Human IgG subclass antibodies to the 19 kilodalton carboxy terminal fragment of Plasmodium falciparum merozoite surface protein 1 (MSP1(19)) and predominance of the MAD20 allelic type of MSP1 in Uganda

Citation
B. Apio et al., Human IgG subclass antibodies to the 19 kilodalton carboxy terminal fragment of Plasmodium falciparum merozoite surface protein 1 (MSP1(19)) and predominance of the MAD20 allelic type of MSP1 in Uganda, E AFR MED J, 77(4), 2000, pp. 189-193
Citations number
20
Categorie Soggetti
General & Internal Medicine
Journal title
EAST AFRICAN MEDICAL JOURNAL
ISSN journal
0012835X → ACNP
Volume
77
Issue
4
Year of publication
2000
Pages
189 - 193
Database
ISI
SICI code
0012-835X(200004)77:4<189:HISATT>2.0.ZU;2-S
Abstract
Objective: To determine the natural human humoral immune responses to the 1 9 kilodalton carboxy terminal fragment of Plasmodium falciparum merozoite s urface protein 1 (MSP1(19)), a malaria candidate vaccine antigen and to det ermine the prevalence of MAD20 and K1 alleles of P. falciparum MSP1, Design: Community based cross-sectional study. Setting: Atopi Parish, Apac District, Uganda, 1995, Subjects: Three hundred and seventy four Ugandans between <1 and 70 years o ld provided serum samples. Main outcome measures: IgG subclass antibodies by ELISA; MAD20 and K1 allel ic types of MSP1 by PCR, Results: Both the prevalence and the mean concentration of serum IgG1, and to a lesser extent IgG3, antibodies increased with age. IgG2 or 1gG4 antibo dies were virtually nonexistent. The cross-reactivity between the 4 sequenc e variants (E-KNG, E-TSR, Q-KNG and Q-TSR) of MSP1(19) was confirmed; howev er, a minority of sera preferentially recognised the KNG but not the TSR va riants. All 33 P,falciparum isolates from different parts of m Uganda carri ed the E-TSR (Mad20) allelic type and 3 isolates were mixed infections with E-TSR (MAD20) and Q-KNG (K1) allelic types, confirming the rarity of the K 1 allele in Uganda, Conclusion: There is a robust IgG1 antibody response to the malaria vaccine candidate antigen MSP119 which begins at an early age. Future cohort studi es are necessary to estblish the impact of these antibodies on clinical imm unity to malaria. The MAD20 allelic type of MSP1 id predominant in Ugandan P, falciparum isolates.