As. Bansal et al., VARIATIONS IN SERUM SCD23 IN CONDITIONS WITH EITHER ENHANCED HUMORAL OR CELL-MEDIATED-IMMUNITY, Immunology, 79(2), 1993, pp. 285-289
Soluble CD23 (sCD23) is increased by interleukin-4 (IL-4) and decrease
d by interferon-gamma (IFN-gamma). On the basis of cytokine profiles T
-helper (Th) cells may be functionally divided into IL-2- and IFN-gamm
a-secreting Th1 cells, which are involved in cell-mediated immunity (C
MI), and IL-4- and IL-5-producing Th2 cells, which arc involved in hum
oral immunity. Compared with sex-matched controls (median 8.5) we foun
d significantly elevated levels of serum sCD23 in patients with rheuma
toid arthritis (median 22.7, P < 0.0002), with the highest levels dete
cted in patients fulfilling an increasing number of the American Assoc
iation revised criteria for rheumatoid arthritis. Soluble CD23 levels
were also significantly raised in autoimmune thyroiditis (median 11.7,
P < 0.02) and myasthenia gravis (median 10.4, P < 0.05). In contrast
patients with either coeliac (median 6.5) or Crohn's disease (median 5
.8) had reduced levels of sCD23 compared to appropriate controls (medi
an 11.8), in both cases significant at P < 0.01. Variations in sCD23 m
ay, therefore, reflect enhanced Th1 activity in the two latter conditi
ons in contrast to heightened Th2 activity within the three classical
autoimmune conditions.