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Journal of Tropical Pediatrics 1996 42(5):287-290; doi:10.1093/tropej/42.5.287
© 1996 by Oxford University Press
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Vitamin A Deficiency and T-cell Subpopulations in Children with Meningococcal Disease

Richard D. Semba, MD, MPH*,, Marc Bulterys, MD, MPH**, Vincent Munyeshuli, MD***, Théophile Gatsinzi, MD***, Alfred Saah, MD, MPH{dagger}, Ann Chao, PhD{dagger}{dagger} and Abel Dushimimana, MD{dagger}{dagger}{dagger}

*Department of Ophthalmology, School of Medicine, Johns Hopkins University Baltimore, MD, USA
**Center for Population Health, University of New Mexico Albuquerque, NM, USA
***Department of Pediatrics, National University of Rwanda Butare, Rwanda
{dagger}Department of Epidemiology, School of Hygiene and Public Health, Johns Hopkins University Baltimore, MD, USA
{dagger}{dagger}Epidemiology and Cancer Control Program, University of New Mexico Albuquerque, NM, USA
{dagger}{dagger}{dagger}University Center for Public Health, School of Medicine, National University of Rwanda Butare, Rwanda

Correspondence: Dr Richard Semba, Ocular Immunology Service, Suite 700, 550 North Broadway, Baltimore, MD 21205. Tel. (410) 955-3572, Fax (410) 955-0629

Although group A meningococcal disease is a major cause of child morbidity and mortality in sub-Saharan Africa, little is known about vitamin A status and T-cell subpopulations in affected children. A prospective study of vitamin A levels and T-cell subpopulations was conducted in 41 children hospitalized for meningococcal meningitis in Butare, Rwanda, during an epidemic from September through November, 1992. The mean age of cases was 3.6±2.7 years (range 0.5–16 years). The casefatality rate was 20 per cent; 73 per cent of the children had serum vitamin A levels consistent with subclinical deficiency (<0.7 µmol/l), and 27 per cent had levels consistent with severe deficiency (<0.35 µmol/l). Mean CD4 per cent was higher and CD8 per cent was lower among children with meningitis compared with known reference populations. These results suggest that meningococcal disease is characterized by T-cell subpopulation alterations and vitamin A deficiency.


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