Myasthenia Gravis News Community › Forums › Healthcare and Treatments › Seronegative MG: are there MG-causing antibodies undiscovered?

  • Seronegative MG: are there MG-causing antibodies undiscovered?

    Posted by Community Member on May 14, 2024 at 6:00 am

    Seronegative MG is defined as an individual with MG who does not have the common MG antibodies: acetylcholine receptor (AChR), Muscle-specific tyrosine kinase (MuSK), and Low-density lipoprotein receptor-related protein 4 (LRP4).

    However, could individuals with seronegative MG have a Myasthenia gravis-causing antibody that science has yet to discover?

    What are your thoughts?

    Community Member replied 11 Members · 12 Replies
  • 12 Replies
  • Community Member

    Member

    Sounds reasonable to me . Medicine is taking new turns every day . Hopefully Myasthenia will be interesting enough for someone to look .

    • Community Member

      Member

      Yes, I do think they will discover other antibodies. I’m seronegative since 1997 and have had every MG symptom in the book including MG crisis on life support for almost a month before actually being diagnosed ( by symptoms). I’ve been on continuous immunosuppressive meds since 1997. Also, Mestinon never worked for me.

  • Community Member

    Member

    When I was initially diagnosed in the 1990s, the only known MG-related antibody was AChR. The MG connection to MuSK was discovered in 2001 and LRP-4 in 2018 (I think). Those are just a few of the possibly thousands of antibodies produced by our bodies. I’m certain there’s more discoveries to come!

    • Community Member

      Member

      Yes!

      Thank You

  • Community Member

    Member

    Yes – check for voltage gated antibodies – aka Lambert Eaton Syndrome. It’s called myasthenic overlap syndrome in the literature. I’m antibody negative MG and antibody positive Lambert Eaton. Also look for striated muscle antibodies, Acetylcholine Receptor Binding Antibody

    And Acetylcholine Receptor Modulating Antibody – Quest has a panel. For MG there is also RYR, titin, LRP4 – Quest has a panel.

  • Community Member

    Member

    My answer: Occam’s razor.

  • Community Member

    Member

    My daughter has MG and positive to striated muscles antibodie called Ryanodin receptor antibodie . It took her neurologist 12 years to meassure that antibody –

  • Community Member

    Member

    YES that’s exactly right. The way the brain’s control signals to muscles are being blocked for MG seronegative individuals isn’t known yet. It’s a matter of research.

    –JSW

  • Community Member

    Member

    pls do get me wrong. my mg is so far seronegative, and i have to wait for a muscle biopsy until the end of August…. is there a chance that it will not show what is in the backgrund of my disease? it is not MuSK or AchR or what, fot sure, i take all the pills as subscribed and really just getting worse.

    • Community Member

      Member

      My daughter has myastenia . She was sero neg for 12 years . Half a year ago they did a test for striated muscles and it showed up that my daughter has Ryanodin receptor antibodie .She do not respond on Mestinon .You could ask for that antibodie plus lrp4 ,titin and agrin

      • Community Member

        Member

        thank you, i definitelly will

  • Community Member

    Member

    Or is it possible the tests simply aren’t good enough to detect the antibodies that are there? I have had great success with Vyvgart even though I am triple seronegative (No AChr, no MuSK, no LRP-4). Mestinon works great for me too.

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