This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Aranzamendi, C., Fransen, F., Langelaar, M., Franssen, F., van der Ley, P., van Putten, J.P., Rutten, V., Pinelli, E. (2012): Trichinella spiralis-secreted products modulate DC functionality and expand regulatory T cells in vitro. Parasite Immunol., 34(4):210–223. 10.1111/j.1365-3024.2012.01353.xAranzamendiC.FransenF.LangelaarM.FranssenF.van der LeyP.van PuttenJ.P.RuttenV.PinelliE.2012Trichinella spiralis-secreted products modulate DC functionality and expand regulatory T cells in vitroParasite Immunol34421022310.1111/j.1365-3024.2012.01353.xOpen DOISearch in Google Scholar
Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., Van Rooijen, N., Plonquet, A., Gherardi, R.K., Chazaud, B. (2007): Inflammatory monocytes recruited after skeletal muscle injury switch into anti-inflammatory macrophages to support myogenesis. J. Exp. Med., 204(5): 1057–1069. 10.1084/jem.20070075ArnoldL.HenryA.PoronF.Baba-AmerY.Van RooijenN.PlonquetA.GherardiR.K.ChazaudB.2007Inflammatory monocytes recruited after skeletal muscle injury switch into anti-inflammatory macrophages to support myogenesisJ. Exp. Med20451057106910.1084/jem.20070075Open DOISearch in Google Scholar
Ashour, D.S. (2013): Trichinella spiralis immunomodulation: an interactive multifactorial process. Expert. Rev. Clin. Immunol., 9(7): 669–675. 10.1586/1744666X.2013.811187AshourD.S.2013Trichinella spiralis immunomodulation: an interactive multifactorial processExpert. Rev. Clin. Immunol9766967510.1586/1744666X.2013.811187Open DOISearch in Google Scholar
Bai, X., Wu, X., Wang, X., Liu, X., Song, Y., Gao, F., Miao, Y., Yu, L., Tang, B., Wang, X., Radu, B., Valee, I., Boireau, P., Wang, F., Zhao, Y., Liu, M. (2012a): Inhibition of mammalian muscle differentiation by excretory secretory products of muscle larvae of Trichinella spiralis in vitro. Parasitol. Res., 110(6): :2481–2490. 10.1007/s00436-011-2789-2BaiX.WuX.WangX.LiuX.SongY.GaoF.MiaoY.YuL.TangB.WangX.RaduB.ValeeI.BoireauP.WangF.ZhaoY.LiuM.2012aInhibition of mammalian muscle differentiation by excretory secretory products of muscle larvae of Trichinella spiralis in vitroParasitol. Res11062481249010.1007/s00436-011-2789-2Open DOISearch in Google Scholar
Bai, X., Wu, X., Wang, X., Guan, Z., Gao, F., Yu, J., Yu, L., Tang, B., Liu, X., Song, Y., Wang X., Radu, B., Boireau, P., Wang, F., Liu, M. (2012b): Regulation of cytokine expression in murine macrophages stimulated by excretory/secretory products from Trichinella spiralis in vitro. Mol. Cell. Biochem., 360(1–2):79–88. 10.1007/s11010-011-1046-4BaiX.WuX.WangX.GuanZ.GaoF.YuJ.YuL.TangB.LiuX.SongY.WangX.RaduB.BoireauP.WangF.LiuM.2012bRegulation of cytokine expression in murine macrophages stimulated by excretory/secretory products from Trichinella spiralis in vitroMol. Cell. Biochem3601–2798810.1007/s11010-011-1046-4Open DOISearch in Google Scholar
Bautista-Garfias, C.R., Ixta, O., Orduña, M., Martínez, F., Aguilar, B., Cortés, A. (1999): Enhancement of resistance in mice treated with Lactobacillus casei Effect on Trichinella spiralis infection. Vet. Parasitol., 80(3): 251–260. 10.1016/S0304-4017(98)00210-6Bautista-GarfiasC.R.IxtaO.OrduñaM.MartínezF.AguilarB.CortésA.1999Enhancement of resistance in mice treated with Lactobacillus casei Effect on Trichinella spiralis infectionVet. Parasitol80325126010.1016/S0304-4017(98)00210-6Open DOISearch in Google Scholar
Bautista-Garfias, C.R., Ixta-Rodríguez, O., Martínez-Gómez, F., Lopez, M.G., Aguilar-Figueroa, B.R. (2001): Effect of viable or dead Lactobacillus casei organisms administered orally to mice on resistance against Trichinella spiralis infection. Parasite, 8(Suppl.2): 226–228. 10.1051/parasite/200108s2226Bautista-GarfiasC.R.Ixta-RodríguezO.Martínez-GómezF.LopezM.G.Aguilar-FigueroaB.R.2001Effect of viable or dead Lactobacillus casei organisms administered orally to mice on resistance against Trichinella spiralis infectionParasite8Suppl.222622810.1051/parasite/200108s222611484363Open DOISearch in Google Scholar
Berrili, F., Di Cave, D., Cavalero, S., D’amelio, S. (2012): Interactions between parasites and microbial communities in the human gut. Front. Cell. Infect. Microbiol., 2(2012): Article 141. 10.3389/fcimb.2012.00141.BerriliF.Di CaveD.CavaleroS.D’amelioS.2012Interactions between parasites and microbial communities in the human gutFront. Cell. Infect. Microbiol22012Article 14110.3389/fcimb.2012.00141Open DOISearch in Google Scholar
Bruschi, F. (2002): The immune response to the parasitic nematode Trichinella and the ways to escape it. From experimental studies to implications for human infection. Curr. Drug Targets Immune Endocr. Metabol. Disord., 2(3): 269–280.BruschiF.2002The immune response to the parasitic nematode Trichinella and the ways to escape it. From experimental studies to implications for human infectionCurr. Drug Targets Immune Endocr. Metabol. Disord2326928010.2174/156800802334052312476491Search in Google Scholar
Bruschi, F. (2012): Trichinellosis in developing countries: is it neglected? J. Infect. Dev. Ctries., 6(3): 216–222. 10.3855/jidc.2478BruschiF.2012Trichinellosis in developing countries: is it neglected?J. Infect. Dev. Ctries6321622210.3855/jidc.247822421602Open DOISearch in Google Scholar
Bruschi, F., Chiumiento, L. (2011): Trichinella inflammatory myopathy: host or parasite strategy? Parasit. Vectors, 4 (2011): Article number 42. 10.1186/1756-3305-4-42BruschiF.ChiumientoL.2011Trichinella inflammatory myopathy: host or parasite strategy?Parasit. Vectors42011Article number 4210.1186/1756-3305-4-42Open DOISearch in Google Scholar
Bucková, B., Hurniková, Z., Lauková, A., Revajová, V., Dvorožňáková, E. (2018): The anti-parasitic effect of probiotic bacteria via limiting the fecundity of Trichinella spiralis female adults. Helminthologia, 55(2): 102–111. 10.2478/helm-2018-0010BuckováB.HurnikováZ.LaukováA.RevajováV.DvorožňákováE.2018The anti-parasitic effect of probiotic bacteria via limiting the fecundity of Trichinella spiralis female adultsHelminthologia55210211110.2478/helm-2018-0010Open DOISearch in Google Scholar
Donnet-Hughes, A., Rochat, F., Serrant, P., Aeschlimann, J.M., Schifrin, E.J. (1999): Modulation of nonspecific mechanisms of defense by lactic acid bacteria: effective dose. J. Dairy Sci., 82(5): 863–869Donnet-HughesA.RochatF.SerrantP.AeschlimannJ.M.SchifrinE.J.1999Modulation of nonspecific mechanisms of defense by lactic acid bacteria: effective doseJ. Dairy Sci82586386910.3168/jds.S0022-0302(99)75304-XSearch in Google Scholar
Dvorožňáková, E., Porubcová, J., Šnábel, V., Fedoročko, P. (2008): Immunomodulative effect of liposomized muramyltripeptide phosphatidylethanolamine (LMTP-PE) on mice with alveolar echinococcosis and treated with albendazole. Parasitol. Res., 103(4): 919–929. 10.1007/s00436-008-1077-2DvorožňákováE.PorubcováJ.ŠnábelV.FedoročkoP.2008Immunomodulative effect of liposomized muramyltripeptide phosphatidylethanolamine (LMTP-PE) on mice with alveolar echinococcosis and treated with albendazoleParasitol. Res103491992910.1007/s00436-008-1077-218587669Open DOISearch in Google Scholar
Dvorožňáková, E., Bucková, B., Hurníková, Z., Revajová, V., Lauková, A. (2016): Effect of probiotic bacteria on phagocytosis and respiratory burst activity of blood polymorphonuclear leukocytes (PMNL) in mice infected with Trichinella spiralis. Vet. Parasitol., 231(2016): 69–76. 10.1016/j.vetpar.2016.07.004.DvorožňákováE.BuckováB.HurníkováZ.RevajováV.LaukováA.2016Effect of probiotic bacteria on phagocytosis and respiratory burst activity of blood polymorphonuclear leukocytes (PMNL) in mice infected with Trichinella spiralisVet. Parasitol2312016697610.1016/j.vetpar.2016.07.004Open DOISearch in Google Scholar
El Temsahy, M.M., Ibrahim, I.R., Mossalam, S.F., Mahrous, H., Abdel Bary, A., Abdel Salam, S.A. (2015): Evaluation of newly isolated probiotics in the protection against experimental intestinal trichinellosis. Vet. Parasitol., 214(3–4): 303–314. 10.1016/j.vetpar.2015.08.029El TemsahyM.M.IbrahimI.R.MossalamS.F.MahrousH.Abdel BaryA.Abdel SalamS.A.2015Evaluation of newly isolated probiotics in the protection against experimental intestinal trichinellosisVet. Parasitol2143–430331410.1016/j.vetpar.2015.08.02926386829Open DOISearch in Google Scholar
Falduto, G.H., Vila, C.C., Saracino, M.P., Gentilini, M.V., Venturielo, S.M. (2016): Regulatory parameters of the lung immune response during the early phase of experimental trichinellosis. Vet. Parasitol., 231(2016 ): 47–52. 10.1016/j.vetpar.2016.05.009FaldutoG.H.VilaC.C.SaracinoM.P.GentiliniM.V.VenturieloS.M.2016Regulatory parameters of the lung immune response during the early phase of experimental trichinellosisVet. Parasitol2312016475210.1016/j.vetpar.2016.05.00927211081Open DOISearch in Google Scholar
FAO/WHO (2002): Guidelines for the Evaluation of Probiotics in Food. Joint FAO/WHO Working Group Report on Drafting Guidelines for the Evaluation of Probiotics in Food, London, Ontario, Canada https://www.who.int/foodsafety/fs_management/en/probiotic_guidelines.pdfFAO/WHO2002Guidelines for the Evaluation of Probiotics in Food. Joint FAO/WHO Working Group Report on Drafting Guidelines for the Evaluation of Probiotics in FoodLondon, Ontario, Canadahttps://www.who.int/foodsafety/fs_management/en/probiotic_guidelines.pdfSearch in Google Scholar
Franken, L., Schiwon, M., Kurts, C. (2016): Macrophages: sentinels and regulators of the immune system. Cell. Microbiol., 18(4): 475–487. 10.1111/cmi.12580FrankenL.SchiwonM.KurtsC.2016Macrophages: sentinels and regulators of the immune systemCell. Microbiol18447548710.1111/cmi.1258026880038Open DOISearch in Google Scholar
Goudarzi, M., Goudarzi, H., Rashidan, M. (2014): Probiotics: an update on mechanisms of action and clinical applications. Novel. Biomed., 2(1): 22–30. https://pdfs.semanticscholar.org/4be2/d39cb4db77212490dcad3c7fd0e616a2eecc.pdfGoudarziM.GoudarziH.RashidanM.2014Probiotics: an update on mechanisms of action and clinical applicationsNovel. Biomed212230https://pdfs.semanticscholar.org/4be2/d39cb4db77212490dcad3c7fd0e616a2eecc.pdfSearch in Google Scholar
Goździk, K., Odoevskaya, I.M., Movsesyan, S.O., Cabaj, W. (2017): Molecular identification of Trichinella isolates from wildlife animals of the Russian Arctic territories. Helminthologia, 54(1): 11–16. 10.1515/helm-2017-0002GoździkK.OdoevskayaI.M.MovsesyanS.O.CabajW.2017Molecular identification of Trichinella isolates from wildlife animals of the Russian Arctic territoriesHelminthologia541111610.1515/helm-2017-0002Open DOISearch in Google Scholar
Gruden-Movsesijan, A., Ilic, N., Colic, M., Majstorovic, I., Vasilev, S., Radovic, I., Sofronic-Milosavljevic, L. (2011): The impact of Trichinella spiralis excretory-secretory products on dendritic cells. Comp. Immunol. Microbiol. Infect. Dis., 34(5):429–439. 10.1016/j.cimid.2011.08.004Gruden-MovsesijanA.IlicN.ColicM.MajstorovicI.VasilevS.RadovicI.Sofronic-MilosavljevicL.2011The impact of Trichinella spiralis excretory-secretory products on dendritic cellsComp. Immunol. Microbiol. Infect. Dis34542943910.1016/j.cimid.2011.08.00421903269Open DOISearch in Google Scholar
Han, C., Xu, J., Liu, Ch., Li, X., Zhai, P., Hashan, A., Song, M. (2018): Modulation of TLR2 and TLR4 in macrophages following Trichinella spiralis infection. Helminthologia 55(3): 195–203. 10.2478/helm-2018-0015HanC.XuJ.LiuCh.LiX.ZhaiP.HashanA.SongM.2018Modulation of TLR2 and TLR4 in macrophages following Trichinella spiralis infectionHelminthologia55319520310.2478/helm-2018-0015Open DOISearch in Google Scholar
Han, C., Yu, J., Zhang, Z., Zhai, P., Zhang, Y., Meng, S., Yu, Y., Li, X., Song, M. (2019): Immunomodulatory effects of Trichinella spiralis excretory-secretory antigens on macrophages. Exp. Parasitol., 196(January 2019):68–72. 10.1016/j.exppara.2018.10.001HanC.YuJ.ZhangZ.ZhaiP.ZhangY.MengS.YuY.LiX.SongM.2019Immunomodulatory effects of Trichinella spiralis excretory-secretory antigens on macrophagesExp. Parasitol196January 2019687210.1016/j.exppara.2018.10.001Open DOISearch in Google Scholar
Hasby Sad, M., Safwat, O., El-Guindy, D., Raafat, R., Elgendy, D., Hasby, E. (2018): Biomolecular changes and cortical neurodegenerative lesions in Trichinella spiralis infected BALB/c mice: a preliminary study elucidating a potential relationship between systemic helminthic infections and idiopathic Parkinson’s. Helminthologia 55(4): 261–274. 10.2478/helm-2018-0029Hasby SadM.SafwatO.El-GuindyD.RaafatR.ElgendyD.HasbyE.2018Biomolecular changes and cortical neurodegenerative lesions in Trichinella spiralis infected BALB/c mice: a preliminary study elucidating a potential relationship between systemic helminthic infections and idiopathic Parkinson’sHelminthologia55426127410.2478/helm-2018-0029Open DOISearch in Google Scholar
Ilic, N., Worthington, J.J., Gruden-Movsesijan, A., Travis, M.A., Sofronic-Milosavljevic, L., Grencis, R.K. (2011): Trichinella spiralis antigens prime mixed Th1/Th2 response but do not induce de novo generation of Foxp3+ T cells in vitro. Parasite Immunol., 33(10): 572–582. 10.1111/j.1365-3024.2011.01322.xIlicN.WorthingtonJ.J.Gruden-MovsesijanA.TravisM.A.Sofronic-MilosavljevicL.GrencisR.K.2011Trichinella spiralis antigens prime mixed Th1/Th2 response but do not induce de novo generation of Foxp3+ T cells in vitroParasite Immunol331057258210.1111/j.1365-3024.2011.01322.xOpen DOISearch in Google Scholar
Ilic, N., Gruden-Movsesijan, A., Sofronic-Milosavljevic, L. (2012): Trichinella spiralis shaping the immune response. Immunol. Res., 52(1-2): 111–119. 10.1007/s12026-012-8287-5IlicN.Gruden-MovsesijanA.Sofronic-MilosavljevicL.2012Trichinella spiralis shaping the immune responseImmunol. Res521-211111910.1007/s12026-012-8287-5Open DOISearch in Google Scholar
James, S.L. (1995): Role of nitric oxide in parasitic infections. Microbiol. Rev., 59(4):533–547.JamesS.L.1995Role of nitric oxide in parasitic infectionsMicrobiol. Rev59453354710.1128/mr.59.4.533-547.1995Search in Google Scholar
Kapel, C.M.O., Gamble, H.R. (2000): Infectivity, persistence, and antibody response to domestic and sylvatic Trichinella spp. in experimentally infected pigs. Int. J. Parasitol., 30(2): 215–221. 10.1016/S0020-7519(99)00202-7KapelC.M.O.GambleH.R.2000Infectivity, persistence, and antibody response to domestic and sylvatic Trichinella spp. in experimentally infected pigsInt. J. Parasitol30221522110.1016/S0020-7519(99)00202-7Open DOISearch in Google Scholar
Kapila, R., Sebastian, R., Varma, D.V.P., Sharma, R., Kapasiya, M., Salingati, V., Kapila, S., Dang, A.K. (2013): Comparison of innate immune activation after prolonged feeding of milk fermented with three species of Lactobacilli. Microbiol. Immunol., 57(11): 778–784. 10.1111/1348-0421.12092KapilaR.SebastianR.VarmaD.V.P.SharmaR.KapasiyaM.SalingatiV.KapilaS.DangA.K.2013Comparison of innate immune activation after prolonged feeding of milk fermented with three species of LactobacilliMicrobiol. Immunol571177878410.1111/1348-0421.12092Open DOISearch in Google Scholar
Kazura, J.W., Meshnick, S.R. (1984): Scavenger enzymes and resistance to oxygen mediated damage in Trichinella spiralis. Mol. Biochem. Parasitol., 10(1): 1–10.KazuraJ.W.MeshnickS.R.1984Scavenger enzymes and resistance to oxygen mediated damage in Trichinella spiralisMol. Biochem. Parasitol10111010.1016/0166-6851(84)90013-6Search in Google Scholar
Kołodz iej-Sobocińska, M., Dvorožňáková, E., Dziemian, E., Machnicka-R owińska, B. (2007): Trichinella spiralis reinfection: Macrophage activity in BALB/c mice. Parasitol. Res., 101(3): 629–637. 10.2478/s11687-012-0039-5Kołodz iej-SobocińskaM.DvorožňákováE.DziemianE.Machnicka-R owińskaB.2007Trichinella spiralis reinfection: Macrophage activity in BALB/c miceParasitol. Res101362963710.2478/s11687-012-0039-5Open DOISearch in Google Scholar
Lauková, A., Strompfová, V., Ouwehand, A. (2004): Adhesion properties of enterococci to intestinal mucus of different hosts. Vet. Res. Commun., 28(8): 647–655. 10.1023/B:VERC.0000045948.04027.a7LaukováA.StrompfováV.OuwehandA.2004Adhesion properties of enterococci to intestinal mucus of different hostsVet. Res. Commun28864765510.1023/B:VERC.0000045948.04027.a7Open DOISearch in Google Scholar
Lebeer, S., Vanderleyden, J., De Keersmaecker, S.C.J. (2010): Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens. Nat. Rev. Microbiol., 8(2010) 171–184. 10.1038/nrmicro2297LebeerS.VanderleydenJ.De KeersmaeckerS.C.J.2010Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogensNat. Rev. Microbiol8201017118410.1038/nrmicro229720157338Open DOISearch in Google Scholar
Martinez, F.O., Gordon, S. (2014): The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000Prime Rep., 6(2014): 13. 10.12703/P6-13MartinezF.O.GordonS.2014The M1 and M2 paradigm of macrophage activation: time for reassessmentF1000Prime Rep620141310.12703/P6-13394473824669294Open DOISearch in Google Scholar
Martinez, J., Merino, S., Rodríquez-Cabeiro F. (2004): Physiological responses to Trichinella spiralis infection in Wistar rats: is immune response costly? Helminthologia, 41(2): 67–71.MartinezJ.MerinoS.Rodríquez-CabeiroF.2004Physiological responses to Trichinella spiralis infection in Wistar rats: is immune response costly?Helminthologia4126771Search in Google Scholar
Martínez-Gómez, F., Santiago-Rosales, R., Ramón Bautista-Garfias, C.R. (2009): Effect of Lactobacillus casei Shirota strain intraperitoneal administration in CD1 mice on the establishment of Trichinella spiralis adult worms and on IgA anti-T. spiralis production. Vet. Parasitol., 162(1–2): 171–175. 10.1016/j.vetpar.2009.02.010Martínez-GómezF.Santiago-RosalesR.Ramón Bautista-GarfiasC.R.2009Effect of Lactobacillus casei Shirota strain intraperitoneal administration in CD1 mice on the establishment of Trichinella spiralis adult worms and on IgA anti-T. spiralis productionVet. Parasitol1621–217117510.1016/j.vetpar.2009.02.01019269100Open DOISearch in Google Scholar
Martínez-Gómez, F., Fuentes-Castro, B.E., Bautista-Garfias, C.R. (2011): The intraperitoneal inoculation of Lactobacillus casei in mice induces total protection against Trichinella spiralis infection. Parasitol. Res., 109(6): 1609–1617. 10.1007/s00436-011-2432-2Martínez-GómezF.Fuentes-CastroB.E.Bautista-GarfiasC.R.2011The intraperitoneal inoculation of Lactobacillus casei in mice induces total protection against Trichinella spiralis infectionParasitol. Res10961609161710.1007/s00436-011-2432-221541750Open DOISearch in Google Scholar
Mikeš, Z., Ferenčík, M., Jahnová, E., Ebringer, L., Čižnár, I. (1995): Hypocholesterolemic and immunomodulatory effects of orally applied Enterococcus faecium M‐74 in man. Folia Microbiol., 40(6): 639–646. 10.1007/BF02818522MikešZ.FerenčíkM.JahnováE.EbringerL.ČižnárI.1995Hypocholesterolemic and immunomodulatory effects of orally applied Enterococcus faecium M‐74 in manFolia Microbiol40663964610.1007/BF028185228768254Open DOISearch in Google Scholar
Miler, H.R. (1987): Gastrointestinal mucus, a medium for survival and for elimination of parasitic nematodes and protozoa. Parasitology, 94(Suppl): S77 – S100MilerH.R.1987Gastrointestinal mucus, a medium for survival and for elimination of parasitic nematodes and protozoaParasitology94SupplS77S10010.1017/S0031182000085838Search in Google Scholar
Piskoríková, M. (2010): Quality and characterization of existing and new probiotics (EFSA QPS). In Proceedings of Regulatory Framework Workshop Health Claim Approval of Probiotics in the European Union Issusses, 18. June, 2010. Košice, The Slovak RepublicPiskoríkováM.2010Quality and characterization of existing and new probiotics (EFSA QPS)InProceedings of Regulatory Framework Workshop Health Claim Approval of Probiotics in the European Union Issusses, 18. June, 2010Košice, The Slovak RepublicSearch in Google Scholar
Rodríguez-Sosa, M., Satoskar, A.R., Calderón, R., Gomez-Garcia, L., Savedra, R., Bojalil, R., Terrazas, L.I. (2002): Chronic helminth infection induces alternatively activated macrophages expressing high levels of CCR5 with low interleukin-12 production and Th2-biasing ability. Infect. Immun., 70(7): 3656–3664. 10.1128/IAI.70.7.3656-3664.2002Rodríguez-SosaM.SatoskarA.R.CalderónR.Gomez-GarciaL.SavedraR.BojalilR.TerrazasL.I.2002Chronic helminth infection induces alternatively activated macrophages expressing high levels of CCR5 with low interleukin-12 production and Th2-biasing abilityInfect. Immun7073656366410.1128/IAI.70.7.3656-3664.200212809512065507Open DOISearch in Google Scholar
Rolot, M., Dewals, B.G. (2018): Macrophage activation and functions during helminth infection: Recent advances from the laboratory mouse. J. Immunol. Res., 2018: Article ID 2790627. 10.1155/2018/2790627RolotM.DewalsB.G.2018Macrophage activation and functions during helminth infection: Recent advances from the laboratory mouseJ. Immunol. Res2018Article ID 279062710.1155/2018/2790627605108630057915Open DOISearch in Google Scholar
Singh, V.P., Sharma, J., Babu, S., Rizwanula, Singla, A. (2013): Role of probiotics in health and disease: a review. J. Pak. Med. Assoc., 63(2):253–257.SinghV.P.SharmaJ.BabuS.RizwanulaSingla, A.2013Role of probiotics in health and disease: a reviewJ. Pak. Med. Assoc632253257Search in Google Scholar
Sofronic-Milosavljevic, L., Ilic, N., Pineli, E., Gruden-Movsesijan, A. (2015): Secretory products of Trichinella spiralis muscle larvae and immunomodulation: implication for autoimmune diseases, allergies, and malignancies. J. Immunol. Res., 2015: Article ID 523875. 10.1155/2015/523875Sofronic-MilosavljevicL.IlicN.PineliE.Gruden-MovsesijanA.2015Secretory products of Trichinella spiralis muscle larvae and immunomodulation: implication for autoimmune diseases, allergies, and malignanciesJ. Immunol. Res2015: Article ID 52387510.1155/2015/523875446584526114122Open DOISearch in Google Scholar
Travers, M.A., Florent, I., Kohl, L., Grelier, P. (2011): Probiotics for the control of parasites: an overview. J. Parasitol. Res., 2011: Article ID 610769. 10.1155/2011/610769TraversM.A.FlorentI.KohlL.GrelierP.2011Probiotics for the control of parasites: an overviewJ. Parasitol. Res2011: Article ID 61076910.1155/2011/610769318233121966589Open DOISearch in Google Scholar
Tsai, Y.T., Cheng, P.Ch., Pan, T.M. (2012): The immunomodulatory effects of lactic acid bacteria for improving immune functions and benefits. Appl. Microbiol. Biotechnol., 96(4): 853–862. 10.1007/s00253-012-4407-3TsaiY.T.ChengP.Ch.PanT.M.2012The immunomodulatory effects of lactic acid bacteria for improving immune functions and benefitsAppl. Microbiol. Biotechnol96485386210.1007/s00253-012-4407-323001058Open DOISearch in Google Scholar
Vitetta, L., Saltzman, E.T., Nikov, T., Ibrahim, I., Hal, S. (2016): Modulating the gut micro-environment in the treatment of intestinal parasites J. Clin. Med., 5(11): 102.VitettaL.SaltzmanE.T.NikovT.IbrahimI.HalS.2016Modulating the gut micro-environment in the treatment of intestinal parasitesJ. Clin. Med51110210.3390/jcm5110102512679927854317Open DOISearch in Google Scholar
Wang, Y., Liu, H., Zhao, J. (2019): Macrophage polarization induced by probiotic bacteria: a concise review. Probiotics & Antimicro. Prot., (2019). 10.1007/s12602-019-09612-yWangY.LiuH.ZhaoJ.2019Macrophage polarization induced by probiotic bacteria: a concise reviewProbiotics & Antimicro. Prot201910.1007/s12602-019-09612-y31741313Open DOISearch in Google Scholar
Wing, E.J., Krahenbuhl, J.L., Remington, J.S. (1979): Studies of macrophage function during Trichinella spiralis infection in mice. Immunology, 36(3):479–85.WingE.J.KrahenbuhlJ.L.RemingtonJ.S.1979Studies of macrophage function during Trichinella spiralis infection in miceImmunology36347985Search in Google Scholar
Yadav A. K., Temjenmongla N. (2012): Efficacy of Lasia spinosa leaf extract in treating mice infected with Trichinella spiralis. Parasitol. Res., 110(1): 493–498. 10.1007/s00436-011-2551-9YadavA. K.TemjenmonglaN.2012Efficacy of Lasia spinosa leaf extract in treating mice infected with Trichinella spiralisParasitol. Res110149349810.1007/s00436-011-2551-921748345Open DOISearch in Google Scholar
Zhao, L., Shao, S., Chen, Y., Sun, X., Sun, R., Huang, J., Zhan, B., Zhu, X. (2017): Trichinella spiralis calreticulin binds human complement C1q as an immune evasion strategy. Front. Immunol., 8(2017): Article 636. 10.3389/fimmu.2017.00636ZhaoL.ShaoS.ChenY.SunX.SunR.HuangJ.ZhanB.ZhuX.2017Trichinella spiralis calreticulin binds human complement C1q as an immune evasion strategyFront. Immunol8(2017): Article 63610.3389/fimmu.2017.00636544950528620388Open DOISearch in Google Scholar
