Hannover Medical School February 15 th 2010 The gut microbiota shapes intestinal immune response during health and disease Round and Mazmanian, Nature.

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Presentation transcript:

Hannover Medical School February 15 th 2010 The gut microbiota shapes intestinal immune response during health and disease Round and Mazmanian, Nature Reviews Immunology, Vol

Hannover Medical School Gut microbiota more than 1000 species collective weight of about 1kg in human intestine colonization begins immediately after birth symbiotic bacteria provide benefits to the host: –nutrient supply –pathogen defense –immune system development/ function O´Hara and Shanahan, EMBO reports, 2006

Hannover Medical School Gut-associated lymphoid tissue (GALT) GALT Peyer`s patches appendix isolated lymphoid follicles intestinal epithelial cell (IEC) = T-cell areas = B-cell follicles

Hannover Medical School Developmental defects in germ-free mice IEC show decreased rates of cell-turnover and reduced expression of MHC class II molecules, TLR9 and antimicrobial proteins fewer lymphocytes in lamina propria and epithelium fewer and smaller Peyer`s patches, isolated lymphoid follicles and mesenteric lymph nodes reduced levels of secretory IgA Macpherson and Harris, Nat rev Immunol., 2004

Hannover Medical School Defects in immune response in germ-free mice decreased immune resistance to infection with Shigella flexneri decreased bacterial clearence upon Listeria monocytogenes infection Salmonella enterica serovar Typhimurium exploits deficiency in colonization resistance to establish infection

Hannover Medical School Inflammatory bowel disease (IBD) chronic inflammation of the gastointestinal tract two main forms: 1. Crohn`s disease –affects all layers of the bowel wall –granuloma formation in up to 60% of patients 2. Ulcerative colitis –affects superficial mucosal layers no pathogen has been conclusively shown to be the causative agent incidence is the highest in developed countries Crohn´s disease Janeway, Immunobiology, 7ed.

Hannover Medical School IBD is driven by T cells mucosal homeostasis  cytokine production by regulatory (T Reg ) T cells supresses pro-inflammatory responses mucosal inflammation  increased production of pro-inflammatory cytokines by T helper (T H ) cells T H 1, T H 2, T H 17 T Reg TNF, IFNγ, IL-17  T Reg transfer can prevent the induction of experimental colitis adapted from Bouma and Strober, Nat rev Immunol., 2003 and Vignali et al., Nat rev Immunol., 2008

Hannover Medical School Involvement of the microbiota in regulating the balance between T H and T Reg cell subsets in the gut germ-free animals show defective T H 17 cell development in the small intestine ATP generated by intestinal bacteria increases the production of IL-17 in the colon germ-free mice have reduced numbers of T Reg cells in the mesenteric lymph nodes increased numbers of T reg cells in the small intestine of germ- free mice  Intestinal bacteria direct the differentiation of both pro- and anti- inflammatory T cell populations and may therefore play a crucial role in IBD T Reg THTH

Hannover Medical School Evidence for the involvement of commensal bacteria in IBD IBD patients have increased antibody titres against indigenous bacteria inflammatory lesions are pronounced in areas with high numbers of bacteria genetic variants that are highly linked to IBD include mutations in genes that are involved in bacterial sensing (NOD2) and T cell immunity (IL23R) IBD patients show abnormal microbial composition (= dysbiosis) mice studies showed that dysbiosis alone may be important for the induction of IBD

Hannover Medical School Immunological dysregulation associated with dysbiosis of the microbiota Symbionts  health promoting functions Commensals  provide no benefit or detriment Pathobionts  have the potential to induce pathology  Inflammatory responses in IBD are directed towards pathobionts

Hannover Medical School Different bacterial species ameliorate the symptoms of IBD Probiotics dietary microorgansims that are beneficial to the health of the host act on serveral cell types (epithelial cells, DCs, T cells) ability to limit inflammation by induction of T Reg cells VSL#3: mixture of Lactobacillus spp., Bifidobacterium spp., Streptococcus salivarius

Hannover Medical School Model for Bacteroides fragilis-mediated protection from disease induced by Heliobacter hepaticus PSA: polysaccharid A (= symbiotic factor)  symbiotic factors actively maintain health

Hannover Medical School Proposed causes of dysbiosis of the microbiota  Increased incidence of immune-mediated disorders in developed countries could be due to alterations in the microbiota

Hannover Medical School Summary the microbiota promote the appropriate development of the immune system immune-mediated disorders seem to involve reduced T Reg cell activity absence of beneficial microorganisms (owing to dysbiosis) can lead to the induction of inflammatory responses and immune- mediated diseases  the microbiota plays an important role in supporting health

Hannover Medical School Thank you for your attention!