Abstract | OBJECTIVE: METHOD: The study population consisted of 26 Zambian children < 6 years of age who presented with cerebral malaria to a rural hospital in 1994 and who were treated with quinine for seven days. Six children (23%) were anaemic (haemoglobin < 11 g/dl) one month after completing antimalarial therapy. RESULTS: On admission, concentrations of neopterin were markedly elevated in all patients. During the seven days of anti-malarial therapy, neopterin levels remained elevated in the 6 children who proved to have persistent anaemia one month after finishing treatment but declined significantly (P = 0.008) in the 20 children who corrected their haemoglobin levels by that time. Conversely, interleukin-4 levels declined in the children with persistent anaemia (P = 0.043) but not in the other children. CONCLUSION: Persistence of the TH-1 mediated immune response and associated activation of macrophages may be involved in the pathogenesis of lingering anaemia after treatment of malaria.
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Authors | G Biemba, V R Gordeuk, P E Thuma, G F Mabeza, G Weiss |
Journal | Tropical medicine & international health : TM & IH
(Trop Med Int Health)
Vol. 3
Issue 1
Pg. 60-5
(Jan 1998)
ISSN: 1360-2276 [Print] England |
PMID | 9484971
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antimalarials
- Hemoglobins
- Interleukin-6
- Interleukin-10
- Interleukin-4
- Neopterin
- Sulfadoxine
- Quinine
- Deferoxamine
- Pyrimethamine
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Topics |
- Analysis of Variance
- Anemia
(complications, immunology)
- Antimalarials
(therapeutic use)
- Child, Preschool
- Deferoxamine
(therapeutic use)
- Drug Therapy, Combination
- Female
- Follow-Up Studies
- Hemoglobins
(analysis)
- Humans
- Infant
- Interleukin-10
(blood)
- Interleukin-4
(blood)
- Interleukin-6
(blood)
- Macrophage Activation
- Malaria, Cerebral
(complications, drug therapy, immunology)
- Male
- Neopterin
(blood)
- Pyrimethamine
(therapeutic use)
- Quinine
(therapeutic use)
- Retrospective Studies
- Sulfadoxine
(therapeutic use)
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