Microbial Translocation Disorders: Assigning an Etiology to Idiopathic Illnesses

Author:

Sfera Adonis1ORCID,Hazan Sabine2,Klein Carolina3,del Campo Carlos Manuel Zapata-Martín4,Sasannia Sarvin5,Anton Johnathan J.6,Rahman Leah7,Andronescu Christina V.8,Sfera Dan O.1,Kozlakidis Zisis9ORCID,Nicolson Garth L.10

Affiliation:

1. Department of Psychiatry, Patton State Hospital, University of California, Riverside, CA 92521, USA

2. ProgenaBiome, 1845 Knoll Dr, Ventura, CA 93003, USA

3. Napa State Hospital, 2100 Napa Vallejo Hwy, Napa, CA 94558, USA

4. Instituto National de Cardiologia, Juan Badiano 1, Belisario Domínguez Secc 16, Tlalpan, Ciudad de México 14080, Mexico

5. Department of Medicine, Shiraz University of Medical Sciences, Shiraz 14336-71348, Iran

6. Department of Biology, California Baptist University, 8432 Magnolia Ave., Riverside, CA 92504, USA

7. Department of Neuroscience, University of Oregon, 1585 E 13th Ave., Eugene, OR 97403, USA

8. Medical Anthropology, Stanford University, 450 Serra Mall, Stanford, CA 94305, USA

9. International Agency for Research on Cancer, 69000 Lyon, France

10. Department of Molecular Pathology, The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA

Abstract

Gut microbes are immunologically tolerated in the gastrointestinal tract but trigger aggressive immune responses upon translocation across the gut barrier. Although oral tolerance, a physiological process that dampens immune responses to food proteins and commensal microbiota, remains poorly defined, significant progress was made during and after the Human Immunodeficiency Virus epidemic in the 1980s and the discovery of regulatory T cells in 1995. Additional insight was gained after the discoveries of innate lymphoid cells in 2008 and the functional elucidation of mucosal mast cells. Prior to the historical discovery of human pathogens, the etiologies of most human diseases were considered unknown. The same was true about many genetic disorders prior to the Human Genome Project. Here, we hypothesize that many of the remaining idiopathic conditions, including autoimmune, fibroproliferative, and neuropsychiatric diseases as well as some cancers, can be considered microbial translocation disorders triggered by the host immune responses to extraintestinal gut microbes and/or their constituent parts. In addition to microbial translocation, we also discuss potential interventions for intestinal barrier rehabilitation, including antibodies against tumor necrosis factor-like ligand 1A and membrane lipid replacement supplements.

Funder

Institute for Molecular Medicine

Nutritional Therapeutics, Inc.

Publisher

MDPI AG

Subject

General Earth and Planetary Sciences,General Environmental Science

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