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An Interview With Ian Lipkin - An Ambitious Project to Study the ME/CFS Microbiome

  [ 43 votes ]   [ 2 Comments ]
By Simon McGrath • • February 20, 2014

An Interview With Ian Lipkin - An Ambitious Project to Study the ME/CFS Microbiome
Dr. Lipkin is raising money for this potentially ground-breaking study. If successful, it could provide an explanation for the chronic immune activation found in ME/CFS patients. It could also lead to effective treatments. The total cost of the study is $1 million. Because NIH has not funded the research, Dr. Lipkin is relying on independent sources for support. You can donate HERE.

By Simon McGrath

Dr W. Ian Lipkin has demonstrated a clear commitment to ME/CFS research. First came his study looking at Borna virus in the 1990?s, and then the landmark study that ruled out XMRV as a cause, and most recently we have heard about the huge pathogen and immune study – a vast collaboration with many key clinicians and researchers, including Dr Dan Peterson and Professor Jose Montoya.

That research had already found clear signs of immune activation in patients and, when I spoke to him, Lipkin was clearly excited about the very latest results to emerge from the study – I wish I could reveal more, but a paper has just been submitted and details are embargoed until publication.

Lipkin believes that immune activation may be responsible for driving the symptoms associated with ME/CFS. And that the immune activation and could itself be triggered by bugs, not in the blood, but found in the vast ecosystem of bacteria, viruses and fungi, that constitute the gut microbiome.

However, he doesn’t have the funds to pursue this research and so he’s appealing to the patient community for the one million dollars he needs to get the work done. The payoff? A better understanding of the illness and the possibility of new treatments.

Dr Lipkin on ME/CFS

Lipkin made a splash in the world of ME/CFS when he led the XMRV study that both disproved its role in the illness and also managed to unite the patient community. At the press conference for that study he said his first brush with CFS was a large study in the 1990s that demonstrated no connection between the Borna virus (one of many viruses he’s discovered) and CFS. But he stressed that their findings in the same study of B-cell activation in CFS patients was a clear sign that this was not a psychosomatic disorder.  The findings in his new study have only confirmed his views:

“There is no question in my mind that this is a physical disorder. The fact that we haven‘t been smart enough or invested enough in it to sort that, doesn’t mean that this is anything else.”

The smoking gun

The immune activation he’s found could explain fatigue – it’s almost a universal symptom of infections like flu, and is actually a consequence of immune activation rather than caused by pathogens themselves.

The same could be true of other ME/CFS symptoms including disturbed sleep and brain dysfunction which again are typical symptoms of immune activation.

Lipkin is eager to build on this work. He believes the immune activation is a smoking gun and now wants to track down who or what pulled the trigger.

There are several credible places to look for the culprits triggering the activation. One is white blood cells: some viruses could be hiding out in cells and so wouldn’t have been found by the initial search in the blood plasma – and Lipkin already has a white blood cell study lined up.

However, his attention is particularly focused on the microbiome, the large ecosystem of bugs that live on our skin and within our ‘inner tube‘ that leads from mouth to bottom.

There are at least one trillion bugs in the gut microbiome – and there are more immune cells in the gut than anywhere else: it’s a great place to hunt for bugs that might be triggering immune activation.

Click HERE to read more.

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Article Comments Post a Comment

article reference
Posted by: SusanSimon
Feb 24, 2014
"Professor Montoya" is an M.D. and should be credited as such. Thank you for the article.
Reply Reply

Lipkin Effort
Posted by: reino
Mar 26, 2014
When will CFS researchers ever figure out that they will never have enough funding to figure this disease out on their own. There have been hundreds of millions of dollars spent on the American Gut project sequencing the gut biome. Why doesn't he simply call Rob Knight, the director of the project and piggy back on what's been done already instead of reinvest the wheel all the time....very very frustrating. These people need to crawl out of academia an figure out how the real world works and try reaching out to other people who know more than they do about a given subject.

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