Recently, we reported that IL-12 increased expression and function of
CD26/DPPIV, this may be a new cellular pathway of the Th1-like immune
responses. Here, we looked for a specific subset which would respond t
o CD26 upregulation by IL-12. Contrary to previously described results
, under our culture conditions (1 mu g/ml of PHA), IL-12 enhanced pref
erentially the CD8 cell proliferation. By using dual fluorescence anal
ysis, IL-12-dependent CD26 expression was found in both CD4 and CD8 (p
reviously CD26(+) or CD26(-)) activated T cells and, moreover, the CD4
5RO percentage was unaffected. However, the density of CD45RO Ag (whic
h was reported to coexpress with CD26) was impaired. These effects can
be implicated in the biological functions of IL-12 and provide some c
linical possibilities. (C) 1998 Elsevier Science B.V. All rights reser
ved.