Irritant contact dermatitis (ICD) is a multifactorial disease, the ons
et and modulation of which depend on both endogenous and exogenous fac
tors. Among the former, age, race, site, sex and history of dermatitis
may all be important. Such variables can now readily be quantified by
objective noninvasive techniques, such as measurement of transepiderm
al water loss (TEWL). Moreover, effects of irritants on the epidermis
are related to the particular chemical properties of each molecule, co
ntributing further to clinical heterogeneity. Release of cytokines and
mediators may be initiated by a number of cells, including living ker
atinocytes and those of the stratum corneum, thus modulating inflammat
ion and repair. Furthermore, differences in mechanisms of inflammation
between acute and chronic ICD may exist, the former being characteriz
ed predominantly by inflammation, the latter by hyperproliferation and
transient hyperkeratosis. These findings may explain the complexity a
nd difficulty of investigating ICD. Better understanding and quantific
ation of these mechanisms may lead to identification of high-risk indi
viduals and more effective prevention and treatment.