HIV-1 Infection and Antibodies to Plasmodium falciparum in Adults

Background. Coinfection with human immunodeficiency virus (HIV) may increase susceptibility to malaria by compromising naturally acquired immunity. Methods. In 339 adults (64% HIV infected), we measured antibodies to Plasmodium falciparum variant surface antigens (VSA) and antibodies that opsonise i...

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Veröffentlicht in:The Journal of infectious diseases 2014-11, Vol.210 (9), p.1407-1414
Hauptverfasser: Hasang, Wina, Dembo, Edson G., Wijesinghe, Rushika, Molyneux, Malcolm E., Kublin, James G., Rogerson, Stephen
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container_end_page 1414
container_issue 9
container_start_page 1407
container_title The Journal of infectious diseases
container_volume 210
creator Hasang, Wina
Dembo, Edson G.
Wijesinghe, Rushika
Molyneux, Malcolm E.
Kublin, James G.
Rogerson, Stephen
description Background. Coinfection with human immunodeficiency virus (HIV) may increase susceptibility to malaria by compromising naturally acquired immunity. Methods. In 339 adults (64% HIV infected), we measured antibodies to Plasmodium falciparum variant surface antigens (VSA) and antibodies that opsonise infected erythrocytes using parasite lines FCR3, E8B, and R29, and antibodies to merozoite antigens AMA-1 and MSP2. We determined the relationship between malaria antibodies, HIV infection, markers of immune compromise, and risk of incident parasitemia. Results. HIV-infected adults had significantly lower mean levels of opsonizing antibody to all parasite lines (P < .0001), and lower levels of antibody to AMA-1 (P = .01) and MSP2 (P < .0001). Levels of immunoglobulin G (IgG) to VSA were not affected by HIV status. Opsonising antibody titres against some isolates were positively correlated with CD4 count. There were negative associations between human immunodeficiency virus type 1 (HIV-1) viral load and opsonizing antibodies to FCR3 (P = .04), and levels of IgG to AMA-1 (P ≤ .03) and MSP2-3D7 (P = .05). Lower opsonizing antibody levels on enrollment were seen in those who became parasitemic during follow-up, independent of HIV infection (P < .04 for each line). Conclusions. HIV-1 infection decreases opsonizing antibodies to VSA, and antibody to merozoite antigens. Opsonizing antibodies were associated with lack of parasitemia during follow up, suggesting a role in protection.
doi_str_mv 10.1093/infdis/jiu262
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Coinfection with human immunodeficiency virus (HIV) may increase susceptibility to malaria by compromising naturally acquired immunity. Methods. In 339 adults (64% HIV infected), we measured antibodies to Plasmodium falciparum variant surface antigens (VSA) and antibodies that opsonise infected erythrocytes using parasite lines FCR3, E8B, and R29, and antibodies to merozoite antigens AMA-1 and MSP2. We determined the relationship between malaria antibodies, HIV infection, markers of immune compromise, and risk of incident parasitemia. Results. HIV-infected adults had significantly lower mean levels of opsonizing antibody to all parasite lines (P &lt; .0001), and lower levels of antibody to AMA-1 (P = .01) and MSP2 (P &lt; .0001). Levels of immunoglobulin G (IgG) to VSA were not affected by HIV status. Opsonising antibody titres against some isolates were positively correlated with CD4 count. There were negative associations between human immunodeficiency virus type 1 (HIV-1) viral load and opsonizing antibodies to FCR3 (P = .04), and levels of IgG to AMA-1 (P ≤ .03) and MSP2-3D7 (P = .05). Lower opsonizing antibody levels on enrollment were seen in those who became parasitemic during follow-up, independent of HIV infection (P &lt; .04 for each line). Conclusions. HIV-1 infection decreases opsonizing antibodies to VSA, and antibody to merozoite antigens. Opsonizing antibodies were associated with lack of parasitemia during follow up, suggesting a role in protection.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiu262</identifier><identifier>PMID: 24795481</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adolescent ; Adult ; Aged ; Antibodies ; Antibodies, Protozoan - immunology ; Antigens ; Antigens, Protozoan - immunology ; Case-Control Studies ; CD4 Lymphocyte Count ; Coinfection - immunology ; Coinfection - parasitology ; Coinfection - virology ; Erythrocytes ; Female ; HIV ; HIV 1 ; HIV infections ; HIV Infections - complications ; HIV Infections - immunology ; HIV Infections - parasitology ; HIV/AIDS ; Human immunodeficiency virus ; Human immunodeficiency virus 1 ; Humans ; Immunoglobulin G - immunology ; Malaria ; Malaria, Falciparum - complications ; Malaria, Falciparum - immunology ; Malaria, Falciparum - virology ; Male ; Merozoites ; Middle Aged ; Parasitemia ; Parasites ; Plasmodium falciparum ; Plasmodium falciparum - immunology ; Young Adult</subject><ispartof>The Journal of infectious diseases, 2014-11, Vol.210 (9), p.1407-1414</ispartof><rights>Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. 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Coinfection with human immunodeficiency virus (HIV) may increase susceptibility to malaria by compromising naturally acquired immunity. Methods. In 339 adults (64% HIV infected), we measured antibodies to Plasmodium falciparum variant surface antigens (VSA) and antibodies that opsonise infected erythrocytes using parasite lines FCR3, E8B, and R29, and antibodies to merozoite antigens AMA-1 and MSP2. We determined the relationship between malaria antibodies, HIV infection, markers of immune compromise, and risk of incident parasitemia. Results. HIV-infected adults had significantly lower mean levels of opsonizing antibody to all parasite lines (P &lt; .0001), and lower levels of antibody to AMA-1 (P = .01) and MSP2 (P &lt; .0001). Levels of immunoglobulin G (IgG) to VSA were not affected by HIV status. Opsonising antibody titres against some isolates were positively correlated with CD4 count. 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Coinfection with human immunodeficiency virus (HIV) may increase susceptibility to malaria by compromising naturally acquired immunity. Methods. In 339 adults (64% HIV infected), we measured antibodies to Plasmodium falciparum variant surface antigens (VSA) and antibodies that opsonise infected erythrocytes using parasite lines FCR3, E8B, and R29, and antibodies to merozoite antigens AMA-1 and MSP2. We determined the relationship between malaria antibodies, HIV infection, markers of immune compromise, and risk of incident parasitemia. Results. HIV-infected adults had significantly lower mean levels of opsonizing antibody to all parasite lines (P &lt; .0001), and lower levels of antibody to AMA-1 (P = .01) and MSP2 (P &lt; .0001). Levels of immunoglobulin G (IgG) to VSA were not affected by HIV status. Opsonising antibody titres against some isolates were positively correlated with CD4 count. 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subjects Adolescent
Adult
Aged
Antibodies
Antibodies, Protozoan - immunology
Antigens
Antigens, Protozoan - immunology
Case-Control Studies
CD4 Lymphocyte Count
Coinfection - immunology
Coinfection - parasitology
Coinfection - virology
Erythrocytes
Female
HIV
HIV 1
HIV infections
HIV Infections - complications
HIV Infections - immunology
HIV Infections - parasitology
HIV/AIDS
Human immunodeficiency virus
Human immunodeficiency virus 1
Humans
Immunoglobulin G - immunology
Malaria
Malaria, Falciparum - complications
Malaria, Falciparum - immunology
Malaria, Falciparum - virology
Male
Merozoites
Middle Aged
Parasitemia
Parasites
Plasmodium falciparum
Plasmodium falciparum - immunology
Young Adult
title HIV-1 Infection and Antibodies to Plasmodium falciparum in Adults
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