Journal article
Antigenic cartography of immune responses to Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1)
- Abstract:
- Naturally acquired clinical immunity to Plasmodium falciparum is partly mediated by antibodies directed at parasite-derived antigens expressed on the surface of red blood cells which mediate disease and are extremely diverse. Unlike children, adults recognize a broad range of variant surface antigens (VSAs) and are protected from severe disease. Though crucial to the design and feasibility of an effective malaria vaccine, it is not yet known whether immunity arises through cumulative exposure to each of many antigenic types, cross-reactivity between antigenic types, or some other mechanism. In this study, we measured plasma antibody responses of 36 children with symptomatic malaria to a diverse panel of 36 recombinant proteins comprising part of the DBLα domain (the 'DBLα-tag') of PfEMP1, a major class of VSAs. We found that although plasma antibody responses were highly specific to individual antigens, serological profiles of responses across antigens fell into one of just two distinct types. One type was found almost exclusively in children that succumbed to severe disease (19 out of 20) while the other occurred in all children with mild disease (16 out of 16). Moreover, children with severe malaria had serological profiles that were narrower in antigen specificity and shorter-lived than those in children with mild malaria. Borrowing a novel technique used in influenza-antigenic cartography-we mapped these dichotomous serological profiles to amino acid sequence variation within a small sub-region of the PfEMP1 DBLα domain. By applying our methodology on a larger scale, it should be possible to identify epitopes responsible for eliciting the protective version of serological profiles to PfEMP1 thereby accelerating development of a broadly effective anti-disease malaria vaccine.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 709.2KB, Terms of use)
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- Publisher copy:
- 10.1371/journal.ppat.1007870
Authors
- Publisher:
- Public Library of Science
- Journal:
- PLoS Pathogens More from this journal
- Volume:
- 15
- Issue:
- 7
- Pages:
- e1007870
- Publication date:
- 2019-07-01
- Acceptance date:
- 2019-05-24
- DOI:
- EISSN:
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1553-7374
- ISSN:
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1553-7366
- Pmid:
-
31260501
- Language:
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English
- Pubs id:
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pubs:1028450
- UUID:
-
uuid:6d9f1454-d195-403a-bd40-d9caa44b8b98
- Local pid:
-
pubs:1028450
- Source identifiers:
-
1028450
- Deposit date:
-
2019-07-29
- ARK identifier:
Terms of use
- Copyright holder:
- Tuju et al
- Copyright date:
- 2019
- Rights statement:
- © 2019 Tuju et al. This is an open access article distributed under the terms of the Creative Commons Attribution License
- Notes:
- A correction has been published for this article which is available to download here or from the publisher's website at: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008018
- Licence:
- CC Attribution (CC BY)
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