCrossRef
3.
go back to reference Orme IM. Development of new vaccines and drugs for TB: limitations and potential strategic errors. Future Microbiol. 2011;6:161–77.PubMedCrossRef Orme IM. Development of new vaccines and drugs for TB: limitations and potential strategic errors. Future Microbiol. 2011;6:161–77.PubMedCrossRef
4.
go back to reference Orme IM. New vaccines against tuberculosis: the status of current research. Infect Dis Clin North Am. 1999;13:169–85.PubMedCrossRef Orme IM. New vaccines against tuberculosis: the status of current research. Infect Dis Clin North Am. 1999;13:169–85.PubMedCrossRef
6.
7.
go back to reference Tameris MD, Hatherill M, Landry BS, et al. Safety and efficacy of MVA85A, a new tuberculosis vaccine, in infants previously vaccinated with BCG: a randomised, placebo-controlled phase 2b trial. Lancet. 1 Feb 2013 (Epub ahead of print). Tameris MD, Hatherill M, Landry BS, et al. Safety and efficacy of MVA85A, a new tuberculosis vaccine, in infants previously vaccinated with BCG: a randomised, placebo-controlled phase 2b trial. Lancet. 1 Feb 2013 (Epub ahead of print).
8.
go back to reference McShane H. Tuberculosis vaccines: beyond bacille Calmette-Guerin. Philos Trans R Soc Lond B Biol Sci. 2013;366:2782–9. McShane H. Tuberculosis vaccines: beyond bacille Calmette-Guerin. Philos Trans R Soc Lond B Biol Sci. 2013;366:2782–9.
9.
go back to reference Abel B, Tameris M, Mansoor N, et al. The novel tuberculosis vaccine, AERAS-402, induces robust and polyfunctional CD4+ and CD8+ T cells in adults. Am J Respir Crit Care Med. 2010;181:1407–17.PubMedCrossRef Abel B, Tameris M, Mansoor N, et al. The novel tuberculosis vaccine, AERAS-402, induces robust and polyfunctional CD4+ and CD8+ T cells in adults. Am J Respir Crit Care Med. 2010;181:1407–17.PubMedCrossRef
10.
go back to reference Skeiky YA, Alderson MR, Ovendale PJ, et al. Differential immune responses and protective efficacy induced by components of a tuberculosis polyprotein vaccine, Mtb72F, delivered as naked DNA or recombinant protein. J Immunol. 2004;172:7618–28.PubMed Skeiky YA, Alderson MR, Ovendale PJ, et al. Differential immune responses and protective efficacy induced by components of a tuberculosis polyprotein vaccine, Mtb72F, delivered as naked DNA or recombinant protein. J Immunol. 2004;172:7618–28.PubMed
11.
go back to reference Brandt L, Skeiky YA, Alderson MR, et al. The protective effect of the Mycobacterium bovis BCG vaccine is increased by coadministration with the Mycobacterium tuberculosis 72-kilodalton fusion polyprotein Mtb72F in M. tuberculosis-infected guinea pigs. Infect Immun. 2004;72:6622–32.PubMedCrossRef Brandt L, Skeiky YA, Alderson MR, et al. The protective effect of the Mycobacterium bovis BCG vaccine is increased by coadministration with the Mycobacterium tuberculosis 72-kilodalton fusion polyprotein Mtb72F in M. tuberculosis-infected guinea pigs. Infect Immun. 2004;72:6622–32.PubMedCrossRef
12.
go back to reference Spertini F, Audran R, Lurati F, et al. The candidate tuberculosis vaccine Mtb72F/AS02 in PPD positive adults: a randomized controlled phase I/II study. Tuberculosis (Edinb). 2012;93:179–88.CrossRef Spertini F, Audran R, Lurati F, et al. The candidate tuberculosis vaccine Mtb72F/AS02 in PPD positive adults: a randomized controlled phase I/II study. Tuberculosis (Edinb). 2012;93:179–88.CrossRef
13.
go back to reference Day CL, Tameris M, Mansoor N, et al. Induction and Regulation of T Cell Immunity by the Novel TB Vaccine M72/AS01 in South African Adults. Am J Respir Crit Care Med. 10 Jan 2013 (Epub ahead of print). Day CL, Tameris M, Mansoor N, et al. Induction and Regulation of T Cell Immunity by the Novel TB Vaccine M72/AS01 in South African Adults. Am J Respir Crit Care Med. 10 Jan 2013 (Epub ahead of print).
14.
go back to reference Aagaard C, Hoang T, Dietrich J, et al. A multistage tuberculosis vaccine that confers efficient protection before and after exposure. Nat Med. 2011;17:189–94.PubMedCrossRef Aagaard C, Hoang T, Dietrich J, et al. A multistage tuberculosis vaccine that confers efficient protection before and after exposure. Nat Med. 2011;17:189–94.PubMedCrossRef
15.
go back to reference Lin PL, Dietrich J, Tan E, et al. The multistage vaccine H56 boosts the effects of BCG to protect cynomolgus macaques against active tuberculosis and reactivation of latent Mycobacterium tuberculosis infection. J Clin Invest. 2012;122:303–14.PubMedCrossRef Lin PL, Dietrich J, Tan E, et al. The multistage vaccine H56 boosts the effects of BCG to protect cynomolgus macaques against active tuberculosis and reactivation of latent Mycobacterium tuberculosis infection. J Clin Invest. 2012;122:303–14.PubMedCrossRef
16.
go back to reference Bertholet S, Ireton GC, Ordway DJ, et al. A defined tuberculosis vaccine candidate boosts BCG and protects against multidrug resistant Mycobacterium tuberculosis. Sci Transl Med. 2010;2(53):53ra74. Bertholet S, Ireton GC, Ordway DJ, et al. A defined tuberculosis vaccine candidate boosts BCG and protects against multidrug resistant Mycobacterium tuberculosis. Sci Transl Med. 2010;2(53):53ra74.
17.
go back to reference Baldwin SL, Bertholet S, Reese VA, Ching LK, Reed SG, Coler RN. The importance of adjuvant formulation in the development of a tuberculosis vaccine. J Immunol. 2012;188:2189–97.PubMedCrossRef Baldwin SL, Bertholet S, Reese VA, Ching LK, Reed SG, Coler RN. The importance of adjuvant formulation in the development of a tuberculosis vaccine. J Immunol. 2012;188:2189–97.PubMedCrossRef
18.
go back to reference Billeskov R, Elvang TT, Andersen PL, Dietrich J. The HyVac4 subunit vaccine efficiently boosts BCG-primed anti-mycobacterial protective immunity. PLoS One. 2012;7:e39909.PubMedCrossRef Billeskov R, Elvang TT, Andersen PL, Dietrich J. The HyVac4 subunit vaccine efficiently boosts BCG-primed anti-mycobacterial protective immunity. PLoS One. 2012;7:e39909.PubMedCrossRef
19.
go back to reference Goonetilleke NP, McShane H, Hannan CM, Anderson RJ, Brookes RH, Hill AV. Enhanced immunogenicity and protective efficacy against Mycobacterium tuberculosis of bacille Calmette-Guerin vaccine using mucosal administration and boosting with a recombinant modified vaccinia virus Ankara. J Immunol. 2003;171:1602–9.PubMed Goonetilleke NP, McShane H, Hannan CM, Anderson RJ, Brookes RH, Hill AV. Enhanced immunogenicity and protective efficacy against Mycobacterium tuberculosis of bacille Calmette-Guerin vaccine using mucosal administration and boosting with a recombinant modified vaccinia virus Ankara. J Immunol. 2003;171:1602–9.PubMed
20.
go back to reference McShane H. Developing an improved vaccine against tuberculosis. Expert Rev Vaccines. 2004;3:299–306.PubMedCrossRef McShane H. Developing an improved vaccine against tuberculosis. Expert Rev Vaccines. 2004;3:299–306.PubMedCrossRef
21.
go back to reference McShane H, Brookes R, Gilbert SC, Hill AV. Enhanced immunogenicity of CD4(+) T-cell responses and protective efficacy of a DNA-modified vaccinia virus Ankara prime-boost vaccination regimen for murine tuberculosis. Infect Immun. 2001;69:681–6.PubMedCrossRef McShane H, Brookes R, Gilbert SC, Hill AV. Enhanced immunogenicity of CD4(+) T-cell responses and protective efficacy of a DNA-modified vaccinia virus Ankara prime-boost vaccination regimen for murine tuberculosis. Infect Immun. 2001;69:681–6.PubMedCrossRef
22.
go back to reference McShane H, Hill A. Prime-boost immunisation strategies for tuberculosis. Microbes Infect. 2005;7:962–7.PubMedCrossRef McShane H, Hill A. Prime-boost immunisation strategies for tuberculosis. Microbes Infect. 2005;7:962–7.PubMedCrossRef
23.
go back to reference Williams A, Goonetilleke NP, McShane H, et al. Boosting with poxviruses enhances Mycobacterium bovis BCG efficacy against tuberculosis in guinea pigs. Infect Immun. 2005;73:3814–6.PubMedCrossRef Williams A, Goonetilleke NP, McShane H, et al. Boosting with poxviruses enhances Mycobacterium bovis BCG efficacy against tuberculosis in guinea pigs. Infect Immun. 2005;73:3814–6.PubMedCrossRef
24.
go back to reference White AD, Sibley L, Dennis MJ, et al. An evaluation of the safety and immunogenicity of a candidate TB vaccine, MVA85A, delivered by aerosol to the lungs of macaques. Clin Vaccine Immunol. 2013;20(5):663-72. White AD, Sibley L, Dennis MJ, et al. An evaluation of the safety and immunogenicity of a candidate TB vaccine, MVA85A, delivered by aerosol to the lungs of macaques. Clin Vaccine Immunol. 2013;20(5):663-72.
25.
go back to reference Meyer J, Harris SA, Satti I, et al. Comparing the safety and immunogenicity of a candidate TB vaccine MVA85A administered by intramuscular and intradermal delivery. Vaccine. 2013;31:1026–33.PubMedCrossRef Meyer J, Harris SA, Satti I, et al. Comparing the safety and immunogenicity of a candidate TB vaccine MVA85A administered by intramuscular and intradermal delivery. Vaccine. 2013;31:1026–33.PubMedCrossRef
26.
go back to reference Kato-Maeda M, Shanley CA, Ackart D, et al. Beijing sublineages of Mycobacterium tuberculosis differ in pathogenicity in the guinea pig. Clin Vacc Immunol. 2012;19:1–10.CrossRef Kato-Maeda M, Shanley CA, Ackart D, et al. Beijing sublineages of Mycobacterium tuberculosis differ in pathogenicity in the guinea pig. Clin Vacc Immunol. 2012;19:1–10.CrossRef
27.
go back to reference Ordway DJ, Shang S, Henao-Tamayo M, et al. Mycobacterium bovis BCG-mediated protection against W-Beijing strains of Mycobacterium tuberculosis is diminished concomitant with the emergence of regulatory T cells. Clin Vaccine Immunol. 2011;18:1527–35.PubMedCrossRef Ordway DJ, Shang S, Henao-Tamayo M, et al. Mycobacterium bovis BCG-mediated protection against W-Beijing strains of Mycobacterium tuberculosis is diminished concomitant with the emergence of regulatory T cells. Clin Vaccine Immunol. 2011;18:1527–35.PubMedCrossRef
28.
go back to reference Shang S, Harton M, Tamayo MH, et al. Increased Foxp3 expression in guinea pigs infected with W-Beijing strains of M. tuberculosis. Tuberculosis (Edinb). 2011;91:378–85.CrossRef Shang S, Harton M, Tamayo MH, et al. Increased Foxp3 expression in guinea pigs infected with W-Beijing strains of M. tuberculosis. Tuberculosis (Edinb). 2011;91:378–85.CrossRef
29.
go back to reference Grode L, Seiler P, Baumann S, et al. Increased vaccine efficacy against tuberculosis of recombinant Mycobacterium bovis bacille Calmette-Guerin mutants that secrete listeriolysin. J Clin Invest. 2005;115:2472–9.PubMedCrossRef Grode L, Seiler P, Baumann S, et al. Increased vaccine efficacy against tuberculosis of recombinant Mycobacterium bovis bacille Calmette-Guerin mutants that secrete listeriolysin. J Clin Invest. 2005;115:2472–9.PubMedCrossRef
30.
go back to reference Grode L, Ganoza CA, Brohm C, Weiner J 3rd, Eisele B, Kaufmann SH. Safety and immunogenicity of the recombinant BCG vaccine VPM1002 in a phase 1 open-label randomized clinical trial. Vaccine. 2013;31:1340–8.PubMedCrossRef Grode L, Ganoza CA, Brohm C, Weiner J 3rd, Eisele B, Kaufmann SH. Safety and immunogenicity of the recombinant BCG vaccine VPM1002 in a phase 1 open-label randomized clinical trial. Vaccine. 2013;31:1340–8.PubMedCrossRef
31.
go back to reference Nambiar JK, Pinto R, Aguilo JI, et al. Protective immunity afforded by attenuated, PhoP-deficient Mycobacterium tuberculosis is associated with sustained generation of CD4+ T-cell memory. Eur J Immunol. 2012;42:385–92.PubMedCrossRef Nambiar JK, Pinto R, Aguilo JI, et al. Protective immunity afforded by attenuated, PhoP-deficient Mycobacterium tuberculosis is associated with sustained generation of CD4+ T-cell memory. Eur J Immunol. 2012;42:385–92.PubMedCrossRef
32.
go back to reference Verreck FA, Vervenne RA, Kondova I, et al. MVA.85A boosting of BCG and an attenuated, phoP deficient M. tuberculosis vaccine both show protective efficacy against tuberculosis in rhesus macaques. PLoS One. 2009;4:e5264.PubMedCrossRef Verreck FA, Vervenne RA, Kondova I, et al. MVA.85A boosting of BCG and an attenuated, phoP deficient M. tuberculosis vaccine both show protective efficacy against tuberculosis in rhesus macaques. PLoS One. 2009;4:e5264.PubMedCrossRef
33.
34.
go back to reference Hinchey J, Jeon BY, Alley H, et al. Lysine auxotrophy combined with deletion of the SecA2 gene results in a safe and highly immunogenic candidate live attenuated vaccine for tuberculosis. PLoS One. 2011;6:e15857.PubMedCrossRef Hinchey J, Jeon BY, Alley H, et al. Lysine auxotrophy combined with deletion of the SecA2 gene results in a safe and highly immunogenic candidate live attenuated vaccine for tuberculosis. PLoS One. 2011;6:e15857.PubMedCrossRef
35.
go back to reference Sambandamurthy VK, Derrick SC, Hsu T, et al. Mycobacterium tuberculosis DeltaRD1 DeltapanCD: a safe and limited replicating mutant strain that protects immunocompetent and immunocompromised mice against experimental tuberculosis. Vaccine. 2006;24:6309–20.PubMedCrossRef Sambandamurthy VK, Derrick SC, Hsu T, et al. Mycobacterium tuberculosis DeltaRD1 DeltapanCD: a safe and limited replicating mutant strain that protects immunocompetent and immunocompromised mice against experimental tuberculosis. Vaccine. 2006;24:6309–20.PubMedCrossRef
36.
go back to reference Sambandamurthy VK, Derrick SC, Jalapathy KV, et al. Long-term protection against tuberculosis following vaccination with a severely attenuated double lysine and pantothenate auxotroph of Mycobacterium tuberculosis. Infect Immun. 2005;73:1196–203.PubMedCrossRef Sambandamurthy VK, Derrick SC, Jalapathy KV, et al. Long-term protection against tuberculosis following vaccination with a severely attenuated double lysine and pantothenate auxotroph of Mycobacterium tuberculosis. Infect Immun. 2005;73:1196–203.PubMedCrossRef
37.
go back to reference Sambandamurthy VK, Jacobs WR Jr. Live attenuated mutants of Mycobacterium tuberculosis as candidate vaccines against tuberculosis. Microbes Infect. 2005;7:955–61.PubMedCrossRef Sambandamurthy VK, Jacobs WR Jr. Live attenuated mutants of Mycobacterium tuberculosis as candidate vaccines against tuberculosis. Microbes Infect. 2005;7:955–61.PubMedCrossRef
38.
go back to reference Sampson SL, Dascher CC, Sambandamurthy VK, et al. Protection elicited by a double leucine and pantothenate auxotroph of Mycobacterium tuberculosis in guinea pigs. Infect Immun. 2004;72:3031–7.PubMedCrossRef Sampson SL, Dascher CC, Sambandamurthy VK, et al. Protection elicited by a double leucine and pantothenate auxotroph of Mycobacterium tuberculosis in guinea pigs. Infect Immun. 2004;72:3031–7.PubMedCrossRef
39.
go back to reference Zimmerman DM, Waters WR, Lyashchenko KP, et al. Safety and immunogenicity of the Mycobacterium tuberculosis DeltalysA DeltapanCD vaccine in domestic cats infected with feline immunodeficiency virus. Clin Vaccine Immunol. 2009;16:427–9.PubMedCrossRef Zimmerman DM, Waters WR, Lyashchenko KP, et al. Safety and immunogenicity of the Mycobacterium tuberculosis DeltalysA DeltapanCD vaccine in domestic cats infected with feline immunodeficiency virus. Clin Vaccine Immunol. 2009;16:427–9.PubMedCrossRef
40.
go back to reference Hinchey J, Lee S, Jeon BY, et al. Enhanced priming of adaptive immunity by a proapoptotic mutant of Mycobacterium tuberculosis. J Clin Invest. 2007;117:2279–88.PubMedCrossRef Hinchey J, Lee S, Jeon BY, et al. Enhanced priming of adaptive immunity by a proapoptotic mutant of Mycobacterium tuberculosis. J Clin Invest. 2007;117:2279–88.PubMedCrossRef
41.
go back to reference Sweeney KA, Dao DN, Goldberg MF, et al. A recombinant Mycobacterium smegmatis induces potent bactericidal immunity against Mycobacterium tuberculosis. Nat Med. 2011;17:1261–8.PubMedCrossRef Sweeney KA, Dao DN, Goldberg MF, et al. A recombinant Mycobacterium smegmatis induces potent bactericidal immunity against Mycobacterium tuberculosis. Nat Med. 2011;17:1261–8.PubMedCrossRef
42.
go back to reference Turner J, Rhoades ER, Keen M, Belisle JT, Frank AA, Orme IM. Effective preexposure tuberculosis vaccines fail to protect when they are given in an immunotherapeutic mode. Infect Immun. 2000;68:1706–9.PubMedCrossRef Turner J, Rhoades ER, Keen M, Belisle JT, Frank AA, Orme IM. Effective preexposure tuberculosis vaccines fail to protect when they are given in an immunotherapeutic mode. Infect Immun. 2000;68:1706–9.PubMedCrossRef
43.
go back to reference Cardona PJ. RUTI: a new chance to shorten the treatment of latent tuberculosis infection. Tuberculosis (Edinb). 2006;86:273–89.CrossRef Cardona PJ. RUTI: a new chance to shorten the treatment of latent tuberculosis infection. Tuberculosis (Edinb). 2006;86:273–89.CrossRef
44.
go back to reference Gil O, Vilaplana C, Guirado E, et al. Enhanced gamma interferon responses of mouse spleen cells following immunotherapy for tuberculosis relapse. Clin Vaccine Immunol. 2008;15:1742–4.PubMedCrossRef Gil O, Vilaplana C, Guirado E, et al. Enhanced gamma interferon responses of mouse spleen cells following immunotherapy for tuberculosis relapse. Clin Vaccine Immunol. 2008;15:1742–4.PubMedCrossRef
45.
go back to reference Vilaplana C, Montane E, Pinto S, et al. Double-blind, randomized, placebo-controlled phase I clinical trial of the therapeutical antituberculous vaccine RUTI. Vaccine. 2010;28:1106–16.PubMedCrossRef Vilaplana C, Montane E, Pinto S, et al. Double-blind, randomized, placebo-controlled phase I clinical trial of the therapeutical antituberculous vaccine RUTI. Vaccine. 2010;28:1106–16.PubMedCrossRef
46.
go back to reference Coler RN, Bertholet S, Pine SO, et al. Therapeutic immunization against Mycobacterium tuberculosis is an effective adjunct to antibiotic treatment. J Infect Dis. 2013;207(8):1242–52. Coler RN, Bertholet S, Pine SO, et al. Therapeutic immunization against Mycobacterium tuberculosis is an effective adjunct to antibiotic treatment. J Infect Dis. 2013;207(8):1242–52.
47.
go back to reference Turner OC, Keefe RG, Sugawara I, Yamada H, Orme IM. SWR mice are highly susceptible to pulmonary infection with Mycobacterium tuberculosis. Infect Immun. 2003;71:5266–72.PubMedCrossRef Turner OC, Keefe RG, Sugawara I, Yamada H, Orme IM. SWR mice are highly susceptible to pulmonary infection with Mycobacterium tuberculosis. Infect Immun. 2003;71:5266–72.PubMedCrossRef
48.
go back to reference Faujdar J, Gupta P, Natrajan M, et al. Mycobacterium indicus pranii as stand-alone or adjunct immunotherapeutic in treatment of experimental animal tuberculosis. Indian J Med Res. 2012;134:696–703. Faujdar J, Gupta P, Natrajan M, et al. Mycobacterium indicus pranii as stand-alone or adjunct immunotherapeutic in treatment of experimental animal tuberculosis. Indian J Med Res. 2012;134:696–703.
49.
go back to reference Gupta A, Ahmad FJ, Ahmad F, et al. Efficacy of Mycobacterium indicus pranii immunotherapy as an adjunct to chemotherapy for tuberculosis and underlying immune responses in the lung. PLoS One. 2012;7:e39215.PubMedCrossRef Gupta A, Ahmad FJ, Ahmad F, et al. Efficacy of Mycobacterium indicus pranii immunotherapy as an adjunct to chemotherapy for tuberculosis and underlying immune responses in the lung. PLoS One. 2012;7:e39215.PubMedCrossRef
50.
go back to reference Ordway DJ, Shanley CA, Caraway ML, et al. Evaluation of standard chemotherapy in the guinea pig model of tuberculosis. Antimicrob Agents Chemother. 2010;54:1820–33.PubMedCrossRef Ordway DJ, Shanley CA, Caraway ML, et al. Evaluation of standard chemotherapy in the guinea pig model of tuberculosis. Antimicrob Agents Chemother. 2010;54:1820–33.PubMedCrossRef
51.
go back to reference Rawat KD, Chahar M, Reddy PV, et al. Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig. Infect Genet Evol. 2012;13:11–7.PubMedCrossRef Rawat KD, Chahar M, Reddy PV, et al. Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig. Infect Genet Evol. 2012;13:11–7.PubMedCrossRef
52.
go back to reference Gupta A, Ahmad FJ, Ahmad F, et al. Protective efficacy of Mycobacterium indicus pranii against tuberculosis and underlying local lung immune responses in guinea pig model. Vaccine. 2012;30:6198–209.PubMedCrossRef Gupta A, Ahmad FJ, Ahmad F, et al. Protective efficacy of Mycobacterium indicus pranii against tuberculosis and underlying local lung immune responses in guinea pig model. Vaccine. 2012;30:6198–209.PubMedCrossRef
53.
go back to reference von Reyn CF, Mtei L, Arbeit RD, et al. Prevention of tuberculosis in Bacille Calmette-Guerin-primed, HIV-infected adults boosted with an inactivated whole-cell mycobacterial vaccine. AIDS. 2012;24:675–85.CrossRef von Reyn CF, Mtei L, Arbeit RD, et al. Prevention of tuberculosis in Bacille Calmette-Guerin-primed, HIV-infected adults boosted with an inactivated whole-cell mycobacterial vaccine. AIDS. 2012;24:675–85.CrossRef
54.
go back to reference Orme IM. The mouse as a useful model of tuberculosis. Tuberculosis (Edinb). 2003;83:112–5.CrossRef Orme IM. The mouse as a useful model of tuberculosis. Tuberculosis (Edinb). 2003;83:112–5.CrossRef
55.
go back to reference Rhoades ER, Frank AA, Orme IM. Progression of chronic pulmonary tuberculosis in mice aerogenically infected with virulent Mycobacterium tuberculosis. Tuber Lung Dis. 1997;78:57–66.PubMedCrossRef Rhoades ER, Frank AA, Orme IM. Progression of chronic pulmonary tuberculosis in mice aerogenically infected with virulent Mycobacterium tuberculosis. Tuber Lung Dis. 1997;78:57–66.PubMedCrossRef
56.
go back to reference Turner OC, Basaraba RJ, Frank AA, Orme IM. Granuloma formation in mouse and guinea pig models of experimental tuberculosis. In: Boros DL, editor. Granulomatous infections and inflammation: cellular and molecular mechanisms. Washington DC: ASM Press; 2003. p. 65–84. Turner OC, Basaraba RJ, Frank AA, Orme IM. Granuloma formation in mouse and guinea pig models of experimental tuberculosis. In: Boros DL, editor. Granulomatous infections and inflammation: cellular and molecular mechanisms. Washington DC: ASM Press; 2003. p. 65–84.
57.
go back to reference Driver ER, Ryan GJ, Hoff DR, et al. Evaluation of a mouse model of necrotic granuloma formation using C3HeB/FeJ mice for testing of drugs against Mycobacterium tuberculosis. Antimicrob Agents Chemother. 2012;56:3181–95.PubMedCrossRef Driver ER, Ryan GJ, Hoff DR, et al. Evaluation of a mouse model of necrotic granuloma formation using C3HeB/FeJ mice for testing of drugs against Mycobacterium tuberculosis. Antimicrob Agents Chemother. 2012;56:3181–95.PubMedCrossRef
58.
go back to reference Kramnik I. Genetic dissection of host resistance to Mycobacterium tuberculosis: the sst1 locus and the Ipr1 gene. Curr Top Microbiol Immunol. 2008;321:123–48.PubMedCrossRef Kramnik I. Genetic dissection of host resistance to Mycobacterium tuberculosis: the sst1 locus and the Ipr1 gene. Curr Top Microbiol Immunol. 2008;321:123–48.PubMedCrossRef
59.
go back to reference Pichugin AV, Yan BS, Sloutsky A, Kobzik L, Kramnik I. Dominant role of the sst1 locus in pathogenesis of necrotizing lung granulomas during chronic tuberculosis infection and reactivation in genetically resistant hosts. Am J Pathol. 2009;174:2190–201.PubMedCrossRef Pichugin AV, Yan BS, Sloutsky A, Kobzik L, Kramnik I. Dominant role of the sst1 locus in pathogenesis of necrotizing lung granulomas during chronic tuberculosis infection and reactivation in genetically resistant hosts. Am J Pathol. 2009;174:2190–201.PubMedCrossRef
60.
go back to reference Basaraba RJ, Orme IM. Pulmonary tuberculosis in the guinea pig. In: Leong FY, Dartois V, Dick T, editors. A color Atlas of comparative pathology of pulmonary tuberculosis. Baton Rouge: CRC Press; 2010. Basaraba RJ, Orme IM. Pulmonary tuberculosis in the guinea pig. In: Leong FY, Dartois V, Dick T, editors. A color Atlas of comparative pathology of pulmonary tuberculosis. Baton Rouge: CRC Press; 2010.
61.
go back to reference Basaraba RJ. Experimental tuberculosis: the role of comparative pathology in the discovery of improved tuberculosis treatment strategies. Tuberculosis (Edinb). 2008;88(Suppl 1):S35–47.CrossRef Basaraba RJ. Experimental tuberculosis: the role of comparative pathology in the discovery of improved tuberculosis treatment strategies. Tuberculosis (Edinb). 2008;88(Suppl 1):S35–47.CrossRef
62.
go back to reference Ordway DJ, Orme IM. Animal models of mycobacteria infection. Curr Protoc Immunol. Chapter 19: Unit 19 5. Ordway DJ, Orme IM. Animal models of mycobacteria infection. Curr Protoc Immunol. Chapter 19: Unit 19 5.
63.
go back to reference Hoff DR, Ryan GJ, Driver ER, et al. Location of intra- and extracellular M. tuberculosis populations in lungs of mice and guinea pigs during disease progression and after drug treatment. PLoS One. 2011;6:e17550.PubMedCrossRef Hoff DR, Ryan GJ, Driver ER, et al. Location of intra- and extracellular M. tuberculosis populations in lungs of mice and guinea pigs during disease progression and after drug treatment. PLoS One. 2011;6:e17550.PubMedCrossRef
64.
go back to reference Ryan GJ, Hoff DR, Driver ER, et al. Multiple M. tuberculosis phenotypes in mouse and guinea pig lung tissue revealed by a dual-staining approach. PLoS One. 2010;5:e11108.PubMedCrossRef Ryan GJ, Hoff DR, Driver ER, et al. Multiple M. tuberculosis phenotypes in mouse and guinea pig lung tissue revealed by a dual-staining approach. PLoS One. 2010;5:e11108.PubMedCrossRef
65.
go back to reference Barry CE 3rd, Boshoff HI, Dartois V, et al. The spectrum of latent tuberculosis: rethinking the biology and intervention strategies. Nat Rev Microbiol. 2009;7:845–55.PubMed Barry CE 3rd, Boshoff HI, Dartois V, et al. The spectrum of latent tuberculosis: rethinking the biology and intervention strategies. Nat Rev Microbiol. 2009;7:845–55.PubMed
66.
go back to reference Orme M. The latent tuberculosis bacillus (I’ll let you know if I ever meet one). Int J Tuberc Lung Dis. 2001;5:589–93.PubMed Orme M. The latent tuberculosis bacillus (I’ll let you know if I ever meet one). Int J Tuberc Lung Dis. 2001;5:589–93.PubMed
67.
go back to reference Lin PL, Rodgers M, Smith L, et al. Quantitative comparison of active and latent tuberculosis in the cynomolgus macaque model. Infect Immun. 2009;77:4631–42.PubMedCrossRef Lin PL, Rodgers M, Smith L, et al. Quantitative comparison of active and latent tuberculosis in the cynomolgus macaque model. Infect Immun. 2009;77:4631–42.PubMedCrossRef
68.
go back to reference Sharpe SA, McShane H, Dennis MJ, et al. Establishment of an aerosol challenge model of tuberculosis in rhesus macaques and an evaluation of endpoints for vaccine testing. Clin Vaccine Immunol. 2010;17:1170–82.PubMedCrossRef Sharpe SA, McShane H, Dennis MJ, et al. Establishment of an aerosol challenge model of tuberculosis in rhesus macaques and an evaluation of endpoints for vaccine testing. Clin Vaccine Immunol. 2010;17:1170–82.PubMedCrossRef
69.
go back to reference Williams A, Hall Y, Orme IM. Evaluation of new vaccines for tuberculosis in the guinea pig model. Tuberculosis (Edinb). 2009;89:389–97.CrossRef Williams A, Hall Y, Orme IM. Evaluation of new vaccines for tuberculosis in the guinea pig model. Tuberculosis (Edinb). 2009;89:389–97.CrossRef
70.
go back to reference Checkley AM, McShane H. Tuberculosis vaccines: progress and challenges. Trends Pharmacol Sci. 2011;32:601–6.PubMedCrossRef Checkley AM, McShane H. Tuberculosis vaccines: progress and challenges. Trends Pharmacol Sci. 2011;32:601–6.PubMedCrossRef
71.
go back to reference Comas I, Chakravartti J, Small PM, et al. Human T cell epitopes of Mycobacterium tuberculosis are evolutionarily hyperconserved. Nat Genet. 2010;42:498–503.PubMedCrossRef Comas I, Chakravartti J, Small PM, et al. Human T cell epitopes of Mycobacterium tuberculosis are evolutionarily hyperconserved. Nat Genet. 2010;42:498–503.PubMedCrossRef
72.
go back to reference McShane H, Jacobs WR, Fine PE, et al. BCG: myths, realities, and the need for alternative vaccine strategies. Tuberculosis (Edinb). 2012;92:283–8.CrossRef McShane H, Jacobs WR, Fine PE, et al. BCG: myths, realities, and the need for alternative vaccine strategies. Tuberculosis (Edinb). 2012;92:283–8.CrossRef
Metadata
Title
Vaccine Development for Tuberculosis: Current Progress
Author
Ian M. Orme
Publication date
01-07-2013
Publisher
Springer International Publishing
Published in
Drugs / Issue 10/2013
Print ISSN: 0012-6667
Electronic ISSN: 1179-1950
DOI
https://doi.org/10.1007/s40265-013-0081-8

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