Trypanosoma cruzi: H2 complex and genetic background influence on the humoral immune response against epimastigotes

• Published in: International journal for parasitology 2000-08, Vol.30 (9), p.981-984
• Main Authors: Aguillón, Juan Carlos, Hermosilla, Tamara, Molina, Marı́a Carmen, Morello, Antonio, Repetto, Yolanda, Örn, Anders, Ferreira, Arturo
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Protozoan - biosynthesis; Biological and medical sciences; Chagas Disease - immunology; Experimental protozoal diseases and models; Female; Haplotypes; histocompatibility loci H-2; Immune response; Immunization; Immunoglobulin G - biosynthesis; Immunoradiometric Assay; Infectious diseases; Major histocompatibility; Medical sciences; Medicin och hälsovetenskap; Mice; Mice, Congenic; Parasitic diseases; Protozoal diseases; Trypanosoma cruzi; Trypanosoma cruzi - genetics; Trypanosoma cruzi - immunology
• ISSN: 0020-7519; 1879-0135
• DOI: 10.1016/S0020-7519(00)00078-3

Using A.SW, A.CA, B10.S and B10.M congenic mouse strains, we measured the IgG specific humoral immune responses against sonicated and live Trypanosoma cruzi epimastigotes. Genes located in the A background (A.SW and A.CA strains) mediate higher IgG responses against the parasite antigenic complexes than those located in the B background (strains B10.S and B10.M), regardless of the H2 haplotypes. Thus, non H2 genetic elements seem to be more important in determining differences in the total IgG immune response against T. cruzi. Whether a detectable H2 effect, in favor of the H2 s haplotype, occurred in the A or B background, was contingent on the immunisation protocol used. Thus, the H2 s haplotype mediates a higher IgG response in the A background, if immunised with live epimastigotes, and in the B background against sonicated epimastigotes. Most likely this represents a complex sequence of events, controlled by non-MHC genes, involving antigen handling and processing and depending on the physical form of antigen delivery.