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Infection and Immunity, September 2004, p. 5135-5142, Vol. 72, No. 9
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.9.5135-5142.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Gamma Interferon Responses to Plasmodium falciparum Liver-Stage Antigen 1 and Thrombospondin-Related Adhesive Protein and Their Relationship to Age, Transmission Intensity, and Protection against Malaria

Chandy C. John,^1,2,* Ann M. Moormann,^1, Peter O. Sumba,³ Ayub V. Ofulla,⁴ Daniel C. Pregibon,¹ and James W. Kazura¹

Center for Global Health and Diseases,¹ Division of Pediatric Infectious Diseases, Case Western Reserve University, and Rainbow Center for International Child Health, Rainbow Babies and Children's Hospital, Cleveland, Ohio,² Center for Vector Biology and Control Research, Kenya Medical Research Institute, Kisian,³ Department of Biomedical Sciences and Technology, Maseno University, Maseno, Kenya⁴

Received 1 April 2004/ Returned for modification 22 May 2004/ Accepted 1 June 2004

Gamma interferon (IFN-) responses to the Plasmodium falciparum antigens liver-stage antigen 1 (LSA-1) and thrombospondin-related adhesive protein (TRAP) are thought to be important in protection against malaria. Optimal methods of testing and the effects of age and transmission intensity on these responses are unknown. IFN- responses to LSA-1 and TRAP peptides were assessed by the enzyme-linked immunospot assay (ELISPOT) and enzyme-linked immunosorbent assay (ELISA) in children and adults from areas of stable and unstable malaria transmission in Kenya. Adults in the areas of stable and unstable transmission had similar frequencies and levels of IFN- responses to LSA-1 and TRAP as determined by ELISPOT and ELISA. In contrast, IFN- responses to the LSA-1 T3 peptide (assessed by ELISPOT) and to any LSA-1 peptide (assessed by ELISA) were less frequent in children in the area of unstable transmission than in children in the area of stable transmission. IFN- responses to LSA-1 were more frequently detected by ELISA than by ELISPOT in the stable-transmission area. IFN- responses detected by ELISA and ELISPOT did not correlate with each other. In children in the stable-transmission area, IFN- responses to LSA-1 peptides assessed by ELISA, but not by ELISPOT, were associated with protection against clinical malaria and anemia. IFN- responses to LSA-1 appear to require repeated P. falciparum exposure and/or increased age and, as measured by ELISA, are associated with protection against clinical malaria and anemia.

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* Corresponding author. Mailing address: Rainbow Center for International Child Health, Rainbow Babies and Children's Hospital, RBC 487, 11100 Euclid Ave., MS6008, Cleveland, OH 44106. Phone: (216) 844-3645. Fax: (216) 368-4825. E-mail: chandy.john{at}case.edu.

Editor: W. A. Petri, Jr.

C.C.J. and A.M.M. contributed equally to this work.

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Infection and Immunity, September 2004, p. 5135-5142, Vol. 72, No. 9
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.9.5135-5142.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

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