Debate has surrounded the subject of B cell life span since it was fir
st measured in mice in the early 1970s. In the 25 years which have pas
sed since then, it has become increasingly apparent that the methods e
mployed to measure rates of B cell turnover, such as [H-3]-thymidine l
abelling, cell transfer or cell ablation, brought about significant di
sruptions to normal physiology which in themselves might have affected
B cell turnover. More recently the use of bromodeoxyuridine has overc
ome many of these methodological difficulties and has allowed rates of
B cell renewal to be measured within B cell subpopulations defined by
multiparameter flow cytometry. Such studies have largely resolved the
issue, concluding that about 85% of peripheral B cells are phenotypic
ally mature and display first-order exponential kinetics defined by a
half-life of 5-6 weeks, whilst the remainder are short-lived with a li
fe span of several days. This review examines both traditional and rec
ent methods and discusses the influence of age, self-tolerance and ran
domnes in the overall shaping of a kinetically stable mature B cell po
pulation.