• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To become a member, simply click the Register button at the top right.

Probiotics Signal Host Immune Cells

kolowesi

Senior Member
Messages
267
Location
Central Texas
This is from the latest Swanson newsletter:


Lee Swanson Research Update
Could Probiotics Protect Us From Gut Parasites?
September 2009

The gut-health benefits of probiotics may also extend to preventing and eradicating parasitic infections, according to early data from researchers at the University of Texas Southwestern.

Scientists studying Toxoplasma gondii, the parasite responsible for toxoplasmosis, found that bacteria present in the human gut help stimulate the body's defense mechanisms.

"While this is very early data, our results suggest that looking at the bacteria present in each patient's gut could help physicians understand their susceptibility to infectious diseases," said Dr. Felix Yarovinski from the University of Texas Southwestern. "It also suggests the possibility of developing novel probiotic strategies for treating parasitic infections such as toxoplasmosis and cryptosporidiosis, a related disease caused by the parasite Cryptosporidum."

The UT Southwestern researchers published their findings in Cell Host & Microbe.

Dr. Yarovinsky said that probiotics may occupy space in the intestine and thus reduce or prevent potentially pathogenic bacteria attaching to the intestinal wall.

"In our work we revealed a novel feature of the beneficial relationship between commensal microorganisms and the host immune system," he said. "We found that gut commensal bacteria function as a molecular adjuvant, providing toll-like receptor (TLR)-dependent immunostimulatory signals to dendritic cells, which are the active mechanism of defense."

The researchers used mice that had an inactivated form of a specific immune protein, called toll-like receptor 11 (TLR-11), which plays a role in controlling the animals' immune response to the parasite. While TLR-11 is normally active in mice, humans do not have an active form of the receptor. It has therefore remained unclear quite how the human body "senses" T gondii.

Despite a lack of normal defense mechanisms, the researchers noted that the animals immune systems did react to T gondii infection.

The researchers found that the commensalor goodbacteria in the gut activated the immune systems, thereby inducing various inflammatory responses against the invading pathogen. "This seems to be the first example of direct pathogen recognition in vivo where activation of the immune system depends on indirect rather than direct sensing of a pathogen," said Dr. Yarovinsky.

And the potential benefits of the gut microflora appear to outweigh the benefits of having a full-functioning TLR-11, said Dr. Yarovinsky. In mice the receptor appears to do more harm than good.

TLR-11-deficient mice were able to mobilize enough signaling proteins, with the help of their commensal bacteria, to defeat the parasite, while mice with the receptor activated too many signaling proteins and developed severe inflammation in their small intestines.

Cell Host & Microbe 6(2):187-196, 2009