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.

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