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Chronic, patent Plasmodium berghei malaria in splenectomized mice
Infection and Immunity
|March 1, 1982
Summary
Splenectomized mice develop resistance, not immunity, to Plasmodium berghei infections, which become chronic. Suppressing infection rather than curing it enhances resistance to superinfection in these Plasmodium berghei models.
Area of Science:
- Immunology
- Parasitology
- Infectious Diseases
Background:
- Splenectomy in mice can lead to chronic Plasmodium berghei infections, often with high parasitemia.
- True immunity is typically not achieved, but a degree of resistance can develop.
Purpose of the Study:
- To investigate the development of resistance and immunity to Plasmodium berghei in splenectomized mice.
- To compare the effects of infection suppression versus radical cure on subsequent resistance.
Main Methods:
- Splenectomized mice were infected with Plasmodium berghei.
- Infections were either suppressed (sulfonamide) or cured (chloroquine) after 2 weeks of patency.
- Resistance to superinfection was assessed.
Main Results:
- A patent infection of at least 2 weeks was required for resistance development.
- Sulfonamide treatment resulted in a higher proportion of resistant mice compared to chloroquine treatment.
- Some mouse strains (B10LP) spontaneously cleared chronic infections, unlike others (C57BL/Rij, BALB/c).
- Chronic infections caused limited anemia, elevated liver enzymes, and reduced immune reactivity compared to acute lethal infections.
Conclusions:
- Splenectomy-associated Plasmodium berghei infection in mice leads to chronic states with limited pathology.
- Infection suppression strategies may be more effective than radical cure for inducing resistance to superinfection in this model.
- Strain-specific differences exist in the ability to clear chronic Plasmodium berghei infections.