Tetanus immunity after diphtheria, tetanus toxoids, and acellular pertussis vaccination in children with clinically stable HIV infection

HIV infection often impairs the immune response to childhood vaccines. We sought to study the ability of HIV-infected children receiving highly active antiretroviral therapy (HAART) to generate a booster response to immunization with a recall antigen to which they had lost humoral immunity. Diphther...

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Veröffentlicht in:Journal of Allergy and Clinical Immunology 2005-09, Vol.116 (3), p.698-703
Hauptverfasser: Rosenblatt, Howard M., Song, Lin Y., Nachman, Sharon A., Stanley, Kenneth E., Krogstad, Paul A., Johnson, George M., Wiznia, Andrew A.
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container_issue 3
container_start_page 698
container_title Journal of Allergy and Clinical Immunology
container_volume 116
creator Rosenblatt, Howard M.
Song, Lin Y.
Nachman, Sharon A.
Stanley, Kenneth E.
Krogstad, Paul A.
Johnson, George M.
Wiznia, Andrew A.
description HIV infection often impairs the immune response to childhood vaccines. We sought to study the ability of HIV-infected children receiving highly active antiretroviral therapy (HAART) to generate a booster response to immunization with a recall antigen to which they had lost humoral immunity. Diphtheria, tetanus toxoids, and acellular pertussis (DTaP) vaccination was given at either 16 or 36 weeks after initiation of HAART to 37 HIV-infected children 2 to 9 years of age with a history of DTaP or diphtheria-tetanus-pertussis receipt who had negative tetanus antibody titers (≤1:243) at baseline. There was a clear increase in tetanus titers after vaccination, with an increase of 27-fold over the baseline values at weeks 4 and 8. The effect on tetanus titers faded to a 9-fold and 3-fold increase over baseline values at weeks 18 and 32, respectively. DTaP vaccination did not affect HIV-1 RNA viral load or CD4 percentage or cell count. There was no increase in either acute or long-term adverse events associated with the DTaP vaccination. Although children with stable HIV infection receiving HAART can mount antigen-specific responses to tetanus immunization, the durability of these responses might be limited. Long-term monitoring of specific immune function in such children is indicated.
doi_str_mv 10.1016/j.jaci.2005.05.016
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We sought to study the ability of HIV-infected children receiving highly active antiretroviral therapy (HAART) to generate a booster response to immunization with a recall antigen to which they had lost humoral immunity. Diphtheria, tetanus toxoids, and acellular pertussis (DTaP) vaccination was given at either 16 or 36 weeks after initiation of HAART to 37 HIV-infected children 2 to 9 years of age with a history of DTaP or diphtheria-tetanus-pertussis receipt who had negative tetanus antibody titers (≤1:243) at baseline. There was a clear increase in tetanus titers after vaccination, with an increase of 27-fold over the baseline values at weeks 4 and 8. The effect on tetanus titers faded to a 9-fold and 3-fold increase over baseline values at weeks 18 and 32, respectively. DTaP vaccination did not affect HIV-1 RNA viral load or CD4 percentage or cell count. There was no increase in either acute or long-term adverse events associated with the DTaP vaccination. 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Long-term monitoring of specific immune function in such children is indicated.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.1016/j.jaci.2005.05.016</identifier><identifier>PMID: 16159645</identifier><identifier>CODEN: JACIBY</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Animals ; Antibodies, Bacterial - blood ; Antiretroviral drugs ; Antiretroviral Therapy, Highly Active ; Biological and medical sciences ; Child ; Child, Preschool ; Children &amp; youth ; Clostridium tetani - immunology ; diphtheria-tetanus-acellular pertussis vaccines ; Diphtheria-Tetanus-Pertussis Vaccine - immunology ; Drug therapy ; Female ; Flow Cytometry ; Fundamental and applied biological sciences. 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We sought to study the ability of HIV-infected children receiving highly active antiretroviral therapy (HAART) to generate a booster response to immunization with a recall antigen to which they had lost humoral immunity. Diphtheria, tetanus toxoids, and acellular pertussis (DTaP) vaccination was given at either 16 or 36 weeks after initiation of HAART to 37 HIV-infected children 2 to 9 years of age with a history of DTaP or diphtheria-tetanus-pertussis receipt who had negative tetanus antibody titers (≤1:243) at baseline. There was a clear increase in tetanus titers after vaccination, with an increase of 27-fold over the baseline values at weeks 4 and 8. The effect on tetanus titers faded to a 9-fold and 3-fold increase over baseline values at weeks 18 and 32, respectively. DTaP vaccination did not affect HIV-1 RNA viral load or CD4 percentage or cell count. There was no increase in either acute or long-term adverse events associated with the DTaP vaccination. 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source MEDLINE; Wiley Journals; Elsevier ScienceDirect Journals Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; IngentaConnect Free/Open Access Journals; PubMed Central
subjects Animals
Antibodies, Bacterial - blood
Antiretroviral drugs
Antiretroviral Therapy, Highly Active
Biological and medical sciences
Child
Child, Preschool
Children & youth
Clostridium tetani - immunology
diphtheria-tetanus-acellular pertussis vaccines
Diphtheria-Tetanus-Pertussis Vaccine - immunology
Drug therapy
Female
Flow Cytometry
Fundamental and applied biological sciences. Psychology
Fundamental immunology
HIV
HIV infections
HIV Infections - drug therapy
HIV Infections - immunology
Human immunodeficiency virus
Human immunodeficiency virus 1
Humans
immune response
Immunization, Secondary
Immunodeficiencies
Immunodeficiencies. Immunoglobulinopathies
Immunopathology
Laboratories
Male
Medical sciences
Tetanus - immunology
Vaccines
title Tetanus immunity after diphtheria, tetanus toxoids, and acellular pertussis vaccination in children with clinically stable HIV infection
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