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The V gene repertoire as revealed by polyclonal B cell activators
Annales D'Immunologie
|June 1, 1976
Summary
B lymphocytes are activated by non-specific signals, not just Ig receptors. This challenges the idea that thymus-dependent antigens control B cell activation and tolerance.
Area of Science:
- Immunology
- Cell Biology
Background:
- The one non-specific signal hypothesis proposes B lymphocyte activation via non-clonal receptors, distinct from Ig receptors.
- Protein A acts as a polyclonal B cell activator but not through Ig receptor Fc regions.
Purpose of the Study:
- To summarize evidence supporting the one non-specific signal hypothesis for B lymphocyte activation.
- To investigate the role of thymus-dependent antigens in B cell activation and tolerance.
Main Methods:
- Review of existing evidence on B cell activation mechanisms.
- Experimental induction of tolerance to thymus-dependent protein antigens.
- Activation of tolerant B cells using polyclonal B cell activators (e.g., LPS, PPD).
Main Results:
- Polyclonal B cell activators can activate B cells tolerant to thymus-dependent antigens, inducing autoantibody production.
- Experimentally induced tolerance in B cells mirrors self-antigen tolerance.
- LPS and PPD induced autoantibodies capable of lysing autologous cells.
Conclusions:
- B lymphocytes lack the ability to distinguish self from non-self antigens.
- T cells possess the capacity for self/non-self discrimination, unlike B cells.