Publication | Closed Access
The asynchronous development of immunological memory in helper (T) and precursor (B) cell lines
106
Citations
51
References
1971
Year
ImmunohematologyLymphocyte DevelopmentAdaptive Immune SystemImmunodeficienciesImmunologyImmune RegulationImmunodominanceAntigen ProcessingImmune SystemImmunotherapyPrecursor MemoryAsynchronous DevelopmentNeuroimmunologyImmunological MemorySmall InjectionsCell LinesAutoimmunityT Cell ImmunityHumoral ImmunityImmune FunctionCell BiologyT MemoryDevelopmental BiologyImmune Cell DevelopmentDevelopmental ImmunologyMedicine
Abstract A simple method is described for distinguishing helper (T) and precursor (B) immunological memory: it depends on the sequential use of 2 cross‐reacting antigens for priming and challenge. Using cow and sheep erythrocytes, we have followed the asynchronous development of helper and precursor memory. Helper (T) memory is optimal 4 – 6 days after a wide range of antigen doses (2 × 10 4 –2 × 10 9 red blood cells). It reaches rather higher levels after very small injections, but persists longer after high doses. Precursor (B) memory requires a large amount of antigen for optimal development (2 × 10 7 – 2 × 10 9 red blood cells). It increases for at least 2 months after priming. B‐memory cells defined by the cross‐reactive criterion are insensitive to anti‐theta serum but require the presence of T cells for their effective stimulation by antigen. Precursor memory does not appear to be carried by the antibody‐forming cells themselves. It is more sensitive to irradiation damage than T memory. Memory of either kind leads to increased production of both IgM and IgG antibody‐forming cells. Helper memory cells seem to be able to interact with virgin B cells in the normal spleen.
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