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Acquisition of Growth-Inhibitory Antibodies against Blood-Stage Plasmodium falciparum

McCallum, F. J. ; Persson, Kristina LU ; Mugyenyi, C. K. ; Fowkes, F. J. I. ; Simpson, J. A. ; Richards, J. S. ; Williams, T. N. ; Marsh, K. and Beeson, J. G. (2008) In PLoS ONE 3(10).
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... (More)
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. (Less)
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author
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publishing date
type
Contribution to journal
publication status
published
subject
keywords
recombinant merozoite surface protein 1, parasite antibody, merozoite surface protein 1, immunoglobulin G, unclassified drug, protozoon antibody
in
PLoS ONE
volume
3
issue
10
article number
e3571
publisher
Public Library of Science (PLoS)
external identifiers
  • scopus:55849109645
ISSN
1932-6203
DOI
10.1371/journal.pone.0003571
language
English
LU publication?
no
additional info
10
id
5b271f37-9915-49e8-86fd-336f8d505bfc (old id 8726609)
date added to LUP
2016-04-01 13:45:05
date last changed
2022-04-21 23:26:40
@article{5b271f37-9915-49e8-86fd-336f8d505bfc,
  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.}},
  author       = {{McCallum, F. J. and Persson, Kristina and Mugyenyi, C. K. and Fowkes, F. J. I. and Simpson, J. A. and Richards, J. S. and Williams, T. N. and Marsh, K. and Beeson, J. G.}},
  issn         = {{1932-6203}},
  keywords     = {{recombinant merozoite surface protein 1; parasite antibody; merozoite surface protein 1; immunoglobulin G; unclassified drug; protozoon antibody}},
  language     = {{eng}},
  number       = {{10}},
  publisher    = {{Public Library of Science (PLoS)}},
  series       = {{PLoS ONE}},
  title        = {{Acquisition of Growth-Inhibitory Antibodies against Blood-Stage Plasmodium falciparum}},
  url          = {{http://dx.doi.org/10.1371/journal.pone.0003571}},
  doi          = {{10.1371/journal.pone.0003571}},
  volume       = {{3}},
  year         = {{2008}},
}