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Cell mediated immunity in childhood malaria.
S Rajajee1, V Pushpa, P R Narayanan
1Department of Immunology, Tuberculosis Research Centre, Madras, Tamil-Nadu.
Indian Journal of Pediatrics
|March 1, 1990
Summary
Childhood malaria, caused by Plasmodium vivax and Plasmodium falciparum, does not appear to suppress cell-mediated immunity (CMI). Lymphocyte proliferation responses remained comparable between infected children and healthy controls, both during and after treatment.
Area of Science:
- Immunology
- Infectious Diseases
- Pediatrics
Background:
- Childhood malaria is a significant global health concern.
- Understanding the impact of malaria on the immune system is crucial for effective treatment and prevention strategies.
- Cell-mediated immunity (CMI) plays a vital role in controlling parasitic infections like malaria.
Purpose of the Study:
- To investigate the status of cell-mediated immunity (CMI) in children with Plasmodium vivax and Plasmodium falciparum malaria.
- To compare CMI responses during active infection and after treatment with those of healthy controls.
Main Methods:
- Assessed CMI using lymphocyte proliferative response assays.
- Tested responses to mitogens phytohaemagglutinin (PHA) and poke weed mitogen (PWM).
- Evaluated responses to the antigen purified protein derivative (PPD) in malaria patients and 19 healthy controls.
Main Results:
- No significant differences were observed in PHA, PWM, or PPD responses between children with malaria and healthy controls.
- Lymphocyte proliferative responses did not differ significantly between the period of parasitemia and after antimalarial treatment.
- These findings suggest that CMI, as measured by lymphocyte proliferation, is not depressed during childhood malaria.
Conclusions:
- Childhood malaria, including infections with P. vivax and P. falciparum, does not appear to cause a significant depression in cell-mediated immunity.
- Lymphocyte proliferative responses remain largely unaffected, indicating preserved immune function despite malarial infection.
- Further research may explore other aspects of immune response in pediatric malaria.