CIRCULATING GROUP-II PHOSPHOLIPASE A(2) ACTIVITY AND ANTILIPOCORTIN ANTIBODIES IN SYSTEMIC LUPUS-ERYTHEMATOSUS - CORRELATIVE STUDY WITH DISEASE-ACTIVITY
W. Pruzanski et al., CIRCULATING GROUP-II PHOSPHOLIPASE A(2) ACTIVITY AND ANTILIPOCORTIN ANTIBODIES IN SYSTEMIC LUPUS-ERYTHEMATOSUS - CORRELATIVE STUDY WITH DISEASE-ACTIVITY, Journal of rheumatology, 21(2), 1994, pp. 252-257
Objective. Lipocortin (LC) and phospholpase A(2) (PLA(2)) are involved
in phospholipid metabolism, and on the cellular level LC seems to be
an antagonist of PLA(2). Since anti-LC1 autoantibodies were found in s
ystemic lupus erythematosus (SLE), we undertook a study of the relatio
nship between PLA(2), anti-LC1, and disease activity in a large group
of patients with SLE. Methods. Sera from 81 patients with SLE were tes
ted for the activity of extracellular PLA(2) and the presence and leve
l of antilipocortin 1 [anti-LC1 (IgM) and anti-LC1 (IgG)I antibodies.
Both were compared to SLE activity. Results. Mean PLA(2) activity was
4.6-fold higher in patients with SLE than in healthy controls (707 +/-
219 vs 154 +/- 6 u/ml, p < 0.01). PLA(2) activity correlated signific
antly with PLA(2) immunoreactivity as estimated by an ELISA method usi
ng monoclonal antibodies against ''synovial type'' PLA(2) (n = 21, r =
0.984, p < 0.001). Anti-LC1 IgM and IgG antibody levels were signific
antly higher in SLE than in healthy individuals [anti-LC1 (IgM) 54.5 /- 4.6 vs 22.6 +/- 2.3 EU/ml, p < 0.001 and anti-LC1 (IgG) 54.3 +/- 3.
4 vs 22.9 +/- 2.3 EU/ml, p < 0.001]. There was no correlation between
PLA(2) activity and anti-LC1 antibody titers. Elevated levels of PLA(2
) [> normal mean + 2 SD (i.e., > 300 u/ml)] were found in 41/81 patien
ts with SLE. Anti-LC1 antibody titers were high (> 64 EU/ml) in 23/41
patients; 14/40 patients with SLE with normal PLA(2)0 (<300 u/ml) also
had higher titers of anti-LC1 antibodies. PLA, activity was significa
ntly associated with the presence of synovitis, being markedly increas
ed in 1 1/12 patients. Mean PLA, in this group of patients (1593 +/- 9
57 u/ml) was significantly higher (p < 0.001) than that (553 +/- 188 u
/ml) in the group of 69 patients with SLE without synovitis. Conclusio
ns. There was no correlation of PLA(2) activity with the Systemic Lupu
s Erythematosus Disease Activity Index (SLEDAI) or the Lupus Activity
Criteria Count (LACC). Circulating PLA(2) activity in SLE correlated o
nly with active synovitis. There was no correlation of anti-LC 1 titer
s with duration of the disease, age, steroid dosage, SLEDAI, or LACC o
r any individual clinical or laboratory variable included in the asses
sment of SLEDAI and LACC.