Dendritic cells have the remarkable property of presenting any incomin
g antigen(1). To do so they must not only capture antigens with high e
fficiency and broad specificity, but must also maximize their capacity
to load class II molecules of the major histocompatibility complex (M
HC) with antigenic peptides in order to present a large array of epito
pes from different proteins, each at a sufficient copy number. Here we
show that formation of peptide-MHC class II complexes is boosted by i
nflammatory stimuli that induce maturation of dendritic cells. In imma
ture dendritic cells, class II molecules are rapidly internalized and
recycled, turning over with a half-life of about 10 hours. Inflammator
y stimuli induce a rapid and transient boost of class II synthesis, wh
ile the half-life of dass II molecules increases to over 100 hours. Th
ese coordinated changes result in the rapid accumulation of a large nu
mber of long-lived peptide-loaded MHC dass II molecules capable of sti
mulating T cells even after several days, The capacity of dendritic ce
lls to load many antigenic peptides over a short period of initial exp
osure to inflammatory stimuli could favour presentation of infectious
antigens.