Acquisition of antibodies to merozoite surface protein 3 among residents of Korogwe, north eastern Tanzania
- PMID: 20205959
- PMCID: PMC2841183
- DOI: 10.1186/1471-2334-10-55
Acquisition of antibodies to merozoite surface protein 3 among residents of Korogwe, north eastern Tanzania
Abstract
Background: A polymorphic malaria parasite antigen, merozoite surface protein 3 (MSP3), is among the blood stage malaria vaccine candidates. It is believed to induce immunity through cytophilic antibodies that disrupt the process of erythrocytes invasion by merozoites. This study aimed at assessing natural acquisition of antibodies to MSP3 in individuals living in an area with different malaria transmission intensity in preparation for malaria vaccine trials.
Methods: The study was conducted in individuals aged 0-19 years from villages located in lowland, intermediate and highland strata in Korogwe district, northeastern Tanzania. Blood samples from 492 study participants were collected between May and June 2006 for malaria diagnosis and immunological investigations. Reactivity of MSP3 to different types of antibodies (immunoglobulin M, G and IgG subclass 1 and 3) were analysed by Enzyme Linked ImmunoSorbent Assay (ELISA).
Results: Malaria parasite prevalence was higher in the lowland (50%) compared to the intermediate (23.1%) and highland (9.8%) strata. Immunogloblin G subclasses 1 and 3 (IgG1 & IgG3), total IgG and IgM were found to increase with increasing age. IgG3 levels were significantly higher than IgG1 (p < 0.001). Furthermore, Plasmodium falciparum infection was associated with higher IgG3 levels (p = 0.008). Adjusting by strata and age in individuals who had positive blood smears, both IgG and IgM were associated with parasite density, whereby IgG levels decreased by 0.227 (95%CI: 0.064 - 0.391; p = 0.007) while IgM levels decreased by 0.165 (95%CI: 0.044 - 0.286; p = 0.008).
Conclusion: Individuals with higher levels of IgG3 might be partially protected from malaria infection. Higher levels of total IgG and IgM in highlands might be due to low exposure to malaria infection, recent infection or presence of cross-reactive antigens. Further studies of longitudinal nature are recommended. Data obtained from this study were used in selection of one village (Kwashemshi) for conducting MSP3 phase 1b malaria vaccine trial in Korogwe.
Figures

Similar articles
-
Plasmodium falciparum merozoite surface antigen-specific cytophilic IgG and control of malaria infection in a Beninese birth cohort.Malar J. 2019 Jun 11;18(1):194. doi: 10.1186/s12936-019-2831-x. Malar J. 2019. PMID: 31185998 Free PMC article.
-
Evaluation of host humoral antibody production against Plasmodium falciparum recombinant circumsporozoite antigen in Nigerian children.J Vector Borne Dis. 2012 Sep;49(3):151-6. J Vector Borne Dis. 2012. PMID: 23135009
-
IgG3 antibodies to Plasmodium falciparum merozoite surface protein 2 (MSP2): increasing prevalence with age and association with clinical immunity to malaria.Am J Trop Med Hyg. 1998 Apr;58(4):406-13. doi: 10.4269/ajtmh.1998.58.406. Am J Trop Med Hyg. 1998. PMID: 9574783
-
Plasmodium falciparum merozoite surface protein 3 as a vaccine candidate: a brief review.Rev Inst Med Trop Sao Paulo. 2022 Mar 11;64:e23. doi: 10.1590/S1678-9946202264023. eCollection 2022. Rev Inst Med Trop Sao Paulo. 2022. PMID: 35293561 Free PMC article. Review.
-
Chapter 5. Potential contribution of sero-epidemiological analysis for monitoring malaria control and elimination: historical and current perspectives.Adv Parasitol. 2009;69:299-352. doi: 10.1016/S0065-308X(09)69005-9. Adv Parasitol. 2009. PMID: 19622411 Review.
Cited by
-
Using community-owned resource persons to provide early diagnosis and treatment and estimate malaria burden at community level in north-eastern Tanzania.Malar J. 2012 May 3;11:152. doi: 10.1186/1475-2875-11-152. Malar J. 2012. PMID: 22554149 Free PMC article.
-
Differing rates of antibody acquisition to merozoite antigens in malaria: implications for immunity and surveillance.J Leukoc Biol. 2017 Apr;101(4):913-925. doi: 10.1189/jlb.5MA0716-294R. Epub 2016 Nov 11. J Leukoc Biol. 2017. PMID: 27837017 Free PMC article.
-
Protein microarray analysis of antibody responses to Plasmodium falciparum in western Kenyan highland sites with differing transmission levels.PLoS One. 2013 Dec 2;8(12):e82246. doi: 10.1371/journal.pone.0082246. eCollection 2013. PLoS One. 2013. PMID: 24312649 Free PMC article.
-
Humoral immune response to Plasmodium falciparum vaccine candidate GMZ2 and its components in populations naturally exposed to seasonal malaria in Ethiopia.Malar J. 2013 Feb 5;12:51. doi: 10.1186/1475-2875-12-51. Malar J. 2013. PMID: 23383869 Free PMC article.
-
Standardization and validation of a cytometric bead assay to assess antibodies to multiple Plasmodium falciparum recombinant antigens.Malar J. 2012 Dec 21;11:427. doi: 10.1186/1475-2875-11-427. Malar J. 2012. PMID: 23259607 Free PMC article.
References
-
- Breman JG. The ears of the hippopotamus: manifestations, determinants, and estimates of the malaria burden. Am J Trop Med Hyg. 2001;64:1–11. - PubMed
-
- Soe S, Theisen M, Roussilhon C, Aye KS, Druilhe P. Association between protection against clinical malaria and antibodies to merozoite surface antigens in an area of hyperendemicity in Myanmar: complementarity between responses to merozoite surface protein 3 and the 220-kilodalton glutamate-rich protein. Infect Immun. 2004;72:247–252. doi: 10.1128/IAI.72.1.247-252.2004. - DOI - PMC - PubMed
-
- Riley EM, Allen SJ, Wheeler JG, Blackman MJ, Bennett S, Takacs B. Naturally acquired cellular and humoral immune responses to the major merozoite surface antigen (PfMSP1) of Plasmodium falciparum are associated with reduced malaria morbidity. Parasite Immunol. 1992;14:321–337. doi: 10.1111/j.1365-3024.1992.tb00471.x. - DOI - PubMed
-
- Perignon JL, Druilhe P. Immune mechanisms underlying the premunition against Plasmodium falciparum malaria. Mem Inst Oswaldo Cruz. 1994;89(Suppl 2):51–53. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources