colitis;
mucosal inflammation;
T helper 1 cell;
T helper 2 cell;
D O I:
10.1097/01.mog.0000245545.80160.0f
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Purpose of review Abrogation of mucosal T cell homeostasis by exaggerated not only T helper 1, but also T helper 2 cells is a major problem that leads to intestinal inflammation. In this regard, it is important to understand these different aspects of mucosal inflammation. Recent findings Both T helper 1 and 2 cells play central roles in the induction of mucosal immune responses including secretory IgA antibody production, which would be the most beneficial aspect for the host defense mechanism. T helper 1- and 2-type responses, however, exhibit other roles in the abrogation of intestinal homeostasis. Although it has been shown that T helper 1-type immune responses are key players in the induction of intestinal inflammation in mice colitis models and also in inflammatory bowel diseases in humans, studies in murine colitis models clearly show that T helper 2-type responses are also involved in the pathophysiology of the intestinal inflammation. Both regulatory type T cells and T helper 17 cells are involved to down- or upregulate aberrant T helper 1 and 2 cell responses. Summary Understanding the cellular and molecular mechanisms of crosstalk among T helper 1, 2, 17 and T regulatory 1 cells is central for the prevention or treatment of inflammatory bowel diseases.
机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Chi, Xinxin
Jin, Wei
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Jin, Wei
Bai, Xue
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Bai, Xue
Zhao, Xiaohong
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Zhao, Xiaohong
Shao, Jing
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Shao, Jing
Li, Jiaqi
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Li, Jiaqi
Sun, Qinli
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Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Sun, Qinli
Su, Bing
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机构:
Shanghai Jiao Tong Univ, Shanghai Inst Immunol, Dept Immunol & Microbiol, Sch Med, Shanghai 200025, Peoples R China
Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Sch Med, Shanghai 200025, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Su, Bing
Wang, Xiaohu
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Wang, Xiaohu
Yang, Xuexian O.
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机构:
Univ New Mexico, Dept Mol Genet & Microbiol, Sch Med, Albuquerque, NM 87131 USATsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Yang, Xuexian O.
Dong, Chen
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机构:
Tsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China
Shanghai Jiao Tong Univ, Affiliated Renji Hosp, Sch Med, Shanghai Immune Therapy Inst, Shanghai 200127, Peoples R ChinaTsinghua Univ, Inst Immunol, Beijing 100084, Peoples R China