Decreased specific antibody synthesis in old adults: Decreased potency of antigen-specific B cells with aging
The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparin...
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Published in | Mechanisms of ageing and development Vol. 53; no. 3; pp. 229 - 241 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Shannon
Elsevier Ireland Ltd
30.04.1990
Elsevier Science |
Subjects | |
Online Access | Get full text |
ISSN | 0047-6374 1872-6216 |
DOI | 10.1016/0047-6374(90)90041-D |
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Abstract | The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparing adults over age 60 to young adults aged 18–40, using tetanus toxoid (TT) as an immunologic probe.
A culture system which does not require TT booster immunizations of study subjects was used to induce
in vitro specific antibody responses. The amount of anti-TT antibody (Ab) produced in serum and in culture was measured by a TT-specific enzyme-linked immunosorbent assay (ELISA). The numbers of anti-TT Ab-secreting B cells were measured by a TT-specific ELISA-plaque assay. The TT-specific responses of old subjects were significantly less than that seen for young control subjects in the following measures: (1) serum anti-TT Ab titers (mean ± S.E. log 2 titer = 3.3 ± 1.1
vs. 9.5 ± 1.4,
P < 0.01); (2) anti-TT Ab produced by peripheral blood lymphocytes (PBL) in cultures stimulated with TT (6 ± 2.1 ng/ml
vs. 22 ± 8.4 ng/ml,
P < 0.01); (3) numbers of anti-TT Ab secreting B cells per million cells culured (6.7 ± 3.4
vs. 26.6 ± 7.6,
P < 0.001) and (4) mean ng Ab secreted per anti-TT Ab-secreting B cell (0.6 ± 0.4 ng
vs. 12.7 ± 7.8 ng,
P < 0.01). This study shows that both decreased numbers of Ag-specific immune B cells and decreased potency on a per cell basis contribute to the impaired immune responses to immunizations in older adults. |
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AbstractList | The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparing adults over age 60 to young adults aged 18-40, using tetanus toxoid (TT) as an immunologic probe. A culture system which does not require TT booster immunizations of study subjects was used to induce in vitro specific antibody responses. The amount of anti-TT antibody (Ab) produced in serum and in culture was measured by a TT-specific enzyme-linked immunosorbent assay (ELISA). The numbers of anti-TT Ab-secreting B cells were measured by a TT-specific ELISA-plaque assay. The TT-specific responses of old subjects were significantly less than that seen for young control subjects in the following measures: (1) serum anti-TT Ab titers (mean +/- S.E. log 2 titer = 3.3 +/- 1.1 vs. 9.5 +/- 1.4, P less than 0.01); (2) anti-TT Ab produced by peripheral blood lymphocytes (PBL) in cultures stimulated with TT (6 +/- 2.1 ng/ml vs. 22 +/- 8.4 ng/ml, P less than 0.01); (3) numbers of anti-TT Ab secreting B cells per million cells cultured (6.7 +/- 3.4 vs. 26.6 +/- 7.6, P less than 0.001) and (4) mean ng Ab secreted per anti-TT Ab-secreting B cell (0.6 +/- 0.4 ng vs. 12.7 +/- 7.8 ng, P less than 0.01). This study shows that both decreased numbers of Ag-specific immune B cells and decreased potency on a per cell basis contribute to the impaired immune responses to immunizations in older adults.The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparing adults over age 60 to young adults aged 18-40, using tetanus toxoid (TT) as an immunologic probe. A culture system which does not require TT booster immunizations of study subjects was used to induce in vitro specific antibody responses. The amount of anti-TT antibody (Ab) produced in serum and in culture was measured by a TT-specific enzyme-linked immunosorbent assay (ELISA). The numbers of anti-TT Ab-secreting B cells were measured by a TT-specific ELISA-plaque assay. The TT-specific responses of old subjects were significantly less than that seen for young control subjects in the following measures: (1) serum anti-TT Ab titers (mean +/- S.E. log 2 titer = 3.3 +/- 1.1 vs. 9.5 +/- 1.4, P less than 0.01); (2) anti-TT Ab produced by peripheral blood lymphocytes (PBL) in cultures stimulated with TT (6 +/- 2.1 ng/ml vs. 22 +/- 8.4 ng/ml, P less than 0.01); (3) numbers of anti-TT Ab secreting B cells per million cells cultured (6.7 +/- 3.4 vs. 26.6 +/- 7.6, P less than 0.001) and (4) mean ng Ab secreted per anti-TT Ab-secreting B cell (0.6 +/- 0.4 ng vs. 12.7 +/- 7.8 ng, P less than 0.01). This study shows that both decreased numbers of Ag-specific immune B cells and decreased potency on a per cell basis contribute to the impaired immune responses to immunizations in older adults. The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparing adults over age 60 to young adults aged 18–40, using tetanus toxoid (TT) as an immunologic probe. A culture system which does not require TT booster immunizations of study subjects was used to induce in vitro specific antibody responses. The amount of anti-TT antibody (Ab) produced in serum and in culture was measured by a TT-specific enzyme-linked immunosorbent assay (ELISA). The numbers of anti-TT Ab-secreting B cells were measured by a TT-specific ELISA-plaque assay. The TT-specific responses of old subjects were significantly less than that seen for young control subjects in the following measures: (1) serum anti-TT Ab titers (mean ± S.E. log 2 titer = 3.3 ± 1.1 vs. 9.5 ± 1.4, P < 0.01); (2) anti-TT Ab produced by peripheral blood lymphocytes (PBL) in cultures stimulated with TT (6 ± 2.1 ng/ml vs. 22 ± 8.4 ng/ml, P < 0.01); (3) numbers of anti-TT Ab secreting B cells per million cells culured (6.7 ± 3.4 vs. 26.6 ± 7.6, P < 0.001) and (4) mean ng Ab secreted per anti-TT Ab-secreting B cell (0.6 ± 0.4 ng vs. 12.7 ± 7.8 ng, P < 0.01). This study shows that both decreased numbers of Ag-specific immune B cells and decreased potency on a per cell basis contribute to the impaired immune responses to immunizations in older adults. The rise in rates of infection in adults over the age of 60 is accompanied by a decreased ability of older adults to make specific immune responses after immunization with a variety of specific antigens (Ag). This investigation delineates age-related changes in Ag-specific humoral immunity, comparing adults over age 60 to young adults aged 18-40, using tetanus toxoid (TT) as an immunologic probe. A culture system which does not require TT booster immunizations of study subjects was used to induce in vitro specific antibody responses. The amount of anti-TT antibody (Ab) produced in serum and in culture was measured by a TT-specific enzyme-linked immunosorbent assay (ELISA). The numbers of anti-TT Ab-secreting B cells were measured by a TT-specific ELISA-plaque assay. The TT-specific responses of old subjects were significantly less than that seen for young control subjects in the following measures: (1) serum anti-TT Ab titers (mean +/- S.E. log 2 titer = 3.3 +/- 1.1 vs. 9.5 +/- 1.4, P less than 0.01); (2) anti-TT Ab produced by peripheral blood lymphocytes (PBL) in cultures stimulated with TT (6 +/- 2.1 ng/ml vs. 22 +/- 8.4 ng/ml, P less than 0.01); (3) numbers of anti-TT Ab secreting B cells per million cells cultured (6.7 +/- 3.4 vs. 26.6 +/- 7.6, P less than 0.001) and (4) mean ng Ab secreted per anti-TT Ab-secreting B cell (0.6 +/- 0.4 ng vs. 12.7 +/- 7.8 ng, P less than 0.01). This study shows that both decreased numbers of Ag-specific immune B cells and decreased potency on a per cell basis contribute to the impaired immune responses to immunizations in older adults. |
Author | Giddings, Bernadette R. Burns, Edith A. Goodwin, James S. Seigneuret, Margaret C. Lum, Lawrence G. |
Author_xml | – sequence: 1 givenname: Edith A. surname: Burns fullname: Burns, Edith A. organization: Division of Geriatrics, Department of Medicine, University of Wisconsin School of Medicine, Miwaukee Clinical Campus, Milwaukee, WI U.S.A – sequence: 2 givenname: Lawrence G. surname: Lum fullname: Lum, Lawrence G. organization: Division of Hematology/Oncology, Departments of Medicine and Pediatrics, Medical College of Wisconsin, Milwaukee, WI U.S.A – sequence: 3 givenname: Margaret C. surname: Seigneuret fullname: Seigneuret, Margaret C. organization: Division of Hematology/Oncology, Departments of Medicine and Pediatrics, Medical College of Wisconsin, Milwaukee, WI U.S.A – sequence: 4 givenname: Bernadette R. surname: Giddings fullname: Giddings, Bernadette R. organization: Division of Hematology/Oncology, Departments of Medicine and Pediatrics, Medical College of Wisconsin, Milwaukee, WI U.S.A – sequence: 5 givenname: James S. surname: Goodwin fullname: Goodwin, James S. organization: Division of Geriatrics, Department of Medicine, University of Wisconsin School of Medicine, Miwaukee Clinical Campus, Milwaukee, WI U.S.A |
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Keywords | Aging Immunity Vaccination Antibody synthesis Tetanus toxoid Human Senescence Immune response Antibody Toxoid Clostridiales Clostridium tetani Biosynthesis Infection Clostridiaceae Bacteriosis Bacteria Tetanus Elderly |
Language | English |
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SubjectTerms | Adolescent Adult Aged Aging Aging - immunology Antibody Specificity Antibody synthesis B-Lymphocytes - immunology Biological and medical sciences Cells, Cultured Development. Metamorphosis. Moult. Ageing Enzyme-Linked Immunosorbent Assay Fundamental and applied biological sciences. Psychology Humans Immunity Immunoglobulins - biosynthesis Middle Aged Tetanus Toxoid Vaccination Vertebrates: anatomy and physiology, studies on body, several organs or systems |
Title | Decreased specific antibody synthesis in old adults: Decreased potency of antigen-specific B cells with aging |
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