Lamprecht P, Moosig F, Csernok E, Seitzer U, Schnabel A, Mueller A, Gross W L
Department of Rheumatology, University of Luebeck, 23538 Luebeck, Germany.
Thorax. 2001 Oct;56(10):751-7. doi: 10.1136/thorax.56.10.751.
Lack of CD28 expression on peripheral blood CD4+ and CD8+ T cells has been reported in patients with Wegener's granulomatosis (WG), suggesting a pathogenetic role of CD28- T cells in WG.
Ten patients with WG and six with sarcoidosis (disease control) were analysed. Fluorescence activated cell sorter (FACS) analysis was used to detect CD28 expression on T cells from peripheral venous blood and from bronchoalveolar lavage (BAL) fluid. T cells in biopsy specimens from granulomatous lesions of the upper respiratory tract were analysed for CD28 expression by double immunofluorescence staining.
A significantly higher fraction of CD28- T cells was found in the CD4+ and CD8+ T cell compartment in BAL fluid (65.6 (5.4)% and 76.3 (4.1)%, respectively) than in blood (13.4 (6.2)% and 42.9 (6.2)%; p<0.001) in patients with WG but not in those with acute sarcoidosis (6.7 (2.2)% and 53.4 (7.3)% in BAL fluid v 4.1 (2.5)% and 52.0 (9.4)% in blood). The total number of CD4+/CD28- T cells but not of CD8+/CD28- T cells was also significantly higher in BAL fluid than in blood in patients with WG (p<0.05). Patients with WG had a significantly higher fraction of CD28- T cells in the CD4+ and CD8+ T cell compartment in BAL fluid than patients with acute sarcoidosis (65.6 (5.4)% v 6.7 (2.2)%; p<0.001; and 76.3 (4.1)% v 53.4 (7.3)%; p<0.05). The total number of CD4+/CD28- and CD8+/CD28- T cells was also significantly higher in patients with WG than in those with sarcoidosis (p<0.01). An abundance of CD28- T cells was found in granulomatous lesions by double immunofluorescence staining in patients with WG.
Our data indicate enrichment of CD28- T cells in BAL fluid and suggest recruitment of CD28- T cells into granulomatous lesions in WG. Further analysis of the phenotype and function of T cell subsets in WG is needed to better understand leucocyte homing in WG and to find new therapeutic targets.
据报道,韦格纳肉芽肿(WG)患者外周血CD4+和CD8+ T细胞缺乏CD28表达,提示CD28阴性T细胞在WG发病机制中起作用。
分析了10例WG患者和6例结节病患者(疾病对照)。采用荧光激活细胞分选仪(FACS)分析外周静脉血和支气管肺泡灌洗(BAL)液中T细胞的CD28表达。通过双重免疫荧光染色分析上呼吸道肉芽肿性病变活检标本中的T细胞CD28表达。
在WG患者中,BAL液中CD4+和CD8+ T细胞亚群中CD28阴性T细胞的比例(分别为65.6(5.4)%和76.3(4.1)%)显著高于血液中的比例(13.4(6.2)%和42.9(6.2)%;p<0.001),而急性结节病患者则不然(BAL液中为6.7(2.2)%和53.4(7.3)%,血液中为4.1(2.5)%和52.0(9.4)%)。WG患者BAL液中CD4+/CD28阴性T细胞的总数显著高于血液中的总数,但CD8+/CD28阴性T细胞则不然(p<0.05)。WG患者BAL液中CD4+和CD8+ T细胞亚群中CD28阴性T细胞的比例显著高于急性结节病患者(65.6(5.4)%对6.7(2.2)%;p<0.001;76.3(4.1)%对53.4(7.3)%;p<0.05)。WG患者中CD4+/CD28阴性和CD8+/CD28阴性T细胞的总数也显著高于结节病患者(p<0.01)。通过双重免疫荧光染色在WG患者的肉芽肿性病变中发现大量CD28阴性T细胞。
我们的数据表明BAL液中CD28阴性T细胞富集,并提示CD28阴性T细胞被募集到WG的肉芽肿性病变中。需要进一步分析WG中T细胞亚群的表型和功能,以更好地了解WG中的白细胞归巢并找到新的治疗靶点。