Considering the ‘Alternatives’ for Next-Generation Anti-Staphylococcus aureus Vaccine Development
Tài liệu tham khảo
Laupland, 2013, The changing epidemiology of Staphylococcus aureus bloodstream infection: a multinational population-based surveillance study, Clin. Microbiol. Infect., 19, 465, 10.1111/j.1469-0691.2012.03903.x
Williamson, 2013, Incidence, trends and demographics of Staphylococcus aureus infections in Auckland, New Zealand, 2001–2011, BMC Infect. Dis., 13, 569, 10.1186/1471-2334-13-569
Hassoun, 2017, Incidence, prevalence, and management of MRSA bacteremia across patient populations—a review of recent developments in MRSA management and treatment, Crit. Care, 21, 211, 10.1186/s13054-017-1801-3
Andreassen, 2017, The impact of methicillin-resistant S. aureus on length of stay, readmissions and costs: a register based case-control study of patients hospitalized in Norway, Antimicrob. Resist. Infect. Control, 6, 74, 10.1186/s13756-017-0232-x
Lee, 2018, Methicillin-resistant Staphylococcus aureus, Nat. Rev. Dis. Primers, 4, 18033, 10.1038/nrdp.2018.33
Acree, 2017, S. aureus infections in Chicago, 2006–2014: increase in CA MSSA and decrease in MRSA incidence, Infect. Control Hosp. Epidemiol., 38, 1226, 10.1017/ice.2017.177
Crowley, 2017, UK Renal Registry 19th Annual Report: Chapter 10. Epidemiology of reported infections in patients receiving dialysis in England between January 2015 and December 2015: a joint report from Public Health England and the UK Renal Registry, Nephron, 137, 251, 10.1159/000481372
Delorme, 2017, A longitudinal analysis of methicillin-resistant and sensitive Staphylococcus aureus incidence in respect to specimen source, patient location, and temperature variation, Int. J. Infect. Dis., 54, 50, 10.1016/j.ijid.2016.11.405
Fowler, 2014, Where does a Staphylococcus aureus vaccine stand?, Clin. Microbiol. Infect., 20, 66, 10.1111/1469-0691.12570
Giersing, 2016, Status of vaccine research and development of vaccines for Staphylococcus aureus, Vaccine, 34, 2962, 10.1016/j.vaccine.2016.03.110
Bagnoli, 2012, Inferring reasons for the failure of Staphylococcus aureus vaccines in clinical trials, Front. Cell. Infect. Microbiol., 2, 16, 10.3389/fcimb.2012.00016
Krishna, 2012, Innate and adaptive immune responses against Staphylococcus aureus skin infections, Semin. Immunopathol., 34, 261, 10.1007/s00281-011-0292-6
Fattom, 2015, Efficacy profile of a bivalent Staphylococcus aureus glycoconjugated vaccine in adults on hemodialysis: Phase III randomized study, Hum. Vaccin. Immunother., 11, 632, 10.4161/hv.34414
Fowler, 2013, Effect of an investigational vaccine for preventing Staphylococcus aureus infections after cardiothoracic surgery: a randomized trial, JAMA, 309, 1368, 10.1001/jama.2013.3010
McNeely, 2014, Mortality among recipients of the Merck V710 Staphylococcus aureus vaccine after postoperative S. aureus infections: an analysis of possible contributing host factors, Hum. Vaccin. Immunother., 10, 3513, 10.4161/hv.34407
Levy, 2015, Safety and immunogenicity of an investigational 4-component Staphylococcus aureus vaccine with or without AS03B adjuvant: results of a randomized phase I trial, Hum. Vaccin. Immunother., 11, 620, 10.1080/21645515.2015.1011021
Begier, 2017, SA4Ag, a 4-antigen Staphylococcus aureus vaccine, rapidly induces high levels of bacteria-killing antibodies, Vaccine, 35, 1132, 10.1016/j.vaccine.2017.01.024
Spellberg, 2008, The antifungal vaccine derived from the recombinant N terminus of Als3p protects mice against the bacterium Staphylococcus aureus, Infect. Immun., 76, 4574, 10.1128/IAI.00700-08
Misstear, 2014, Targeted nasal vaccination provides antibody-independent protection against Staphylococcus aureus, J. Infect. Dis., 209, 1479, 10.1093/infdis/jit636
von Kockritz-Blickwede, 2008, Immunological mechanisms underlying the genetic predisposition to severe Staphylococcus aureus infection in the mouse model, Am. J. Pathol., 173, 1657, 10.2353/ajpath.2008.080337
Wiese, 2013, A nationwide study of comorbidity and risk of reinfection after Staphylococcus aureus bacteraemia, J. Infect., 67, 199, 10.1016/j.jinf.2013.04.018
McDonald, 2012, TH17 deficiency in human disease, J. Allergy Clin. Immunol., 129, 1429, 10.1016/j.jaci.2012.03.034
Joshi, 2012, Immunization with Staphylococcus aureus iron regulated surface determinant B (IsdB) confers protection via Th17/IL17 pathway in a murine sepsis model, Hum. Vaccin. Immunother., 8, 336, 10.4161/hv.18946
Ishigame, 2009, Differential roles of interleukin-17A and -17F in host defense against mucoepithelial bacterial infection and allergic responses, Immunity, 30, 108, 10.1016/j.immuni.2008.11.009
Holley, 2012, Th1 and Th17 cells regulate innate immune responses and bacterial clearance during central nervous system infection, J. Immunol., 188, 1360, 10.4049/jimmunol.1101660
Lin, 2009, Th1-Th17 cells mediate protective adaptive immunity against Staphylococcus aureus and Candida albicans infection in mice, PLoS Pathog., 5, 10.1371/journal.ppat.1000703
Cho, 2010, IL-17 is essential for host defense against cutaneous Staphylococcus aureus infection in mice, J. Clin. Invest., 120, 1762, 10.1172/JCI40891
Zhang, 2018, Protection against Staphylococcus aureus colonization and infection by B- and T-cell-mediated mechanisms, mBio, 9, 10.1128/mBio.01949-18
Cox, 2011, Cytokines and the inception of CD8 T cell responses, Trends Immunol., 32, 180, 10.1016/j.it.2011.01.004
Cruz-Adalia, 2017, Conventional CD4+ T cells present bacterial antigens to induce cytotoxic and memory CD8+ T cell responses, Nat. Commun., 8, 1591, 10.1038/s41467-017-01661-7
Lin, 2015, CD8 T cells and Mycobacterium tuberculosis infection, Semin. Immunopathol., 37, 239, 10.1007/s00281-015-0490-8
Behar, 2013, Antigen-specific CD8(+) T cells and protective immunity to tuberculosis, Adv. Exp. Med. Biol., 783, 141, 10.1007/978-1-4614-6111-1_8
Lee, 2012, MHC class-I-restricted CD8 T cells play a protective role during primary Salmonella infection, Immunol. Lett., 148, 138, 10.1016/j.imlet.2012.10.009
Rollin, 2017, Intracellular survival of Staphylococcus aureus in endothelial cells: a matter of growth or persistence, Front. Microbiol., 8, 1354, 10.3389/fmicb.2017.01354
Lacoma, 2017, Investigating intracellular persistence of Staphylococcus aureus within a murine alveolar macrophage cell line, Virulence, 8, 1761, 10.1080/21505594.2017.1361089
Brown, 2015, Memory Th1 cells are protective in invasive Staphylococcus aureus infection, PLoS Pathog., 11, 10.1371/journal.ppat.1005226
Uebele, 2017, Antigen delivery to dendritic cells shapes human CD4(+) and CD8(+) T cell memory responses to Staphylococcus aureus, PLoS Pathog., 13, 10.1371/journal.ppat.1006387
Xiao, 2017, Mucosal-associated invariant T cells: new insights into antigen recognition and activation, Front. Immunol., 8, 1540, 10.3389/fimmu.2017.01540
McCarthy, 2018, Human γδ T-cell control of mucosal immunity and inflammation, Front. Immunol., 9, 985, 10.3389/fimmu.2018.00985
Triggianese, 2016, Evidence of IL-17 producing innate lymphoid cells in peripheral blood from patients with enteropathic spondyloarthritis, Clin. Exp. Rheumatol., 34, 1085
Nielsen, 2017, γδ T cells in homeostasis and host defence of epithelial barrier tissues, Nat. Rev. Immunol., 17, 733, 10.1038/nri.2017.101
Lalor, 2016, Memory γδ T cells-newly appreciated protagonists in infection and immunity, Trends Immunol., 37, 690, 10.1016/j.it.2016.07.006
Sutton, 2009, Interleukin-1 and IL-23 induce innate IL-17 production from gammadelta T cells, amplifying Th17 responses and autoimmunity, Immunity, 31, 331, 10.1016/j.immuni.2009.08.001
Martin, 2009, Interleukin-17-producing gammadelta T cells selectively expand in response to pathogen products and environmental signals, Immunity, 31, 321, 10.1016/j.immuni.2009.06.020
Harly, 2012, Key implication of CD277/butyrophilin-3 (BTN3A) in cellular stress sensing by a major human γδ T-cell subset, Blood, 120, 2269, 10.1182/blood-2012-05-430470
Tyler, 2015, Human Vγ9/Vδ2 T cells: innate adaptors of the immune system, Cell. Immunol., 296, 10, 10.1016/j.cellimm.2015.01.008
Gu, 2015, Sensing of pyrophosphate metabolites by Vγ9Vδ2 T cells, Front. Immunol., 5, 688, 10.3389/fimmu.2014.00688
Misiak, 2017, IL-17-producing innate and pathogen-specific tissue resident memory γδ T cells expand in the lungs of Bordetella pertussis-infected mice, J. Immunol., 198, 363, 10.4049/jimmunol.1601024
Simonian, 2009, IL-17A-expressing T cells are essential for bacterial clearance in a murine model of hypersensitivity pneumonitis, J. Immunol., 182, 6540, 10.4049/jimmunol.0900013
Sun, 2018, Vγ4+ T cells: a novel IL-17-producing γδ T subsets during the early phase of chlamydial airway infection in mice, Mediators Inflamm., 2018, 10.1155/2018/6265746
Dalton, 2004, Fas-Fas ligand interactions are essential for the binding to and killing of activated macrophages by γδ T cells, J. Immunol., 173, 3660, 10.4049/jimmunol.173.6.3660
Tuero, 2016, Mucosal and systemic γδ+ T cells associated with control of simian immunodeficiency virus infection, J. Immunol., 197, 4686, 10.4049/jimmunol.1600579
Hess, 2003, Intracellular survival of Staphylococcus aureus within cultured enterocytes, J. Surg. Res., 114, 42, 10.1016/S0022-4804(03)00314-7
Spencer, 2013, Granzyme A produced by γ9δ2 T cells induces human macrophages to inhibit growth of an intracellular pathogen, PLoS Pathog., 9, 10.1371/journal.ppat.1003119
Peng, 2008, Interleukin 17-producing γδ T cells increased in patients with active pulmonary tuberculosis, Cell. Mol. Immunol., 5, 203, 10.1038/cmi.2008.25
Ma, 2008, Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3, J. Exp. Med., 205, 1551, 10.1084/jem.20080218
Maher, 2013, Nlrp-3-driven interleukin 17 production by γδT cells controls infection outcomes during Staphylococcus aureus surgical site infection, Infect. Immun., 81, 4478, 10.1128/IAI.01026-13
Murphy, 2014, Staphylococcus aureus infection of mice expands a population of memory γδ T cells that are protective against subsequent infection, J. Immunol., 192, 3697, 10.4049/jimmunol.1303420
Cheng, 2012, Role of gamma-delta T cells in host response against Staphylococcus aureus-induced pneumonia, BMC Immunol., 13, 38, 10.1186/1471-2172-13-38
Dillen, 2018, Clonally expanded γδ T cells protect against Staphylococcus aureus skin reinfection, J. Clin. Invest., 128, 1026, 10.1172/JCI96481
Wang, 2001, Antibacterial effect of human Vγ2Vδ2 T cells in vivo, J. Clin. Invest., 108, 1349, 10.1172/JCI200113584
Romagnoli, 2016, IL-17A–producing resident memory γδ T cells orchestrate the innate immune response to secondary oral Listeria monocytogenes infection, Proc. Natl. Acad. Sci. U. S. A., 113, 8502, 10.1073/pnas.1600713113
Sun, 2009, Adaptive immune features of natural killer cells, Nature, 457, 557, 10.1038/nature07665
Sheridan, 2013, γδ T cells exhibit multifunctional and protective memory in intestinal tissues, Immunity, 39, 184, 10.1016/j.immuni.2013.06.015
Godfrey, 2018, Unconventional T cell targets for cancer immunotherapy, Immunity, 48, 453, 10.1016/j.immuni.2018.03.009
Wilhelm, 2014, Successful adoptive transfer and in vivo expansion of haploidentical γδ T cells, J. Transl. Med., 12, 45, 10.1186/1479-5876-12-45
Qaqish, 2017, Adoptive transfer of phosphoantigen-specific γδ T cell subset attenuates Mycobacterium tuberculosis infection in nonhuman primates, J. Immunol., 198, 4753, 10.4049/jimmunol.1602019
Markovits, 2017, Immune-mediated syndromes following intravenous bisphosphonate therapy, Inflammopharmacology, 25, 665, 10.1007/s10787-017-0365-9
Spits, 2013, Innate lymphoid cells—a proposal for uniform nomenclature, Nat. Rev. Immunol., 13, 145, 10.1038/nri3365
Cherrier, 2018, Innate lymphoid cell development: a T cell perspective, Immunity, 48, 1091, 10.1016/j.immuni.2018.05.010
Mortha, 2018, Cytokine Networks between Innate Lymphoid Cells and Myeloid Cells, Frontiers in Immunology, 9
Sonnenberg, 2012, Innate lymphoid cell interactions with microbiota: implications for intestinal health and disease, Immunity, 37, 601, 10.1016/j.immuni.2012.10.003
Hepworth, 2013, Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria, Nature, 498, 113, 10.1038/nature12240
Klose, 2013, A T-bet gradient controls the fate and function of CCR6-RORγt+ innate lymphoid cells, Nature, 494, 261, 10.1038/nature11813
Simoni, 2017, Human innate lymphoid cell subsets possess tissue-type based heterogeneity in phenotype and frequency, Immunity, 46, 148, 10.1016/j.immuni.2016.11.005
Kim, 2016, Migration and tissue tropism of innate lymphoid cells, Trends Immunol., 37, 68, 10.1016/j.it.2015.11.003
Klose, 2014, Differentiation of type 1 ILCs from a common progenitor to all helper-like innate lymphoid cell lineages, Cell, 157, 340, 10.1016/j.cell.2014.03.030
Abt, 2015, Innate immune defenses mediated by two ILC subsets are critical for protection against acute Clostridium difficile infection, Cell Host Microbe, 18, 27, 10.1016/j.chom.2015.06.011
Goto, 2014, Innate lymphoid cells regulate intestinal epithelial cell glycosylation, Science, 345, 10.1126/science.1254009
Hasegawa, 2014, Interleukin-22 regulates the complement system to promote resistance against pathobionts after pathogen-induced intestinal damage, Immunity, 41, 620, 10.1016/j.immuni.2014.09.010
Satoh-Takayama, 2008, Microbial flora drives interleukin 22 production in intestinal NKp46+ cells that provide innate mucosal immune defense, Immunity, 29, 958, 10.1016/j.immuni.2008.11.001
Van Maele, 2014, Activation of type 3 innate lymphoid cells and interleukin 22 secretion in the lungs during Streptococcus pneumoniae infection, J. Infect. Dis., 210, 493, 10.1093/infdis/jiu106
Yang, 2015, Type 1 innate lymphoid cells contribute to the pathogenesis of chronic hepatitis B, Innate Immun., 21, 665, 10.1177/1753425915586074
Kramer, 2017, Compartment-specific distribution of human intestinal innate lymphoid cells is altered in HIV patients under effective therapy, PLoS Pathog., 13, 10.1371/journal.ppat.1006373
Rak, 2016, IL-33-dependent group 2 innate lymphoid cells promote cutaneous wound healing, J. Invest. Dermatol., 136, 487, 10.1038/JID.2015.406
Yin, 2013, IL-33 promotes Staphylococcus aureus-infected wound healing in mice, Int. Immunopharmacol., 17, 432, 10.1016/j.intimp.2013.07.008
Gauguet, 2015, Intestinal microbiota of mice influences resistance to Staphylococcus aureus pneumonia, Infect. Immun., 83, 4003, 10.1128/IAI.00037-15
Mulcahy, 2016, Interleukin-22 regulates antimicrobial peptide expression and keratinocyte differentiation to control Staphylococcus aureus colonization of the nasal mucosa, Mucosal Immunol., 9, 1429, 10.1038/mi.2016.24
McKenzie, 2006, Perforin and Fas induced by IFNgamma and TNFalpha mediate beta cell death by OT-I CTL, Int. Immunol., 18, 837, 10.1093/intimm/dxl020
van de Pavert, 2014, Maternal retinoids control type 3 innate lymphoid cells and set the offspring immunity, Nature, 508, 123, 10.1038/nature13158
Perry, 2012, Inhibition of LTi cell development by CD25 blockade is associated with decreased intrathecal inflammation in multiple sclerosis, Sci. Transl. Med., 4, 10.1126/scitranslmed.3004140
Corren, 2011, Lebrikizumab treatment in adults with asthma, N. Engl. J. Med., 365, 1088, 10.1056/NEJMoa1106469
Pavord, 2012, Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial, Lancet, 380, 651, 10.1016/S0140-6736(12)60988-X
Eberl, 2015, Innate lymphoid cells: a new paradigm in immunology, Science, 348, 10.1126/science.aaa6566
Gherardin, 2018, Human blood MAIT cell subsets defined using MR1 tetramers, Immunol. Cell Biol., 96, 507, 10.1111/imcb.12021
Treiner, 2005, Mucosal-associated invariant T (MAIT) cells: an evolutionarily conserved T cell subset, Microbes Infect., 7, 552, 10.1016/j.micinf.2004.12.013
Tsukamoto, 2013, Exceptionally high conservation of the MHC class I-related gene, MR1, among mammals, Immunogenetics, 65, 115, 10.1007/s00251-012-0666-5
Mori, 2016, The immunology of CD1- and MR1-restricted T cells, Annu. Rev. Immunol., 34, 479, 10.1146/annurev-immunol-032414-112008
Kjer-Nielsen, 2012, MR1 presents microbial vitamin B metabolites to MAIT cells, Nature, 491, 717, 10.1038/nature11605
Ussher, 2014, CD161++ CD8+ T cells, including the MAIT cell subset, are specifically activated by IL-12+IL-18 in a TCR-independent manner, Eur. J. Immunol., 44, 195, 10.1002/eji.201343509
Loh, 2016, Human mucosal-associated invariant T cells contribute to antiviral influenza immunity via IL-18-dependent activation, Proc. Natl. Acad. Sci. U. S. A., 113, 10133, 10.1073/pnas.1610750113
Jiang, 2016, Enhanced immune response of MAIT cells in tuberculous pleural effusions depends on cytokine signaling, Sci. Rep., 6
Chiba, 2018, Mucosal-associated invariant T cells in autoimmune diseases, Front. Immunol., 9, 1333, 10.3389/fimmu.2018.01333
Chiba, 2017, Activation status of mucosal-associated invariant T cells reflects disease activity and pathology of systemic lupus erythematosus, Arthritis Res. Ther., 19, 58, 10.1186/s13075-017-1257-5
Meierovics, 2013, MAIT cells are critical for optimal mucosal immune responses during in vivo pulmonary bacterial infection, Proc. Natl. Acad. Sci. U. S. A., 110, E3119, 10.1073/pnas.1302799110
Chua, 2012, Polyclonal mucosa-associated invariant T cells have unique innate functions in bacterial infection, Infect. Immun., 80, 3256, 10.1128/IAI.00279-12
Georgel, 2011, The non-conventional MHC class I MR1 molecule controls infection by Klebsiella pneumoniae in mice, Mol. Immunol., 48, 769, 10.1016/j.molimm.2010.12.002
Chen, 2016, Mucosal-associated invariant T-cell activation and accumulation after in vivo infection depends on microbial riboflavin synthesis and co-stimulatory signals, Mucosal Immunol., 10, 58, 10.1038/mi.2016.39
Wang, 2018, MAIT cells protect against pulmonary Legionella longbeachae infection, Nat. Commun., 9
Grimaldi, 2014, Specific MAIT cell behaviour among innate-like T lymphocytes in critically ill patients with severe infections, Intensive Care Med., 40, 192, 10.1007/s00134-013-3163-x
Wong, 2014, Low levels of peripheral CD161++CD8+ mucosal associated invariant T (MAIT) cells are found in HIV and HIV/TB co-infection, PLoS One, 8
Cui, 2015, Mucosal-associated invariant T cell–rich congenic mouse strain allows functional evaluation, J. Clin. Invest., 125, 4171, 10.1172/JCI82424
Le Bourhis, 2010, Antimicrobial activity of mucosal-associated invariant T cells, Nat. Immunol., 11, 701, 10.1038/ni.1890
Gold, 2010, Human mucosal associated invariant T cells detect bacterially infected cells, PLoS Biol., 8, 10.1371/journal.pbio.1000407
Sandberg, 2017, Bacterial deception of MAIT cells in a cloud of superantigen and cytokines, PLoS Biol., 15, 10.1371/journal.pbio.2003167
Le Bourhis, 2013, MAIT cells detect and efficiently lyse bacterially-infected epithelial cells, PLoS Pathog., 9, 10.1371/journal.ppat.1003681
Kurioka, 2014, MAIT cells are licensed through granzyme exchange to kill bacterially sensitized targets, Mucosal Immunol., 8, 429, 10.1038/mi.2014.81
Fernandez, 2015, MAIT cells are depleted early but retain functional cytokine expression in HIV infection, Immunol. Cell Biol., 93, 177, 10.1038/icb.2014.91
Wakao, 2017, Mucosal-associated invariant T cells in regenerative medicine, Front. Immunol., 8, 1711, 10.3389/fimmu.2017.01711
Howson, 2018, MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A, Nat. Commun., 9, 10.1038/s41467-017-02540-x
Greenberg, 2018, Distinct T-helper cell responses to Staphylococcus aureus bacteremia reflect immunologic comorbidities and correlate with mortality, Crit. Care, 22, 107, 10.1186/s13054-018-2025-x