Cited by 529

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Regulation of the host immune system by helminth parasites

Maizels, Rick M., McSorley, Henry J.·2016·Journal of Allergy and Clinical Immunology

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.jaci.2016.07.007

Cites

7 of 7 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig 1 Immune system–parasite interactions during helminth infections. A, Blockade of innate sensing and alarmin production, such as inhibiting Toll-like receptor (TLR) responses of dendritic cells, thereby impairing inflammatory TH1/TH17 development, and abrogating epithelial cell production of IL-33, thereby pre-empting the type 2 response. ILC2, Type 2 innate lymphoid cell. B, Modulation of the adaptive immune response, promoting Treg cell differentiation either directly through production of TGF-β–like mimics (TGM) or indirectly by inducing host TGF-β and retinoic acid (RA) from DCs and macrophages. C, Modification of bystander immune responses in the infected host.
Fig 1 Immune system–parasite interactions during helminth infections. A, Blockade of innate sensing and alarmin production, such as inhibiting Toll-like receptor (TLR) responses of dendritic cells, thereby impairing inflammatory TH1/TH17 development, and abrogating epithelial cell production of IL-33, thereby pre-empting the type 2 response. ILC2, Type 2 innate lymphoid cell. B, Modulation of the adaptive immune response, promoting Treg cell differentiation either directly through production of TGF-β–like mimics (TGM) or indirectly by inducing host TGF-β and retinoic acid (RA) from DCs and macrophages. C, Modification of bystander immune responses in the infected host.CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Research works printed but not linked: 159

  1. McSorley, 2012, Helminth infections and host immune regulation, Clin Microbial Rev, 25, 585, 10.1128/CMR.05040-11 · DOI · Paper page
  2. Johnston, 2014, Helminths and immunological tolerance, Transplantation, 97, 127, 10.1097/TP.0b013e3182a53f59 · DOI
  3. Mishra, 2014, Systemic impact of intestinal helminth infections, Mucosal Immunol, 7, 753, 10.1038/mi.2014.23 · DOI
  4. Hotez, 2008, Helminth infections: the great neglected tropical diseases, J Clin Invest, 118, 1311, 10.1172/JCI34261 · DOI
  5. Nutman, 1987, Parasite-specific anergy in human filariasis. Insights after analysis of parasite antigen-driven lymphokine production, J Clin Invest, 79, 1516, 10.1172/JCI112982 · DOI
  6. Maizels, 1991, Immunological tolerance: the key feature in human filariasis?, Parasitol Today, 7, 271, 10.1016/0169-4758(91)90093-4 · DOI
  7. King, 1992, Immunologic tolerance in lymphatic filariasis. Diminished parasite-specific T and B cell lymphocyte precursor frequency in the microfilaremic state, J Clin Invest, 89, 1403, 10.1172/JCI115729 · DOI
  8. Piessens, 1980, Immune responses in human infections with Brugia malayi. Specific cellular unresponsiveness to filarial antigens, J Clin Invest, 65, 172, 10.1172/JCI109648 · DOI
  9. Colley, 1986, Immune responses during human schistosomiasis. XII. Differential responsiveness in patients with hepatosplenic disease, Am J Trop Med Hyg, 35, 793, 10.4269/ajtmh.1986.35.793 · DOI
  10. Sartono, 1995, Elevated cellular responses and interferon-γ release after long-term diethylcarbamazine treatment of patients with human lymphatic filariasis, J Infect Dis, 171, 1683, 10.1093/infdis/171.6.1683 · DOI
  11. Grogan, 1996, Elevated proliferation and interleukin-4 release from CD4+ cells after chemotherapy in human Schistosoma haematobium infection, Eur J Immunol, 26, 1365, 10.1002/eji.1830260628 · DOI
  12. Mahanty, 1996, High levels of spontaneous and parasite antigen-driven interleukin-10 production are associated with antigen-specific hyporesponsiveness in human lymphatic filariasis, J Infect Dis, 173, 769, 10.1093/infdis/173.3.769 · DOI · Paper page
  13. Doetze, 2000, Antigen-specific cellular hyporesponsiveness in a chronic human helminth infection is mediated by Th3/Tr1-type cytokines IL-10 and transforming growth factor-b but not by a Th1 to Th2 shift, Int Immunol, 12, 623, 10.1093/intimm/12.5.623 · DOI · Paper page
  14. Mbow, 2013, T-helper 17 cells are associated with pathology in human schistosomiasis, J Infect Dis, 207, 186, 10.1093/infdis/jis654 · DOI
  15. Babu, 2009, Filarial lymphedema is characterized by antigen-specific Th1 and Th17 proinflammatory responses and a lack of regulatory T cells, PLoS Negl Trop Dis, 3, e420, 10.1371/journal.pntd.0000420 · DOI
  16. Sakaguchi, 2000, Regulatory T cells: key controllers of immunologic self-tolerance, Cell, 101, 455, 10.1016/S0092-8674(00)80856-9 · DOI
  17. Maizels, 2011, Regulatory T cells in infection, Adv Immunol, 112, 73, 10.1016/B978-0-12-387827-4.00003-6 · DOI
  18. Ludwig-Portugall, 2012, TLRs, Treg, and B cells, an interplay of regulation during helminth infection, Front Immunol, 3, 8, 10.3389/fimmu.2012.00008 · DOI
  19. Metenou, 2013, Regulatory T cell subsets in filarial infection and their function, Front Immunol, 4, 305, 10.3389/fimmu.2013.00305 · DOI
  20. Labeaud, 2009, Do antenatal parasite infections devalue childhood vaccination?, PLoS Negl Trop Dis, 3, e442, 10.1371/journal.pntd.0000442 · DOI · Paper page
  21. Salgame, 2013, Effect of helminth-induced immunity on infections with microbial pathogens, Nat Immunol, 14, 1118, 10.1038/ni.2736 · DOI
  22. Hartgers, 2009, Responses to malarial antigens are altered in helminth-infected children, J Infect Dis, 199, 1528, 10.1086/598687 · DOI
  23. Dolo, 2012, Filariasis attenuates anemia and proinflammatory responses associated with clinical malaria: a matched prospective study in children and young adults, PLoS Negl Trop Dis, 6, e1890, 10.1371/journal.pntd.0001890 · DOI
  24. Nash, 2011, Diagnosis and treatment of neurocysticercosis, Nat Rev Neurol, 7, 584, 10.1038/nrneurol.2011.135 · DOI
  25. Verma, 2011, Immune response in symptomatic and asymptomatic neurocysticercosis, Med Microbiol Immunol, 200, 255, 10.1007/s00430-011-0198-x · DOI
  26. Tuero, 2015, A comparative study of peripheral immune responses to Taenia solium in individuals with parenchymal and subarachnoid neurocysticercosis, PLoS Negl Trop Dis, 9, e0004143, 10.1371/journal.pntd.0004143 · DOI
  27. Lammie, 1991, Maternal filarial infection as risk factor for infection in children, Lancet, 337, 1005, 10.1016/0140-6736(91)92661-K · DOI
  28. Steel, 1994, Long-term effect of prenatal exposure to maternal microfilaraemia on immune responsiveness to filarial antigens, Lancet, 343, 890, 10.1016/S0140-6736(94)90009-4 · DOI
  29. Mpairwe, 2014, Pregnancy and helminth infections, Parasite Immunol, 36, 328, 10.1111/pim.12101 · DOI
  30. Straubinger, 2014, Maternal immune response to helminth infection during pregnancy determines offspring susceptibility to allergic airway inflammation, J Allergy Clin Immunol, 134, 1271, 10.1016/j.jaci.2014.05.034 · DOI · Paper page
  31. Weinstock, 2014, Helminth infections decrease host susceptibility to immune-mediated diseases, J Immunol, 193, 3239, 10.4049/jimmunol.1400927 · DOI
  32. Li, 2015, Intestinal helminths regulate lethal acute graft-versus-host disease and preserve the graft-versus-tumor effect in mice, J Immunol, 194, 1011, 10.4049/jimmunol.1303099 · DOI
  33. Finlay, 2014, Induction of regulatory cells by helminth parasites: exploitation for the treatment of inflammatory diseases, Immunol Rev, 259, 206, 10.1111/imr.12164 · DOI
  34. Watanabe, 2007, T regulatory cell levels decrease in people infected with Schistosoma mansoni on effective treatment, Am J Trop Med Hyg, 77, 676, 10.4269/ajtmh.2007.77.676 · DOI
  35. Wammes, 2012, Regulatory T cells in human lymphatic filariasis: stronger functional activity in microfilaremics, PLoS Negl Trop Dis, 6, e1655, 10.1371/journal.pntd.0001655 · DOI
  36. Metenou, 2010, At homeostasis filarial infections have expanded adaptive T regulatory but not classical Th2 cells, J Immunol, 184, 5375, 10.4049/jimmunol.0904067 · DOI
  37. Katawa, 2015, Hyperreactive onchocerciasis is characterized by a combination of Th17-Th2 immune responses and reduced regulatory T cells, PLoS Negl Trop Dis, 9, e3414, 10.1371/journal.pntd.0003414 · DOI
  38. Turner, 2008, Intensity of intestinal infection with multiple worm species is related to regulatory cytokine output and immune hyporesponsiveness, J Infect Dis, 197, 1204, 10.1086/586717 · DOI
  39. Figueiredo, 2010, Chronic intestinal helminth infections are associated with immune hyporesponsiveness and induction of a regulatory network, Infect Immun, 78, 3160, 10.1128/IAI.01228-09 · DOI
  40. Satoguina, 2002, Antigen-specific T regulatory-1 cells are associated with immunosuppression in a chronic helminth infection (onchocerciasis), Microbes Infect, 4, 1291, 10.1016/S1286-4579(02)00014-X · DOI
  41. Satoguina, 2005, T regulatory-1 cells induce IgG4 production by B cells: role of IL-10, J Immunol, 174, 4718, 10.4049/jimmunol.174.8.4718 · DOI
  42. Satoguina, 2008, Tr1 and naturally occurring regulatory T cells induce IgG4 in B cells through GITR/GITR-L interaction, IL-10 and TGF-β, Eur J Immunol, 38, 3101, 10.1002/eji.200838193 · DOI
  43. van der Neut Kolfschoten, 2007, Anti-inflammatory activity of human IgG4 antibodies by dynamic Fab arm exchange, Science, 317, 1554, 10.1126/science.1144603 · DOI
  44. Grogan, 1996, Antischistosome IgG4 and IgE responses are affected differentially by chemotherapy in children versus adults, J Infect Dis, 173, 1242, 10.1093/infdis/173.5.1242 · DOI
  45. Zaccone, 2009, Schistosoma mansoni egg antigens induce Treg that participate in diabetes prevention in NOD mice, Eur J Immunol, 39, 1098, 10.1002/eji.200838871 · DOI
  46. Blankenhaus, 2011, Strongyloides ratti infection induces expansion of Foxp3+ regulatory T cells that interfere with immune response and parasite clearance in BALB/c mice, J Immunol, 186, 4295, 10.4049/jimmunol.1001920 · DOI
  47. Sawant, 2014, Regulatory T cells limit induction of protective immunity and promote immune pathology following intestinal helminth infection, J Immunol, 192, 2904, 10.4049/jimmunol.1202502 · DOI · Paper page
  48. Smith, 2016, Low level regulatory T cell activity is essential for functional type-2 effector immunity to expel gastrointestinal helminths, Mucosal Immunol, 9, 428, 10.1038/mi.2015.73 · DOI
  49. Taylor, 2005, Removal of regulatory T cell activity reverses hyporesponsiveness and leads to filarial parasite clearance in vivo, J Immunol, 174, 4924, 10.4049/jimmunol.174.8.4924 · DOI · Paper page
  50. Taylor, 2012, T cells in helminth infection: the regulators and the regulated, Trends Immunol, 33, 181, 10.1016/j.it.2012.01.001 · DOI
  51. Wilson, 2005, Suppression of allergic airway inflammation by helminth-induced regulatory T cells, J Exp Med, 202, 1199, 10.1084/jem.20042572 · DOI
  52. Layland, 2013, Schistosoma mansoni-mediated suppression of allergic airway inflammation requires patency and Foxp3+ Treg cells, PLoS Negl Trop Dis, 7, e2379, 10.1371/journal.pntd.0002379 · DOI · Paper page
  53. D'Elia, 2009, Regulatory T cells: a role in the control of helminth driven intestinal pathology and worm survival, J Immunol, 182, 2340, 10.4049/jimmunol.0802767 · DOI
  54. Wammes, 2010, Regulatory T cell in human geohelminth infection suppress immune responses to BCG and Plasmodium falciparum, Eur J Immunol, 40, 437, 10.1002/eji.200939699 · DOI
  55. Elias, 2008, Poor immunogenicity of BCG in helminth infected population is associated with increased in vitro TGF-β production, Vaccine, 26, 3897, 10.1016/j.vaccine.2008.04.083 · DOI
  56. Toulza, 2016, Mycobacterium tuberculosis-specific CD4+ T-cell response is increased, and Treg cells decreased, in anthelmintic-treated patients with latent TB, Eur J Immunol, 46, 752, 10.1002/eji.201545843 · DOI
  57. Hussaarts, 2011, Regulatory B-cell induction by helminths: implications for allergic disease, J Allergy Clin Immunol, 128, 733, 10.1016/j.jaci.2011.05.012 · DOI · Paper page
  58. Wilson, 2010, Helminth-induced CD19+CD23hi B cells modulate experimental allergic and autoimmune inflammation, Eur J Immunol, 40, 1682, 10.1002/eji.200939721 · DOI
  59. van der Vlugt, 2012, Schistosomes induce regulatory features in human and mouse CD1d B cells: inhibition of allergic inflammation by IL-10 and regulatory T cells, PLoS One, 7, e30883, 10.1371/journal.pone.0030883 · DOI
  60. Correale, 2008, Helminth infections associated with multiple sclerosis induce regulatory B cells, Ann Neurol, 64, 187, 10.1002/ana.21438 · DOI
  61. Akdis, 2014, Mechanisms of allergen-specific immunotherapy: multiple suppressor factors at work in immune tolerance to allergens, J Allergy Clin Immunol, 133, 621, 10.1016/j.jaci.2013.12.1088 · DOI
  62. Perona-Wright, 2006, Dendritic cell activation and function in response to Schistosoma mansoni, Int J Parasitol, 36, 711, 10.1016/j.ijpara.2006.02.003 · DOI
  63. Everts, 2010, Sensing of helminth infections by dendritic cells via pattern recognition receptors and beyond: consequences for T helper 2 and regulatory T cell polarization, Eur J Immunol, 40, 1525, 10.1002/eji.200940109 · DOI
  64. Tussiwand, 2015, Klf4 expression in conventional dendritic cells is required for T helper 2 cell responses, Immunity, 42, 916, 10.1016/j.immuni.2015.04.017 · DOI
  65. Jenkins, 2007, Dendritic cell expression of OX40 ligand acts as a costimulatory, not polarizing, signal for optimal Th2 priming and memory induction in vivo, J Immunol, 179, 3515, 10.4049/jimmunol.179.6.3515 · DOI
  66. Smith, 2011, Chronic helminth infection mediates tolerance in vivo through dominance of CD11clo CD103− DC population, J Immunol, 186, 7098, 10.4049/jimmunol.1003636 · DOI
  67. Blum, 2012, Heligmosomoides polygyrus bakeri induces tolerogenic dendritic cells that block colitis and prevent antigen-specific gut T cell responses, J Immunol, 189, 2512, 10.4049/jimmunol.1102892 · DOI
  68. Balic, 2004, Selective maturation of dendritic cells by Nippostrongylus brasiliensis secreted proteins drives T helper type 2 immune responses, Eur J Immunol, 34, 3047, 10.1002/eji.200425167 · DOI
  69. Cervi, 2004, Dendritic cells copulsed with microbial and helminth antigens undergo modified maturation, segregate the antigens to distinct intracellular compartments, and concurrently induce microbe-specific Th1 and helminth-specific Th2 responses, J Immunol, 172, 2016, 10.4049/jimmunol.172.4.2016 · DOI
  70. Segura, 2007, Impairment of dendritic cell function by excretory-secretory products: a potential mechanism for nematode-induced immunosuppression, Eur J Immunol, 37, 1887, 10.1002/eji.200636553 · DOI
  71. Matisz, 2015, Adoptive transfer of helminth antigen-pulsed dendritic cells protects against the development of experimental colitis in mice, Eur J Immunol, 45, 3126, 10.1002/eji.201545579 · DOI
  72. Everts, 2012, Schistosome-derived omega-1 drives Th2 polarization by suppressing protein synthesis following internalization by the mannose receptor, J Exp Med, 209, 1753, 10.1084/jem.20111381 · DOI · Paper page
  73. Martinez, 2009, Alternative activation of macrophages: an immunologic functional perspective, Annu Rev Immunol, 27, 451, 10.1146/annurev.immunol.021908.132532 · DOI · Paper page
  74. Nair, 2005, Chitinase and Fizz family members are a generalized feature of nematode infection with selective upregulation of Ym1 and Fizz1 by antigen-presenting cells, Infect Immun, 73, 385, 10.1128/IAI.73.1.385-394.2005 · DOI
  75. Filbey, 2014, Innate and adaptive type 2 immune cell responses in genetically controlled resistance to intestinal helminth infection, Immunol Cell Biol, 92, 436, 10.1038/icb.2013.109 · DOI · Paper page
  76. Gause, 2013, Type 2 immunity and wound healing: evolutionary refinement of adaptive immunity by helminths, Nat Rev Immunol, 13, 607, 10.1038/nri3476 · DOI
  77. MacDonald, 1998, Requirement for in vivo production of IL-4, but not IL-10, in the induction of proliferative suppression by filarial parasites, J Immunol, 160, 4124, 10.4049/jimmunol.160.8.4124 · DOI
  78. Terrazas, 2005, Role of the programmed death-1 pathway in the suppressive activity of alternatively activated macrophages in experimental cysticercosis, Int J Parasitol, 35, 1349, 10.1016/j.ijpara.2005.06.003 · DOI
  79. Broadhurst, 2012, Upregulation of retinal dehydrogenase 2 in alternatively activated macrophages during retinoid-dependent Type-2 immunity to helminth infection in mice, PLoS Pathog, 8, e1002883, 10.1371/journal.ppat.1002883 · DOI
  80. Hewitt, 2003, The MHC class I antigen presentation pathway: strategies for viral immune evasion, Immunology, 110, 163, 10.1046/j.1365-2567.2003.01738.x · DOI
  81. Greenwood, 1968, Autoimmune disease and parasitic infections in Nigerians, Lancet, 2, 380, 10.1016/S0140-6736(68)90595-3 · DOI
  82. van den Biggelaar, 2004, Long-term treatment of intestinal helminths increases mite skin-test reactivity in Gabonese schoolchildren, J Infect Dis, 189, 892, 10.1086/381767 · DOI · Paper page
  83. Feary, 2011, Atopy and current intestinal parasite infection: a systematic review and meta-analysis, Allergy, 66, 569, 10.1111/j.1398-9995.2010.02512.x · DOI · Paper page
  84. Mutapi, 2011, Schistosome infection intensity is inversely related to auto-reactive antibody levels, PLoS One, 6, e19149, 10.1371/journal.pone.0019149 · DOI
  85. McKay, 2015, Not all parasites are protective, Parasite Immunol, 37, 324, 10.1111/pim.12160 · DOI
  86. Smits, 2005, Helminth infections: protection from atopic disorders, Curr Allergy Asthma Rep, 5, 42, 10.1007/s11882-005-0053-5 · DOI
  87. Maizels, 2014, Helminths in the hygiene hypothesis—sooner or later?, Clin Exp Immunol, 177, 38, 10.1111/cei.12353 · DOI
  88. Weinstock, 2013, Translatability of helminth therapy in inflammatory bowel diseases, Int J Parasitol, 43, 245, 10.1016/j.ijpara.2012.10.016 · DOI · Paper page
  89. Correale, 2007, Association between parasite infection and immune responses in multiple sclerosis, Ann Neurol, 61, 97, 10.1002/ana.21067 · DOI
  90. Correale, 2011, The impact of parasite infections on the course of multiple sclerosis, J Neuroimmunol, 233, 6, 10.1016/j.jneuroim.2011.01.002 · DOI · Paper page
  91. Smits, 2010, Chronic helminth infections protect against allergic diseases by active regulatory processes, Curr Allergy Asthma Rep, 10, 3, 10.1007/s11882-009-0085-3 · DOI · Paper page
  92. Evans, 2015, Worms as therapeutics for allergy: understanding why benefits in animal studies have not translated into clinical success, J Allergy Clin Immunol, 135, 343, 10.1016/j.jaci.2014.07.007 · DOI
  93. Amu, 2010, Regulatory B cells prevent and reverse allergic airway inflammation via FoxP3-positive T regulatory cells in a murine model, J Allergy Clin Immunol, 125, 1114, 10.1016/j.jaci.2010.01.018 · DOI
  94. Smith, 2007, Infection with a helminth parasite prevents experimental colitis via a macrophage-mediated mechanism, J Immunol, 178, 4557, 10.4049/jimmunol.178.7.4557 · DOI
  95. Summers, 2005, Trichuris suis therapy for active ulcerative colitis: a randomized controlled trial, Gastroenterology, 128, 825, 10.1053/j.gastro.2005.01.005 · DOI · Paper page
  96. Bager, 2010, Trichuris suis ova therapy for allergic rhinitis: A randomized, double-blind, placebo-controlled clinical trial, J Allergy Clin Immunol, 125, 123, 10.1016/j.jaci.2009.08.006 · DOI
  97. Garg, 2014, Helminth therapy (worms) for induction of remission in inflammatory bowel disease, Cochrane Database Syst Rev, CD009400
  98. Daniłowicz-Luebert, 2011, Modulation of specific and allergy-related immune responses by helminths, J Biomed Biotechnol, 2011, 821578
  99. McSorley, 2013, Immunomodulation by helminth parasites: Defining mechanisms and mediators, Int J Parasitol, 43, 301, 10.1016/j.ijpara.2012.11.011 · DOI
  100. Shepherd, 2015, Identifying the immunomodulatory components of helminths, Parasite Immunol, 37, 293, 10.1111/pim.12192 · DOI · Paper page
  101. Schnoeller, 2008, A helminth immunomodulator reduces allergic and inflammatory responses by induction of IL-10-producing macrophages, J Immunol, 180, 4265, 10.4049/jimmunol.180.6.4265 · DOI
  102. Hams, 2016, The helminth T2 RNase omega1 promotes metabolic homeostasis in an IL-33- and group 2 innate lymphoid cell-dependent mechanism, FASEB J, 30, 824, 10.1096/fj.15-277822 · DOI
  103. Marshall, 2008, Effect of activated antigen-specific B cells on ES-62-mediated modulation of effector function of heterologous antigen-specific T cells in vivo, Immunology, 123, 411, 10.1111/j.1365-2567.2007.02706.x · DOI
  104. Harnett, 2012, Receptor usage by the Acanthocheilonema viteae-derived immunomodulator, ES-62, Exp Parasitol, 132, 97, 10.1016/j.exppara.2011.09.001 · DOI
  105. Aprahamian, 2015, The immunomodulatory parasitic worm product ES-62 reduces lupus-associated accelerated atherosclerosis in a mouse model, Int J Parasitol, 45, 203, 10.1016/j.ijpara.2014.12.006 · DOI
  106. Zaccone, 2011, The S. mansoni glycoprotein ω-1 induces Foxp3 expression in NOD mouse CD4+ T cells, Eur J Immunol, 41, 2709, 10.1002/eji.201141429 · DOI
  107. Robinson, 2011, A family of helminth molecules that modulate innate cell responses via molecular mimicry of host antimicrobial peptides, PLOS Pathogens, 7, e1002042, 10.1371/journal.ppat.1002042 · DOI
  108. Robinson, 2012, A helminth cathelicidin-like protein suppresses antigen processing and presentation in macrophages via inhibition of lysosomal vATPase, FASEB J, 26, 4614, 10.1096/fj.12-213876 · DOI
  109. Dainichi, 2001, Nippocystatin, a cysteine protease inhibitor from Nippostrongylus brasiliensis, inhibits antigen processing and modulates antigen- specific immune response, Infect Immun, 69, 7380, 10.1128/IAI.69.12.7380-7386.2001 · DOI · Paper page
  110. Klotz, 2011, A helminth immunomodulator exploits host signaling events to regulate cytokine production in macrophages, PLoS Pathog, 7, e1001248, 10.1371/journal.ppat.1001248 · DOI
  111. Ziegler, 2015, A novel regulatory macrophage Induced by a helminth molecule instructs IL-10 in CD4+ T cells and protects against mucosal inflammation, J Immunol, 194, 1555, 10.4049/jimmunol.1401217 · DOI · Paper page
  112. Huang, 2016, Eosinophils in helminth infection: defenders and dupes, Trends Parasitol, 10.1016/j.pt.2016.05.004 · DOI
  113. McSorley, 2012, Suppression of type 2 immunity and allergic airway inflammation by secreted products of the helminth Heligmosomoides polygyrus, Eur J Immunol, 42, 2667, 10.1002/eji.201142161 · DOI
  114. Trujillo-Vargas, 2007, Helminth derived products inhibit the development of allergic responses in mice, Am J Respir Cell Mol Biol, 175, 336
  115. Schabussova, 2013, Oesophagostomum dentatum extract modulates T cell-dependent immune responses to bystander antigens and prevents the development of allergy in mice, PLoS One, 8, e67544, 10.1371/journal.pone.0067544 · DOI
  116. Reynolds, 2015, Cohabitation in the intestine: interactions among helminth parasites, bacterial microbiota, and host immunity, J Immunol, 195, 4059, 10.4049/jimmunol.1501432 · DOI · Paper page
  117. Gause, 2016, Macrobiota—helminths as active participants and partners of the microbiota in host intestinal homeostasis, Curr Opin Microbiol, 32, 14, 10.1016/j.mib.2016.04.004 · DOI
  118. Zaiss, 2016, Interactions between the intestinal microbiome and helminth parasites, Parasite Immunol, 38, 5, 10.1111/pim.12274 · DOI
  119. Walk, 2010, Alteration of the murine gut microbiota during infection with the parasitic helminth Heligmosomoides polygyrus, Inflamm Bowel Dis, 16, 1841, 10.1002/ibd.21299 · DOI
  120. Reynolds, 2014, Commensal-pathogen interactions in the intestinal tract: lactobacilli promote infection with, and are promoted by, helminth parasites, Gut Microbes, 5, 10, 10.4161/gmic.32155 · DOI
  121. Holm, 2015, Chronic Trichuris muris infection decreases diversity of the intestinal microbiota and concomitantly increases the abundance of lactobacilli, PLoS One, 10, e0125495, 10.1371/journal.pone.0125495 · DOI
  122. Houlden, 2015, Chronic Trichuris muris infection in C57BL/6 mice causes significant changes in host microbiota and metabolome: effects reversed by pathogen clearance, PLoS One, 10, e0125945, 10.1371/journal.pone.0125945 · DOI
  123. Zaiss, 2015, The intestinal microbiota contributes to the ability of helminths to modulate allergic inflammation, Immunity, 43, 998, 10.1016/j.immuni.2015.09.012 · DOI · Paper page
  124. Brestoff, 2015, Immune regulation of metabolic homeostasis in health and disease, Cell, 161, 146, 10.1016/j.cell.2015.02.022 · DOI
  125. Odegaard, 2015, Type 2 responses at the interface between immunity and fat metabolism, Curr Opin Immunol, 36, 67, 10.1016/j.coi.2015.07.003 · DOI
  126. Wiria, 2014, Helminth infections, type-2 immune response, and metabolic syndrome, PLoS Pathog, 10, e1004140, 10.1371/journal.ppat.1004140 · DOI
  127. Wu, 2011, Eosinophils sustain adipose alternatively activated macrophages associated with glucose homeostasis, Science, 332, 243, 10.1126/science.1201475 · DOI
  128. Hussaarts, 2015, Chronic helminth infection and helminth-derived egg antigens promote adipose tissue M2 macrophages and improve insulin sensitivity in obese mice, FASEB J, 29, 3027, 10.1096/fj.14-266239 · DOI
  129. Herrera, 2001, Do helminths play a role in carcinogenesis?, Trends Parasitol, 17, 172, 10.1016/S1471-4922(00)01942-5 · DOI
  130. Mayer, 2007, The role of helminth infections in carcinogenesis, Adv Parasitol, 65, 239, 10.1016/S0065-308X(07)65004-0 · DOI
  131. Honeycutt, 2014, Controversies and challenges in research on urogenital schistosomiasis-associated bladder cancer, Trends Parasitol, 30, 324, 10.1016/j.pt.2014.05.004 · DOI
  132. Smout, 2015, Carcinogenic parasite secretes growth factor that accelerates wound healing and potentially promotes neoplasia, PLoS Pathog, 11, e1005209, 10.1371/journal.ppat.1005209 · DOI · Paper page
  133. Wang, 2011, The draft genome of the carcinogenic human liver fluke Clonorchis sinensis, Genome Biol, 12, R107, 10.1186/gb-2011-12-10-r107 · DOI
  134. Sripa, 2012, The tumorigenic liver fluke Opisthorchis viverrini—multiple pathways to cancer, Trends Parasitol, 28, 395, 10.1016/j.pt.2012.07.006 · DOI
  135. Saleem, 2012, Cutting edge: mast cells critically augment myeloid-derived suppressor cell activity, J Immunol, 189, 511, 10.4049/jimmunol.1200647 · DOI
  136. Morales, 2014, Myeloid-derived suppressor cells enhance IgE-mediated mast cell responses, J Leukoc Biol, 95, 643, 10.1189/jlb.0913510 · DOI
  137. Valanparambil, 2016, Primary Heligmosomoides polygyrus bakeri infection induces myeloid-derived suppressor cells that suppress CD4+ Th2 responses and promote chronic infection, Mucosal Immunol
  138. Kumar, 2016, The nature of myeloid-derived suppressor cells in the tumor microenvironment, Trends Immunol, 37, 208, 10.1016/j.it.2016.01.004 · DOI · Paper page
  139. van der Burg, 2016, Vaccines for established cancer: overcoming the challenges posed by immune evasion, Nat Rev Cancer, 16, 219, 10.1038/nrc.2016.16 · DOI
  140. Saenz, 2008, Welcome to the neighborhood: epithelial cell-derived cytokines license innate and adaptive immune responses at mucosal sites, Immunol Rev, 226, 172, 10.1111/j.1600-065X.2008.00713.x · DOI
  141. Hammad, 2015, Barrier epithelial cells and the control of type 2 immunity, Immunity, 43, 29, 10.1016/j.immuni.2015.07.007 · DOI · Paper page
  142. Hammad, 2009, House dust mite allergen induces asthma via Toll-like receptor 4 triggering of airway structural cells, Nat Med, 15, 410, 10.1038/nm.1946 · DOI
  143. Willart, 2012, Interleukin-1α controls allergic sensitization to inhaled house dust mite via the epithelial release of GM-CSF and IL-33, J Exp Med, 209, 1505, 10.1084/jem.20112691 · DOI
  144. Maizels, 2012, Susceptibility and immunity to helminth parasites, Curr Opin Immunol, 25, 459, 10.1016/j.coi.2012.06.003 · DOI
  145. Ajendra, 2014, ST2 deficiency does not impair type 2 immune responses during chronic filarial infection but leads to an increased microfilaremia due to an impaired splenic microfilarial clearance, PLoS One, 9, e93072, 10.1371/journal.pone.0093072 · DOI
  146. Hung, 2013, IL-33 drives biphasic IL-13 production for noncanonical Type 2 immunity against hookworms, Proc Natl Acad Sci U S A, 110, 282, 10.1073/pnas.1206587110 · DOI
  147. Scalfone, 2013, Participation of MyD88 and interleukin-33 as innate drivers of Th2 immunity to Trichinella spiralis, Infect Immun, 81, 1354, 10.1128/IAI.01307-12 · DOI
  148. Yang, 2013, Macrophages as IL-25/IL-33-responsive cells play an important role in the induction of type 2 immunity, PLoS One, 8, e59441, 10.1371/journal.pone.0059441 · DOI
  149. Bouchery, 2015, ILC2s and T cells cooperate to ensure maintenance of M2 macrophages for lung immunity against hookworms, Nat Commun, 6, 6970, 10.1038/ncomms7970 · DOI · Paper page
  150. Yasuda, 2012, Contribution of IL-33-activated type II innate lymphoid cells to pulmonary eosinophilia in intestinal nematode-infected mice, Proc Natl Acad Sci U S A, 109, 3451, 10.1073/pnas.1201042109 · DOI
  151. Humphreys, 2008, IL-33, a potent inducer of adaptive immunity to intestinal nematodes, J Immunol, 180, 2443, 10.4049/jimmunol.180.4.2443 · DOI
  152. Hewitson, 2015, Concerted activity of IgG1 antibodies and IL-4/IL-25-dependent effector cells trap helminth larvae in the tissues following vaccination with defined secreted antigens, providing sterile immunity to challenge infection, PLoS Pathog, 11, e1004676, 10.1371/journal.ppat.1004676 · DOI
  153. Zaiss, 2013, IL-1β suppresses innate IL-25 and IL-33 production and maintains helminth chronicity, PLoS Pathog, 9, e1003531, 10.1371/journal.ppat.1003531 · DOI · Paper page
  154. Mearns, 2014, IL-25 exhibits disparate roles during Th2-cell differentiation versus effector function, Eur J Immunol, 44, 1976, 10.1002/eji.201344400 · DOI
  155. Gerbe, 2016, Intestinal epithelial tuft cells initiate type 2 mucosal immunity to helminth parasites, Nature, 529, 226, 10.1038/nature16527 · DOI
  156. von Moltke, 2016, Tuft-cell-derived IL-25 regulates an intestinal ILC2-epithelial response circuit, Nature, 529, 221, 10.1038/nature16161 · DOI · Paper page
  157. Howitt, 2016, Tuft cells, taste-chemosensory cells, orchestrate parasite type 2 immunity in the gut, Science, 351, 1329, 10.1126/science.aaf1648 · DOI
  158. Diemert, 2012, Generalized urticaria induced by the Na-ASP-2 hookworm vaccine: implications for the development of vaccines against helminths, J Allergy Clin Immunol, 130, 169, 10.1016/j.jaci.2012.04.027 · DOI
  159. Hewitson, 2011, Heligmosomoides polygyrus elicits a dominant nonprotective antibody response directed at restricted glycan and peptide epitopes, J Immunol, 187, 4764, 10.4049/jimmunol.1004140 · DOI

Cited by

Sorted by citations

See all 529

Metadata

Authors
Maizels, R. M., & McSorley, H. J.
Venue
Journal of Allergy and Clinical Immunology
Publisher
Elsevier BV
Published
2016-09
Volume
138
Issue
3
Pages
666-675
ISSN
0091-6749
Cited by
529
References
7
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review