Blockade of IL-10 Signaling during Bacillus Calmette-Guérin Vaccination Enhances and Sustains Th1, Th17, and Innate Lymphoid IFN-γ and IL-17 Responses and Increases Protection to <i>Mycobacterium tuberculosis</i> Infection

Journal of Immunology - Tập 189 Số 8 - Trang 4079-4087 - 2012
Jonathan M. Pitt1, Evangelos Stavropoulos1, Paul S. Redford1, Amy M. Beebe2, Gregory J. Bancroft3, Douglas B. Young4, Anne O’Garra1
1*Division of Immunoregulation, Medical Research Council National Institute for Medical Research, London NW7 1AA, United Kingdom;
2†Merck Research Laboratories, Palo Alto, CA 94304;
3‡Department of Immunology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1B 3DG, United Kingdom; and
4Division of Mycobacterial Research, Medical Research Council National Institute for Medical Research, London NW7 1AA, United Kingdom

Tóm tắt

Abstract Vaccination with Mycobacterium bovis bacillus Calmette-Guérin (BCG) remains the only prophylactic vaccine against tuberculosis, caused by Mycobacterium tuberculosis, but gives variable protection against pulmonary disease. The generation of host Th1 responses following BCG vaccination is accepted as the major mechanism of protection against M. tuberculosis infection. Early production of IL-17 in the lungs following M. tuberculosis challenge of mice previously vaccinated with M. tuberculosis peptides in adjuvant has been shown to be required for efficient Th1 cell recruitment. IL-10 regulates various processes involved in generation of Th1 and Th17 responses. Previous studies have shown IL-10 as a negative regulator of the immune response to primary M. tuberculosis infection, with Il10−/− mice having reduced lung bacterial loads. In this study we show that inhibition of IL-10 signaling during BCG vaccination enhances host-generated Ag-specific IFN-γ and IL-17A responses, and that this regimen gives significantly greater protection against aerogenic M. tuberculosis challenge in both susceptible and relatively resistant strains of mice. In M. tuberculosis-susceptible CBA/J mice, Ab blockade of IL-10R specifically during BCG vaccination resulted in additional protection against M. tuberculosis challenge of &gt;1-log10 compared with equivalent isotype-treated controls. The protection observed following BCG vaccination concurrent with anti–IL-10R mAb treatment was sustained through chronic M. tuberculosis infection and correlated with enhanced lung Th1 and Th17 responses and increased IFN-γ and IL-17A production by γδ T cells and an innate-like Thy1.2+CD3− lymphoid population. We show that IL-10 inhibits optimal BCG-elicited protection, therefore suggesting that antagonists of IL-10 may be of great benefit as adjuvants in preventive vaccination against tuberculosis.

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Tài liệu tham khảo

World Health Organization. 2011. Global Tuberculosis Control 2011. World Health Organization, Geneva, Switzerland. Available at: http://www.who.int/tb/publications/global_report/en/.

Dorman, 2007, From magic bullets back to the magic mountain: the rise of extensively drug-resistant tuberculosis., Nat. Med., 13, 295, 10.1038/nm0307-295

Kaufmann, 2010, Future vaccination strategies against tuberculosis: thinking outside the box., Immunity, 33, 567, 10.1016/j.immuni.2010.09.015

Fine, 1995, Variation in protection by BCG: implications of and for heterologous immunity., Lancet, 346, 1339, 10.1016/S0140-6736(95)92348-9

Young, 2008, Confronting the scientific obstacles to global control of tuberculosis., J. Clin. Invest., 118, 1255, 10.1172/JCI34614

Cooper, 2009, Cell-mediated immune responses in tuberculosis., Annu. Rev. Immunol., 27, 393, 10.1146/annurev.immunol.021908.132703

Dye, 1999, Consensus statement. Global burden of tuberculosis: estimated incidence, prevalence, and mortality by country. WHO Global Surveillance and Monitoring Project., JAMA, 282, 677, 10.1001/jama.282.7.677

Barry, 2009, The spectrum of latent tuberculosis: rethinking the biology and intervention strategies., Nat. Rev. Microbiol., 7, 845, 10.1038/nrmicro2236

Keane, 2001, Tuberculosis associated with infliximab, a tumor necrosis factor α-neutralizing agent., N. Engl. J. Med., 345, 1098, 10.1056/NEJMoa011110

Flynn, 1995, Tumor necrosis factor-α is required in the protective immune response against Mycobacterium tuberculosis in mice., Immunity, 2, 561, 10.1016/1074-7613(95)90001-2

Cooper, 1993, Disseminated tuberculosis in interferon γ gene-disrupted mice., J. Exp. Med., 178, 2243, 10.1084/jem.178.6.2243

Flynn, 1993, An essential role for interferon γ in resistance to Mycobacterium tuberculosis infection., J. Exp. Med., 178, 2249, 10.1084/jem.178.6.2249

Casanova, 2002, Genetic dissection of immunity to mycobacteria: the human model., Annu. Rev. Immunol., 20, 581, 10.1146/annurev.immunol.20.081501.125851

Khader, 2006, Interleukin 12p40 is required for dendritic cell migration and T cell priming after Mycobacterium tuberculosis infection., J. Exp. Med., 203, 1805, 10.1084/jem.20052545

Cooper, 2007, Interleukin-12 and tuberculosis: an old story revisited., Curr. Opin. Immunol., 19, 441, 10.1016/j.coi.2007.07.004

Fremond, 2007, IL-1 receptor-mediated signal is an essential component of MyD88-dependent innate response to Mycobacterium tuberculosis infection., J. Immunol., 179, 1178, 10.4049/jimmunol.179.2.1178

Mayer-Barber, 2010, Caspase-1 independent IL-1β production is critical for host resistance to mycobacterium tuberculosis and does not require TLR signaling in vivo., J. Immunol., 184, 3326, 10.4049/jimmunol.0904189

Mayer-Barber, 2011, Innate and adaptive interferons suppress IL-1α and IL-1β production by distinct pulmonary myeloid subsets during Mycobacterium tuberculosis infection., Immunity, 35, 1023, 10.1016/j.immuni.2011.12.002

Jung, 2005, Properties and protective value of the secondary versus primary T helper type 1 response to airborne Mycobacterium tuberculosis infection in mice., J. Exp. Med., 201, 1915, 10.1084/jem.20050265

Jung, 2008, “Immunization” against airborne tuberculosis by an earlier primary response to a concurrent intravenous infection., Immunology, 124, 514, 10.1111/j.1365-2567.2007.02803.x

Wolf, 2008, Initiation of the adaptive immune response to Mycobacterium tuberculosis depends on antigen production in the local lymph node, not the lungs., J. Exp. Med., 205, 105, 10.1084/jem.20071367

Reiley, 2008, ESAT-6-specific CD4 T cell responses to aerosol Mycobacterium tuberculosis infection are initiated in the mediastinal lymph nodes., Proc. Natl. Acad. Sci. USA, 105, 10961, 10.1073/pnas.0801496105

Khader, 2007, IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge., Nat. Immunol., 8, 369, 10.1038/ni1449

Gopal, 2012, IL-23-dependent IL-17 drives Th1-cell responses following Mycobacterium bovis BCG vaccination., Eur. J. Immunol., 42, 364, 10.1002/eji.201141569

Cruz, 2010, Pathological role of interleukin 17 in mice subjected to repeated BCG vaccination after infection with Mycobacterium tuberculosis, J. Exp. Med., 207, 1609, 10.1084/jem.20100265

Torrado, 2010, IL-17 and Th17 cells in tuberculosis., Cytokine Growth Factor Rev., 21, 455, 10.1016/j.cytogfr.2010.10.004

Cooper, 2010, Editorial: be careful what you ask for: is the presence of IL-17 indicative of immunity?, J. Leukoc. Biol., 88, 221, 10.1189/jlb.0310146

Moore, 2001, Interleukin-10 and the interleukin-10 receptor., Annu. Rev. Immunol., 19, 683, 10.1146/annurev.immunol.19.1.683

Belkaid, 2001, The role of interleukin (IL)-10 in the persistence of Leishmania major in the skin after healing and the therapeutic potential of anti-IL-10 receptor antibody for sterile cure., J. Exp. Med., 194, 1497, 10.1084/jem.194.10.1497

Murray, 2002, Interleukin-10 (IL-10) in experimental visceral leishmaniasis and IL-10 receptor blockade as immunotherapy., Infect. Immun., 70, 6284, 10.1128/IAI.70.11.6284-6293.2002

Brooks, 2006, Interleukin-10 determines viral clearance or persistence in vivo., Nat. Med., 12, 1301, 10.1038/nm1492

Ejrnaes, 2006, Resolution of a chronic viral infection after interleukin-10 receptor blockade., J. Exp. Med., 203, 2461, 10.1084/jem.20061462

Roach, 2001, Endogenous inhibition of antimycobacterial immunity by IL-10 varies between mycobacterial species., Scand. J. Immunol., 54, 163, 10.1046/j.1365-3083.2001.00952.x

Turner, 2002, In vivo IL-10 production reactivates chronic pulmonary tuberculosis in C57BL/6 mice., J. Immunol., 169, 6343, 10.4049/jimmunol.169.11.6343

Beamer, 2008, Interleukin-10 promotes Mycobacterium tuberculosis disease progression in CBA/J mice., J. Immunol., 181, 5545, 10.4049/jimmunol.181.8.5545

Redford, 2010, Enhanced protection to Mycobacterium tuberculosis infection in IL-10-deficient mice is accompanied by early and enhanced Th1 responses in the lung., Eur. J. Immunol., 40, 2200, 10.1002/eji.201040433

Redford, 2011, The role of IL-10 in immune regulation during M. tuberculosis infection., Mucosal Immunol., 4, 261, 10.1038/mi.2011.7

Castro, 2000, Anti-interleukin 10 receptor monoclonal antibody is an adjuvant for T helper cell type 1 responses to soluble antigen only in the presence of lipopolysaccharide., J. Exp. Med., 192, 1529, 10.1084/jem.192.10.1529

Darrah, 2010, IL-10 production differentially influences the magnitude, quality, and protective capacity of Th1 responses depending on the vaccine platform., J. Exp. Med., 207, 1421, 10.1084/jem.20092532

Roberts, 2005, Interleukin-4 (IL-4) and IL-10 collude in vaccine failure for novel exacerbatory antigens in murine Leishmania major infection., Infect. Immun., 73, 7620, 10.1128/IAI.73.11.7620-7628.2005

Tabbara, 2005, Conditions influencing the efficacy of vaccination with live organisms against Leishmania major infection., Infect. Immun., 73, 4714, 10.1128/IAI.73.8.4714-4722.2005

Stober, 2005, IL-10 from regulatory T cells determines vaccine efficacy in murine Leishmania major infection., J. Immunol., 175, 2517, 10.4049/jimmunol.175.4.2517

Brooks, 2008, IL-10 blockade facilitates DNA vaccine-induced T cell responses and enhances clearance of persistent virus infection., J. Exp. Med., 205, 533, 10.1084/jem.20071948

Silva, 2001, Blocking the receptor for IL-10 improves antimycobacterial chemotherapy and vaccination., J. Immunol., 167, 1535, 10.4049/jimmunol.167.3.1535

Murray, 1999, Increased antimycobacterial immunity in interleukin-10-deficient mice., Infect. Immun., 67, 3087, 10.1128/IAI.67.6.3087-3095.1999

O’Farrell, 1998, IL-10 inhibits macrophage activation and proliferation by distinct signaling mechanisms: evidence for Stat3-dependent and -independent pathways., EMBO J., 17, 1006, 10.1093/emboj/17.4.1006

Lalor, 2011, BCG vaccination induces different cytokine profiles following infant BCG vaccination in the UK and Malawi., J. Infect. Dis., 204, 1075, 10.1093/infdis/jir515

Soares, 2008, Bacillus Calmette-Guérin vaccination of human newborns induces T cells with complex cytokine and phenotypic profiles., J. Immunol., 180, 3569, 10.4049/jimmunol.180.5.3569

Zhang, 2009, Coactivation of Syk kinase and MyD88 adaptor protein pathways by bacteria promotes regulatory properties of neutrophils., Immunity, 31, 761, 10.1016/j.immuni.2009.09.016

Jacobs, 2000, Increased resistance to mycobacterial infection in the absence of interleukin-10., Immunology, 100, 494, 10.1046/j.1365-2567.2000.00053.x

Flynn, 2001, Immunology of tuberculosis., Annu. Rev. Immunol., 19, 93, 10.1146/annurev.immunol.19.1.93

Apt, 2009, Man and mouse TB: contradictions and solutions., Tuberculosis (Edinb.), 89, 195, 10.1016/j.tube.2009.02.002

North, 2004, Immunity to tuberculosis., Annu. Rev. Immunol., 22, 599, 10.1146/annurev.immunol.22.012703.104635

Medina, 1998, Resistance ranking of some common inbred mouse strains to Mycobacterium tuberculosis and relationship to major histocompatibility complex haplotype and Nramp1 genotype., Immunology, 93, 270, 10.1046/j.1365-2567.1998.00419.x

Marquis, 2008, Fibrotic response as a distinguishing feature of resistance and susceptibility to pulmonary infection with Mycobacterium tuberculosis in mice., Infect. Immun., 76, 78, 10.1128/IAI.00369-07

Lockhart, 2006, IL-17 production is dominated by γδ T cells rather than CD4 T cells during Mycobacterium tuberculosis infection., J. Immunol., 177, 4662, 10.4049/jimmunol.177.7.4662

Okamoto Yoshida, 2010, Essential role of IL-17A in the formation of a mycobacterial infection-induced granuloma in the lung., J. Immunol., 184, 4414, 10.4049/jimmunol.0903332

Wilson, 2011, IL-10 blocks the development of resistance to re-infection with Schistosoma mansoni., PLoS Pathog., 7, e1002171, 10.1371/journal.ppat.1002171

Mittrücker, 2007, Poor correlation between BCG vaccination-induced T cell responses and protection against tuberculosis., Proc. Natl. Acad. Sci. USA, 104, 12434, 10.1073/pnas.0703510104

Majlessi, 2006, An increase in antimycobacterial Th1-cell responses by prime-boost protocols of immunization does not enhance protection against tuberculosis., Infect. Immun., 74, 2128, 10.1128/IAI.74.4.2128-2137.2006

Darrah, 2007, Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major, Nat. Med., 13, 843, 10.1038/nm1592

Huber, 2011, Th17 cells express interleukin-10 receptor and are controlled by Foxp3− and Foxp3+ regulatory CD4+ T cells in an interleukin-10-dependent manner., Immunity, 34, 554, 10.1016/j.immuni.2011.01.020

Chaudhry, 2011, Interleukin-10 signaling in regulatory T cells is required for suppression of Th17 cell-mediated inflammation., Immunity, 34, 566, 10.1016/j.immuni.2011.03.018

Spits, 2011, The expanding family of innate lymphoid cells: regulators and effectors of immunity and tissue remodeling., Nat. Immunol., 12, 21, 10.1038/ni.1962

Monticelli, 2011, Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus., Nat. Immunol., 12, 1045, 10.1038/ni.2131

Gonzalez-Juarrero, 2001, Temporal and spatial arrangement of lymphocytes within lung granulomas induced by aerosol infection with Mycobacterium tuberculosis, Infect. Immun., 69, 1722, 10.1128/IAI.69.3.1722-1728.2001

Miossec, 2009, Interleukin-17 and type 17 helper T cells., N. Engl. J. Med., 361, 888, 10.1056/NEJMra0707449

Lowe, 2012, Neutrophils in tuberculosis: friend or foe?, Trends Immunol., 33, 14, 10.1016/j.it.2011.10.003

Nandi, 2011, Regulation of neutrophils by interferon-γ limits lung inflammation during tuberculosis infection., J. Exp. Med., 208, 2251, 10.1084/jem.20110919