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. 2007 May;75(5):2415-20.
doi: 10.1128/IAI.00951-06. Epub 2007 Feb 5.

Immunoglobulin G antibody reactivity to a group A Plasmodium falciparum erythrocyte membrane protein 1 and protection from P. falciparum malaria

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Immunoglobulin G antibody reactivity to a group A Plasmodium falciparum erythrocyte membrane protein 1 and protection from P. falciparum malaria

Pamela A Magistrado et al. Infect Immun. 2007 May.

Abstract

Variant surface antigens (VSA) on the surface of Plasmodium falciparum-infected red blood cells play a major role in the pathogenesis of malaria and are key targets for acquired immunity. The best-characterized VSA belong to the P. falciparum erythrocyte membrane protein 1 (PfEMP1) family. In areas where P. falciparum is endemic, parasites causing severe malaria and malaria in young children with limited immunity tend to express semiconserved PfEMP1 molecules encoded by group A var genes. Here we investigated antibody responses of Tanzanians who were 0 to 19 years old to PF11_0008, a group A PfEMP1. PF11_0008 has previously been found to be highly transcribed in a nonimmune Dutch volunteer experimentally infected with NF54 parasites. A high proportion of the Tanzanian donors had antibodies against recombinant PF11_0008 domains, and in children who were 4 to 9 years old the presence of antibodies to the PF11_0008 CIDR2beta domain was associated with reduced numbers of malaria episodes. These results indicate that homologues of PF11_0008 are present in P. falciparum field isolates and suggest that PF11_0008 CIDR2beta-reactive antibodies might be involved in protection against malaria episodes.

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Figures

FIG. 1.
FIG. 1.
Point prevalence (circles and error bars showing 95% confidence intervals) and plasma levels (bars and error bars showing geometric means and 95% confidence intervals) of IgG antibodies to PF11_0008 DBL1α, DBL2γ, and CIDR2β domains. Plasma was collected from individuals who were 2 to 19 years old living in Mgome (high malaria transmission) (A), Ubiri (moderate malaria transmission) (B), or Magamba (low malaria transmission) (C).
FIG. 2.
FIG. 2.
Point prevalence (circles and error bars showing 95% confidence intervals) and plasma levels (bars and error bars showing geometric means and 95% confidence intervals) of IgG antibodies reacting to DBL1α (A), DBL2γ (B), and CIDR2β (C) of PF11_0008. Plasma was collected from individuals who were 0 to 19 years old living in Mkokola, a village where the level of malaria transmission is high.
FIG. 3.
FIG. 3.
P. falciparum geometric mean density (bars and error bars showing 95% confidence intervals) and percentage of children and adults with a malaria episode in a high-malaria-transmission village (Mkokola) as defined by fever and the presence of parasites (circles and error bars showing 95% confidence intervals).
FIG. 4.
FIG. 4.
PF11_0008 CIDR2β IgG levels in individuals with (shaded box plots) or without (open box plots) a malaria episode in different age groups in Mkokola. The IgG levels are indicated by box plots with the median and the 25th and 75th percentiles; the error bars indicate the 10th and 90th percentiles, and the circles indicate outliers. P values calculated using the two-sample t test with equal variances are indicated.

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References

    1. Baruch, D. I., B. Gamain, J. W. Barnwell, J. S. Sullivan, A. Stowers, G. G. Galland, L. H. Miller, and W. E. Collins. 2002. Immunization of Aotus monkeys with a functional domain of the Plasmodium falciparum variant antigen induces protection against a lethal parasite line. Proc. Natl. Acad. Sci. USA 99:3860-3865. - PMC - PubMed
    1. Baruch, D. I., J. A. Gormely, C. Ma, R. J. Howard, and B. L. Pasloske. 1996. Plasmodium falciparum erythrocyte membrane protein 1 is a parasitized erythrocyte receptor for adherence to CD36, thrombospondin, and intercellular adhesion molecule 1. Proc. Natl. Acad. Sci. USA 93:3497-3502. - PMC - PubMed
    1. Baruch, D. I., X. C. Ma, B. Pasloske, R. J. Howard, and L. H. Miller. 1999. CD36 peptides that block cytoadherence define the CD36 binding region for Plasmodium falciparum-infected erythrocytes. Blood 94:2121-2127. - PubMed
    1. Baruch, D. I., B. L. Pasloske, H. B. Singh, X. Bi, X. C. Ma, M. Feldman, T. F. Taraschi, and R. J. Howard. 1995. Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes. Cell 82:77-87. - PubMed
    1. Bian, Z., G. Wang, X. Tian, and J. Fan. 1999. Expression of Plasmodium falciparum-infected erythrocyte membrane protein from cerebral malaria patients. Zhongguo Jiehe Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi 17:359-362. [Chinese.] - PubMed

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