Human Infection with Ascaris lumbricoides Is Associated with Suppression of the Interleukin-2 Response to Recombinant Cholera Toxin B Subunit following Vaccination with the Live Oral Cholera Vaccine CVD 103-HgR

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Published inInfection and Immunity Vol. 69; no. 3; pp. 1574 - 1580
Main Authors Cooper, Philip J., Chico, Martha, Sandoval, Carlos, Espinel, Ivan, Guevara, Angel, Levine, Myron M., Griffin, George E., Nutman, Thomas B.
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.03.2001
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Abstract Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue IAI About IAI Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy Connect to IAI IAI RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0019-9567 Online ISSN: 1098-5522 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to IAI .asm.org, visit: IAI       
AbstractList To investigate the potential immunomodulatory effects of concurrent ascariasis on the cytokine response to a live oral vaccine, we measured cytokine responses to cholera toxin B subunit (CT-B) following vaccination with the live oral cholera vaccine CVD 103-HgR in Ascaris lumbricoides -infected subjects randomized in a double-blind study to receive two doses of either albendazole or placebo prior to vaccination and in a group of healthy U.S. controls. Postvaccination cytokine responses to CT-B were characterized by transient increases in the production of interleukin-2 (IL-2; P = 0.02) and gamma interferon (IFN-γ; P = 0.001) in the three study groups combined; however, postvaccination increases in IFN-γ were significant only in the albendazole-treated A. lumbricoides infection group ( P = 0.008). Postvaccination levels of IL-2 were significantly greater in the albendazole-treated group compared with the placebo group ( P = 0.03). No changes in levels of Th1 and Th2 cytokines in response to control ascaris antigens were observed over the same period. These findings indicate that vaccination with CVD 103-HgR is associated with a Th1 cytokine response (IL-2 and IFN-γ) to CT-B, that infection with A. lumbricoides diminishes the magnitude of this response, and that albendazole treatment prior to vaccination was able to partially reverse the deficit in IL-2. The potential modulation of the immune response to oral vaccines by geohelminth parasites has important implications for the design of vaccination campaigns in geohelminth-endemic areas.
To investigate the potential immunomodulatory effects of concurrent ascariasis on the cytokine response to a live oral vaccine, we measured cytokine responses to cholera toxin B subunit (CT-B) following vaccination with the live oral cholera vaccine CVD 103-HgR in Ascaris lumbricoides-infected subjects randomized in a double-blind study to receive two doses of either albendazole or placebo prior to vaccination and in a group of healthy U.S. controls. Postvaccination cytokine responses to CT-B were characterized by transient increases in the production of interleukin-2 (IL-2; P = 0.02) and gamma interferon (IFN-gamma; P = 0.001) in the three study groups combined; however, postvaccination increases in IFN-gamma were significant only in the albendazole-treated A. lumbricoides infection group (P = 0.008). Postvaccination levels of IL-2 were significantly greater in the albendazole-treated group compared with the placebo group (P = 0.03). No changes in levels of Th1 and Th2 cytokines in response to control ascaris antigens were observed over the same period. These findings indicate that vaccination with CVD 103-HgR is associated with a Th1 cytokine response (IL-2 and IFN-gamma) to CT-B, that infection with A. lumbricoides diminishes the magnitude of this response, and that albendazole treatment prior to vaccination was able to partially reverse the deficit in IL-2. The potential modulation of the immune response to oral vaccines by geohelminth parasites has important implications for the design of vaccination campaigns in geohelminth-endemic areas.To investigate the potential immunomodulatory effects of concurrent ascariasis on the cytokine response to a live oral vaccine, we measured cytokine responses to cholera toxin B subunit (CT-B) following vaccination with the live oral cholera vaccine CVD 103-HgR in Ascaris lumbricoides-infected subjects randomized in a double-blind study to receive two doses of either albendazole or placebo prior to vaccination and in a group of healthy U.S. controls. Postvaccination cytokine responses to CT-B were characterized by transient increases in the production of interleukin-2 (IL-2; P = 0.02) and gamma interferon (IFN-gamma; P = 0.001) in the three study groups combined; however, postvaccination increases in IFN-gamma were significant only in the albendazole-treated A. lumbricoides infection group (P = 0.008). Postvaccination levels of IL-2 were significantly greater in the albendazole-treated group compared with the placebo group (P = 0.03). No changes in levels of Th1 and Th2 cytokines in response to control ascaris antigens were observed over the same period. These findings indicate that vaccination with CVD 103-HgR is associated with a Th1 cytokine response (IL-2 and IFN-gamma) to CT-B, that infection with A. lumbricoides diminishes the magnitude of this response, and that albendazole treatment prior to vaccination was able to partially reverse the deficit in IL-2. The potential modulation of the immune response to oral vaccines by geohelminth parasites has important implications for the design of vaccination campaigns in geohelminth-endemic areas.
Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue IAI About IAI Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy Connect to IAI IAI RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0019-9567 Online ISSN: 1098-5522 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to IAI .asm.org, visit: IAI       
To investigate the potential immunomodulatory effects of concurrent ascariasis on the cytokine response to a live oral vaccine, we measured cytokine responses to cholera toxin B subunit (CT-B) following vaccination with the live oral cholera vaccine CVD 103-HgR in Ascaris lumbricoides-infected subjects randomized in a double-blind study to receive two doses of either albendazole or placebo prior to vaccination and in a group of healthy U.S. controls. Postvaccination cytokine responses to CT-B were characterized by transient increases in the production of interleukin-2 (IL-2; P = 0.02) and gamma interferon (IFN- gamma ; P = 0.001) in the three study groups combined; however, postvaccination increases in IFN- gamma were significant only in the albendazole-treated A. lumbricoides infection group (P = 0.008). Postvaccination levels of IL-2 were significantly greater in the albendazole-treated group compared with the placebo group (P = 0.03). No changes in levels of Th1 and Th2 cytokines in response to control ascaris antigens were observed over the same period. These findings indicate that vaccination with CVD 103-HgR is associated with a Th1 cytokine response (IL-2 and IFN- gamma ) to CT-B, that infection with A. lumbricoides diminishes the magnitude of this response, and that albendazole treatment prior to vaccination was able to partially reverse the deficit in IL-2. The potential modulation of the immune response to oral vaccines by geohelminth parasites has important implications for the design of vaccination campaigns in geohelminth-endemic areas.
Author Martha Chico
Angel Guevara
Ivan Espinel
Philip J. Cooper
Carlos Sandoval
Thomas B. Nutman
George E. Griffin
Myron M. Levine
AuthorAffiliation Laboratory of Parasitic Diseases, National Institutes of Health, Bethesda, Maryland 20892 1 ; Department of Clinical Investigations, Hospital Vozandes, Quito, Ecuador 2 ; Center for Vaccine Development, University of Maryland, Baltimore, Maryland 21201 3 ; and St. George's Hospital Medical School, Tooting, London, United Kingdom 4
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  organization: <!--label omitted: 2-->Department of Clinical Investigations, Hospital Vozandes, Quito, Ecuador2
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  givenname: George E.
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  fullname: Griffin, George E.
  organization: <!--label omitted: 4-->St. George's Hospital Medical School, Tooting, London, United Kingdom4
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BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14162131$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/11179329$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords Ascaris lumbricoides
Vision disorder
Suppression
Vaccination
Vibrio cholerae
Helper cell
Potential
Subunit
Association
Interleukin 2
Bacteria
Nematoda
Human
Cytokine
Vaccine
Parasitosis
Helminthiasis
Infection
Ascariasis
Toxin
Eye disease
Benzimidazole derivatives
Nematode disease
Blindness
Bacteriosis
Helmintha
Vibrionaceae
Nemathelminthia
Cholera
Invertebrata
Language English
License CC BY 4.0
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Corresponding author. Present address: Division of Infectious Diseases, St. George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, United Kingdom. Phone: 44-20-8725-5827. Fax: 44-20-8725-3487. E-mail: pc102d@hotmail.com.
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PublicationTitle Infection and Immunity
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Snippet Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit...
To investigate the potential immunomodulatory effects of concurrent ascariasis on the cytokine response to a live oral vaccine, we measured cytokine responses...
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StartPage 1574
SubjectTerms Adult
Albendazole - therapeutic use
Animals
Anthelmintics - therapeutic use
Antigens, Helminth - immunology
Ascariasis - drug therapy
Ascariasis - immunology
Ascaris lumbricoides
Ascaris lumbricoides - drug effects
Ascaris lumbricoides - immunology
Bacteriology
Biological and medical sciences
Cholera - prevention & control
Cholera Toxin - immunology
Cholera Vaccines - immunology
Cholera Vaccines - therapeutic use
Double-Blind Method
Female
Fundamental and applied biological sciences. Psychology
Fungal and Parasitic Infections
Humans
Interferon-gamma - blood
Interleukin-2 - blood
Leukocytes, Mononuclear - immunology
Male
Microbiology
Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains
toxin B
Vaccination
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Title Human Infection with Ascaris lumbricoides Is Associated with Suppression of the Interleukin-2 Response to Recombinant Cholera Toxin B Subunit following Vaccination with the Live Oral Cholera Vaccine CVD 103-HgR
URI http://iai.asm.org/content/69/3/1574.abstract
https://www.ncbi.nlm.nih.gov/pubmed/11179329
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Volume 69
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