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IgA and IgA diphtheria antitoxin responses from human tonsil lymphocytes
Journal of Immunology (Baltimore, Md. : 1950)
|March 1, 1975
Summary
Human tonsil lymphocytes produce significant IgG and IgA diphtheria antitoxin after stimulation. Prior immunization, specifically two doses after six months, is crucial for initiating this in vitro antibody response.
Area of Science:
- Immunology
- Cell Biology
Background:
- Tonsils are key sites for immune responses to inhaled or ingested antigens.
- Understanding in vitro antibody production by human lymphocytes is crucial for vaccine development.
Purpose of the Study:
- To investigate the in vitro antibody production of human tonsil lymphocytes against diphtheria toxoid.
- To determine the factors influencing the in vitro antibody response, including prior immunization history.
- To characterize the immunoglobulin classes and polymeric forms of antibodies produced.
Main Methods:
- Human tonsil lymphocytes were stimulated with diphtheria toxoid in a Marbrook culture system.
- Antibody levels (IgG, IgA) in culture supernatants were quantified using radioimmunoassay with radiolabeled antigen.
- Immunoglobulin characterization involved immunodiffusion and sucrose density gradient ultracentrifugation.
- Neutralization assays were performed to confirm antitoxin activity.
Main Results:
- Significant IgG and IgA diphtheria antitoxin responses were observed in culture supernatants.
- Responding supernatants demonstrated toxin-neutralizing capacity.
- At least two diphtheria toxoid immunizations after six months of age were necessary to prime tonsils for an in vitro response.
- Approximately 40% of the produced IgA was polymeric (greater than 7S).
- Secretory piece was not detected on the produced IgA or specific IgA antitoxin.
Conclusions:
- Human tonsil lymphocytes can produce functional IgG and IgA diphtheria antitoxin in vitro.
- Prior immunization history significantly impacts the ability of tonsil lymphocytes to mount an in vitro antibody response.
- Human tonsil lymphocytes produce polymeric IgA in vitro, but it lacks secretory piece.