Membrane-bound antibodies to bloodstream Trypanosoma cruzi in mice: strain differences in susceptibility to complement-mediated lysis
- PMID: 116784
- PMCID: PMC1537771
Membrane-bound antibodies to bloodstream Trypanosoma cruzi in mice: strain differences in susceptibility to complement-mediated lysis
Abstract
The Y, CL and other strains of Trypanosoma cruzi display different morphological and immunological characteristics. Such observations are here extended to the interaction of bloodstream forms of different strains of T. cruzi with components of the complement system. We demonstrate that the bloodstream forms of the Y and B strains, but not those of the CL strain, are lysed by normal human serum. Lysis is mediated by combined activities of the alternative and classical complement pathways. These activities are triggered by antibodies on the surface of the parasites as shown by: (a) binding of fluorescein or radiolabelled anti-mouse immunoglobulin to the parasite's membrane and (b) the finding that bloodstream forms from lethally irradiated mice can be sensitized and rendered susceptible to complement-mediated lysis by incubation with sera from acutely infected animals. Bloodstream forms of the CL strain also bear surface immunoglobulin and sensitizing antibodies are present in the sera of mice infected with this strain. However, CL trypomastigotes from acutely infected mice fail to be lysed by human or mouse complement unless the parasites are pre-incubated with sera from chronically infected animals. The basis of the different interactions between CL and Y trypomastigotes with antibodies and the complement system, and their biological significance are discussed.
Similar articles
-
Relative resistance of Brazil strain trypomastigote forms of Trypanosoma cruzi to in vitro antibody-dependent complement-mediated lysis.J Parasitol. 1988 Dec;74(6):1046-50. J Parasitol. 1988. PMID: 3057163
-
Protective effects of specific antibodies in Trypanosoma cruzi infections.J Immunol. 1976 Mar;116(3):755-60. J Immunol. 1976. PMID: 815433
-
Differentiation between Trypanosoma cruzi and T. rangeli by their different complement sensitivity.Tropenmed Parasitol. 1982 Sep;33(3):147-50. Tropenmed Parasitol. 1982. PMID: 6814023
-
Anti-alpha-galactosyl antibodies in chagasic patients. Possible biological significance.Braz J Med Biol Res. 1988;21(6):1275-86. Braz J Med Biol Res. 1988. PMID: 2471563 Review.
-
Immunological consequences of infection and vaccination in South American trypanosomiasis.Philos Trans R Soc Lond B Biol Sci. 1984 Nov 13;307(1131):51-61. doi: 10.1098/rstb.1984.0108. Philos Trans R Soc Lond B Biol Sci. 1984. PMID: 6151688 Review.
Cited by
-
Occurrence of foamy macrophages during the innate response of zebrafish to trypanosome infections.Elife. 2021 Jun 11;10:e64520. doi: 10.7554/eLife.64520. Elife. 2021. PMID: 34114560 Free PMC article.
-
ASP-2/Trans-sialidase chimeric protein induces robust protective immunity in experimental models of Chagas' disease.NPJ Vaccines. 2023 May 31;8(1):81. doi: 10.1038/s41541-023-00676-0. NPJ Vaccines. 2023. PMID: 37258518 Free PMC article.
-
Performance of TcI/TcVI/TcII Chagas-Flow ATE-IgG2a for universal and genotype-specific serodiagnosis of Trypanosoma cruzi infection.PLoS Negl Trop Dis. 2017 Mar 23;11(3):e0005444. doi: 10.1371/journal.pntd.0005444. eCollection 2017 Mar. PLoS Negl Trop Dis. 2017. PMID: 28333926 Free PMC article.
-
Inefficient complement system clearance of Trypanosoma cruzi metacyclic trypomastigotes enables resistant strains to invade eukaryotic cells.PLoS One. 2010 Mar 16;5(3):e9721. doi: 10.1371/journal.pone.0009721. PLoS One. 2010. PMID: 20300530 Free PMC article.
-
A DTU-dependent blood parasitism and a DTU-independent tissue parasitism during mixed infection of Trypanosoma cruzi in immunosuppressed mice.Parasitol Res. 2014 Jan;113(1):375-85. doi: 10.1007/s00436-013-3665-z. Epub 2013 Nov 1. Parasitol Res. 2014. PMID: 24178748
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources