Effects of pregnancy and intensity of Plasmodium falciparum transmission on immunoglobulin G subclass responses to variant surface antigens
- PMID: 15972500
- PMCID: PMC1168589
- DOI: 10.1128/IAI.73.7.4112-4118.2005
Effects of pregnancy and intensity of Plasmodium falciparum transmission on immunoglobulin G subclass responses to variant surface antigens
Abstract
Placenta-sequestering Plasmodium falciparum involved in the pathogenesis of pregnancy-associated malaria (PAM) in otherwise clinically immune women expresses particular variant surface antigens (VSA(PAM)) on the surface of infected erythrocytes that differ from VSA found in parasitized nonpregnant individuals (non-PAM type VSA). We studied levels of immunoglobulin G (IgG) and IgG subclasses with specificity for VSA(PAM) and for non-PAM type VSA in pregnant and nonpregnant women from two sites with different endemicities in Cameroon. We found that VSA(PAM)-specific responses depended on the pregnancy status, parity, gestational age, and parasite transmission intensity, whereas only the parasite transmission intensity influenced the levels of IgG specific for non-PAM type VSA. For both types of VSA, the responses were dominated by the cytophilic subclass IgG1, followed by IgG3. In pregnant women, the levels of VSA(PAM)-specific antibodies either were very low or negative or were very high, whereas the levels of the antibodies specific for non-PAM type VSA were uniformly high. Interestingly, the levels of VSA(PAM)-specific IgG1 increased with increasing gestational age, while the levels of the corresponding IgG3 tended to decrease with increasing gestational age. The IgG subclass responses with specificity for non-PAM type VSA did not vary significantly with gestational age. Taken together, our data indicate that IgG1 and to a lesser extent IgG3 are the main subclasses involved in acquired VSA(PAM)-specific immunity to pregnancy-associated malaria.
Figures


Similar articles
-
Variant surface antigen-specific IgG and protection against clinical consequences of pregnancy-associated Plasmodium falciparum malaria.Lancet. 2004 Jan 24;363(9405):283-9. doi: 10.1016/S0140-6736(03)15386-X. Lancet. 2004. PMID: 14751701
-
Antibodies from malaria-exposed pregnant women recognize trypsin resistant epitopes on the surface of Plasmodium falciparum-infected erythrocytes selected for adhesion to chondroitin sulphate A.Malar J. 2004 Sep 6;3:31. doi: 10.1186/1475-2875-3-31. Malar J. 2004. PMID: 15350207 Free PMC article.
-
Expression of variant surface antigens by Plasmodium falciparum parasites in the peripheral blood of clinically immune pregnant women indicates ongoing placental infection.Infect Immun. 2003 Mar;71(3):1584-6. doi: 10.1128/IAI.71.3.1584-1586.2003. Infect Immun. 2003. PMID: 12595482 Free PMC article.
-
VAR2CSA and protective immunity against pregnancy-associated Plasmodium falciparum malaria.Parasitology. 2007;134(Pt 13):1871-6. doi: 10.1017/S0031182007000121. Parasitology. 2007. PMID: 17958922 Review.
-
Cytoadhesion of Plasmodium falciparum-infected erythrocytes and the infected placenta: a two-way pathway.Braz J Med Biol Res. 2006 Dec;39(12):1525-36. doi: 10.1590/s0100-879x2006001200003. Braz J Med Biol Res. 2006. PMID: 17160261 Review.
Cited by
-
Opsonization of malaria-infected erythrocytes activates the inflammasome and enhances inflammatory cytokine secretion by human macrophages.Malar J. 2012 Oct 9;11:343. doi: 10.1186/1475-2875-11-343. Malar J. 2012. PMID: 23046548 Free PMC article.
-
Differential evolution of anti-VAR2CSA- IgG3 in primigravidae and multigravidae pregnant women infected by Plasmodium falciparum.Malar J. 2008 Jan 11;7:10. doi: 10.1186/1475-2875-7-10. Malar J. 2008. PMID: 18190692 Free PMC article.
-
Evasion of Classical Complement Pathway Activation on Plasmodium falciparum-Infected Erythrocytes Opsonized by PfEMP1-Specific IgG.Front Immunol. 2019 Jan 7;9:3088. doi: 10.3389/fimmu.2018.03088. eCollection 2018. Front Immunol. 2019. PMID: 30666256 Free PMC article.
-
Antibodies to variant surface antigens of Plasmodium falciparum-infected erythrocytes are associated with protection from treatment failure and the development of anemia in pregnancy.J Infect Dis. 2009 Jul 15;200(2):299-306. doi: 10.1086/599841. J Infect Dis. 2009. PMID: 19500037 Free PMC article. Clinical Trial.
-
Progress and Insights Toward an Effective Placental Malaria Vaccine.Front Immunol. 2021 Feb 25;12:634508. doi: 10.3389/fimmu.2021.634508. eCollection 2021. Front Immunol. 2021. PMID: 33717176 Free PMC article. Review.
References
-
- Aguiar, J. C., G. R. Albrecht, P. Cegielski, B. M. Greenwood, J. B. Jensen, G. Lallinger, A. Martinez, I. A. McGregor, J. N. Minjas, J. Neequaye, M. E. Patarroyo, J. A. Sherwood, and R. J. Howard. 1992. Agglutination of Plasmodium falciparum-infected erythrocytes from East and West African isolates by human sera from distant geographic regions. Am. J. Trop. Med. Hyg. 47:621-632. - PubMed
-
- Altman, D. G., D. Machin, T. N. Bryant, and M. J. Gardner (ed.). 2000. Statistics with confidence. British Medical Journal, London, United Kingdom.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous