Infectious diseases continue to be the leading cause of morbidity and
mortality worldwide. Increased awareness of the fact that mucosal memb
ranes are the most frequent portals of entry of pathogenic microorgani
sms has prompted studies aimed at the development of vaccination proto
cols and antigen delivery systems that would lead to an increased prot
ection of mucosae. Although systemic and strictly local (e.g., intrava
ginal or conjunctival) immunizations are of limited effectiveness in t
he induction of generalized mucosal protection, ingestion or inhalatio
n of antigens results in a disseminated immune response manifested by
the appearance of specific antibodies of the secretory immunoglobulin
(Ig) A isotype in external secretions due to the dissemination of IgA
precursor cells from IgA-inductive lymphoid tissues. Furthermore, addi
tional inductive sites strategically positioned at the opening of the
respiratory and digestive tracts may also be suitable targets for indu
ction of immune responses at desired effector sites. To prevent degrad
ation and increase the absorption of ingested antigens, novel strategi
es including enclosure of antigens in biodegradable microspheres or li
posomes, or their expression in viral and bacterial vectors and in pla
nts, are currently being considered. Forthcoming technological advance
s in antigen preparation and routes of delivery will undoubtedly have
a profound impact on immunization practices in the future. (C) 1997 El
sevier Science B.V.