In the past few years, considerable evidence has accumulated to suggest the
existence of functionally polarized responses by the CD4(+) T helper (Th)-
and the CD8(+) T cytotoxic (Tc)-cell subsets that depend on the cytokines t
hey produce. The Th1 and Th2 cellular immune response provide a useful mode
l for explaining not only the different types of protection, but also the p
athogenic mechanisms of several immunopathological disorders. The factors r
esponsible for the polarization of specific immune response into a predomin
ant Th1 or Th2 profile have been extensively investigated in mice and human
s. Evidence has accumulated from animal models to suggest that Th1-type lym
phokines are involved in the genesis of organ-specific autoimmune diseases,
such as experimental autoimmune uveitis, experimental allergic encephalomy
elitis, or insulin-dependent diabetes mellitus. Accordingly, data so far av
ailable in human diseases favor a prevalent Th1 lymphokine profile in targe
t organs of patients with organ-specific autoimmunity. By contrast, Th2-cel
l predominance was found in the skin of patients with chronic graft-versus
host disease, progressive systemic sclerosis, systemic lupus erythematosus
and allergic diseases. The Th1/Th2 concept suggests that modulation of rela
tive contribution of Th1- or Th2-type cytokines regulate the balance betwee
n protection and immunopathology, as well as the development and/or the sev
erity of some immunologic disorders, In this review, we have discussed the
paradigm of Th1 and Th2 cytokines in relation to autoimmunity and allergy.