LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » New Virus detected in CFS and MS

 - UBBFriend: Email this page to someone!    
Author Topic: New Virus detected in CFS and MS
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi everyone,

I am posting an interesting article that was on the ImmuneSupport website - a good website for Chronic Fatigue Syndrome and Fibromyalgia, and now they are finally recognizing Lyme.

Anyway, this is regarding a previously undetected virus that they are hypothesizing could be among the culprits for CFS and perhaps MS.

I had CFS in 1984 when the few CFS doctors were speculating that the disease might be Epstein-Barr, HHV6, a retrovirus, Post-polio syndrome, etc.so I realize they are always looking for the one magic bullet and it's probably a very complex syndrome. And many CFS and Fibromyalgia patients seem to turn out to be Lyme patients in reality.

But given that multiple pathogens activate in CFS and Lyme patients, I thought I'd give us one more to worry about!

ARTICLE FROM www.immunesupport.com on 7/22/06:


``Previously Undetected'' Virus Implicated In Developmentof Chronic Fatigue Syndrome and other Conditions
by Editor
ImmuneSupport.com

06-27-2006

Note: This article includes our follow-up suggestions regarding its implications for Chronic Fatigue Syndrome patients.

Medical science may be just a few research steps away from cracking the secret of Chronic Fatigue Syndrome (CFS), according to news from the National CFIDS Foundation (NCF). Bottom line, states NCF's Medical Committee: ``Parainfluenza Virus-5 plays what the Foundation sees as a predominant and primary role in the development of CFS.''

This is news that the NCF believes can ``change the very nature of this disease.'' CFS has been an unexplained ailment, characterized by chronic debilitating fatigue and a combination of flulike symptoms.

Virus in the Cross-Hairs

Independent research and detective work funded by the nonprofit NCF has confirmed evidence of a ``previously undetected'' viral infection in patients with CFS. The research ``dovetails'' with work by virologists at the private biotechnology research firm Cryptic Afflictions, LLC. It also builds on years of NCF sleuthing for clues in the work of dozens of scientists around the globe, both published and held proprietary.

The NCF defines the CFS culprit as a strain of the recently named Parainfluenza Virus-5 (PIV-5); formerly called Simian Virus-5, or SV5, owing to its initial isolation in monkey tissue. It is an RNA virus, or ``rubulavirus'' in the category of viruses known to be associated with diseases such as mumps, encephalitis, and meningitis. And, as an RNA virus, it might be a mutating ``chameleon.'' At least a dozen strains of mumps virus have been identified, for example.

It is further defined as a "zoonotic" virus - one that in mutating can be transmitted between animals and people. And, at least as found in an initial CFS patient test performed by NCF-funded researchers, it exactly matches the ``SER'' strain of PIV-5 virus isolated in diseased swine by German researchers in 1994.

The Research-Detective Story So Far

NCF-funded scientists identified a new viral ``footprint'' in the blood of Chronic Fatigue Syndrome patients, in the form of a deficiency of the Stat-1 protein, which ``plays a vital role in immunity.'' The researchers then created a ``short list'' of viruses known to ``directly attack and degrade the Stat-1 protein'' as part of a viral strategy for evading the host's immune response. PIV-5 was on that list.

Meanwhile, they learned that Steven Robbins, MD, a virologist and CEO of Cryptic Afflictions, LLC, had tested blood samples from 56 CFS patients, and cerebrospinal fluid samples from 11 CFS patients, for antibodies specific to an RNA virus he calls ``Cryptovirus.'' Dr. Robbins found that the vast majority (96 percent) of his CFS blood samples and 91 percent of the CFS spinal fluid samples tested positively for ``Cryptovirus-specific'' antibodies.

The NCF also learned that a recent medical journal article suggests Cryptovirus ``is most similar to PIV-5'' - and that Cryptic Afflictions has ``extensive U.S. and international patents pending and owns the intellectual property rights'' for Cryptovirus, according to a report from its parent company, Century Pacific Financial Corp.

Dr. Robbins also found that the Cryptovirus could ``cause virtually identical disease in experimentally-infected animals,'' according to Century Pacific. Further, he found that ``nucleotide sequence data indicate that the virus is pandemic and represents a single virus `species' more akin to measles virus than hypervariable viruses like HIV.''

In addition to the Cryptovirus's association with Chronic Fatigue Syndrome, Cryptic Afflictions reports it is also believed implicated in other neurological disorders, including multiple sclerosis and idiopathic (unexplained) epilepsy. For example, the company reports it found Cryptovirus antibodies ``in the cerebrospinal fluid and blood of over 90 percent of patients tested with multiple sclerosis.''

Next Steps for CFS Research?

At a minimum, Century Pacific says Cryptic Afflictions is now pursuing tests of brain lesions in multiple sclerosis patients, and next plans to ask the FDA for approval of the diagnostic tests. Their testing plans for CFS seem to be unstated.

The National CFIDS Foundation, meanwhile, reports it is working to get this information out to ``medical and health groups that may be interested in further research,'' and says it is ``interested in funding those researchers who have expertise in the area.''

The NCF is an all-volunteer patient organization with no paid employees, and is funded solely by individual donations for the primary purpose of funding CFS research.

To review the NCF press release on this discovery, as well as a highly detailed, sourced report on the National CFIDS Foundation Medical Committee's detective work, titled ``Parainfluenza Virus-5: A new paradigm and a serious host challenge,'' visit the Foundation's site at http://www.ncf-net.org/Discoveries.htm

What does this mean for you?

1. Clearly, this and further research that may establish Chronic Fatigue Syndrome as a pathogen-triggered disease would lend medical validity to the condition.

2. Further, increasing knowledge regarding this virus or viruses may lead to preventive measures such as vaccines and epidemic surveillance, and/or effective treatments.

3. This news of the dedicated efforts by NCF-funded researchers and others underscores the importance of contributions to CFS research. We at Pro Health are proud to report that as a patient-owned company we have raised and donated more than $2.5 million to CFS and Fibromyalgia research to date, and contribute a portion of all our product sales to this cause.

--
Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

Icon 1 posted      Profile for Michelle M   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
VERY interesting, Jill. Thanks for posting.

I do have one question.

Who in the world would volunteer to have their brain lesions biopsied???

NOT ME!!!

Post-mortem, yep! Right now, nope!

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.