Abstract
Kinetics and family transmission of antigen-specific in vitro cell-mediated responses were investigated in 68, and serum-antibody responses to tetanus toxoid (TT) in 73 individuals from a total of 12 families. Proliferative responses to highly purified TT monomer were studied in 6- to 7-day lymphocyte cultures. The effect of booster immunization was detectable 7(D7) and 30 (D30), but not 120 days (D120) later. The sex of donors was not found to have any influence. A significant influence of the time interval since the last immunization was found for the responses at D7 and D30. Data were correspondingly adjusted for segregation and linkage analyses. Several transmission hypotheses for the data obtained at D7 and D30 were evaluated by likelihood ratio tests. Observations at D30 were compatible with the hypothesis of a control by a dominant genetic determinant for high responses closely linked to the major histocompatibility complex region. No such evidence could be found for D7. Afterbooster immunization, mean antibody levels determined on D7, D30 (peak of response), and D120 were found to be higher than those prior to immunization (D0). The sex of the donors was found to have no influence on antibody responses. The time interval since the last immunization and the age of donors both had a slight influence, and data were correspondingly adjusted for segregation and linkage analyses, which showed no evidence of genetic control of the antibody responses or of linkage to HLA.
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Abbreviations
- TT:
-
tetanus toxoid
- D0, D7, D30, D120 :
-
day of booster immunization and 7th, 30th and 120th day following booster immunization
- cpm:
-
counts per minute
- 3H-thymidine, 3H-T:
-
Δ=difference between 3H-T (1n cpm) incorporated in to stimulated cultures and 3H-T (1n cpm) incorporated in nonstimulated cultures
- MHC:
-
major histocompatibility complex
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Ballet, J.J., Rabian-Herzog, C., Lathrop, M. et al. Specific immune responses after booster immunization with tetanus toxoid in man: Study of kinetics, family segregation, and linkage to HLA of in vitro lymphocyte proliferative responses and serum-antibody responses. Immunogenetics 18, 343–358 (1983). https://doi.org/10.1007/BF00372467
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DOI: https://doi.org/10.1007/BF00372467