» Articles » PMID: 18958278

Acquisition of Growth-inhibitory Antibodies Against Blood-stage Plasmodium Falciparum

Overview
Journal PLoS One
Date 2008 Oct 30
PMID 18958278
Citations 67
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Antibodies that inhibit the growth of blood-stage Plasmodium falciparum may play an important role in acquired and vaccine-induced immunity in humans. However, the acquisition and activity of these antibodies is not well understood.

Methods: We tested dialysed serum and purified immunoglobulins from Kenyan children and adults for inhibition of P. falciparum blood-stage growth in vitro using different parasite lines. Serum antibodies were measured by ELISA to blood-stage parasite antigens, extracted from P. falciparum schizonts, and to recombinant merozoite surface protein 1 (42 kDa C-terminal fragment, MSP1-42).

Results: Antibodies to blood-stage antigens present in schizont protein extract and to recombinant MSP1-42 significantly increased with age and were highly correlated. In contrast, growth-inhibitory activity was not strongly associated with age and tended to decline marginally with increasing age and exposure, with young children demonstrating the highest inhibitory activity. Comparison of growth-inhibitory activity among samples collected from the same population at different time points suggested that malaria transmission intensity influenced the level of growth-inhibitory antibodies. Antibodies to recombinant MSP1-42 were not associated with growth inhibition and high immunoglobulin G levels were poorly predictive of inhibitory activity. The level of inhibitory activity against different isolates varied.

Conclusions: Children can acquire growth-inhibitory antibodies at a young age, but once they are acquired they do not appear to be boosted by on-going exposure. Inhibitory antibodies may play a role in protection from early childhood malaria.

Citing Articles

Antibody responses in Burkinabe children against proteins associated with reduced risk of clinical malaria.

Yuguchi T, Dankyi B, Rojrung R, Nagaoka H, Kanoi B, Tiono A Front Immunol. 2025; 16:1521082.

PMID: 40079008 PMC: 11896993. DOI: 10.3389/fimmu.2025.1521082.


Bi-isotype immunoglobulins enhance antibody-mediated neutrophil activity against parasites.

Ogwang R, Murugu L, Nkumama I, Nyamako L, Kai O, Mwai K Front Immunol. 2024; 15:1360220.

PMID: 38650925 PMC: 11033408. DOI: 10.3389/fimmu.2024.1360220.


Atypical memory B cell frequency correlates with antibody breadth and function in malaria immune adults.

Partey F, Dowuona J, Pobee A, Walker M, Aculley B, Prah D Sci Rep. 2024; 14(1):4888.

PMID: 38418831 PMC: 10902325. DOI: 10.1038/s41598-024-55206-2.


IgG Subclass Switch in Volunteers Repeatedly Immunized with the Full-Length Merozoite Surface Protein 1 (MSP1).

Rathay V, Furle K, Kiehl V, Ulmer A, Lanzer M, Thomson-Luque R Vaccines (Basel). 2024; 12(2).

PMID: 38400191 PMC: 10893298. DOI: 10.3390/vaccines12020208.


Mouse Models for Unravelling Immunology of Blood Stage Malaria.

Olatunde A, Cornwall D, Roedel M, Lamb T Vaccines (Basel). 2022; 10(9).

PMID: 36146602 PMC: 9501382. DOI: 10.3390/vaccines10091525.


References
1.
Cohen S, Butcher G, CRANDALL R . Action of malarial antibody in vitro. Nature. 1969; 223(5204):368-71. DOI: 10.1038/223368a0. View

2.
Elliott S, Beeson J . Estimating the burden of global mortality in children aged <5 years by pathogen-specific causes. Clin Infect Dis. 2008; 46(11):1794-5. DOI: 10.1086/588049. View

3.
Mbogo C, Snow R, Khamala C, Kabiru E, Ouma J, Githure J . Relationships between Plasmodium falciparum transmission by vector populations and the incidence of severe disease at nine sites on the Kenyan coast. Am J Trop Med Hyg. 1995; 52(3):201-6. DOI: 10.4269/ajtmh.1995.52.201. View

4.
Blackman M, Shai S, Holder A . Antibodies inhibit the protease-mediated processing of a malaria merozoite surface protein. J Exp Med. 1994; 180(1):389-93. PMC: 2191569. DOI: 10.1084/jem.180.1.389. View

5.
Duraisingh M, Maier A, Triglia T, Cowman A . Erythrocyte-binding antigen 175 mediates invasion in Plasmodium falciparum utilizing sialic acid-dependent and -independent pathways. Proc Natl Acad Sci U S A. 2003; 100(8):4796-801. PMC: 153635. DOI: 10.1073/pnas.0730883100. View