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American Journal of Clinical Nutrition, Vol. 79, No. 3, 444-450, March 2004
© 2004 American Society for Clinical Nutrition


ORIGINAL RESEARCH COMMUNICATION

Effect of zinc supplementation on immune and inflammatory responses in pediatric patients with shigellosis1,2,3

Rubhana Raqib, Swapan Kumar Roy, Muhammad Jubayer Rahman, Tasnim Azim, Syeda Shegufta Ameer, Jobayer Chisti and Jan Andersson

1 From the International Centre for Diarrhoeal Diseases Research, Bangladesh (ICDDR,B): Centre for Health and Population Research, Dhaka, Bang-ladesh (RR, SKR, MJR, TA, SSA, and JC), and the Center for Infectious Medicine, Karolinska Institutet, Huddinge University Hospital, Huddinge, Sweden (JA)

Background: Several studies showed benefits of long-term zinc supplementation on the incidence, severity, and duration of diarrhea and on the incidence of respiratory infections. Prolonged zinc supplementation also improves cell-mediated immunity in severely malnourished children.

Objective: We studied the effect of short-term zinc supplementation on intrinsic and specific immune and inflammatory responses in moderately malnourished children with acute shigellosis.

Design: A randomized, double-blind, placebo-controlled trial was conducted in Shigella-infected children aged 12-59 mo. Elemental zinc (20 mg) and a multivitamin containing vitamins A and D, thiamine, riboflavin, nicotinamide, and calcium at twice the recommended dietary allowance were given daily for 2 wk to the zinc group (n = 28), whereas the multivitamin alone was given to the control group (n = 28). Standard antibiotic therapy was given to all patients.

Results: Serum zinc concentrations increased in both groups during convalescence; however, zinc supplementation showed a significant effect. The lymphocyte proliferation response in the zinc group increased relative to that in the control group (P = 0.002), but no significant effects were seen on concentrations of cytokines (interleukin 2 and interferon {gamma}) released from mitogen-stimulated mononuclear cells or on concentrations of cytokines (interleukin 2, interferon {gamma}, and interleukin 1ß) in feces. Among the antigen [lipopolysaccharide and invasion plasmid-encoded antigen (Ipa)]-specific antibodies, plasma Ipa-specific immunoglobulin G responses at day 30 were significantly higher in the zinc group than in the control group. However, the 2 groups did not differ significantly in the other antigen-specific responses in plasma and stool.

Conclusion: A 14-d course of zinc supplementation during acute shigellosis increases the lymphocyte proliferation response and the Ipa-specific immunoglobulin G response.

Key Words: Zinc • Shigella • specific immunity • cellular immunity




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