Clancy R, Ren Z, Turton J, Pang G, Wettstein A
Hunter Immunology Unit, Hunter New England Area Health Service, John Hunter Hospital, Newcastle, NSW, Australia.
Dig Liver Dis. 2007 May;39(5):445-51. doi: 10.1016/j.dld.2006.12.006. Epub 2007 Feb 21.
Support for a role of Mycobacterium avium subspecies paratuberculosis in Crohn's disease is largely based on epidemiological evidence, as no data on mechanisms linking the presence of M. avium subspecies paratuberculosis with gut damage is available.
To determine whether the presence of M. avium subspecies paratuberculosis contributes to the pathogenesis of Crohn's disease by promoting cytokine secretion within gut mucosa.
A total of 235 subjects were recruited: 63 with Crohn's disease, 53 with ulcerative colitis, 45 with irritable bowel syndrome and 74 normal controls. M. avium subspecies paratuberculosis status was defined by nested PCR using IS900 sequence. Gut mucosal organ cultures were established to detect cytokine secretion patterns.
Significantly higher tumour necrosis factor-alpha concentrations were found in culture supernatants for Crohn's disease compared to ulcerative colitis (p<0.05), irritable bowel syndrome (p<0.01) and controls (p<0.0001). When tumour necrosis factor-alpha levels were correlated with the presence of M. avium subspecies paratuberculosis, significantly greater concentrations were only found in M. avium subspecies paratuberculosis-positive Crohn's disease patients (p<0.05). Tumour necrosis factor-alpha levels in M. avium subspecies paratuberculosis-positive Crohn's disease were significantly higher than in M. avium subspecies paratuberculosis-positive ulcerative colitis (p<0.01), M. avium subspecies paratuberculosis-positive irritable bowel syndrome (p<0.05) and M. avium subspecies paratuberculosis-positive controls (p<0.01) and all M. avium subspecies paratuberculosis-negative specimens.
The data link M. avium subspecies paratuberculosis with a pathogenic mechanism in Crohn's disease and is consistent with abnormal macrophage handling of M. avium subspecies paratuberculosis.
支持副结核分枝杆菌在克罗恩病中发挥作用的证据主要基于流行病学,因为目前尚无关于副结核分枝杆菌的存在与肠道损伤之间联系机制的数据。
通过促进肠道黏膜内细胞因子分泌,确定副结核分枝杆菌的存在是否有助于克罗恩病的发病机制。
共招募了235名受试者:63例克罗恩病患者、53例溃疡性结肠炎患者、45例肠易激综合征患者和74名正常对照者。采用基于IS900序列的巢式PCR定义副结核分枝杆菌状态。建立肠道黏膜器官培养以检测细胞因子分泌模式。
与溃疡性结肠炎(p<0.05)、肠易激综合征(p<0.01)和对照者(p<0.0001)相比,克罗恩病患者培养上清液中的肿瘤坏死因子-α浓度显著更高。当肿瘤坏死因子-α水平与副结核分枝杆菌的存在相关时,仅在副结核分枝杆菌阳性的克罗恩病患者中发现显著更高的浓度(p<0.05)。副结核分枝杆菌阳性的克罗恩病患者的肿瘤坏死因子-α水平显著高于副结核分枝杆菌阳性的溃疡性结肠炎患者(p<0.01)、副结核分枝杆菌阳性的肠易激综合征患者(p<0.05)、副结核分枝杆菌阳性的对照者(p<0.01)以及所有副结核分枝杆菌阴性标本。
数据表明副结核分枝杆菌与克罗恩病的致病机制相关,并且与巨噬细胞对副结核分枝杆菌的异常处理一致。