Identification of Plasmodium falciparum Antigens by Antigenic Analysis of Genomic and Proteomic Data
The recent explosion in genomic sequencing has made available a wealth of data that can now be analyzed to identify protein antigens, potential targets for vaccine development. Here we present, in the context of Plasmodium falciparum, a strategy that rapidly identifies target antigens from large and...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 100; no. 17; pp. 9952 - 9957 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
19.08.2003
National Acad Sciences |
Subjects | |
Online Access | Get full text |
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Summary: | The recent explosion in genomic sequencing has made available a wealth of data that can now be analyzed to identify protein antigens, potential targets for vaccine development. Here we present, in the context of Plasmodium falciparum, a strategy that rapidly identifies target antigens from large and complex genomes. Sixteen antigenic proteins recognized by volunteers immunized with radiation-attenuated P. falciparum sporozoites, but not by mock immunized controls, were identified. Several of these were more antigenic than previously identified and well characterized P. falciparum-derived protein antigens. The data suggest that immune responses to Plasmodium are dispersed on a relatively large number of parasite antigens. These studies have implications for our understanding of immunodominance and breadth of responses to complex pathogens. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Present address: Unidad de Epidemiologia y Bioestadistica, Hospital Clinic, Universitat de Barcelona, Barcelona E-08036, Spain. To whom correspondence should be addressed. E-mail: alex@liai.org. Communicated by Howard M. Grey, La Jolla Institute for Allergy and Immunology, San Diego, CA, May 29, 2003 Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. PF10_0179, PFL0800c, PFI0165c, PFC0210c, PF14_0372, PF11_0341, mal4T2c4.p1t1, PF13_0278, PFE0765w, PF11_0479, PFC0450w, PF14_0074, PFC0700c, PF14_0291, MAL8P1.78, MAL13P1.218, PFD0425w, PF13_0320, PF11_0435, PFI0260, PF11_0226, PFA0515w, MAL6P1.252, PF14_0236, PF14_0751, PF14_0648, and PF11_0456). Present address: La Jolla Institute for Allergy and Immunology, San Diego, CA 92121. Present address: Department of Medical Microbiology, St. George's Hospital Medical School, London SW17 0RE, United Kingdom. Present address: Sanaria, Gaithersburg, MD 20878. Abbreviations: PBMC, peripheral blood mononuclear cells; ELISPOT, enzyme-linked immunospot; CSP, circumsporozoite protein; EXP-1, exported protein 1; LSA-1, liver-stage antigen 1; MIC, measured IC50 nM value; MudPIT, multidimensional protein identification technology; SFC, spot-forming cells; SSP2, sporozoite surface protein 2; PIC, predicted IC50 nM value. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1633254100 |