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Universidade Federal do Rio de Janeiro Centro de Ciências da Saúde Instituto de Biofísica Carlos Chagas Filho The importance of apoptosis for immune regulation in Chagas’ disease George A. DosReis
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Fabrício Montalvão. IBCCF-UFRJ Landi V. Guillermo. IBCCF-UFRJ Geisy M. de Almeida. IBCCF-UFRJ Elizabeth M. Silva. IBCCF-UFRJ Marise P. Nunes. IOC-Fiocruz-RJ Juliana de Meis. IOC-Fiocruz-RJ Christina M. Takiya. Dept. Histologia-UFRJ Richard Siegel. NIAID-NIH, USA Celio Freire-de-Lima. IBCCF-UFRJ Marcela F. Lopes. IBCCF-UFRJ
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Lopes MF et al. Immunol. Today 21; 489-494, 2000 Freire-de-Lima CG et al. Nature 403; 199-203, 2000 Phagocytosis of apoptotic cells (efferocytosis) inactivates macrophages and exacerbates parasite replication through TGF-β, ODC and polyamine synthesis X Efferocytosis
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T. cruzi infection: Consequences of apoptosis Efferocytosis
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Apoptosis in T. cruzi infection Modify efferocytosis by: 1. Caspase inhibition 2. Anti-FasL treatment 3. Antibodies to apoptotic cells Efferocytosis
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Blocking apoptosis in T. cruzi infection Caspase inhibition Efferocytosis
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Caspase inhibition reduces lymphocyte apopotosis in vivo Silva, E. M. et al. Caspase inhibition reduces lymphocyte apoptosis and improves host immune responses to Trypanosoma cruzi infection. Eur. J. Immunol. 2007, 37 (3), 738-746.
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Treatment with zVAD reduces parasitemia Silva, E. M. et al. Caspase inhibition reduces lymphocyte apoptosis and improves host immune responses to Trypanosoma cruzi infection. Eur. J. Immunol. 2007, 37 (3), 738-746.
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Treatment with zVAD in vivo increases macrophage activation
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The general caspase inhibitor zVAD reduces apoptosis of T lymphocytes in vitro and in vivo Treatment with zVAD increases immunity to T. cruzi infection
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Blocking apoptosis in T. cruzi infection Anti-FasL Efferocytosis
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Increased immunity to T. cruzi after treatment with anti-FasL in vivo Guillermo, L.V. et al. The Fas death pathway controls coordinated expansions of type 1 CD8 and type 2 CD4 T cells in Trypanosoma cruzi infection. J. Leukoc. Biol. 2007, 81, 942-951.
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Anti-FasL in vivo accelerates and increases type 1 cytokine responses
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Anti-FasL reduces apoptosis of CD4 and CD8 T cells Anti-FasL increases type 1 cytokine responses, increases macrophage NO production and reduces parasitemia Lymphocyte apoptosis is deleterious for T. cruzi Infection in vivo
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Modifying immune regulation through opsonization of apoptotic cells Antibodies Efferocytosis
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Differential reaction of chagasic IgG with apoptotic lymphocytes 1101001000 0 20 40 60 80 100 % of Max Annexin V + CHA CT - 26.1% CHA - 36.3% IgG (H+L) A 10000 OD (Arbitrary Units) Migration Distance (Arbitrary Units) CT 400 600 800 1000 50 40 30 20 10 0 B C Position 403 Peak values (AU) Position 901 Position 1055Position 1022 Cha
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Opsonization of apoptotic cells with chagasic IgG reduces the effect of efferocytosis on replication of T. cruzi IgG purified from T. cruzi infection (90 days) or age matched serum
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Control of parasite replication is mediated by increased TNF-α production Apoptotic cells opsonized with chagasic IgG increase TNF-α production
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Control of parasite replication requires engagement of FcγRs
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Previous immunization with apoptotic cells reduces parasitemia in vivo Dm28c dpi
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Conclusions Chagasic IgG opsonizes apoptotic cells and reduces the effect of efferocytosis on parasite replication The protective effect is mediated by increased TNF-α production The protective effect requires FcγRs Generation of autoantibodies against apoptotic cell antigens could play a protective role against parasite infection
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