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Published on: September 22, 2019
Intestinal amebiasis: cyclic suppression of the immune response
P K Ghosh1, C Castellanos-Barba, L Ortiz-Ortiz
1Departamento de Inmunología, Universidad Nacional Autónoma de México, México, D. F.
Insights
Entamoeba histolytica infection impairs spleen lymphocyte function in mice, causing cyclic depression in DNA synthesis and potential signal-transduction defects, which may aid parasite invasion.
Area of Science:
- Immunology
- Parasitology
- Cellular Biology
Background:
- Intestinal amebiasis is caused by Entamoeba histolytica.
- The cellular immune response to E. histolytica infection is not fully understood.
- Understanding immune evasion strategies is crucial for developing treatments.
Purpose of the Study:
- To evaluate the cellular immune response in a mouse model of intestinal amebiasis.
- To investigate the impact of Entamoeba histolytica infection on spleen lymphocyte function.
Main Methods:
- C3H/HeJ mice were inoculated with E. histolytica.
- Spleen lymphocytes were isolated at various time points post-infection.
- Lymphocytes were stimulated with mitogens (Concanavalin A, pokeweed mitogen) or parasite antigen.
- DNA synthesis and interleukin-2 production were measured.
- Signal transduction was assessed using phorbol myristate acetate and ionomycin.
Main Results:
- E. histolytica infection caused a cyclic depression in spleen lymphocyte DNA synthesis.
- Reduced DNA synthesis was observed with T-cell, T- and B-cell mitogens, and ameba antigen stimulation.
- Interleukin-2 production was decreased in stimulated spleen cells from infected mice.
- A signal-transduction defect was identified in spleen cells from infected mice.
Conclusions:
- Entamoeba histolytica infection significantly alters spleen lymphocyte function in mice.
- These cellular immune alterations may contribute to the parasite's ability to invade the host.
- Further research into immune modulation by E. histolytica is warranted.
Abstract:
The cellular immune response was evaluated in a C3H/HeJ mouse model of intestinal amebiasis at 5-60 days postinoculation with Entamoeba histolytica. At various intervals, spleen lymphocytes were obtained from infected and noninfected control mice and cultured with concanavalin A (Con A), pokeweed mitogen (PWM), or ameba antigen. E. histolytica infection induced a cyclic depression of DNA synthesis when spleen lymphocytes were stimulated with a T-cell mitogen (Con A), a T- and B-cell (PWM) mitogen, or an ameba antigen. A similar response was observed in the determinations of interleukin-2 in the supernatants of Con A-stimulated spleen cells from infected mice. When spleen cells from E. histolytica-infected mice were stimulated with phorbol myristate acetate plus ionomycin, results indicated a signal-transduction defect. These alterations, observed at the cellular level, might facilitate invasion of the host by the parasite.
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