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Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria

The antigenicity of altered structures induced by Plasmodium falciparum in the membranes of infected Aotus monkey and human erythrocytes was examined. Antisera were obtained from monkeys made immune to malaria. Bound antibodies were shown to be localized on the knob protrusions of infected erythrocy...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1979
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185704/
https://www.ncbi.nlm.nih.gov/pubmed/91658
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description The antigenicity of altered structures induced by Plasmodium falciparum in the membranes of infected Aotus monkey and human erythrocytes was examined. Antisera were obtained from monkeys made immune to malaria. Bound antibodies were shown to be localized on the knob protrusions of infected erythrocytes of both human and monkey origin and from both in vitro and in vivo infections. Therefore, P. falciparum infection has produced similar antigenic changes in the erythrocyte surfaces of both man and monkey. Uninfected erythrocytes and all knobless-infected erythrocytes bound no antibody from immune sera. Strains of P. falciparum from widely different geographic areas that were cultured in vitro in human erythrocytes induced structures (knobs) which have common antigenicity. Merozoites were agglutinated by cross-linking of their cell coats when incubated with immune sera. The binding of ferritin-labeled antibody was heavy on the coats of both homologous and heterologous strains of the parasite, indicating that the merozoite surfaces of these strains share common antigens.
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spelling pubmed-21857042008-04-17 Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria J Exp Med Articles The antigenicity of altered structures induced by Plasmodium falciparum in the membranes of infected Aotus monkey and human erythrocytes was examined. Antisera were obtained from monkeys made immune to malaria. Bound antibodies were shown to be localized on the knob protrusions of infected erythrocytes of both human and monkey origin and from both in vitro and in vivo infections. Therefore, P. falciparum infection has produced similar antigenic changes in the erythrocyte surfaces of both man and monkey. Uninfected erythrocytes and all knobless-infected erythrocytes bound no antibody from immune sera. Strains of P. falciparum from widely different geographic areas that were cultured in vitro in human erythrocytes induced structures (knobs) which have common antigenicity. Merozoites were agglutinated by cross-linking of their cell coats when incubated with immune sera. The binding of ferritin-labeled antibody was heavy on the coats of both homologous and heterologous strains of the parasite, indicating that the merozoite surfaces of these strains share common antigens. The Rockefeller University Press 1979-11-01 /pmc/articles/PMC2185704/ /pubmed/91658 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title_full Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title_fullStr Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title_full_unstemmed Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title_short Antigenicity of the infected-erythrocyte and merozoite surfaces in Falciparum malaria
title_sort antigenicity of the infected-erythrocyte and merozoite surfaces in falciparum malaria
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185704/
https://www.ncbi.nlm.nih.gov/pubmed/91658