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Layers of mutualism with commensal bacteria protect us from intestinal inflammation
  1. C Mueller1,
  2. A J Macpherson2
  1. 1Department of Pathology, University of Bern, Switzerland
  2. 2Department of Medicine, McMaster University, Ontario, Canada
  1. Correspondence to:
    Dr A J Macpherson
    Room 4W8, McMaster University Medical Centre, 1200 Main St West, Hamilton, Ontario L8N 3Z5, Canada; macpher{at}mcmaster.ca

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Mammals are highly adapted to their very high densities of non-pathogenic bacteria which inhabit the lower small intestine and colon. This is achieved by a series of functional and cellular layers that normally avoid the inflammatory consequences of immune activation by bacterial molecules. In this review we set out the layers of mucosal immune defence to show the many ways in which mutualism with the commensal flora can break down to trigger chronic intestinal inflammation in animal models and inflammatory bowel disease (IBD) in humans.

SPECIAL PROBLEMS FACED BY INTESTINAL MUCOSAL IMMUNITY—LAYERS OF PROTECTION

The immune system of the intestine is phylogenetically ancient, and its development appears to have preceded most other lymphoid structures, including the thymus.1 The intestinal mucosal immune system is also of immense size. Approximately 70% of all lymphocytes in the body are within the mucosal immune system and most of the antibody produced in healthy individuals is IgA, which is secreted across mucous membranes. Intestinal immunity must be finally balanced between the capacity for mounting protective immune responses to infectious agents and yet tolerate the enormous load of antigens and immunostimulatory molecules that constitute the commensal intestinal bacteria.

Commensal bacteria are present in vast numbers.2 The colon is colonised with approximately 1012 organisms/g intestinal contents, making us walking culture media because the bacteria outnumber our own cells! The benefits of commensal bacteria are well known: they help us digest cellulose and salvage energy, synthesise vitamin K, and fill up the microbiological niche that might otherwise be exploited by less benign microbes. Of course, commensals can become pathogens in the right setting, such as debilitated or immunocompromised patients, but on the whole it is impressive how well we coexist with our microbial passengers.

Our bodies have adapted in many ways to achieve this harmonious mutualism with our commensals. The evidence for this comes …

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