The Role of Mycobacteria in Crohn's Disease
The Role of Mycobacteria in Crohn's Disease
批准号:
6622766
负责人:
DAVID Y GRAHAM
金额:
$22.58万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-05-01 至 2006-04-30
关键词:
Crohn's disease Mycobacterium antibiotics bacterial disease clinical research diagnosis design /evaluation disease /disorder etiology gastrointestinal disorder chemotherapy gastrointestinal infection human subject human therapy evaluation in situ hybridization patient oriented research polymerase chain reaction serology /serodiagnosis
中文摘要
描述(由申请人提供):克罗恩病是一种特发性非-
干酪性肉芽肿病 提出的病因之一是感染
鸟分枝杆菌(Mycobacterium avium subsp.)副结核分枝杆菌(M.副结核病)
反刍动物克罗恩病(Johne病)的病原体。
最近的证据支持克罗恩病中副结核杆菌感染
包括:1)从克罗恩病组织和母乳中分离,
培养,2)通过PCR测定法在组织中鉴定,3)作为
通过原位杂交,在组织中形成细胞壁缺陷,4)长的
在越来越多的克罗恩病患者中,
使用抗分枝杆菌疗法,和5)通过与M
副结核抗原p35、p36和32 k分枝杆菌相关抗原
称为HupB蛋白。 这些数据表明,
在至少一部分克罗恩病患者中存在分枝杆菌。
克罗恩病患者中M-杆菌感染亚群的鉴定
由于缺乏简单而具体的方法,
血清诊断试验,以确定谁将是候选人的抗-
分枝杆菌治疗 这项建议的长远目标是
确认副结核分枝杆菌p35/ p36抗原作为血清学标志物,
是否存在特定的临床/病理分层,
与他们的存在有关。 我们将评估M的存在
克罗恩病患者副结核杆菌感染的血清学检测
来自患者和对照的血清和原位杂交用于检测
细胞壁缺陷型副结核分枝杆菌涉及病变
组织中 我们还将使用激光捕获显微切割技术来测试
克罗恩病肉芽肿中是否存在副结核分枝杆菌
患者 血清学和分子生物学研究的结果将进行比较
根据临床/病理学信息以及人口统计学和流行病学
收集的每例患者的数据以及抗分枝杆菌治疗的结果
疗法 这项研究的结果应该证实或反驳
提出了M.副结核病和克罗恩病,
以及克罗恩病和M.
副结核病
英文摘要
DESCRIPTION (provided by applicant): Crohn's disease is an idiopathic non-
caseating granulomatous disease. One of the proposed etiologies is infection
with Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis), the
causative agent of Crohn's-like disease in ruminants (Johne's disease).
Recent evidences to support M paratuberculosis infection in Crohn's disease
include: 1) its isolation from Crohn's disease tissues and breast milk by
culture, 2) its identification in tissues by PCR assays, 3) its detection as
cell wall deficient forms in tissues by in situ hybridization, 4) the long
term remission (possibly cure) in an increasing number of Crohn's patients by
using anti-mycobacterial therapies, and 5) by an association with the M
paratuberculosis antigens p35, p36 and the 32k mycobacterial associated
antigen termed HupB protein. These data suggest a causal role for
mycobacteria in at least a proportion of patients with Crohn's disease.
Identification of the subgroup of Crohn's disease patients infected with M
paratuberculosis has been hampered due to the lack of a simple and specific
serodiagnostic test to identify those who would be candidates for anti-
mycobacterial therapy. The long-range objective of this proposal is to
confirm M paratuberculosis p35/ p36 antigens as serologic markers and to test
whether there are specific clinical/pathologic stratification(s) that
correlate with their presence. We will assess the presence of M
paratuberculosis infection in Crohn's disease patients by serologic testing of
sera from patients and controls and in situ hybridization for the detection of
the cell wall-deficient form of M paratuberculosis in involved diseased
tissues. We will also use the laser capture microdissection technique to test
whether M paratuberculosis are present in granulomas of Crohn's disease
patients. The results from serology and molecular studies will be compared
with the clinical/pathological information and demographic and epidemiologic
data gathered about each patient as well as with outcome of anti-mycobacterial
therapy. The results of this study should either confirm or refute the
proposed etiologic association of M. paratuberculosis and Crohn's disease as
well as the identification of patients with Crohn's disease and M.
paratuberculosis.
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