A New Decade of ME Research: The 11th Invest in ME International ME Conference 2016
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Riley: Droplet digital PCR for evaluation of associations btw human herpesvirus infection and ME/CFS

Discussion in 'General ME/CFS News' started by mango, Sep 2, 2016.

  1. mango

    mango Senior Member

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    Droplet digital PCR for evaluation of associations between human herpesvirus infection and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)

    Eleanor Riley, London School of Hygiene & Tropical Medicine

    Abstract
    Project Summary:

    Our hypothesis is that Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has a viral aetiology and that the characteristic persistent remitting and relapsing nature of the syndrome is the result of poorly controlled infection with one or more known viruses, possibly due to an underlying immune deficiency.

    We further hypothesise that the causative viruses will be human herpesviruses as they have the key characteristics of being highly prevalent, giving rise to lifelong infections, and undergoing prolonged periods of dormancy/latency with periodic reactivation at times of stress or immune compromise.

    Linking viral infections to ME/CFS has been difficult due to the cross-sectional nature of most epidemiological studies of this disease. Thus, although differences in prevalence of some viruses have been reported, causal inference is lacking. We believe that the development of highly sensitive, specific and quantitative nucleic acid based tests for quantification of human herpesviruses in non-invasive samples (e.g. saliva, urine), will allow us to conduct large scale prospective studies that will provide robust evidence for or against a link between herpesvirus reactivation and ME/CFS.

    The purpose of this R21 application is to conduct exploratory/ developmental work that will underpin future, large scale, epidemiological studies. Our specific objectives are:

    1) To develop and validate highly sensitive and specific, quantitative digital droplet PCR (ddPCR) tests to detect all 8 human herpes viruses in blood and in more easily accessible biological samples (e.g. saliva, urine).

    2) To use these assays to test samples from 250 ME/CFS cases, 200 healthy controls, and 50 controls with confirmed multiple sclerosis (MS), in the UK and Norwegian ME/CFS biobanks and look for associations between herpes virus infection, ME/CFS status and clinical parameters.

    3) In a subset of virus positive and negative participants, to conduct a pilot study to monitor changes in herpesvirus viral load over time (monthly sampling) and correlate this with clinical and biological markers.

    This study is novel in that it will use highly sensitive and specific molecular assays to detect and very accurately quantify circulating viral loads from noninvasively collected samples. When combined with our ongoing recruitment and follow up of ME/CFS cases and controls in the UK (funded by 1R01AI103629-01A1) and our collaboration with the Norwegian ME/CFS biobank, this study will allow us, for the very first time, to correlate virus infection and reactivation with remission and relapse of clinical symptoms.

    If our hypotheses are found to be supported by the evidence, this will offer insights in to the underlying pathophysiology of the disease and open up new avenues for treatment and management of ME/CFS.

    Project Start Date: 4-AUG-2016
    Project End Date: 31-JUL-2018

    https://projectreporter.nih.gov/project_info_description.cfm?aid=9182215
     
    JohnCB, cfs6691, Simon and 6 others like this.
  2. Hutan

    Hutan Senior Member

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    Hmm, I'll be interested to see the results but i'm not sure that correlating increased herpes viral load in blood and saliva with ME symptoms will tell us much about the pathophysiology of the disease.

    About 6 months in to my ME illness, I started getting continuous cold sores ie I always had one. 18 months of Valtrex stopped them - which was nice - but it didn't fix my ME. Now a year or so later, I am in a bad patch of my illness (winter, series of visitors), and I have another cold sore. Could it not be that, just like everyone else, when we are run down and our immune defences are low, latent herpes infections reactivate? It's just the percentage of time that we are vulnerable that is different i.e. most of the time.

    If the study is precise enough to identify different strains of herpes viruses to potentially identify more pathogenic variants, that might add new knowledge. But they just talk about 8 herpes viruses, not strains of each.

    Don't get me wrong, I'm grateful for any ME research that doesn't have a patient blaming agenda. If the illness is prodded from enough directions long enough, we will learn more. I guess even just confirming that people with ME are vulnerable to herpes reactivations would help ensure mainstream doctors provide better care.
     
    mango, Bob, Valentijn and 2 others like this.

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