Kahan A, Collantes-Estevez E, Barel M, Frade R, Amor B
INSERM U 283, Cochin Hospital, Paris, France.
Clin Exp Rheumatol. 1993 Jan-Feb;11(1):27-34.
We assessed the expression of complement receptors (CR1 and CR3) and Fc gamma RIII on unstimulated and FMLP activated polymorphonuclears (PMNs) by indirect immunofluorescence and flow cytometry using CD35 (CR1), CD11b (CR3) and CD16 (Fc gamma RIII) monoclonal antibodies in 24 patients with spondylarthropathies (SpA) and in 18 healthy subjects. SpA patients were classified into 3 groups according to the severity of the disease (severe = asymmetrical peripheral joint involvement and permanent limitation of spine motion; moderate = one of the two items, mild = none of the items). CR1 and Fc gamma RIII expression were significantly decreased in patients with mild SpA, whereas CR1 and CR3 expression were significantly increased in patients with severe disease as compared to control subjects. In patients with mild disease, CR1 expression increased after FMLP activation, but remained significantly lower than in control subjects. The results were confirmed by immunoelectroblotting. These findings suggest that membrane and intracellular pools of CR1 and CR3 may contribute to the clinical modulation of the spondylarthropathies.
我们采用间接免疫荧光法和流式细胞术,使用CD35(CR1)、CD11b(CR3)和CD16(FcγRIII)单克隆抗体,评估了24例脊柱关节病(SpA)患者和18名健康受试者中未受刺激及经N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)激活的多形核白细胞(PMN)上补体受体(CR1和CR3)及FcγRIII的表达。根据疾病严重程度,SpA患者被分为3组(严重=不对称性外周关节受累及脊柱运动永久性受限;中度=两项中的一项;轻度=两项均无)。与对照组相比,轻度SpA患者的CR1和FcγRIII表达显著降低,而重度疾病患者的CR1和CR3表达显著升高。在轻度疾病患者中,FMLP激活后CR1表达增加,但仍显著低于对照组。免疫印迹法证实了这些结果。这些发现表明,CR1和CR3的膜池和细胞内池可能参与了脊柱关节病的临床调节。