A controlled human Schistosoma mansoni infection model to advance novel drugs, vaccines and diagnostics.
Adolescent
Adult
Animals
Antigens, Helminth
/ blood
Antiparasitic Agents
/ pharmacology
Cytokines
/ blood
Female
Humans
Immunity, Humoral
/ drug effects
Immunoglobulin M
/ blood
Male
Middle Aged
Models, Biological
Praziquantel
/ pharmacology
Schistosoma mansoni
/ drug effects
Schistosomiasis mansoni
/ blood
Vaccines
/ immunology
Young Adult
Journal
Nature medicine
ISSN: 1546-170X
Titre abrégé: Nat Med
Pays: United States
ID NLM: 9502015
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
06
06
2019
accepted:
09
01
2020
pubmed:
19
2
2020
medline:
9
4
2020
entrez:
19
2
2020
Statut:
ppublish
Résumé
Schistosomiasis treatment relies on the use of a single drug, praziquantel, which is insufficient to control transmission in highly endemic areas
Identifiants
pubmed: 32066978
doi: 10.1038/s41591-020-0759-x
pii: 10.1038/s41591-020-0759-x
doi:
Substances chimiques
Antigens, Helminth
0
Antiparasitic Agents
0
Cytokines
0
Immunoglobulin M
0
Vaccines
0
Praziquantel
6490C9U457
Banques de données
ClinicalTrials.gov
['NCT02755324']
Types de publication
Clinical Trial, Phase I
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
326-332Références
King, C. H. et al. Utility of repeated praziquantel dosing in the treatment of schistosomiasis in high-risk communities in Africa: a systematic review. PLoS Negl. Trop. Dis. 5, e1321 (2011).
doi: 10.1371/journal.pntd.0001321
pubmed: 21949893
pmcid: 21949893
Tukahebwa, E. M., Vennervald, B. J., Nuwaha, F., Kabatereine, N. B. & Magnussen, P. Comparative efficacy of one versus two doses of praziquantel on cure rate of Schistosoma mansoni infection and re-infection in Mayuge District, Uganda. Trans. R. Soc. Trop. Med. Hyg. 107, 397–404 (2013).
doi: 10.1093/trstmh/trt024
pubmed: 23596262
pmcid: 23596262
Bergquist, R., Utzinger, J. & Keiser, J. Controlling schistosomiasis with praziquantel: how much longer without a viable alternative? Infect. Dis. Poverty 6, 74 (2017).
doi: 10.1186/s40249-017-0286-2
pubmed: 28351414
pmcid: 28351414
Global Burden of Disease Study 2013 Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet 386, 743–800 (2015).
doi: 10.1016/S0140-6736(15)60692-4
Colley, D. G., Bustinduy, A. L., Secor, W. E. & King, C. H. Human schistosomiasis. Lancet 383, 2253–2264 (2014).
doi: 10.1016/S0140-6736(13)61949-2
pubmed: 24698483
pmcid: 24698483
Merrifield, M. et al. Advancing a vaccine to prevent human schistosomiasis. Vaccine 34, 2988–2991 (2016).
doi: 10.1016/j.vaccine.2016.03.079
pubmed: 27036511
pmcid: 27036511
Santini-Oliveira, M. et al. Schistosomiasis vaccine candidate Sm14/GLA-SE: phase 1 safety and immunogenicity clinical trial in healthy male adults. Vaccine 34, 586–594 (2016).
doi: 10.1016/j.vaccine.2015.10.027
pubmed: 26571311
pmcid: 26571311
Zhang, W. et al. Sm-p80-based schistosomiasis vaccine: double-blind preclinical trial in baboons demonstrates comprehensive prophylactic and parasite transmission-blocking efficacy. Ann. NY Acad. Sci. 1425, 38–51 (2018).
doi: 10.1111/nyas.13942
pubmed: 30133707
pmcid: 30133707
Status of Vaccine Research and Development of Vaccines for Schistosomiasis (World Health Organization, 2014); http://who.int/immunization/research/meetings_workshops/Schistosomiasis_VaccineRD_Sept2014.pdf
Mo, A. X. & Colley, D. G. Workshop report: schistosomiasis vaccine clinical development and product characteristics. Vaccine 34, 995–1001 (2016).
doi: 10.1016/j.vaccine.2015.12.032
pubmed: 26721329
pmcid: 26721329
Siddiqui, A. J. et al. Sm-p80-based vaccine trial in baboons: efficacy when mimicking natural conditions of chronic disease, praziquantel therapy, immunization, and Schistosoma mansoni re-encounter. Ann. NY Acad. Sci. 1425, 19–37 (2018).
doi: 10.1111/nyas.13866
pubmed: 29888790
pmcid: 29888790
Roestenberg, M., Hoogerwerf, M. A., Ferreira, D. M., Mordmuller, B. & Yazdanbakhsh, M. Experimental infection of human volunteers. Lancet Infect. Dis. 18, e312–e322 (2018).
doi: 10.1016/S1473-3099(18)30177-4
pubmed: 29891332
pmcid: 29891332
Langenberg, M. C. C. et al. Katayama syndrome without Schistosoma mansoni eggs. Ann. Intern. Med. 170, 732–733 (2019).
doi: 10.7326/L18-0438
pubmed: 30615787
pmcid: 30615787
Balasingam, S. & Wilder-Smith, A. Randomized controlled trials for influenza drugs and vaccines: a review of controlled human infection studies. Int. J. Infect. Dis. 49, 18–29 (2016).
doi: 10.1016/j.ijid.2016.05.013
pubmed: 27208631
pmcid: 27208631
Walk, J. et al. Diagnosis and treatment based on quantitative PCR after controlled human malaria infection. Malar. J. 15, 398 (2016).
doi: 10.1186/s12936-016-1434-z
pubmed: 27495296
pmcid: 27495296
Jin, C. et al. Efficacy and immunogenicity of a Vi-tetanus toxoid conjugate vaccine in the prevention of typhoid fever using a controlled human infection model of Salmonella typhi: a randomised controlled, phase 2b trial. Lancet 390, 2472–2480 (2017).
doi: 10.1016/S0140-6736(17)32149-9
pubmed: 28965718
pmcid: 28965718
Chen, W. H. et al. Single-dose live oral cholera vaccine CVD 103-HgR protects against human experimental infection with Vibrio cholerae O1 El Tor. Clin. Infect. Dis. 62, 1329–1335 (2016).
doi: 10.1093/cid/ciw145
pubmed: 27001804
pmcid: 27001804
Rocha, M. O. et al. Pathogenetic factors of acute Schistosomia mansoni: correlation of worm burden, IgE, blood eosinophilia and intensity of clinical manifestations. Trop. Med. Int. Health 1, 213–220 (1996).
doi: 10.1111/j.1365-3156.1996.tb00029.x
pubmed: 8665387
pmcid: 8665387
van Grootveld, R. et al. Improved diagnosis of active Schistosoma infection in travellers and migrants using the ultra-sensitive in-house lateral flow test for detection of circulating anodic antigen (CAA) in serum. Eur. J. Clin. Microbiol. Infect. Dis. 37, 1709–1716 (2018).
doi: 10.1007/s10096-018-3303-x
pubmed: 29974279
pmcid: 29974279
Meltzer, E. & Schwartz, E. Schistosomiasis: current epidemiology and management in travelers. Curr. Infect. Dis. Rep. 15, 211–215 (2013).
doi: 10.1007/s11908-013-0329-1
Visser, L. G., Polderman, A. M. & Stuiver, P. C. Outbreak of schistosomiasis among travelers returning from Mali, West Africa. Clin. Infect. Dis. 20, 280–285 (1995).
doi: 10.1093/clinids/20.2.280
Sousa, M. S. et al. Performance of an ultra-sensitive assay targeting the circulating anodic antigen (CAA) for detection of Schistosoma mansoni infection in a low endemic area in Brazil. Front. Immunol. 10, 682 (2019).
doi: 10.3389/fimmu.2019.00682
pubmed: 6458306
pmcid: 6458306
Kariuki, T. M. et al. Parameters of the attenuated schistosome vaccine evaluated in the olive baboon. Infect. Immun. 72, 5526–5529 (2004).
doi: 10.1128/IAI.72.9.5526-5529.2004
pubmed: 517471
pmcid: 517471
Corstjens, P. L. et al. Tools for diagnosis, monitoring and screening of Schistosoma infections utilizing lateral-flow based assays and upconverting phosphor labels. Parasitology 141, 1841–1855 (2014).
doi: 10.1017/S0031182014000626
pubmed: 4265670
pmcid: 4265670
Colley, D. G. et al. A five-country evaluation of a point-of-care circulating cathodic antigen urine assay for the prevalence of Schistosoma mansoni. Am. J. Trop. Med. Hyg. 88, 426–432 (2013).
doi: 10.4269/ajtmh.12-0639
pubmed: 3592520
pmcid: 3592520
Caldas, I. R. et al. Human Schistosoma mansoni: immune responses during acute and chronic phases of the infection. Acta Trop. 108, 109–117 (2008).
doi: 10.1016/j.actatropica.2008.05.027
Thompson, L. J. et al. Conditioning of naive CD4(
doi: 10.1038/ni.3329
pubmed: 4757503
pmcid: 4757503
Kariuki, T. M. & Farah, I. O. Resistance to re-infection after exposure to normal and attenuated schistosome parasites in the baboon model. Parasite Immunol. 27, 281–288 (2005).
doi: 10.1111/j.1365-3024.2005.00783.x
Soonawala, D., Geerts, J. W., de Mos, M., Yazdanbakhsh, M. & Visser, L. G. The immune response to schistosome antigens in formerly infected travelers. Am. J. Trop. Med. Hyg. 84, 43–47 (2011).
doi: 10.4269/ajtmh.2011.10-0260
pubmed: 3005525
pmcid: 3005525
Parrino, T. A., Schreiber, D. S., Trier, J. S., Kapikian, A. Z. & Blacklow, N. R. Clinical immunity in acute gastroenteritis caused by Norwalk agent. N. Engl. J. Med. 297, 86–89 (1977).
doi: 10.1056/NEJM197707142970204
pubmed: 405590
pmcid: 405590
Sombetzki, M. et al. Host defense versus immunosuppression: unisexual infection with male or female Schistosoma mansoni differentially impacts the immune response against invading cercariae. Front. Immunol. 9, 861 (2018).
doi: 10.3389/fimmu.2018.00861
pubmed: 29743881
pmcid: 29743881
Richter, D., Harn, D. A. & Matuschka, F. R. The irradiated cercariae vaccine model: looking on the bright side of radiation. Parasitol. Today 11, 288–293 (1995).
doi: 10.1016/0169-4758(95)80041-7
pubmed: 15275325
pmcid: 15275325
Agnew, A. et al. The relationship between worm burden and levels of a circulating antigen (CAA) of five species of Schistosoma in mice. Parasitology 111, 67–76 (1995).
doi: 10.1017/S0031182000064611
pubmed: 7609992
pmcid: 7609992
Janse, J. J. et al. Establishing the production of male Schistosoma mansoni cercariae for a controlled human infection model. J. Infect. Dis. 218, 1142–1146 (2018).
doi: 10.1093/infdis/jiy275
pubmed: 29905805
pmcid: 29905805
Winkel, B. M. F. et al. Early induction of human regulatory dermal antigen presenting cells by skin-penetrating Schistosoma mansoni cercariae. Front. Immunol. 9, 2510 (2018).
doi: 10.3389/fimmu.2018.02510
pubmed: 30429854
pmcid: 30429854
World Medical Association. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA 310, 2191–2194 (2013).
doi: 10.1001/jama.2013.281053
European Commission. Clinical Trials - Directive 2001/20/EC. Official Journal of the European Communities https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-1/dir_2001_20/dir_2001_20_en.pdf (2001).
Corstjens, P. L. et al. Improved sensitivity of the urine CAA lateral-flow assay for diagnosing active Schistosoma infections by using larger sample volumes. Parasit. Vectors 8, 241 (2015).
doi: 10.1186/s13071-015-0857-7
pubmed: 25896512
pmcid: 25896512
Obeng, B. B. et al. Application of a circulating-cathodic-antigen (CCA) strip test and real-time PCR, in comparison with microscopy, for the detection of Schistosoma haematobium in urine samples from Ghana. Ann. Trop. Med. Parasitol. 102, 625–633 (2008).
doi: 10.1179/136485908X337490
pubmed: 18817603
pmcid: 18817603
Deelder, A. M. et al. Applicability of different antigen preparations in the enzyme-linked immunosorbent assay for Schistosomiasis mansoni. Am. J. Trop. Med. Hyg. 29, 401–410 (1980).
doi: 10.4269/ajtmh.1980.29.401
pubmed: 6992609
pmcid: 6992609
Nash, T. E., Ottesen, E. A. & Cheever, A. W. Antibody response to a polysaccharide antigen present in the schistosome gut. II. Modulation of antibody response. Am. J. Trop. Med. Hyg. 27, 944–950 (1978).
doi: 10.4269/ajtmh.1978.27.944
pubmed: 362958
pmcid: 362958
Deelder, A. M., van Zeyl, R. J., Fillie, Y. E., Rotmans, J. P. & Duchenne, W. Recognition of gut-associated antigens by immunoglobulin M in the indirect fluorescent antibody test for Schistosoma mansoni. Trans. R. Soc. Trop. Med. Hyg. 83, 364–367 (1989).
doi: 10.1016/0035-9203(89)90506-3
pubmed: 2515624
pmcid: 2515624
Dalton, J. P., Day, S. R., Drew, A. C. & Brindley, P. J. A method for the isolation of schistosome eggs and miracidia free of contaminating host tissues. Parasitology 115, 29–32 (1997).
doi: 10.1017/S0031182097001091
pubmed: 9226954
pmcid: 9226954
Deelder, A. M. Immunology of experimental infections with Schistosoma mansoni in the Swiss mouse and with Fasciola hepatica in the rabbit. Acta Leiden 39, 5–107 (1973).
pubmed: 4573511
pmcid: 4573511
van den Biggelaar, A. H., Borrmann, S., Kremsner, P. & Yazdanbakhsh, M. Immune responses induced by repeated treatment do not result in protective immunity to Schistosoma haematobium: interleukin (IL)-5 and IL-10 responses. J. Infect. Dis. 186, 1474–1482 (2002).
doi: 10.1086/344352
pubmed: 12404164
pmcid: 12404164
Faulkner, H. et al. Antibody responses in onchocerciasis as a function of age and infection intensity. Parasite Immunol. 23, 509–516 (2001).
doi: 10.1046/j.1365-3024.2001.00408.x
pubmed: 11589780
pmcid: 11589780
Staal, S. L. et al. Prevalence of atopy following mass drug administration with albendazole: a study in school children on Flores Island, Indonesia. Int. Arch. Allergy Immunol. 177, 192–198 (2018).
doi: 10.1159/000490952
pubmed: 30130756
pmcid: 30130756
van Dam, G. J. et al. Antibody response patterns against Schistosoma mansoni in a recently exposed community in Senegal. J. Infect. Dis. 173, 1232–1241 (1996).
doi: 10.1093/infdis/173.5.1232
pubmed: 8627077
pmcid: 8627077
Bates, D., Machler, M., Bolker, B. M. & Walker, S. C. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48 (2015).
doi: 10.18637/jss.v067.i01
Kuznetsova, A., Brockhoff, P. B. & Christensen, R. H. B. lmerTest package: tests in linear mixed effects models. J. Stat. Softw. 82, 1–26 (2017).
doi: 10.18637/jss.v082.i13
Wickham, H. ggplot2: Elegant Graphics for Data Analysis 2nd edn (Springer, 2016).
Rohart, F., Gautier, B., Singh, A. & Le Cao, K. A. mixOmics: an R package for ‘omics feature selection and multiple data integration. PLoS Comput. Biol. 13, e1005752 (2017).
doi: 10.1371/journal.pcbi.1005752
pubmed: 5687754
pmcid: 5687754
Singh, A. et al. DIABLO: an integrative approach for identifying key molecular drivers from multi-omic assays. Bioinformatics 35, 3055–3062 (2019).
doi: 10.1093/bioinformatics/bty1054