In a clinical study, researchers demonstrate a model for developing targeted probiotic therapies to modulate the microbiome
Researchers from Case Western Reserve University School of Medicine and University Hospitals (UH) Cleveland Medical Center have demonstrated a new model for developing probiotics to modulate the microbiome.
The research team reviewed studies about the microbiome’s role in disease and health and illustrated their approach by using Crohn’s disease (CD) as an example. The study was published online Jan. 25 in the journal Gastroenterology.
The team included senior author Mahmoud Ghannoum, director of the Integrated Microbiome and the Center for Medical Mycology at UH and Case Western Reserve, who has been studying the microbiome for decades.
According to the authors, gut microbes may influence a number of health-related issues, including diseases such as CD and other degenerative diseases, including obesity, diabetes, cancer, autism and cardiovascular disease.
“The microbiome consists of bacteria, fungal and viral constituents in the gut. We have come to learn how the interaction between these communities, as well as potential interaction with the body can affect health and disease,” Ghannoum said.
“An imbalance of the gut microbiota composition, called dysbiosis, may initiate or exacerbate several diseases,” Ghannoum added. “Furthermore, the imbalance may form a biofilm, which can create a barrier to the absorption of medications and create an environment encouraging growth of harmful bacteria and fungal components.”
Identifying beneficial microbial strains
In their paper, intestinal biofilms that developed in CD were targeted for modulation, and then beneficial microbial strains that could potentially interrupt and disrupt the biofilms were identified.
Through further analysis, four biotherapeutic strains of beneficial bacteria and fungi were selected due to their efficacy in neutralizing the organisms creating the biofilms.
“These strains were shown to have anti-biofilm activity and to interfere with epithelial cell damage caused by the bacteria and fungus found in CD,” said Ghannoum.
In addition to the selected microorganisms, the enzyme amylase was added to the formulation to enhance biofilm abrogation.
The researchers studied the effects in mice and humans. In humans, 49 healthy volunteers enrolled to participate in four weeks of once-a-day formulation consumption.
The comprehensive intestinal microbiome, representing bacterial and fungal communities, profiles were assessed at the start of the study and following four weeks of probiotic consumption.
“The microbiome (both bacteria and fungi) of our subjects was compared with those reported by the Human Microbiome Project (HMP) for healthy subjects as a control for bacterial abundance,” said Ghannoum.
“When the volunteers’ microbiome profiles were analyzed, the changes indicated the effects could be of great benefit to healthy individuals with digestive issues,” he said.
Second clinical study
Following this preliminary study, another clinical study was conducted (recently completed and submitted for publication) to test effects of the formulation on healthy individuals with self-reported gastrointestinal symptoms such as flatulence, bloating and abdominal discomfort.
“The second study showed that the formulation reduced the severity and frequency of overall GI symptoms and positively modulated specific symptoms, such as flatulence, bloating, stool regularity, constipation and abdominal discomfort to a statistically significant degree compared to placebo,” said Ghannoum said. “In addition, the formulation appeared to improve irritability while possibly reducing anxiety, emotional stress and improving overall score on an anxiety symptom questionnaire. Importantly, the research subjects tolerated the formulation very well in comparison to individuals who had received a placebo.
“Studies such as these and additional studies demonstrating that changes in the gut microbiome balance following probiotic modulation can be sustained by either diet modification or maintenance dietary supplementation that has been designed to address the specific microbiome profile of the target condition,” he said.
Ghannoum said that the rational design and appropriate experimental and clinical studies could be applied to other cohorts of individuals based on health and demographic factors to provide insights into gut microbiota composition, microbial interplay with probiotics and potential effects on host organisms.
Through the analysis of big microbiome data sets, researchers have started to appreciate the microbiome composition differences between different cohorts of individuals. That has led to the opportunity to leverage such data insights for targeted microbiome solution development.
“Introducing an additional or adjuvant/supporting therapy that can modulate the gut microbiota and/or prevent gut microbiome dysbiosis may be a new approach to targeted microbiome product development. Not only does this approach have the potential of restoring the microbiome balance, but it may also help achieve better response to the currently used approaches,” Ghannoum said.
Probotic from BIOHM Health Inc.
The probiotic formulation developed through this data-powered design process was launched in market by BIOHM Health Inc. as a general wellness probiotic. Ghannoum is co-founder of BIOHM.
“We launched BIOHM to build off this process of utilizing microbiome data to create nutritional solutions that are built off the actual microbiome profiles of thousands and metadata of real individuals, allowing for truly targeted innovation,” said Afif Ghannoum, CEO of BIOHM Health Inc. and Mahmoud Ghannoum’s son.
Importantly Afif Ghannoum strongly noted that the probiotic currently in market has not been proven to, nor is not intended to prevent, treat or cure CD or any other condition or disease.
“It’s very exciting to see the data-powered approach to microbiome innovation validated by a leading journal such as Gastroenterology, and we’ve had incredible scientific partners in University Hospitals Cleveland Medical Center and Case Western Reserve University School of Medicine.” said Afif Ghannoum, a biotechnology attorney by training.
Authors of the study, called “Modulating the Microbiome for Disease Treatment,” are Rachael Gowen and Ahmed Gamal, from the Department of Dermatology at UH and CWRU, who contributed equally to the paper; Luca Di Martino, UH/CWRU Department of Medicine and Case Digestive Health Research Institute; Thomas S. McCormick and Mahmoud A. Ghannoum also from the UH/CWRU Department of Dermatology
This work was supported by National Institutes of Health grant.
News release courtesy of University Hospitals.
For more information, contact Mike Scott at mike.scott@case.edu.
This article was originally published Jan. 27, 2023.