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Helminth-Tuberculosis Co-infection: An Immunologic Perspective

Babu, Subash, Nutman, Thomas B.·2016·Trends in Immunology
DOI 10.1016/j.it.2016.07.005PMC PMC5003706
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  1. Hotez, 2008, Helminth infections: the great neglected tropical diseases, J. Clin. Invest., 118, 1311, 10.1172/JCI34261 · DOI
  2. Nutman, 2001, Lymphatic filariasis: new insights and prospects for control, Curr. Opin. Infect. Dis., 14, 539, 10.1097/00001432-200110000-00006 · DOI
  3. Dheda, 2016, Tuberculosis, Lancet, 387, 1211, 10.1016/S0140-6736(15)00151-8 · DOI
  4. O’Garra, 2013, The immune response in tuberculosis, Annu. Rev. Immunol., 31, 475, 10.1146/annurev-immunol-032712-095939 · DOI
  5. Getahun, 2015, Latent Mycobacterium tuberculosis infection, N. Engl. J. Med., 373, 1179
  6. Salgame, 2015, Latent tuberculosis infection -–revisiting and revising concepts, Tuberculosis (Edinb.), 95, 373, 10.1016/j.tube.2015.04.003 · DOI
  7. Grencis, 2015, Immunity to helminths: resistance, regulation, and susceptibility to gastrointestinal nematodes, Annu. Rev. Immunol., 33, 201, 10.1146/annurev-immunol-032713-120218 · DOI
  8. Babu, 2014, Immunology of lymphatic filariasis, Parasite Immunol., 36, 338, 10.1111/pim.12081 · DOI · Paper page
  9. McKenzie, 2014, Innate lymphoid cells in inflammation and immunity, Immunity, 41, 366, 10.1016/j.immuni.2014.09.006 · DOI
  10. McSorley, 2013, Immunomodulation by helminth parasites: defining mechanisms and mediators, Int. J. Parasitol., 43, 301, 10.1016/j.ijpara.2012.11.011 · DOI
  11. Metenou, 2013, Regulatory T cell subsets in filarial infection and their function, Front. Immunol., 4, 305, 10.3389/fimmu.2013.00305 · DOI
  12. Semnani, 2004, Filaria-induced immune evasion: suppression by the infective stage of Brugia malayi at the earliest host–parasite interface, J. Immunol., 172, 6229, 10.4049/jimmunol.172.10.6229 · DOI
  13. Semnani, 2004, Toward an understanding of the interaction between filarial parasites and host antigen-presenting cells, Immunol. Rev., 201, 127, 10.1111/j.0105-2896.2004.00196.x · DOI
  14. King, 1993, Cytokine control of parasite-specific anergy in human lymphatic filariasis. Preferential induction of a regulatory T helper type 2 lymphocyte subset, J. Clin. Invest., 92, 1667, 10.1172/JCI116752 · DOI
  15. Gaze, 2014, Immunology of experimental and natural human hookworm infection, Parasite Immunol., 36, 358, 10.1111/pim.12088 · DOI
  16. Maizels, 2003, Immune regulation by helminth parasites: cellular and molecular mechanisms, Nat. Rev. Immunol., 3, 10.1038/nri1183 · DOI
  17. Mishra, 2014, Systemic impact of intestinal helminth infections, Mucosal Immunol., 7, 753, 10.1038/mi.2014.23 · DOI
  18. Allen, 2011, Evolution of Th2 immunity: a rapid repair response to tissue destructive pathogens, PLoS Pathog., 7, e1002003, 10.1371/journal.ppat.1002003 · DOI
  19. Babu, 2013, Immunopathogenesis of lymphatic filarial disease, Semin. Immunopathol., 34, 847, 10.1007/s00281-012-0346-4 · DOI
  20. Strachan, 1999, Lifestyle and atopy, Lancet, 353, 1457, 10.1016/S0140-6736(99)90038-7 · DOI
  21. Yazdanbakhsh, 2002, Allergy, parasites, and the hygiene hypothesis, Science, 296, 490, 10.1126/science.296.5567.490 · DOI
  22. Wilson, 2004, Regulation of allergy and autoimmunity in helminth infection, Clin. Rev. Allergy Immunol., 26, 35, 10.1385/CRIAI:26:1:35 · DOI
  23. Weinstock, 2014, Helminth infections decrease host susceptibility to immune-mediated diseases, J. Immunol., 193, 3239, 10.4049/jimmunol.1400927 · DOI
  24. Levine, 1993, Live oral vaccines against cholera: an update, Vaccine, 11, 207, 10.1016/0264-410X(93)90019-T · DOI
  25. Baily, 1980, Tuberculosis prevention Trial, Madras. Indian J. Med. Res., 72, 1
  26. Suharyono, 1992, Safety and immunogenicity of single-dose live oral cholera vaccine CVD 103-HgR in 5-9-year-old Indonesian children, Lancet, 340, 689, 10.1016/0140-6736(92)92231-4 · DOI
  27. Cooper, 1998, Impaired tetanus-specific cellular and humoral responses following tetanus vaccination in human onchocerciasis: a possible role for interleukin-10, J. Infect. Dis., 178, 1133, 10.1086/515661 · DOI
  28. Prost, 1983, Response to tetanus immunization in onchocerciasis patients, Ann. Trop. Med. Parasitol., 77, 83, 10.1080/00034983.1983.11811675 · DOI
  29. Nookala, 2004, Impairment of tetanus-specific cellular and humoral responses following tetanus vaccination in human lymphatic filariasis, Infect. Immun., 72, 2598, 10.1128/IAI.72.5.2598-2604.2004 · DOI
  30. Elliott, 2010, Effects of maternal and infant coinfections, and of maternal immunisation, on the infant response to BCG and tetanus immunisation, Vaccine, 29, 247, 10.1016/j.vaccine.2010.10.047 · DOI
  31. Barry, 2009, The spectrum of latent tuberculosis: rethinking the biology and intervention strategies, Nat. Rev. Microbiol., 7, 845, 10.1038/nrmicro2236 · DOI
  32. Cooper, 2009, Cell-mediated immune responses in tuberculosis, Annu. Rev. Immunol., 27, 393, 10.1146/annurev.immunol.021908.132703 · DOI
  33. 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 · DOI
  34. Cooper, 2008, The role of cytokines in the initiation, expansion, and control of cellular immunity to tuberculosis, Immunol. Rev., 226, 191, 10.1111/j.1600-065X.2008.00702.x · DOI
  35. Darrah, 2007, Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major, Nat. Med., 13, 843, 10.1038/nm1592 · DOI
  36. Jasenosky, 2015, T cells and adaptive immunity to Mycobacterium tuberculosis in humans, Immunol. Rev., 264, 74, 10.1111/imr.12274 · DOI
  37. Mayer-Barber, 2015, Cytokine and lipid mediator networks in tuberculosis, Immunol. Rev., 264, 264, 10.1111/imr.12249 · DOI
  38. Ottenhoff, 2012, New pathways of protective and pathological host defense to mycobacteria, Trends Microbiol., 20, 419, 10.1016/j.tim.2012.06.002 · DOI
  39. Metenou, 2012, Impact of filarial infections on coincident intracellular pathogens: Mycobacterium tuberculosis and Plasmodium falciparum, Curr. Opin. HIV AIDS, 7, 231, 10.1097/COH.0b013e3283522c3d · DOI
  40. Rougemont, 1977, Tuberculin skin tests and B.C.G. vaccination in hyperendemic area of onchocerciasis, Lancet, 1, 309, 10.1016/S0140-6736(77)91857-8 · DOI
  41. Buck, 1969, Onchocerciasis: some new epidemiologic and clinical findings. Results of an epidemiologic study in the Republic of Chad, Am. J. Trop. Med. Hyg., 18, 217, 10.4269/ajtmh.1969.18.217 · DOI
  42. Stewart, 1999, Onchocerciasis modulates the immune response to mycobacterial antigens, Clin. Exp. Immunol., 117, 517, 10.1046/j.1365-2249.1999.01015.x · DOI
  43. Gebreegziabiher, 2014, Helminth infection increases the probability of indeterminate QuantiFERON gold in tube results in pregnant women, Biomed. Res. Int., 2014, 364137, 10.1155/2014/364137 · DOI
  44. Thomas, 2010, Malnutrition and helminth infection affect performance of an interferon gamma-release assay, Pediatrics, 126, e1522, 10.1542/peds.2010-0885 · DOI
  45. van Soelen, 2012, Effect of Ascaris Lumbricoides specific IgE on tuberculin skin test responses in children in a high-burden setting: a cross-sectional community-based study, BMC Infect. Dis., 12, 211, 10.1186/1471-2334-12-211 · DOI
  46. Lipner, 2006, Coincident filarial, intestinal helminth, and mycobacterial infection: helminths fail to influence tuberculin reactivity, but BCG influences hookworm prevalence, Am. J. Trop. Med. Hyg., 74, 841, 10.4269/ajtmh.2006.74.841 · DOI
  47. Neto, 2009, Enteroparasitosis prevalence and parasitism influence in clinical outcomes of tuberculosis patients with or without HIV coinfection in a reference hospital in Rio de Janeiro (2000-2006), Braz. J. Infect. Dis., 13, 427, 10.1590/S1413-86702009000600008 · DOI
  48. Zevallos, 2010, Tuberculin skin-test reactions are unaffected by the severity of hyperendemic intestinal helminth infections and coinfections, Am. J. Trop. Med. Hyg., 83, 319, 10.4269/ajtmh.2010.10-0073 · DOI
  49. Van der Zalm, 2016, The effect of deworming on tests of tuberculosis infection in children with recent tuberculosis exposure–a randomized controlled trial, Pediatr. Infect. Dis. J., 35, 706, 10.1097/INF.0000000000001115 · DOI
  50. Tristao-Sa, 2002, Intestinal nematodes and pulmonary tuberculosis, Rev. Soc. Bras. Med. Trop., 35, 533, 10.1590/S0037-86822002000500020 · DOI
  51. Elias, 2006, Are intestinal helminths risk factors for developing active tuberculosis?, Trop. Med. Int. Health, 11, 551, 10.1111/j.1365-3156.2006.01578.x · DOI
  52. Brown, 2006, Schistosoma mansoni, nematode infections, and progression to active tuberculosis among HIV-1-infected Ugandans, Am. J. Trop. Med. Hyg., 74, 819, 10.4269/ajtmh.2006.74.819 · DOI
  53. Elliott, 2003, Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans, Trans. R. Soc. Trop. Med. Hyg., 97, 477, 10.1016/S0035-9203(03)90096-4 · DOI
  54. Resende Co, 2007, Intestinal helminth coinfection has a negative impact on both anti-Mycobacterium tuberculosis immunity and clinical response to tuberculosis therapy, Clin. Exp. Immunol., 147, 45, 10.1111/j.1365-2249.2006.03247.x · DOI
  55. Abate, 2015, Asymptomatic helminth infection in active tuberculosis is associated with increased regulatory and Th-2 responses and a lower sputum smear positivity, PLoS Negl. Trop. Dis., 9, e0003994, 10.1371/journal.pntd.0003994 · DOI
  56. Abate, 2015, Effects of albendazole on the clinical outcome and immunological responses in helminth co-infected tuberculosis patients: a double blind randomised clinical trial, Int. J. Parasitol., 45, 133, 10.1016/j.ijpara.2014.09.006 · DOI
  57. Chatterjee, 2014, Incidence of active pulmonary tuberculosis in patients with coincident filarial and/or intestinal helminth infections followed longitudinally in South India, PLoS ONE, 9, e94603, 10.1371/journal.pone.0094603 · DOI
  58. Roy, 2014, Effect of BCG vaccination against Mycobacterium tuberculosis infection in children: systematic review and meta-analysis, Br. Med. J., 349, g4643, 10.1136/bmj.g4643 · DOI
  59. Elias, 2001, Effect of deworming on human T cell responses to mycobacterial antigens in helminth-exposed individuals before and after bacille Calmette-Guerin (BCG) vaccination, Clin. Exp. Immunol., 123, 219, 10.1046/j.1365-2249.2001.01446.x · DOI
  60. Malhotra, 1999, Helminth- and Bacillus Calmette-Guerin-induced immunity in children sensitized in utero to filariasis and schistosomiasis, J. Immunol., 162, 6843, 10.4049/jimmunol.162.11.6843 · DOI
  61. Elias, 2008, Poor immunogenicity of BCG in helminth infected population is associated with increased in vitro TGF-beta production, Vaccine, 26, 3897, 10.1016/j.vaccine.2008.04.083 · DOI
  62. Talaat, 2006, Preexposure to live Brugia malayi microfilariae alters the innate response of human dendritic cells to Mycobacterium tuberculosis, J. Infect. Dis., 193, 196, 10.1086/498912 · DOI
  63. Babu, 2009, Human type 1 and 17 Responses in latent tuberculosis are modulated by coincident filarial infection through cytotoxic T lymphocyte antigen-4 and programmed death-1, J. Infect. Dis., 200, 288, 10.1086/599797 · DOI
  64. Soboslay, 1992, Ivermectin-facilitated immunity in onchocerciasis. Reversal of lymphocytopenia, cellular anergy and deficient cytokine production after single treatment, Clin. Exp. Immunol., 89, 407, 10.1111/j.1365-2249.1992.tb06971.x · DOI
  65. Steel, 1991, Immunologic responses to repeated ivermectin treatment in patients with onchocerciasis, J. Infect. Dis., 164, 581, 10.1093/infdis/164.3.581 · DOI
  66. Babu, 2009, Attenuation of toll-like receptor expression and function in latent tuberculosis by coexistent filarial infection with restoration following antifilarial chemotherapy, PLoS Negl. Trop. Dis., 3, e489, 10.1371/journal.pntd.0000489 · DOI
  67. Chatterjee, 2015, Filarial infection modulates the immune response to Mycobacterium tuberculosis through expansion of CD4+ IL-4 memory T cells, J. Immunol., 194, 2706, 10.4049/jimmunol.1402718 · DOI
  68. George, 2013, Modulation of mycobacterial-specific Th1 and Th17 cells in latent tuberculosis by coincident hookworm infection, J. Immunol., 190, 5161, 10.4049/jimmunol.1203311 · DOI
  69. George, 2015, Modulation of pro- and anti-inflammatory cytokines in active and latent tuberculosis by coexistent Strongyloides stercoralis infection, Tuberculosis (Edinb), 95, 822, 10.1016/j.tube.2015.09.009 · DOI
  70. 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
  71. George, 2014, Helminth infections coincident with active pulmonary tuberculosis inhibit mono- and multifunctional CD4+ and CD8+ T cell responses in a process dependent on IL-10, PLoS Pathog., 10, e1004375, 10.1371/journal.ppat.1004375 · DOI
  72. Pearlman, 1993, Modulation of murine cytokine responses to mycobacterial antigens by helminth-induced T helper 2 cell responses, J. Immunol., 151, 4857, 10.4049/jimmunol.151.9.4857 · DOI
  73. Sacco, 2002, Established T(H1) granulomatous responses induced by active Mycobacterium avium infection switch to T(H2) following challenge with Schistosoma mansoni, Clin. Immunol., 104, 274, 10.1006/clim.2002.5263 · DOI
  74. Frantz, 2010, Helminth coinfection does not affect therapeutic effect of a DNA vaccine in mice harboring tuberculosis, PLoS Negl. Trop. Dis., 4, e700, 10.1371/journal.pntd.0000700 · DOI
  75. Elias, 2005, Low dose chronic Schistosoma mansoni infection increases susceptibility to Mycobacterium bovis BCG infection in mice, Clin. Exp. Immunol., 139, 398, 10.1111/j.1365-2249.2004.02719.x · DOI
  76. Potian, 2011, Preexisting helminth infection induces inhibition of innate pulmonary anti-tuberculosis defense by engaging the IL-4 receptor pathway, J. Exp. Med., 208, 1863, 10.1084/jem.20091473 · DOI
  77. Dias, 2011, Lower production of IL-17A and increased susceptibility to Mycobacterium bovis in mice coinfected with Strongyloides venezuelensis, Mem. Inst. Oswaldo Cruz, 106, 617, 10.1590/S0074-02762011000500015 · DOI
  78. Obieglo, 2016, Chronic gastrointestinal nematode infection mutes immune responses to mycobacterial infection distal to the gut, J. Immunol., 196, 2262, 10.4049/jimmunol.1500970 · DOI
  79. Frantz, 2007, The immune response to toxocariasis does not modify susceptibility to Mycobacterium tuberculosis infection in BALB/c mice, Am. J. Trop. Med. Hyg., 77, 691, 10.4269/ajtmh.2007.77.691 · DOI
  80. Rafi, 2015, Neither primary nor memory immunity to Mycobacterium tuberculosis infection is compromised in mice with chronic enteric helminth infection, Infect. Immun., 83, 1217, 10.1128/IAI.03004-14 · DOI
  81. Hubner, 2012, Chronic helminth infection does not exacerbate Mycobacterium tuberculosis infection, PLoS Negl. Trop. Dis., 6, e1970, 10.1371/journal.pntd.0001970 · DOI
  82. Monin, 2015, Helminth-induced arginase-1 exacerbates lung inflammation and disease severity in tuberculosis, J. Clin. Invest., 125, 4699, 10.1172/JCI77378 · DOI
  83. Hotez, 2014, The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases, PLoS Negl. Trop. Dis., 8, e2865, 10.1371/journal.pntd.0002865 · DOI
  84. Edelman, 1987, Perspective on the development and deployment of rotavirus vaccines, Pediatr. Infect. Dis. J., 6, 704, 10.1097/00006454-198708000-00002 · DOI

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Metadata

Authors
Babu, S., & Nutman, T. B.
Venue
Trends in Immunology
Publisher
Elsevier BV
Published
2016-09
Volume
37
Issue
9
Pages
597-607
ISSN
1471-4906
DOI
10.1016/j.it.2016.07.005
PMC
PMC5003706
Cited by
118
References
3
Language
en
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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