SEARCH

SEARCH BY CITATION

References

  • 1
    Steinmann, P., Keiser, J., Bos, R., Tanner, M. and Utzinger, J., Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect. Dis. 2006. 6: 411425.
  • 2
    Wynn, T. A., Thompson, R. W., Cheever, A. W. and Mentink-Kane, M. M., Immunopathogenesis of schistosomiasis. Immunol. Rev. 2004. 201: 156167.
  • 3
    Zhou, X. N., Wang, L. Y., Chen, M. G., Wu, X. H., Jiang, Q. W., Chen, X. Y., Zheng, J. et al., The public health significance and control of schistosomiasis in China—then and now. Acta Trop. 2005. 96: 97105.
  • 4
    Pearce, E. J. and MacDonald, A. S., The immunobiology of schistosomiasis. Nat. Rev. Immunol. 2002. 2: 499511.
  • 5
    Hsu, C. K., Hsu, S. H., Whitney, R. A., Jr. and Hansen, C. T., Immunopathology of schistosomiasis in athymic mice. Nature 1976. 262: 397399.
  • 6
    Phillips, S. M., DiConza, J. J., Gold, J. A. and Reid, W. A., Schistosomiasis in the congenitally athymic (nude) mouse. I. Thymic dependency of eosinophilia, granuloma formation, and host morbidity. J. Immunol. 1977. 118: 594599.
  • 7
    Mathew, R. C. and Boros, D. L., Anti-L3T4 antibody treatment suppresses hepatic granuloma formation and abrogates antigen-induced interleukin-2 production in Schistosoma mansoni infection. Infect. Immun. 1986. 54: 820826.
  • 8
    Harrington, L. E., Hatton, R. D., Mangan, P. R., Turner, H., Murphy, T. L., Murphy, K. M. and Weaver, C. T., Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages. Nat. Immunol. 2005. 6: 11231132.
  • 9
    Infante-Duarte, C., Horton, H. F., Byrne, M. C. and Kamradt, T., Microbial lipopeptides induce the production of IL-17 in Th cells. J. Immunol. 2000. 165: 61076115.
  • 10
    Korn, T., Bettelli, E., Oukka, M. and Kuchroo, V. K., IL-17 and Th17 cells. Annu. Rev. Immunol. 2009. 27: 485517.
  • 11
    Moseley, T. A., Haudenschild, D. R., Rose, L. and Reddi, A. H., Interleukin-17 family and IL-17 receptors. Cytokine Growth Factor Rev. 2003. 14: 155174.
  • 12
    Annunziato, F., Cosmi, L., Santarlasci, V., Maggi, L., Liotta, F., Mazzinghi, B., Parente, E. et al., Phenotypic and functional features of human Th17 cells. J. Exp. Med. 2007. 204: 18491861.
  • 13
    Lock, C., Hermans, G., Pedotti, R., Brendolan, A., Schadt, E., Garren, H., Langer-Gould, A. et al., Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis. Nat. Med. 2002. 8: 500508.
  • 14
    Matusevicius, D., Kivisakk, P., He, B., Kostulas, N., Ozenci, V., Fredrikson, S. and Link, H., Interleukin-17 mRNA expression in blood and CSF mononuclear cells is augmented in multiple sclerosis. Mult. Scler. 1999. 5: 101104.
  • 15
    Hofstetter, H. H., Ibrahim, S. M., Koczan, D., Kruse, N., Weishaupt, A., Toyka, K. V. and Gold, R., Therapeutic efficacy of IL-17 neutralization in murine experimental autoimmune encephalomyelitis. Cell Immunol. 2005. 237: 123130.
  • 16
    Tzartos, J. S., Friese, M. A., Craner, M. J., Palace, J., Newcombe, J., Esiri, M. M. and Fugger, L., Interleukin-17 production in central nervous system-infiltrating T cells and glial cells is associated with active disease in multiple sclerosis. Am. J. Pathol. 2008. 172: 146155.
  • 17
    Leonaviciene, L., Bradunaite, R. and Astrauskas, V., Proinflammatory cytokine interleukin-17 and its role in pathogenesis of rheumatoid arthritis. Medicina (Kaunas) 2004. 40: 419422.
  • 18
    Nakae, S., Nambu, A., Sudo, K. and Iwakura, Y., Suppression of immune induction of collagen-induced arthritis in IL-17-deficient mice. J. Immunol. 2003. 171: 61736177.
  • 19
    Cruz, A., Khader, S. A., Torrado, E., Fraga, A., Pearl, J. E., Pedrosa, J., Cooper, A. M. et al., Cutting edge: IFN-gamma regulates the induction and expansion of IL-17-producing CD4 T cells during mycobacterial infection. J. Immunol. 2006. 177: 14161420.
  • 20
    Lubberts, E., Joosten, L. A., Chabaud, M., van Den Bersselaar, L., Oppers, B., Coenen-De Roo, C. J., Richards, C. D. et al., IL-4 gene therapy for collagen arthritis suppresses synovial IL-17 and osteoprotegerin ligand and prevents bone erosion. J. Clin. Invest. 2000. 105: 16971710.
  • 21
    Wilson, M. S., Mentink-Kane, M. M., Pesce, J. T., Ramalingam, T. R., Thompson, R. and Wynn, T. A., Immunopathology of schistosomiasis. Immunol. Cell Biol. 2007. 85: 148154.
  • 22
    Rutitzky, L. I., Lopes da Rosa, J. R. and Stadecker, M. J., Severe CD4 T cell-mediated immunopathology in murine schistosomiasis is dependent on IL-12p40 and correlates with high levels of IL-17. J. Immunol. 2005. 175: 39203926.
  • 23
    Warren, K. S. and Domingo, E. O., Granuloma formation around Schistosoma mansoni, S. haematobium, and S. japonicum eggs. Size and rate of development, cellular composition, cross-sensitivity, and rate of egg destruction. Am. J. Trop. Med. Hyg. 1970. 19: 292304.
  • 24
    Warren, K. S., Grove, D. I. and Pelley, R. P., The Schistosoma japonicum egg granuloma. II. Cellular composition, granuloma size, and immunologic concomitants. Am. J. Trop. Med. Hyg. 1978. 27: 271275.
  • 25
    Rutitzky, L. I., Hernandez, H. J. and Stadecker, M. J., Th1-polarizing immunization with egg antigens correlates with severe exacerbation of immunopathology and death in schistosome infection. Proc. Natl. Acad. Sci. USA 2001. 98: 1324313248.
  • 26
    Rutitzky, L. I. and Stadecker, M. J., CD4 T cells producing pro-inflammatory interleukin-17 mediate high pathology in schistosomiasis. Mem. Inst. Oswaldo Cruz 2006. 101(Suppl 1): 327330.
  • 27
    Rutitzky, L. I., Hernandez, H. J., Yim, Y. S., Ricklan, D. E., Finger, E., Mohan, C., Peter, I. et al., Enhanced egg-induced immunopathology correlates with high IFN-gamma in murine schistosomiasis: identification of two epistatic genetic intervals. J. Immunol. 2005. 174: 435440.
  • 28
    Stumhofer, J. S., Laurence, A., Wilson, E. H., Huang, E., Tato, C. M., Johnson, L. M., Villarino, A. V. et al., Interleukin 27 negatively regulates the development of interleukin 17-producing T helper cells during chronic inflammation of the central nervous system. Nat. Immunol. 2006. 7: 937945.
  • 29
    Matsuki, T., Nakae, S., Sudo, K., Horai, R. and Iwakura, Y., Abnormal T cell activation caused by the imbalance of the IL-1/IL-1R antagonist system is responsible for the development of experimental autoimmune encephalomyelitis. Int. Immunol. 2006. 18: 399407.
  • 30
    Sutton, C., Brereton, C., Keogh, B., Mills, K. H. and Lavelle, E. C., A crucial role for interleukin (IL)-1 in the induction of IL-17-producing T cells that mediate autoimmune encephalomyelitis. J. Exp. Med. 2006. 203: 16851691.
  • 31
    Acosta-Rodriguez, E. V., Napolitani, G., Lanzavecchia, A. and Sallusto, F., Interleukins 1beta and 6 but not transforming growth factor-beta are essential for the differentiation of interleukin 17-producing human T helper cells. Nat. Immunol. 2007. 8: 942949.
  • 32
    Rutitzky, L. I., Bazzone, L., Shainheit, M. G., Joyce-Shaikh, B., Cua, D. J. and Stadecker, M. J., IL-23 is required for the development of severe egg-induced immunopathology in schistosomiasis and for lesional expression of IL-17. J. Immunol. 2008. 180: 24862495.
  • 33
    Shainheit, M. G., Smith, P. M., Bazzone, L. E., Wang, A. C., Rutitzky, L. I. and Stadecker, M. J., Dendritic cell IL-23 and IL-1 production in response to schistosome eggs induces Th17 cells in a mouse strain prone to severe immunopathology. J. Immunol. 2008. 181: 85598567.
  • 34
    Smith, P. M., Shainheit, M. G., Bazzone, L. E., Rutitzky, L. I., Poltorak, A. and Stadecker, M. J., Genetic control of severe egg-induced immunopathology and IL-17 production in murine schistosomiasis. J. Immunol. 2009. 183: 33173323.
  • 35
    Shainheit, M. G., Lasocki, K. W., Finger, E., Larkin, B. M., Smith, P. M., Sharpe, A. H., Dinarello, C. A. et al., The pathogenic Th17 cell response to major schistosome egg antigen is sequentially dependent on IL-23 and IL-1beta. J. Immunol. 187: 53285335.
  • 36
    Fossiez, F., Djossou, O., Chomarat, P., Flores-Romo, L., Ait-Yahia, S., Maat, C., Pin, J. J. et al., T cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines. J. Exp. Med. 1996. 183: 25932603.
  • 37
    Molet, S., Hamid, Q., Davoine, F., Nutku, E., Taha, R., Page, N., Olivenstein, R. et al., IL-17 is increased in asthmatic airways and induces human bronchial fibroblasts to produce cytokines. J. Allergy Clin. Immunol. 2001. 108: 430438.
  • 38
    Langrish, C. L., Chen, Y., Blumenschein, W. M., Mattson, J., Basham, B., Sedgwick, J. D., McClanahan, T. et al., IL-23 drives a pathogenic T cell population that induces autoimmune inflammation. J. Exp. Med. 2005. 201: 233240.
  • 39
    Mangan, P. R., Harrington, L. E., O'Quinn, D. B., Helms, W. S., Bullard, D. C., Elson, C. O., Hatton, R. D. et al., Transforming growth factor-beta induces development of the T(H)17 lineage. Nature 2006. 441: 231234.
  • 40
    Kolls, J. K. and Linden, A., Interleukin-17 family members and inflammation. Immunity 2004. 21: 467476.
  • 41
    Veldhoen, M., Hocking, R. J., Flavell, R. A. and Stockinger, B., Signals mediated by transforming growth factor-beta initiate autoimmune encephalomyelitis, but chronic inflammation is needed to sustain disease. Nat. Immunol. 2006. 7: 11511156.
  • 42
    Kotake, S., Udagawa, N., Takahashi, N., Matsuzaki, K., Itoh, K., Ishiyama, S., Saito, S. et al., IL-17 in synovial fluids from patients with rheumatoid arthritis is a potent stimulator of osteoclastogenesis. J. Clin. Invest. 1999. 103: 13451352.
  • 43
    Xu, Y. H., Macedonia, J., Sher, A., Pearce, E. and Cheever, A. W., Dynamic analysis of splenic Th1 and Th2 lymphocyte functions in mice infected with Schistosoma japonicum. Infect. Immun. 1991. 59: 29342940.
  • 44
    Rutitzky, L. I. and Stadecker, M. J., Exacerbated egg-induced immunopathology in murine Schistosoma mansoni infection is primarily mediated by IL-17 and restrained by IFN-gamma. Eur. J. Immunol. 41: 26772687.
  • 45
    Rutitzky, L. I., Smith, P. M. and Stadecker, M. J., T-bet protects against exacerbation of schistosome egg-induced immunopathology by regulating Th17-mediated inflammation. Eur. J. Immunol. 2009. 39: 24702481.
  • 46
    Smith, P. M., Jacque, B., Conner, J. R., Poltorak, A. and Stadecker, M. J., IRAK-2 regulates IL-1-mediated pathogenic Th17 cell development in helminthic infection. PLoS Pathog. 7: e1002272.
  • 47
    Wen, X., He, L., Chi, Y., Zhou, S., Hoellwarth, J., Zhang, C., Zhu, J. et al., Dynamics of Th17 cells and their role in Schistosoma japonicum infection in C57BL/6 mice. PLoS Negl. Trop. Dis. 5: e1399.
  • 48
    Lockhart, E., Green, A. M. and Flynn, J. L., IL-17 production is dominated by gammadelta T cells rather than CD4 T cells during Mycobacterium tuberculosis infection. J. Immunol. 2006. 177: 46624669.
  • 49
    Shibata, K., Yamada, H., Hara, H., Kishihara, K. and Yoshikai, Y., Resident Vdelta1+ gammadelta T cells control early infiltration of neutrophils after Escherichia coli infection via IL-17 production. J. Immunol. 2007. 178: 44664472.
  • 50
    Cua, D. J. and Tato, C. M., Innate IL-17-producing cells: the sentinels of the immune system. Nat. Rev. Immunol. 10: 479489.
  • 51
    Ribot, J. C., Chaves-Ferreira, M., d'Orey, F., Wencker, M., Goncalves-Sousa, N., Decalf, J., Simas, J. P. et al., Cutting edge: adaptive versus innate receptor signals selectively control the pool sizes of murine IFN-gamma- or IL-17-producing gammadelta T cells upon infection. J. Immunol. 185: 64216425.
  • 52
    He, D., Wu, L., Kim, H. K., Li, H., Elmets, C. A. and Xu, H., CD8+ IL-17-producing T cells are important in effector functions for the elicitation of contact hypersensitivity responses. J. Immunol. 2006. 177: 68526858.
  • 53
    Hirata, M., Kage, M., Hara, T., Yoneda, Y., Zhang, M. and Fukuma, T., Schistosoma japonicum egg granuloma formation in the interleukin-4 or interferon-gamma deficient host. Parasite Immunol. 2001. 23: 271280.
  • 54
    Witowski, J., Pawlaczyk, K., Breborowicz, A., Scheuren, A., Kuzlan-Pawlaczyk, M., Wisniewska, J., Polubinska, A. et al., IL-17 stimulates intraperitoneal neutrophil infiltration through the release of GRO alpha chemokine from mesothelial cells. J. Immunol. 2000. 165: 58145821.
  • 55
    Wu, Q., Martin, R. J., Rino, J. G., Breed, R., Torres, R. M. and Chu, H. W., IL-23-dependent IL-17 production is essential in neutrophil recruitment and activity in mouse lung defense against respiratory Mycoplasma pneumoniae infection. Microbes Infect. 2007. 9: 7886.
  • 56
    Zrioual, S., Toh, M. L., Tournadre, A., Zhou, Y., Cazalis, M. A., Pachot, A., Miossec, V. et al., IL-17RA and IL-17RC receptors are essential for IL-17A-induced ELR+ CXC chemokine expression in synoviocytes and are overexpressed in rheumatoid blood. J. Immunol. 2008. 180: 655663.
  • 57
    Khader, S. A., Bell, G. K., Pearl, J. E., Fountain, J. J., Rangel-Moreno, J., Cilley, G. E., Shen, F. et al., IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge. Nat. Immunol. 2007. 8: 369377.
  • 58
    Sergejeva, S., Ivanov, S., Lotvall, J. and Linden, A., Interleukin-17 as a recruitment and survival factor for airway macrophages in allergic airway inflammation. Am. J. Respir. Cell Mol. Biol. 2005. 33: 248253.
  • 59
    Lin, Y., Ritchea, S., Logar, A., Slight, S., Messmer, M., Rangel-Moreno, J., Guglani, L. et al., Interleukin-17 is required for T helper 1 cell immunity and host resistance to the intracellular pathogen Francisella tularensis. Immunity 2009. 31: 799810.
  • 60
    Yang, X. O., Chang, S. H., Park, H., Nurieva, R., Shah, B., Acero, L., Wang, Y. H. et al., Regulation of inflammatory responses by IL-17F. J. Exp. Med. 2008. 205: 10631075.
  • 61
    Martin-Orozco, N., Chung, Y., Chang, S. H., Wang, Y. H. and Dong, C., Th17 cells promote pancreatic inflammation but only induce diabetes efficiently in lymphopenic hosts after conversion into Th1 cells. Eur. J. Immunol. 2009. 39: 216224.
  • 62
    Li, L., Huang, L., Vergis, A. L., Ye, H., Bajwa, A., Narayan, V., Strieter, R. M. et al., IL-17 produced by neutrophils regulates IFN-gamma-mediated neutrophil migration in mouse kidney ischemia-reperfusion injury. J. Clin. Invest. 120: 331342.
  • 63
    Hou, X., Zhou, R., Wei, H., Sun, R. and Tian, Z., NKG2D-retinoic acid early inducible-1 recognition between natural killer cells and Kupffer cells in a novel murine natural killer cell-dependent fulminant hepatitis. Hepatology 2009. 49: 940949.
  • 64
    Ragheb, S. and Boros, D. L., Characterization of granuloma T lymphocyte function from Schistosoma mansoni-infected mice. J. Immunol. 1989. 142: 32393246.