Until recently, mast cells have been viewed primarily as harmful because of
their key role as effector cells of allergic and potentially lethal anaphy
lactic reactions. Their contribution to human health appeared instead to be
limited to the elimination of parasites. There is, however, growing eviden
ce for additional beneficial functions of mast cells, particularly regardin
g the initiation of acquired immune reactions. Thus, mast cells can phagocy
tize diverse particles, take up antigens, and express a number of receptors
, particularly MHC class I and II antigens, ICAM-1 and -3, CD43, CD80, CD86
and CD40L which allow them to interact with T and B lymphocytes. They can
also secrete numerous cytokines that induce and enhance recruitment and fun
ctions of lymphocytes. Finally, there is good evidence that mast cells pres
ent e.g. pollen and bacterial antigens, respond to bacterial superantigens,
but fail to react to endogenously produced antigens or superantigens. Mast
cells can also activate B cells directly to produce Ige, but this activity
and the ability to produce IL-4 or IL-13 is restricted primarily to basoph
il leukocytes and mucosal mast cells. Finally, recent evidence attributes a
pivotal role to the cells in natural immunity to bacteria. There is also e
merging evidence that mast cells can downmodulate the immune response. Whil
e these data require further clarification, the basic ability of mast cells
to initiate innate and acquired immune reactions can no longer be question
ed.