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Published on: July 17, 2014
Immunity in malaria: depression of delayed hypersensitivity reaction in acute Plasmodium falciparum infection
O A Akinwolere1, A I Williams, F M Akinkugbe
1Institute of Child Health, College of Medicine, University College Hospital, Ibadan, Nigeria.
Insights
Acute Plasmodium falciparum malaria significantly impairs cell-mediated immunity in Nigerian children, indicated by a suppressed delayed-type hypersensitivity skin reaction to purified protein derivative (PPD). This immune depression was evident in 90% of infected children, regardless of prior BCG vaccination.
Area of Science:
- Immunology
- Infectious Diseases
- Paediatrics
Background:
- Plasmodium falciparum malaria is a major cause of childhood illness in tropical regions.
- Cell-mediated immunity plays a crucial role in controlling infections and maintaining immune homeostasis.
- Assessing immune responses in children with malaria is vital for understanding disease pathogenesis and developing interventions.
Purpose of the Study:
- To evaluate the impact of acute Plasmodium falciparum malaria on cell-mediated immunity in Nigerian children.
- To determine if malaria infection affects delayed-type hypersensitivity (DTH) responses.
- To explore the clinical and immunopathological significance of these findings in paediatric practice.
Main Methods:
- A controlled study involving 30 Nigerian children with acute malaria and 25 healthy controls.
- Cell-mediated immunity was assessed using the delayed-type hypersensitivity (DTH) skin reaction test.
- The DTH test utilized purified protein derivative (PPD) at a dose of 5 tuberculin units (TU).
Main Results:
- Marked depression of DTH reaction to PPD was observed in 90% of malarious children (27/30).
- Only 16% of healthy control subjects (4/25) showed a depressed DTH response (P < 0.0005).
- Immune suppression occurred despite evidence of previous BCG vaccination in a majority of the children studied.
Conclusions:
- Acute Plasmodium falciparum malaria profoundly suppresses cell-mediated immunity in children.
- The observed immune depression has significant implications for tropical paediatric infectious disease management.
- Further research into the immunopathology of malaria-induced immune suppression is warranted.
Abstract:
The effect of acute Plasmodium falciparum malaria infection on the cell-mediated immune response of 30 Nigerian children attending the General Out-patient (GOP) Clinic of the University College Hospital, Ibadan, Nigeria, was assessed in a controlled study. Delayed-type hypersensitivity skin reaction to five tuberculin units (5 TU) of purified protein derivative (PPD) was used as an indicator of cell-mediated immunity. The results showed marked depression of delayed hypersensitivity reaction to PPD in 27 (90%) of the malarious children, compared with four (16%) of the 25 control healthy subjects (P less than 0.0005). This depression was observed despite evidence of previous BCG vaccination in 38 (69.1%) of the 55 children in the study. The possible clinical significance of these observations in tropical paediatric practice, and the immunopathological implications, are discussed.
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