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The Role of the Microbiome in Immune-Related Diseases

Microbiome Microbes Illness Immune

Kara Fitzgerald, ND
Romilly Hodges, MS CNS CN

“You are not what you think you are. Instead of the form staring back at you when you look in the mirror, what you should imagine is your body as a collection of multiple dynamic ecosystems made up of very tiny, and very biologically diverse, organisms.” – Rob DeSalle

The human intestinal microbiome acts as a signaling hub that integrates environmental inputs, such as diet and lifestyle, with our genetic and metabolic pathways. Its impacts are widespread across host systems, including the immune system,1 which is capable of adapting and responding to a wide range of challenges. How does the microbiome interact with the immune system, and how do these interactions help determine a state of health or disease in the body?

Reciprocal cross-talk between the microbiome and cells in the intestinal mucosal immune system is well-documented.1 We now understand that this cross-talk is important for immune system maturation and modulation across all developmental stages;2 studies of germ-free mice demonstrate that a lack of gut microbiota leads to a significant immune deficiency.3,4 Maintaining a homeostatic balance between microbial activity and host immune response toward it is what allows the immune system to function appropriately to defend against infection but yet demonstrate appropriate tolerance.5

Commensal microbes are symbiotic species, playing a key role in immune homeostasis. Commensal bacteria produce metabolites such as short-chain fatty acids (SCFAs) and amino acid derivatives that enhance the gut barrier integrity, promote immune-balancing T regulatory (Treg) cell formation, and modulate the production of pro-inflammatory mediators.2–4 Species such as Bacteroides fragilis produce polysaccharides with anti-inflammatory effects—specifically the inhibition of interleukin 17 (IL-17) and enhanced activity of Treg cells.3

Conversely, an imbalance between commensal and pathogenic species, known as dysbiosis, activates pathogenic mechanisms. Pathogen activation of toll-like receptors (TLRs), found on intestinal immune cells, creates proinflammatory innate and adaptive immune responses, including Th17 differentiation and recruitment of neutrophils and macrophages to the affected site.1,5,6 These effects can be both acute and chronic, if dysbiosis persists. In patients with inflammatory bowel disease, intestinal dysbiosis triggers an abnormal adaptive immune response that increases the pathological inflammatory processes of the disease and destruction of the gastrointestinal tract.3 Intestinal microbial composition is also implicated in the onset of celiac disease in individuals who carry the susceptible HLA haplotypes.4

Chronic pro-inflammatory signaling is detrimental to the integrity of the intestinal barrier. This allows for the inappropriate translocation of bacterially produced lipopolysaccharides into portal and systemic circulation and provides a mechanism for TLR activation in sites distant to the intestine.1,3,6 This perhaps surprising, and relatively recent, evolution of our knowledge provides an explanation for research that implicates Porphyromonas gingivalis (found in the oral microbiome) and Prevotella copri in the development and progression of rheumatoid arthritis (RA), as just one example.

DNA traces of these bacteria have been found in the synovial fluid of patients with RA, and prolonged antibiotic therapy against specific bacterial infections, as well as probiotic therapy, have been demonstrated to be helpful with RA disease control.6 The intestinal microbiome is also implicated as a triggering or mediating factor in Grave’s disease, Hashimoto’s thyroiditis, multiple sclerosis, type 1 diabetes, systemic lupus erythematosus, and psoriasis.2

Beyond autoimmune conditions, the activation of extraintestinal inflammation pathways may also be traced back to microbial activity in the gut. The flow of bacterial products to the liver in portal circulation can be a trigger of TLRs and a driver of chronic inflammatory liver conditions such as non-alcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH).1 Links have also been made with pancreatitis, pancreatic cancer, and diabetes.1 Microbial DNA analysis of patients with atopic eczema, a chronic inflammatory skin condition, shows altered immune-modulatory properties compared with controls.7,8

Given that environmental factors, including diet and lifestyle, play an important role in shaping the gut microbiome, Functional Medicine provides the perfect opportunity to address dysbiosis and favorably impact the onset and progression of immune-related diseases.

IFM educator Kara Fitzgerald, ND, is a clinician researcher for the Institute for Therapeutic Discovery and maintains a Functional Medicine clinic in Sandy Hook, CT. Romilly Hodges, CNS, is a nutritionist on the team of Dr. Fitzgerald. She has also served as teaching assistant to Deanna Minich, PhD, for the Certified Food and Spirit Practitioner Program and the Food and Spirit Advanced Detoxification Module, which are designed for professionals and incorporate both evidence-based nutrition and holistic well-being.

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References

  1. Cianci R, Pagliari D, Piccirillo CA, Fritz JH, Gambassi G. The microbiota and immune system crosstalk in health and disease. Mediators Inflamm. 2018;2018:2912539. doi:1155/2018/2912539.
  2. Opazo MC, Ortega-Rocha EM, Coronado-Arrázola I, et al. Intestinal microbiota influences non-intestinal related autoimmune diseases. Front Microbiol. 2018;9:432. doi:3389/fmicb.2018.00432.
  3. Shi N, Li N, Duan X, Niu H. Interaction between the gut microbiome and mucosal immune system. Mil Med Res. 2017;4(1):14. doi:1186s40779-017-0122-9.
  4. Sellitto M, Bai G, Serena G, et al. Proof of concept of microbiome-metabolome analysis and delayed gluten exposure on celiac disease autoimmunity in genetically at-risk infants. PLoS One. 2012;7(3):e33387. doi:1371/journal.pone.0033387.
  5. Pagliari D, Gambassi G, Piccirillo CA, Cianci R. The intricate link among gut “immunological niche,” microbiota, and xenobiotics in intestinal pathology. Mediators Inflamm. 2017;2017:8390595. doi:1155/2017/8390595.
  6. Biscetti F, Flex A, Alivernini S, Tolusso B, Gremese E, Ferraccioli G. The role of high-mobility group box-1 and its crosstalk with microbiome in rheumatoid arthritis. Mediators Inflamm. 2017;2017:5230374. doi:1155/2017/5230374.
  7. Oh S, Yap GC, Hong P-Y, et al. Immune-modulatory genomic properties differentiate gut microbiota of infants with and without eczema. PLoS One. 2017;12(10):e0184955. doi:1371/journal.pone.0184955.
  8. Chan CWH, Wong RS, Law PTW, et al. Environmental factors associated with altered gut microbiota in children with eczema: a systematic review. Int J Mol Sci. 2016;17(7):E1147. doi:3390/ijms17071147.

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