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慢性炎症性关节疾病中滑膜浆细胞的免疫球蛋白类别

Immunoglobulin classes in plasma cells of the synovial membrane in chronic inflammatory joint disease.

作者信息

Revell P A, Mayston V J

出版信息

Ann Rheum Dis. 1986 May;45(5):405-8. doi: 10.1136/ard.45.5.405.

Abstract

The histological features of the synovial membrane in rheumatoid arthritis (RA) are shared by other chronic inflammatory joint diseases, so that diagnostic differentiation is impossible. Examination of the immunoglobulin class in the plasma cells present in inflamed synovial membranes, however, has shown differences. Synovial membranes from 12 patients were seropositive RA, eight with seronegative RA, eight with ankylosing spondylitis, five with psoriatic arthritis, and three with Reiter's syndrome have been compared by peroxidase-antiperoxidase (PAP) staining for immunoglobulin classes on routinely paraffin wax embedded sections. There were no significant differences in the percentages of plasma cells containing IgG of IgA between the diseases studied. There were, however, significantly more plasma cells containing IgM in patients with seropositive RA (2-34%) compared with those with seronegative RA (0-10%; p less than 0.002) and with other chronic synovitides (0-9%; p less than 0.002). The results show that it is possible to distinguish seropositive RA from other chronic inflammatory joint diseases by PAP staining for immunoglobulin classes in the plasma cells present in the inflamed synovial membrane.

摘要

类风湿性关节炎(RA)滑膜的组织学特征与其他慢性炎症性关节疾病相同,因此无法进行诊断鉴别。然而,对炎症滑膜中浆细胞免疫球蛋白类别的检测显示出差异。通过过氧化物酶-抗过氧化物酶(PAP)染色法,对12例血清阳性RA患者、8例血清阴性RA患者、8例强直性脊柱炎患者、5例银屑病关节炎患者和3例赖特综合征患者的滑膜常规石蜡包埋切片进行免疫球蛋白类别检测并比较。在所研究的疾病中,含IgG或IgA的浆细胞百分比无显著差异。然而,血清阳性RA患者中含IgM的浆细胞显著多于血清阴性RA患者(0 - 10%;p<0.002)和其他慢性滑膜炎患者(0 - 9%;p<0.002)。结果表明,通过对炎症滑膜中浆细胞免疫球蛋白类别进行PAP染色,有可能将血清阳性RA与其他慢性炎症性关节疾病区分开来。

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1
An Immunofluorescence Study of Rheumatoid Factor.类风湿因子的免疫荧光研究
Ann Rheum Dis. 1963 Jan;22(1):1-10. doi: 10.1136/ard.22.1.1.
3
Diagnostic specificity of synovial lesions.滑膜病变的诊断特异性
Hum Pathol. 1981 Apr;12(4):314-28. doi: 10.1016/s0046-8177(81)80141-4.

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