2017, Number 1
<< Back Next >>
VacciMonitor 2017; 26 (1)
Immunization with excretion-secretion products of Trichinella spiralis combined to CTLA-4 blockade produces a high degree of protection against a challenge with the parasite
Zumaquero-Ríos JL, Pérez-Santos M, Villa-Mancera A, Sarracent-Pérez J
Language: Spanish
References: 20
Page: 24-30
PDF size: 114.62 Kb.
ABSTRACT
Different approaches to vaccination against
T. spiralis using murine experimental models have been used, but the levels
of protection observed in most experimental trials may not be sufficient to provide a good disease control. There is
increasing evidence that inhibitors molecules on T cells are critically involved in the regulation of immune response
against helminths infections, thus negative stimulators represent possible drug targets since their blockade leads to an
increased immune response. Moreover, it has been reported that immunization with excretory-secretory products of
T. spiralis muscular larvae could provide partial protective immunity against parasite infection.
T. spiralis induce a population of cells with elevated levels of known markers of T regulatory, manipulation of which influences the immune
response and parasite load. In the present work we found that immunization with muscle larvae excretory secretory
products of
T. spiralis and blockade of CTLA-4 displayed remarkable high reduction of muscle larvae burdens in a
murine model, showing that elimination of suppressive regulatory pathways results in a more potent and protective The
response which reduces muscle larval establishment.
REFERENCES
Brusca RC, Moore W, Shuster SM. Invertebrates. Third Edition. Sunderland, MA: Sinauer Associates; 2016.
Gottstein B, Pozio E, Nockler K. Epidemiology, diagnosis, treatment and control of trichinellosis. Clin Microbiol Rev 2009;22(1):127-45.
Pozio E, Zarlenga DS. New pieces of the Trichinella puzzle. Int J Parasitol 2013;43(12-13):983-97.
Dea-Ayuela MA, Bolas-Fernández F. Dynamics of the IgG3 responses following immunisation of Balb/c mice with somatic and excretory-secretory antigens from various Trichinella species. Folia Parasitol 2000;47(3):172-80.
Ortega-Pierres G, Vaquero-Vera A, Fonseca-Liñan R, Bermúdez- Cruz RM, Arguello-García R. Induction of protection in murine experimental models against Trichinella spiralis: an up-to date review. J Helminthol 2015;89(5):526-39.
Bruschi F, Chiumiento L. Immunomodulation in trichinellosis: does Trichinella really escape the host immune system? Endocr Metab Immune Disord Drug Targets 2012;12(1):4-15.
Bai X, Wu X, Wang X, Liu X, Song Y, Gao I, et al. Inhibition of mammalian muscle differentiation by excretory secretory products of muscle larvae of Trichinella spiralis in vitro. Parasitol Res 2012;110(6):2481-90.
Robinson MW, Connolly B. Proteomics analysis of the excretorysecretory proteins of the Trichinella spiralis L1 larva, a nematode parasite of skeletal muscle. Proteomics 2005;5(17):4525-32.
Gamble HR. Trichinella spiralis: Immunization of mice using monoclonal antibody affi nity isolated antigens. Exp Parasitol 1985;59(3):394-404.
Ortega-Pierres G, Muñiz E, Coral-Vázquez R, Parkhouse RM. Protection against Trichinella spiralis induced by purifi ed stage- specifi c surface antigens of infective larvae. Parasitol Res 1989;75(7):563-7.
Dea-Ayuela MA, Rama-Iñiguez S, Bolas-Fernandez F. Vaccination of mice against intestinal Trichinella spiralis infections by oral administration of antigens microencapsulated in methacrilic acid copolymers. Vaccine 2006;24(15):2772-80.
Gruden-Movsesijan A, Ilic N, Mostarica-Stojkovics M, Stosic- Grujicic S, Milic M, Sofronic-Milosavljevic L. Mechanism of modulation of experimental autoimmune encephalomyelitis by chronic Trichinella spiralis infection in Dark Agouti rats. Parasite Immunol 2010;32(6):450-9.
Lepenies B, Jacobs T. The role of negative costimulators during parasitic infection. Endocr Metab Immune Disord Drug Targets 2008;8(4):279-88.
Furze RC, Culley FJ, Selkirk ME. Differential roles of the costimulatory molecules GITR and CTLA-4 in the immune response to Trichinella spiralis. Microbes Infect.2006;8(12-13):2803-10.
NOM-062-ZOO-1999. Especifi caciones técnicas para la producción, cuidado y uso de los animales de laboratorio. Ciudad de México: Diario Ofi cial de la Federación; 2001.
De la Rosa-Arana JL, Campos-Rodríguez R, Rivera-Aguilar V, Escobar-Gutiérrez A, Miliar-García A, Herrera- González NE, et al. Comparative effects of levamisole, Staphylococcus, and Freund`s adjuvant on rat immunization with excretory and secretory antigens of Trichinella spiralis muscle larvae. Parasitol Res 2012;111:1599-605.
Wang ZQ, Cui J, Wei HY, Han HM, Zhang HW, Li YL: Vaccination of mice with DNA vaccine induces the immune response and partial protection against T. spiralis infection. Vaccine 2006;24(8):1205-12. Immunization with excretion-secretion products of Trichinella spiralis combined to CTLA-4 blockade produces a high degree of protection against a challenge with the parasite
Hewitson JP, Maizels RM. Vaccination against helminth parasite infection. Expert Rev Vaccines 2014;13(4):473-87.
Bruschi F., Gómez-Morales MA. The translational immunology of trichinellosis: from rodents to humans. En: Jirillo E, Magrone T, Miragliotta G. Inmune response to parasitic infections: Immunity to helminths and novel therapeutic approaches. Sharjah, United Arab Emirates: Bentham Science Publishers; 2014. p.125-61.
Beiting DP, Gagliardo LF, Hesse M, Bliss SK, Meskill D, Appleton JA. Coordinated control of immunity to muscle stage Tichinella spiralis by IL 10 regulatory T cells and TGF β. J Immunol 2007;178(2):1039-47.