结肠炎
免疫系统
生物
免疫学
盲肠
肠系膜淋巴结
小肠结肠炎
微生物学
脆弱类杆菌
医学
抗生素
内科学
生态学
作者
Rance K. Sellon,Susan L. Tonkonogy,Michael Schultz,Levinus A. Dieleman,Wetonia B. Grenther,Ed Balish,D Rennick,R. Balfour Sartor
出处
期刊:Infection and Immunity
[American Society for Microbiology]
日期:1998-11-01
卷期号:66 (11): 5224-5231
被引量:1457
标识
DOI:10.1128/iai.66.11.5224-5231.1998
摘要
ABSTRACT Mice with targeted deletion of the gene for interleukin-10 (IL-10) spontaneously develop enterocolitis when maintained in conventional conditions but develop only colitis when kept in specific-pathogen-free (SPF) environments. This study tested the hypothesis that enteric bacteria are necessary for the development of spontaneous colitis and immune system activation in IL-10-deficient mice. IL-10-deficient mice were maintained in either SPF conditions or germfree conditions or were populated with bacteria known to cause colitis in other rodent models. IL-10-deficient mice kept in SPF conditions developed colitis in all segments of the colon (cecum and proximal and distal colon). These mice exhibited immune system activation as evidenced by increased expression of CD44 on CD4 + T cells; increased mesenteric lymph node cell numbers; and increased production of immunoglobulin A (IgA), IgG1, and IL-12 p40 from colon fragment cultures. Mice populated with bacterial strains, including Bacteroides vulgatus , known to induce colitis in other rodent models had minimal colitis. Germfree IL-10-deficient mice had no evidence of colitis or immune system activation. We conclude therefore that resident enteric bacteria are necessary for the development of spontaneous colitis and immune system activation in IL-10-deficient mice.
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