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 Lyme Study Published Online

 - UBBFriend: Email this page to someone!    
Author Topic: New Lyme Study Published Online
Bugg
Frequent Contributor (1K+ posts)
Member # 8095

Icon 1 posted      Profile for Bugg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Increased IFNα activity and differential antibody response
in patients with a history of Lyme disease and persistent
cognitive deficits.
Jacek E, Fallon BA, Chandra A, Crow MK, Wormser GP, Alaedini A.
Journal of Neuroimmunology, pii: S0165-5728(12)00314-1.
Available online 12 November 2012.

http://dx.doi.org/10.1016/j.jneuroim.2012.10.011

Abstract
Following antibiotic treatment for Lyme disease, some
patients report persistent or relapsing symptoms of pain,
fatigue, and/or cognitive deficits. Factors other than
active infection, including immune abnormalities, have been
suggested, but few clues regarding mechanism have emerged.

Furthermore, the effect of antibiotic treatment on immune
response in affected individuals remains unknown.

In this study, a longitudinal analysis of specific immune
markers of interest was carried out in patients with a
history of Lyme disease and persistent objective memory
impairment, prior to and following treatment with either
ceftriaxone or placebo.

IFNα activity was measured by
detection of serum-induced changes in specific target genes,
using a functional cell-based assay and quantitative
real-time PCR. Level and pattern of antibody reactivity to
brain antigens and to /Borrelia burgdorferi/ proteins were
analyzed by ELISA and immunoblotting. Sera from the patient
cohort induced significantly higher expression of /IFIT1/
and /IFI44/ target genes than those from healthy controls,
indicating increased IFNα activity.

Antibody reactivity to
specific brain and borrelial proteins was significantly
elevated in affected patients. IFNα activity and antibody
profile did not change significantly in response to
ceftriaxone.

The heightened antibody response implies enhanced immune
stimulation, possibly due to prolonged exposure to the
organism prior to the initial diagnosis and antibiotic
treatment of Lyme disease.

The increase in IFNα activity is
suggestive of a mechanism contributing to the ongoing
neuropsychiatric symptoms.

[ 11-16-2012, 12:52 PM: Message edited by: Bugg ]

Posts: 1155 | From Southeast | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Bugg
Frequent Contributor (1K+ posts)
Member # 8095

Icon 1 posted      Profile for Bugg     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know that autoimmunity is not popular on this board. However, for those who are interested, I thought you might like to know that IFN (ie Interferon A) is the antibody that is also found in MS, Sjogrens, lupus, polymyositis, and RA....

As you are aware there are biologics available to treatment aforementioned autoimmune diseases but none of these specifically target interferon A. Currently, two drug companies have developed drugs they are testing in clinical trials in lupus patients that will specifically target Interferon A.

The goal, of course, is to stop the antibody, interferon A, from attacking the body.

Posts: 1155 | From Southeast | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Bugg
Frequent Contributor (1K+ posts)
Member # 8095

Icon 1 posted      Profile for Bugg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just an fyi, as I posted previously on this board I saw the head of neurology at a teaching hospital who is very lyme-friendly. He told me to get my vitamin D levels between 70-100 as that would help to modulate my immune system...ie quell the auotimmunity... He is one of the top MS specialists in the world and he said he has seen an almost absolute reduction in relapsing MS when D levels are between 70-100. A recent controlled study in the Journal of Neurology substantiates this.

I have posted below the results of a study where they are using Vitamin D to suppress the autoantibody effect of IFN. Apparently, those who are higher in IFN activity, as seen in lupus patients, often are also more deficient in Vitamin D.

As some of you with lyme have noted, our levels often drop quickly if we aren't supplementing. I never had this problem pre-lyme disease.

I've been supplementing for months trying to get my levels to 70. I'm at 48.9 right now. I definitely feel better than I did four months ago but my D levels had dropped to 15 so I was really feeling horrible, then.

Here's the study:

http://europepmc.org/articles/PMC3149865/

Posts: 1155 | From Southeast | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
poppy
Frequent Contributor (1K+ posts)
Member # 5355

Icon 1 posted      Profile for poppy     Send New Private Message       Edit/Delete Post   Reply With Quote 
This is D3 you are supplementing?

I have just upped my dose to 4000 i.u. a day without any blood testing for levels. Working in the dark.

Why is Fallon publishing with the chief architect of the IDSA guidelines? Going to lose cred with the patient population this way. There is an autoimmune component of chronic lyme but it is infection driven, and if that is not recognized, then treatment for autoimmunity alone will not work.

Posts: 2888 | From USA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Ditto to poppy:

The union of Fallon & Wormser here is very puzzling and does seem to harm his reputation (in my view). Normally, one would only co-publish with others of high professional and moral standards.

Wormer has neither and has consistently battled lyme patients. It's hard to believe that Fallon seems to be going hand-in-hand with him now.

But, mostly ditto to poppy keen eye for this:

There is an autoimmune component of chronic lyme but it is infection driven, and if that is not recognized, then treatment for autoimmunity alone will not work.

INDEED
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
lightfoot
Frequent Contributor (5K+ posts)
Member # 2536

Icon 1 posted      Profile for lightfoot     Send New Private Message       Edit/Delete Post   Reply With Quote 
Our advocate and researcher for Lyme at Columbia is Brian Fallon MD. I don't think this could be our Fallon.

--------------------
Healing Smiles.....lightfoot [Smile] [Smile] [Smile]

Posts: 7228 | From CO | Registered: May 2002  |  IP: Logged | Report this post to a Moderator
Bugg
Frequent Contributor (1K+ posts)
Member # 8095

Icon 1 posted      Profile for Bugg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Actually, it is Dr. Fallon at Columbia. He believes there is some autoimmune component for some lyme patients...genetics may play a part in this, of course...


Poppy, I took the 50,000 IUs of D2 to get my levels up quickly. After that, I'm taking 5,000 IUs per day of D3. This is what the neurologist told me to do. I had HORRIBLE, EXCRUCIATING BONE PAIN when I first started this regimen that no painkiller would touch. I though I would die for the first three months. Thankfully, the deep bone pain is now much better.. I really believe my bones had become demineralized and were in pain due to remodeling/rebuilding from the Vitamin D....

Posts: 1155 | From Southeast | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
minimonkey
LymeNet Contributor
Member # 8693

Icon 1 posted      Profile for minimonkey     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, this is the same Fallon, and I don't see this as a damage to his reputation, though admittedly it is very weird to see his name and Wormser's together.

I knew that Fallon was willing to work with IDSA members if he felt that their science was good on a particular issue -- (and Fallon is second author here, whereas Wormser is fifth, meaning this is much more Fallon's study than it is Wormser's.)


I have also been supplementing the HECK out of vitamin D for two years, and I can't seem to get it above 44 -- which is a big improvement from where I started, when my doctor said it was "barely measurable."

--------------------
"Looks like freedom but it feels like death..
It's something in between, I guess"

Leonard Cohen, from the song "Closing Time"

Posts: 822 | From California | Registered: Jan 2006  |  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.