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Study of murine experimental Jorge Lobo's disease by analysis of peritoneal lavage cells and footpad histopathology: early versus chronic lesions. | LitMetric

AI Article Synopsis

  • The study investigates the immune response in a murine model of Jorge Lobo's disease, focusing on histological changes and immune cell presence at early (5 months) and late (13 months) stages post-inoculation.
  • At both time points, granulomas were primarily made of macrophages and multinucleated giant cells, with variations in other immune cells; more neutrophils were present at 5 months, while lymphocyte numbers increased by 13 months.
  • A significant decline in fungal viability and quantity was observed over time, alongside increased production of several immune markers (H₂O₂, O₂(-), IL-10, TNF-α) after 13 months, suggesting distinct immune responses during early and

Article Abstract

The murine model of Jorge Lobo's disease is characterized by histological alterations similar to those seen in human disease, including a large number of viable fungi. This study evaluated the immune response of mice with early and late macroscopic lesions (5 and 13 months post-inoculation [p.i.], respectively) by the analysis of peritoneal lavage cells and footpad (FP) histology. The FP of mice were inoculated with 1 × 10(6) fungi (viability index of 41%). At 5 and 13 months p.i., the granuloma mainly consisted of macrophages and multinucleated giant cells, but a larger number of neutrophils was observed at 5 months and lymphocytes at 13 months. The number of fungi in the FP and fungal viability were 1.8 ± 1.1 × 10(6) fungi/ml and 38.5% at 5 months p.i. and 30.8 ± 11.7 × 10(6) fungi/ml and 9% at 13 months (P < .05). Higher production of H₂O₂, O₂(-), IL-10, and TNF-α were observed at 13 months (P < .05), but there was no significant difference in the production of NO, IL-2, IL-4, IL-12 and IFN-γ. The results showed significant differences between early and late lesions and support the use of BALB/c mice for evaluation of the different phases of infection.

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Source
http://dx.doi.org/10.1093/mmy/myv005DOI Listing

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