The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Helminth therapy: Advances in the use of parasitic worms against Inflammatory Bowel Diseases and its challenges
Abstract
Summary: Development of modern medicine and better living conditions in the 20th century helped in reducing a number of cases of infectious diseases. During the same time, expansion of autoimmunological disorders was noticed. Among other are Inflammatory Bowel Diseases (IBD) including ulcerative colitis and Crohn’s disease which are chronic and relapsing inflammation of the gastrointestinal tract. Absence of effective treatment in standard therapies effects the search for alternative opportunities. As per hygienic hypothesis increasing number of cases of autoimmune diseases is as a result of reduced exposure to pathogens, especially parasites. Thus, one of the promising remedial acts against IBD and other allergic and autoimmune disorders is “helminth therapy”. Cure with helminths seems to be the most effective therapy of IBD currently proposed. Helminth therapy focuses on advantageous results that have been obtained from the clinical trials, but its mechanisms are still unclear. Explanation of this phenomenon would help to develop new drugs against IBD based on helminth immunomodulatory molecules.
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.
Integrity signals
Registry
Cites
Statistics
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.
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?
In the citing paper
“Patient acceptability remains an issue, with many reluctant to undergo intentional infection with live parasites due to disgust and concerns about long-term safety”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
In the citing paper
“Rare but serious complications include neurological symptoms, pancreatitis, increased risk of secondary infections, and concerns about aberrant parasite migration, particularly with non-human helminths”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
In the citing paper
“The behavior of live helminths in the human host can be unpredictable, especially with species not naturally adapted to humans, making it difficult to control infection duration and intensity”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
In the citing paper
“Specifically, scientists are now focusing on identifying defined parasite-derived immunomodulatory molecules.”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
In the citing paper
“The deliberate infection of humans with live parasites also raises ethical issues, particularly regarding informed consent and the risk/benefit balance in vulnerable populations”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
In the citing paper
“These substances, which include various proteins and glycoproteins, could, in synthetic or recombinant form, exhibit anti-inflammatory and anti-allergic effects similar to those observed during natural helminth infection”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Maruszewska-Cheruiyot et al. 2018
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
Diversity and dialogue in immunity to helminths
Allen, J. E., & Maizels, R. M. (2011) · Nature reviews. Immunology · doi:10.1038/nri2992 · Cited by 831
Research works printed but not linked: 86
- Adisakwattana, P., Nuamtanong, S., Kusolsuk, T., Chairoj, M., Yenchitsomanas, P.T., Chaisri, U. (2013): Non-encapsulated Trichinella spp., T. papuae, diminishes severity of DSS-induced colitis in mice. Asian Pac. J. Allergy Immunol., 31: 106 – 114. DOI: 10.12932/AP0238.31.2.201310.12932/AP0238.31.2.2013 · DOI
- Barthlott, T., Kassiotis, G., Stockinger, B. (2003): T cell regulation as a side effect of homeostasis and competition. J. Exp. Med., 197: 451 – 460. doi: 10.1084/jem.2002138710.1084/jem.20021387 · DOI
- Bernstein, R.M. (2001): Injections and surgical therapy in chronic pain. Clin. J. Pain., 17: 94 – 10410.1097/00002508-200112001-00018 · DOI
- Biedermann, L., Zeitz, J., Mwinyi, J., Sutter-Minder, E., Rehman, A., Ott, S. J., Steurer-Stey, C., Frei, A., Frei, P., Scharl, M., Loessner, M. J., Vavricka, S. R., Fried, M., Schreiber, S., Schuppler, M., Rogler, G. (2013) : Smoking cessation induces profound changes in the composition of the intestinal microbiota in humans. PLoS One, 8: e59260. DOI: 10.1371/journal.pone.0059260 · DOI
- Bilbo, S.D., Wray, G.A., Perkins, S.E., Parker, W. (2011): Reconstitution of the human biome as the most reasonable solution for epidemics of allergic and autoimmune diseases. Med. Hypotheses., 77: 494 – 504. DOI: 10.1016/j.mehy.2011.06.01910.1016/j.mehy.2011.06.019 · DOI
- Blum, A.M., Hang, L., Setiawan, T.,. Urban, J.P., Stoyanoff, K.M., Leung, J., Weinstock, J.V. (2012): Heligmosomoides polygyrus bakeri induces tolerogenic dendritic cells that block colitis and prevent antigen-specific gut T cell responses. J. Immunol., 189 (5): 2512 – 2520. DOI: 10.4049/jimmunol.110289210.4049/jimmunol.1102892 · DOI
- Bodammer, P., Waitz, G., Loebermann, M., Holtfreter, M.C., Maletzki, C., Krueger, M.R., Nizze, H., Emmrich, J., Reisinger, E.C. (2011): Schistosoma mansoni infection but not egg antigen promotes recovery from colitis in outbred NMRI mice. Dig. Dis. Sci., 56: 70 – 78. DOI: 10.1007/s10620-010-1237-y10.1007/s10620-010-1237-y · DOI
- Brandtzaeg, P., Haraldsen, G., Rugtveit, J. (1997): Immunopathology of human inflammatory bowel disease. Springer Semin. Immunopathol., 18: 555 – 589. DOI: 10.1007/BF0082405810.1007/BF00824058 · DOI
- Broadhurst, M.J., Ardeshir, A., Kanwar, B., Mirpuri, J., Gundra, U.M., Leung, J.M., Wiens, K.E., Vujkovic-Cvijin, I., Kim, C.C., Yarovinsky, F., Lerche, N.W., McCune, J.M., Loke, P. (2012): Therapeutic helminth infection of macaques with idiopathic chronic diarrhea alters the inflammatory signature and mucosal microbiota of the colon. PLoS Pathog., 8: e1003000. DOI: 10.1371/journal.ppat.1003000 · DOI
- Cader, M.Z., Kaser, A. (2013): Recent advances in inflammatory bowel disease: mucosal immune cells in intestinal inflammation. Gut, 62: 1653 – 1664. DOI: 10.1136/gutjnl-2012-30395510.1136/gutjnl-2012-303955 · DOI
- Chandrashekara, S. (2012): The treatment strategies of autoimmune disease may need a different approach from conventional protocol: A review. Indian J. Pharmacol., 44: 665 – 671. DOI: 10.4103/0253-7613.10323510.4103/0253-7613.103235 · DOI
- Chassaing, B., Aitken, J.D., Malleshappa, M., Vijay-Kumar, M. (2015): Dextran sulfate sodium (DSS)-induced colitis in mice. Curr. Protoc. Immunol., 104: 15 – 25. DOI: 10.1002/0471142735.im1525s10410.1002/0471142735.im1525s104 · DOI
- Chen, C.C., Louie, S., McCormick, B., Walker, W.A., Shi, H.N. (2005): Concurrent infection with an intestinal helminth parasite impairs host resistance to enteric Citrobacter rodentium and enhances Citrobacter-induced colitis in mice. Infect. Immun., 73: 5468 – 5481. DOI: 10.1128/IAI.73.9.5468-5481.200510.1128/IAI.73.9.5468-5481.2005 · DOI
- Chen, C.C., Louie, S., McCormick, B.A., Walker, W.A., Shi, H.N. (2006): Helminth primed dendritic cells alter the host response to enteric bacterial infection. J. Immunol.,176: 472 – 483 · DOI
- Cleynen, I., Boucher, G., Jostins, L. et al. (2016): Inherited determinants of Crohn’s disease and ulcerative colitis phenotypes: a genetic association study. Lancet, 9, 156 – 167. DOI: 10.1016/S0140-6736(15)00465-110.1016/S0140-6736(15)00465-1 · DOI
- Correale, J. (2014): Helminth/Parasite treatment of multiple sclerosis. Curr. Treat Options Neurol.,16: 296. DOI: 10.1007/s11940-014-0296-310.1007/s11940-014-0296-3 · DOI
- Croese, J., Giacomin, P., Navarro, S., Clouston, A., McCann, L., Dougall, A., Ferreira, I., Susianto, A., O’Rourke, P., Howlett, M., McCarthy, J., Engwerda, C., Jones, D., Loukas, A. (2015): Experimental hookworm infection and gluten microchallenge promote tolerance in celiac disease. J. Allergy Clin. Immunol.,135: 508 – 516. DOI: 10.1016/j.jaci.2014.07.02210.1016/j.jaci.2014.07.022 · DOI
- Croese, J., O’neil, J., Masson, J., Cooke, S., Melrose, W., Pritchard, D., Speare, R. (2006): A proof of concept study establishing Necator americanus in Crohn’s patients and reservoir donors. Gut, 55: 136 – 137. doi: 10.1136/gut.2005.07912910.1136/gut.2005.079129 · DOI
- Daveson, A.J., Jones, D.M., Gaze, S., McSorley, H., Clouston, A., Pascoe, A., Cooke, S., Speare, R., Macdonald, G.A., Anderson, R., McCarthy, J.S., Loukas, A., Croese, J. (2011): Effect of hookworm infection on wheat challenge in celiac disease – a randomised double-blinded placebo controlled trial. PLoS One, 8: e17366. DOI: 10.1371/journal.pone.0017366 · DOI · Paper page
- Donskow, K., Drela, N., Doligalska, M. (2011): Heligmosomoides bakeri antigen rescues CD4-positive T cells from glucocorticoid-induced apoptosis by Bcl-2 protein expression. Parasite Immunol., 33: 158 – 169. DOI: 10.1111/j.1365-3024.2010.01262.x10.1111/j.1365-3024.2010.01262.x · DOI
- Donskow-Łysoniewska, K., Bien, J., Brodaczewska, K., Krawczak, K., Doligalska, M. (2013b): Colitis promotes adaptation of an intestinal nematode: a Heligmosomoides polygyrus mouse model system. PLoS One, 22: e78034. DOI: 10.1371/journal.pone.0078034 · DOI
- Donskow-Łysoniewska, K., Brodaczewska, K., Doligalska, M. (2013a): Heligmosomoides polygyrus antigens inhibit the intrinsic pathway of apoptosis by overexpression of survivin and Bcl-2 protein in CD4 T cells. Prion, 7: 319 – 327. DOI:10.4161/pri.2500810.4161/pri.25008 · DOI
- Donskow-Lysoniewska, K., Majewski, P., Brodaczewska, K., Jozwicka, K., Doligalska, M. (2012): Heligmosmoides polygyrus fourth stages induce protection against DSS induced colitis and change opioid expression in the intestine. Parasite Immunol., 34: 536 – 546. DOI: 10.1111/pim.1200310.1111/pim.12003 · DOI
- Du, L., Tang, H., Ma, Z., Xu, J., Gao, W., Chen, J., Gan, W., Zhang, Z., Yu, X., Zhou, X., Hu, X. (2011): The protective effect of the recombinant 53-kDa protein of Trichinella spiralis on experimental colitis in mice. Dig. Dis. Sci., 56: 2810 – 2817. DOI: 10.1007/s10620-011-1689-810.1007/s10620-011-1689-8 · DOI
- Elliott, D.E., Li, J., Blum, A., Metwali, A., Qadir, K., Urban, J.F. Jr, Weinstock, J.V. (2003): Exposure to schistosome eggs protects mice from TNBS-induced colitis. Am. J. Physiol. Gastrointest. Liver Physiol., 284: G385 – G391. DOI: 10.1152/ajpgi.00049.200210.1152/ajpgi.00049.2002 · DOI
- Elliott, D.E., Setiawan, T., Metwali, A., Blum, A., Urban, J.F. Jr., Weinstock, J.V. (2004): Heligmosomoides polygyrus inhibits established colitis in IL-10-deficient mice. Eur. J. Immunol., 34: 2690 – 2698. DOI: 10.1002/eji.200324833 · DOI
- Elliott, D.E., Urban, J.F. Jr., Argo, C.K., Weinstock, J.V. (2000): Does the failure to acquire helminthic parasites predispose to Crohn’s disease? FASEB J., 14: 1848 – 1855. doi: 10.1096/fj.99-0885hyp10.1096/fj.99-0885hyp · DOI
- Erb, K.J. (2009): Can helminths or helminth-derived products be used in humans to prevent or treat allergic diseases? Trends Immunol., 30: 75 – 82. DOI: 10.1016/j.it.2008.11.00510.1016/j.it.2008.11.005 · DOI
- Finlay, C.M., Walsh, K.P., Mills, K.H. (2014): Induction of regulatory cells by helminth parasites: exploitation for the treatment of inflammatory diseases. Immunol. Rev., 259: 206 – 230. DOI: 10.1111/imr.1216410.1111/imr.12164 · DOI
- Fleming, J.O., Isaak, A., Lee, J.E., Luzzio, C.C., Carrithers, M.D., Cook, T.D., Field, A.S., Boland, J., Fabry, Z. (2011): Probiotic helminth administration in relapsing-remitting multiple sclerosis: a phase 1 study. Mult. Scler., 17: 743 – 754. DOI: 10.1177/135245851139805410.1177/1352458511398054 · DOI
- Goodridge, H.S., Stepek, G., Harnett, W., Harnett, M.M. (2005): Signalling mechanisms underlying subversion of the immune response by the filarial nematode secreted product ES-62. Immunology, 115: 296 – 304. DOI: 10.1111/j.1365-2567.2005.02167.x10.1111/j.1365-2567.2005.02167.x · DOI
- Gouy De Bellocq, J., Ferte, H., Depaquit, J., Justine, J.L., Tillier, A., Durette-Desset, M.C. (2001): Phylogeny of the Trichostrongylina (Nematoda) inferred from 28S rDNA sequences. Mol. Phylogenet. Evol., 19: 430 – 442. DOI: 10.1006/mpev.2001.092510.1006/mpev.2001.0925 · DOI
- Hadis, U., Wahl, B., Schulz, O., Hardtke-Wolenski, M., Schippers, A., Wagner, N., Müller, W., Sparwasser, T., Förster, R., Pabst, O. (2011): Intestinal tolerance requires gut homing and expansion of FoxP3+ regulatory T cells in the lamina propria. Immunity, 34: 237 – 246. DOI: 10.1016/j.immuni.2011.01.01610.1016/j.immuni.2011.01.016 · DOI
- Hang, L., Setiawan, T., Blum, A.M., Urban, J., Stoyanoff, K., Arihiro, S., Reinecker, H.C., Weinstock, J.V. (2010): Heligmosomoides polygyrus infection can inhibit colitis through direct interaction with innate immunity. J. Immunol, 185: 3184 – 3189. DOI: 10.4049/jimmunol.100094110.4049/jimmunol.1000941 · DOI
- Helmby, H. (2015): Human helminth therapy to treat inflammatory disorders - where do we stand? BMC Immunol., 16: 12. DOI: 10.1186/s12865-015-0074-310.1186/s12865-015-0074-3 · DOI
- Herrera, L.A., Ostrosky-Wegman, P. (2001): Do helminths play a role in carcinogenesis? Trends Parasitol., 17: 172 – 175. DOI: 10.1016/S1471-4922(00)01942-510.1016/S1471-4922(00)01942-5 · DOI
- Hokke, C.H., Deelder, A.M., Hoffmann, K.F., Wuhrer, M. (2007): Glycomics-driven discoveries in schistosome research. Exp. Parasitol., 117: 275 – 283. DOI: 10.1016/j.exppara.2007.06.00310.1016/j.exppara.2007.06.003 · DOI
- Hunter, M.M., Wang, A., Hirota, C.L., Mckay, D.M. (2005): Neutralizing anti-IL-10 antibody blocks the protective effect of tapeworm infection in a murine model of chemically induced colitis. J. Immunol., 174: 7368 – 7375. DOI: 10.4049/jimmunol.174.11.7368 · DOI
- Hunter, M.M., Wang, A., Mckay, D.M. (2007): Helminth infection enhances disease in a murine TH2 model of colitis. Gastroenterology, 132: 1320 – 1330. DOI: 10.1053/j.gastro.2007.01.03810.1053/j.gastro.2007.01.038 · DOI
- Ince, M.N., Elliott, D.E., Setiawan, T., Metwali, A., Blum, A., Chen, H.L., Urban, J.F., Flavell, R.A., Weinstock, J.V. (2009): Role of T cell TGF-beta signaling in intestinal cytokine responses and helminthic immune modulation. J. Immunol., 39: 1870 – 1878. DOI: 10.1002/eji.20083895610.1002/eji.200838956 · DOI
- Kappus, K.D., Lundgren, R.G. Jr., Juranek, D.D., Roberts, J.M., Spencer, H.C. (1994): Intestinal parasitism in the United States: update on a continuing problem. Am. J. Trop. Med. Hyg., 50, 705 – 713. DOI: 10.4269/ajtmh.1994.50.70510.4269/ajtmh.1994.50.705 · DOI
- Keubler, L.M., Buettner, M., Häger, C., Bleich, A. (2015): A multihit model: colitis lessons from the Interleukin-10-deficient mouse. Inflamm. Bowel Dis., 2: 1967 – 1975. DOI: 10.1097/MIB.0000000000000468 · DOI
- Khan, A.R., Fallon, P.G. (2013): Helminth therapies: translating the unknown unknowns to known knowns. Int. J. Parasitol., 43: 293 – 299. DOI: 10.1016/j.ijpara.2012.12.00210.1016/j.ijpara.2012.12.002 · DOI
- Khan, W.I., Blennerhasset, P.A., Varghese, A.K., Chowdhury, S.K., Omsted, P., Deng, Y., Collins, S.M. (2002): Intestinal nematode infection ameliorates experimental colitis in mice. Infect. Immun., 70: 5931 – 5937. doi: 10.1128/IAI.70.11.5931-5937.200210.1128/IAI.70.11.5931-5937.2002 · DOI
- Lakatos, P.L. (2006): Recent trends in the epidemiology of inflammatory bowel diseases: up or down? World J. Gastroenterol., 14: 6102-6108. doi: 10.3748/wjg.v12.i38.610210.3748/wjg.v12.i38.6102 · DOI
- Leitner, G.C., Vogelsang, H. (2016): Pharmacological-and non-pharmacological therapeutic approaches in inflammatory bowel disease in adults. World J. Gastrointest. Pharmacol. Ther., 6: 5 – 20. DOI: 10.4292/wjgpt.v7.i1.510.4292/wjgpt.v7.i1.5 · DOI
- Leong, R.W., Mitrev, N., Ko, Y. (2016): Hygiene hypothesis: Is the evidence the same all over the world? Dig. Dis., 34: 35 – 42. DOI: 10.1159/00044292210.1159/000442922 · DOI
- Leung, J., Hang, L., Blum, A., Setiawan, T., Stoyanoff, K., Weinstock, J. (2012): Heligmosomoides polygyrus abrogates antigen-specific gut injury in a murine model of inflammatory bowel disease. Inflamm. Bowel Dis., 18: 1447 – 1455. DOI: 10.1002/ibd.2285810.1002/ibd.22858 · DOI
- Li, X., Sundquist, J., Hemminki, K., Sundquist, K. (2011): Risk of inflammatory bowel disease in firstand second-generation immigrants in Sweden: a nationwide follow-up study. Inflamm. Bowel Dis., 17: 1784 – 1791. DOI: 10.1002/ibd.2153510.1002/ibd.21535 · DOI
- MacDonald, T.T., Monteleone, G. (2005): Immunity, inflammation, and allergy in the gut. Science, 25: 1920 – 1925. DOI: 10.1126/science.110644210.1126/.1106442 · DOI
- Maizels, R.M., Balic, A., Gomez-Escobar, N., Nair, M., Taylor, M.D., Allen, J.E. (2004): Helminth parasites – masters of regulation. Immunol. Rev., 201, 89 – 116. DOI: 10.1111/j.0105-2896.2004.00191.x10.1111/j.0105-2896.2004.00191.x · DOI
- Maizels, R.M., Hewitson, J.P., Smith, K.A. (2012): Susceptibility and immunity to helminth parasites. Curr. Opin. Immunol., 24: 459 – 466. DOI: 10.1016/j.coi.2012.06.00310.1016/j.coi.2012.06.003 · DOI
- Mann, E.R., Li, X. (2014): Intestinal antigen-presenting cells in mucosal immune homeostasis: crosstalk between dendritic cells, macrophages and B-cells. World J. Gastroenterol., 7: 9653 – 9664. DOI: 10.3748/wjg.v20.i29.965310.3748/wjg.v20.i29.9653 · DOI
- McGuckin, M.A., Eri, R., Simms, L.A., Florin, T.H., Radford-Smith, G. (2009): Intestinal barrier dysfunction in inflammatory bowel diseases. Inflamm. Bowel Dis., 15: 100 – 113. DOI: 10.1002/ibd.2053910.1002/ibd.20539 · DOI
- McSorley, H.J., Hewitson, J.P., Maizels, R.M. (2013): Immunomodulation by helminth parasites: defining mechanisms and mediators. Int. J. Parasitol., 43: 301 – 310. DOI: 10.1016/j.ijpara.2012.11.01110.1016/j.ijpara.2012.11.011 · DOI
- Melon, A., Wang, A., Phan, V., Mckay, D.M. (2010): Infection with Hymenolepis diminuta is more effective than daily corticosteroids in blocking chemically induced colitis in mice. J. Biomed. Biotechnol., 384523. DOI: 10.1155/2010/38452310.1155/2010/384523 · DOI
- Metwali, A., Setiawan, T., Blum, A.M., Urban, J., Elliott, D.E., Hang, L., Weinstock, J.V. (2006): Induction of CD8+ regulatory T cells in the intestine by Heligmosomoides polygyrus infection. Am. J. Physiol. Gastrointest. Liver Physiol., 291: G253 – G259. DOI: 10.1152/ajpgi.00409.2005 · DOI
- Molodecky, N.A., Soon, I.S., Rabi, D.M., Ghali, W.A., Ferris, M., Chernoff, G., Benchimol, E.I., Panaccione, R., Ghosh, S., Barkema, H.W., Kaplan, G.G. (2012): Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology, 142: 46 – 54. DOI: 10.1053/j.gastro.2011.10.00110.1053/j.gastro.2011.10.001 · DOI
- Monroy, F.G., Enriquez, F.J. (1992): Heligmosomoides polygyrus: a model for chronic gastrointestinal helminthiasis. Parasitol. Today, 8: 49 – 54. DOI: 10.1016/0169-4758(92)90084-F10.1016/0169-4758(92)90084- · DOI
- Morampudi, V., Bhinder, G., Wu, X., Dai, C., Sham, H.P., Vallance, B.A., Jacobson, K. (2014): DNBS/TNBS colitis models: providing insights into inflammatory bowel disease and effects of dietary fat. J. Vis. Exp., 84: 51297. DOI:10.3791/51297 · DOI
- Moreels, T.G., Nieuwendijk, R.J., De Man, J.G., De Winter, B.Y., Herman, A.G., Van Marck, E.A., Pelckmans, P.A. (2004): Concurrent infection with Schistosoma mansoni attenuates inflammation induced changes in colonic morphology, cytokine levels, and smooth muscle contractility of trinitrobenzene sulphonic acid induced colitis in rats. Gut, 53: 99 – 107 · DOI
- Mulvenna, J., Hamilton, B., Nagaraj, S.H., Smyth, D., Loukas, A., Gorman, J.J. (2009): Proteomics analysis of the excretory/secretory component of the blood-feeding stage of the hookworm, Ancylostoma caninum. Mol. Cell. Proteomics, 8: 109 – 121. DOI: 10.1074/mcp.M800206-MCP200 · DOI
- Niewiadomski, O., Studd, C., Wilson, J., Williams, J., Hair, C., Knight, R., Prewett, E., Dabkowski, P., Alexander, S., Allen, B., Dowling, D., Connell, W., Desmond, P., Bell, S. (2016): Influence of food and lifestyle on the risk of developing inflammatory bowel disease. Intern. Med. J., 46: 669 – 676. DOI: 10.1111/imj.1309410.1111/imj.13094 · DOI
- Packham, G., Stevenson, F.K. (2005): Bodyguards and assassins: Bcl-2 family proteins and apoptosis control in chronic lymphocytic leukaemia. Immunology, 114: 441 – 449. DOI: 10.1111/j.1365-2567.2005.02117.x10.1111/j.1365-2567.2005.02117.x · DOI
- Prasanphanich, N.S., Mickum, M.L., Heimburg-Molinaro, J., Cummings, R.D. (2013): Glycoconjugates in host-helminth interactions. Front. Immunol., 4: 240. DOI: 10.3389/fimmu.2013.0024010.3389/fimmu.2013.00240 · DOI
- Probert, C.S., Jayanthi, V., Pinder, D., Wicks, A.C., Mayberry, J.F. (1992): Epidemiological study of ulcerative proctocolitis in Indian migrants and the indigenous population of Leicestershire. Gut, 33: 687 – 69310.1136/gut.33.5.687 · DOI
- Reardon, C., Sanchez, A., Hogaboam, C.M., Mckay, D.M. (2001): Tapeworm infection reduces epithelial ion transport abnormalities in murine dextran sulfate sodium induced colitis. Infect. Immun., 69: 4417 – 4423. doi: 10.1128/IAI.69.7.4417-4423.200110.1128/IAI.69.7.4417-4423.2001 · DOI
- Rescigno, M., Di Sabatino, A. (2009): Dendritic cells in intestinal homeostasis and disease. J. Clin. Invest.,119: 2441 – 2450. DOI: 10.1172/JCI3913410.1172/JCI39134 · DOI
- Ruyssers, N.E., De Winter, B.Y., De Man, J.G., Loukas, A., Herman, A.G., Pelckmans, P.A., Moreels, T.G. (2008): Worms and the treatment of inflammatory bowel disease: are molecules the answer? Clin. Dev. Immunol., 567314. DOI: 10.1155/2008/567314 · DOI
- Sandborn, W.J., Elliott, D.E., Weinstock, J., Summers, R.W., Landry-Wheeler, A., Silver, N., Harnett, M.D., Hanauer, S.B. (2013): Randomised clinical trial: the safety and tolerability of Trichuris suis ova in patients with Crohn’s disease. Aliment. Pharmacol. Ther., 38: 255 – 263. DOI: 10.1111/apt.1236610.1111/apt.12366 · DOI
- Satsangi, J., Silverberg, M.S., Vermeire, S., Colombel, J.F. (2006): The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications. Gut, 55: 749 – 753. DOI: 10.1136/gut.2005.08290910.1136/gut.2005.082909 · DOI
- Schnoeller, C., Rausch, S., Pillai, S., Avagyan, A., Wittig, B. M., Loddenkemper, C., Hamann, A., Hamelmann, E., Lucius, R., Hartmann, S. (2008): A helminth immunomodulator reduces allergic and inflammatory responses by induction of IL-10-producing macrophages. J. Immunol., 15: 4265 – 4272. DOI: 10.4049/jimmunol.180.6.4265 · DOI
- Setiawan, T., Metwali, A., Blum, A.M. Nedim Ince, M., Urban Jr., J.F., Elliott, D.E., Weinstock, J.V. (2007): Heligmosomoides polygyrus promotes regulatory T-cell cytokine production in the murine normal distal intestine. Infect. Immun., 75: 4655 – 4663. DOI: 10.1128/IAI.00358-0710.1128/IAI.00358-07 · DOI
- Shorter, R.G., Huizenga, K.A., Spencer, R.J. (1972): A working hypothesis for the etiology and pathogenesis of nonspecific inflammatory bowel disease. Am. J. Dig. Dis., 17: 1024 – 103210.1007/BF02239143 · DOI
- Smith, P., Mangan, N.E., Fallon, P.G. (2009): Generation of parasite antigens for use in Toll-like receptor research. Methods Mol., 517: 401 – 413. DOI: 10.1007/978-1-59745-541-1_2410.1007/978-1-59745-541-1_24 · DOI
- Smith, P., Mangan, N.E., Walsh, C.M., Fallon, R.E., Mckenzie, A.N.J., Van Rooijen, N., Fallon, P.G. (2007): Infection with a helminth parasite prevents experimental colitis via a macrophage-mediated mechanism. J. Immunol., 178: 4557 – 4566. DOI: 10.4049/jimmunol.178.7.455710.4049/jimmunol.178.7.4557 · DOI
- Strachan, D.P. (1989): Hay fever, hygiene and household size. BMJ, 299: 1259 – 1260 · DOI · Paper page
- Summers, R.W., Elliott, D.E., Qadir, K., Urban, J.F., Thompson, R., Weinstock, J.V. (2003): Trichuris suis seems to be safe and possibly effective in the treatment of inflammatory bowel disease. Am. J. Gastroenterol., 98, 2034 – 2041. DOI: 10.1111/j.1572-0241.2003.07660.x10.1111/j.1572-0241.2003.07660.x · DOI
- Summers, R.W., Elliott, D.E., Urban, J.F. Jr., Thompson, R., Weinstock, J.V. (2005a): Trichuris suis therapy in Crohn’s disease. Gut, 54: 87 – 90. DOI: 10.1136/gut.2004.04174910.1136/gut.2004.041749 · DOI
- Summers, R.W., Elliott, D.E., Urban, J.F. Jr., Thompson, R.A., Weinstock, J.V. (2005b): Trichuris suis therapy for active ulcerative colitis: a randomized controlled trial. Gastroenterology, 128: 825 – 832. DOI: 10.1053/j.gastro.2005.01.00510.1053/j.gastro.2005.01.005 · DOI
- Sutton, T.L., Zhao, A., Madden, K.B., Elfrey, J.E., Tuft, B.A., Sullivan, C.A., Urban, Jr., J.F., Shea-Donohue, T. (2008): Antiinflammatory mechanisms of enteric Heligmosomoides polygyrus infection against trinitrobenzene sulfonic acid-induced colitis in a murine model. Infect. Immun., 76: 4772 – 4782. DOI: 10.1128/IAI.00744-0710.1128/IAI.00744-07 · DOI
- Taylor, M.D., Van Der Werf, N., Maizels, R.M. (2012): T cells in helminth infection: the regulators and the regulated. Trends Immunol., 33: 181 – 189. DOI: 10.1016/j.it.2012.01.00110.1016/j.it.2012.01.001 · DOI
- Wilson, M.S., Maizels, R.M. (2004): Regulation of allergy and autoimmunity in helminth infection. Clin. Rev. Allergy Immunol., 26: 35 – 50. DOI: 10.1385/CRIAI:26:1:3510.1385/CRIAI:26:1:35 · DOI
- Wirtz, S., Neurath, M.F. (2007): Mouse models of inflammatory bowel disease. Adv. Drug Deliv. Rev., 59: 1073 – 1083. DOI: 10.1016/j.addr.2007.07.00310.1016/j.addr.2007.07.003 · DOI
- Xia, C.M., Zhao, Y., Jiang, L., Jiang, J., Zhang, S.C. (2011): Schistosoma japonicum ova maintains epithelial barrier function during experimental colitis. World J Gastroenterol., 17: 4810 – 4816.10.3748/wjg.v17.i43.4810 · DOI
- Zhao, Y., Zhang, S., Jiang, L., Jiang, J., Liu, H. (2009): Preventive effects of Schistosoma japonicum ova on trinitrobenzenesulfonic acid-induced colitis and bacterial translocation in mice. J. Gastroenterol. Hepatol., 24: 1775 – 1780. DOI: 10.1111/j.1440-1746.2009.05986.x10.1111/j.1440-1746.2009.05986.x · DOI
Cited by
Sorted by citations
Packi, K., Świerczewski, D., Klimczak, S., Ochab, D., Gałęziewska, J., Gromek, P., Kruczkowska, W., Płuciennik, E., Kałuzińska-Kołat, Ż., & Kołat, D. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02425-4
Metadata
- Authors
- Maruszewska-Cheruiyot, M., Donskow-Łysoniewska, K., & Doligalska, M.
- Venue
- Helminthologia
- Publisher
- Walter de Gruyter GmbH
- Published
- 2018-01-27
- Volume
- 55
- Issue
- 1
- Pages
- 1-11
- ISSN
- 1336-9083
- 0440-6605
- PMC
- PMC6799527
- Cited by
- 38
- References
- 1
- 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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Helminth therapy: Advances in the use of parasitic worms against Inflammatory Bowel Diseases and its challenges. https://app.cochat.ai/papers/10.1515/helm-2017-0048
- The paper
- Maruszewska-Cheruiyot, M., Donskow-Łysoniewska, K., & Doligalska, M. (2018). Helminth therapy: Advances in the use of parasitic worms against Inflammatory Bowel Diseases and its challenges. Helminthologia. https://doi.org/10.1515/helm-2017-0048