Literature DB >> 9176706

The anatomical basis of intestinal immunity.

A M Mowat1, J L Viney.   

Abstract

The lymphoid tissues associated with the intestine are exposed continuously to antigen and are the largest part of the immune system. Many lymphocytes are found in organised tissues such as the Peyer's patches and mesenteric lymph nodes, as well as scattered throughout the lamina propria and epithelium of the mucosa itself. These lymphocyte populations have several unusual characteristics and the intestinal immune system is functionally and anatomically distinct from other, peripheral compartments of the immune system. This review explores the anatomical and molecular basis of these differences, with particular emphasis on the factors which determine how the intestinal lymphoid tissues discriminate between harmful pathogens and antigens which are beneficial, such as food proteins or commensal bacteria. These latter antigens normally provoke immunological tolerance, and inappropriate responses to them are responsible for immunopathologies such as food hypersensitivity and inflammatory bowel disease. We describe how interactions between local immune cells, epithelial tissues and antigen-presenting cells may be critical for the induction of tolerance and the expression of active mucosal immunity. In addition, the possibility that the intestine may act as an extrathymic site for T-cell differentiation is discussed. Finally, we propose that, under physiological conditions, immune responses to food antigens and commensal bacteria are prevented by common regulatory mechanisms, in which transforming growth factor beta plays a critical role.

Entities:  

Mesh:

Year:  1997        PMID: 9176706     DOI: 10.1111/j.1600-065x.1997.tb00966.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  110 in total

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Journal:  Springer Semin Immunopathol       Date:  2000

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Review 3.  Mucosal T cell response to reovirus.

Authors:  D Chen; D H Rubin
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4.  Emergence and kinetics of simian immunodeficiency virus-specific CD8(+) T cells in the intestines of macaques during primary infection.

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Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

5.  T-cell activation occurs simultaneously in local and peripheral lymphoid tissue following oral administration of a range of doses of immunogenic or tolerogenic antigen although tolerized T cells display a defect in cell division.

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7.  Immunodominant HIV-specific CD8+ T-cell responses are common to blood and gastrointestinal mucosa, and Gag-specific responses dominate in rectal mucosa of HIV controllers.

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8.  Identifying the target cell in primary simian immunodeficiency virus (SIV) infection: highly activated memory CD4(+) T cells are rapidly eliminated in early SIV infection in vivo.

Authors:  R S Veazey; I C Tham; K G Mansfield; M DeMaria; A E Forand; D E Shvetz; L V Chalifoux; P K Sehgal; A A Lackner
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Review 9.  Porcine isosporosis: infection dynamics, pathophysiology and immunology of experimental infections.

Authors:  Hanna L Worliczek; Marc Buggelsheim; Armin Saalmüller; Anja Joachim
Journal:  Wien Klin Wochenschr       Date:  2007       Impact factor: 1.704

10.  Total Body Irradiation in the "Hematopoietic" Dose Range Induces Substantial Intestinal Injury in Non-Human Primates.

Authors:  Junru Wang; Lijian Shao; Howard P Hendrickson; Liya Liu; Jianhui Chang; Yi Luo; John Seng; Mylene Pouliot; Simon Authier; Daohong Zhou; William Allaben; Martin Hauer-Jensen
Journal:  Radiat Res       Date:  2015-10-23       Impact factor: 2.841

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