Intrinsic defects in B cell response to seasonal influenza vaccination in elderly humans
We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decrease...
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Published in | Vaccine Vol. 28; no. 51; pp. 8077 - 8084 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
29.11.2010
Elsevier Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0264-410X 1873-2518 1873-2518 |
DOI | 10.1016/j.vaccine.2010.10.023 |
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Abstract | We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine
in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells
in vitro, as measured by AID (activation-induced cytidine deaminase), the
in vivo serum HI (hemagglutination inhibition) response, and the
in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. |
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AbstractList | We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro, as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro, as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccinein vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cellsin vitro, as measured by AID (activation-induced cytidine deaminase), thein vivoserum HI (hemagglutination inhibition) response, and thein vivogeneration of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro . Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro , as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro, as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk.We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro. Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro, as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. Abstract We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to the vaccine in vitro . Although the serum response has previously been shown to decrease with age, this has largely been associated to decreased T cell functions. Our results show that in response to the vaccine, the specific response of B cells in vitro , as measured by AID (activation-induced cytidine deaminase), the in vivo serum HI (hemagglutination inhibition) response, and the in vivo generation of switch memory B cells are decreased with age, as evaluated in the same subjects. This is the first report to demonstrate that intrinsic B cell defects with age contribute to reduced antibody responses to the influenza vaccine. The level of AID in response to CpG before vaccination can also predict the robustness of the vaccine response. These results could contribute to developing more effective vaccines to protect the elderly as well as identifying those most at risk. |
Author | Frasca, Daniela Ryan, John G. Phillips, Mitch Blomberg, Bonnie B. Diaz, Alain Lechner, Suzanne C. Landin, Ana Marie Romero, Maria |
AuthorAffiliation | b Department of Psychiatry, University of Miami Miller School of Medicine, Miami, FL, USA c Department of Family Medicine, University of Miami Miller School of Medicine, Miami, FL, USA a Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA |
AuthorAffiliation_xml | – name: b Department of Psychiatry, University of Miami Miller School of Medicine, Miami, FL, USA – name: c Department of Family Medicine, University of Miami Miller School of Medicine, Miami, FL, USA – name: a Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA |
Author_xml | – sequence: 1 givenname: Daniela surname: Frasca fullname: Frasca, Daniela organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 2 givenname: Alain surname: Diaz fullname: Diaz, Alain organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 3 givenname: Maria surname: Romero fullname: Romero, Maria organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 4 givenname: Ana Marie surname: Landin fullname: Landin, Ana Marie organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 5 givenname: Mitch surname: Phillips fullname: Phillips, Mitch organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 6 givenname: Suzanne C. surname: Lechner fullname: Lechner, Suzanne C. organization: Department of Psychiatry, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 7 givenname: John G. surname: Ryan fullname: Ryan, John G. organization: Department of Family Medicine, University of Miami Miller School of Medicine, Miami, FL, USA – sequence: 8 givenname: Bonnie B. surname: Blomberg fullname: Blomberg, Bonnie B. email: bblomber@med.miami.edu organization: Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23635297$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/20974306$$D View this record in MEDLINE/PubMed |
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Copyright | 2010 Elsevier Ltd Elsevier Ltd 2015 INIST-CNRS Copyright © 2010 Elsevier Ltd. All rights reserved. Copyright Elsevier Limited Nov 29, 2010 |
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Issue | 51 |
Keywords | Aging Immunoglobulin class switch recombination Influenza vaccination B lymphocytes Human Immunoglobulins Recombination Vaccination B-Lymphocyte Infection Viral disease Influenza Elderly Immunoglobulin class switch |
Language | English |
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Snippet | We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell response to... Abstract We have evaluated the serum response to seasonal influenza vaccination in subjects of different ages and associated this with the specific B cell... |
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SubjectTerms | Adult Age Age Factors Aged Aged, 80 and over Aging AICDA (Activation-Induced Cytidine Deaminase) Allergy and Immunology Antibodies, Viral - blood Applied microbiology B lymphocytes B-Lymphocytes - immunology Biological and medical sciences Cytidine Deaminase - metabolism Defects Female Fundamental and applied biological sciences. Psychology Health care Hemagglutination Inhibition Tests Humans Immune system Immunoglobulin class switch recombination Immunologic Memory Influenza Influenza vaccination Influenza Vaccines - immunology Influenza, Human - prevention & control Lymphocytes Male Memory Microbiology Middle Aged Mortality Seasons Vaccines Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) |
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