Comparing immunological signatures between Long Covid and ME/CFS

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Dr. David Putrino and Dr. Jamie Wood, of the Icahn School of Medicine at Mount Sinai, have conducted several landmark studies on Long Covid. Their extensive research has led them to suspect that the immune responses of people with Long Covid differ in important ways from the immune responses of other people. If so, these differences (called immunological signatures) may explain why some people develop Long Covid symptoms and hopefully lead to the development of new therapies. To find this information, the team uses a wide range of cutting-edge technologies to compare blood and saliva samples from people with Long Covid with those from healthy participants.
Because both Long Covid and ME/CFS are post-acute infection syndromes (and have similar symptoms), the team also wants help from people with ME/CFS to find immunological signatures for ME/CFS. Similarities between the ME/CFS and Long Covid signatures may lead to therapeutic options for anyone with a post-acute-infection syndrome.
In this webinar, Dr. Putrino and Dr. Wood explain their ongoing research and the current study, which has a high potential to generate new knowledge and to help people diagnosed with ME/CFS or other post-acute infection syndromes.
The Solve Together Real-World Data Platform (ST-RWD) will soon begin to refer consented ST-RWD users who have relevant profiles to be considered for participating in this study that compares ME/CFS and Long Covid. If you are interested, please consider joining ST-RWD via solvecfs.org/research/solve-t....
You can also email us at research@solvecfs.org if you have any questions.

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8 май 2024

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Комментарии : 24

@pattysmith5989 Месяц назад

Thank you for your excellent work. ME for decades.

@davidburian5095 Месяц назад

Thank you David PutHERO. I love the fact that you are in the field. Please stay!

@annabeldean8276 Месяц назад

Thank you 55 yrs here in Australia

@maryreid2282 Месяц назад

Very interested in this research. After being ill in 1980 I was left with M.E./Chronic Fatigue and would love to know some answers for my illness and symptoms. Thank you for doing your research.

@dansmith9724 Месяц назад

Maybe it wasn't mentioned, but many previous studies on mecfs have shown low natural killer cell function. Was nk function testing done in these long covid studies??

@rrrrrulo Месяц назад

Been suffering with ME for over 35 years. Glad to see some progress. Hope to find cause and cure very soon.

@jewelleryaddict Месяц назад

30 years of CFS this should have been done for us after first outbreaks of CFS at Incline Village. Has surely wasted some of my best years of life with a myriad of horrible symptoms and so much disbelief. Not sure which was the worst.

@ShadowMan66 Месяц назад

I'm into year 32 so know exactly how you feel!

@Gina-dn6xm Месяц назад

Wow! I feel like we are finally getting somewhere with these conditions! In the last 8 years, I have been diagnosed with chronic lyme ( positive test), reactivated Epstein Barr, ME/ CFS, and long covid. Thank you so much!

@riptaylor5862 Месяц назад

Yeah right. We”ll be dead by the time they figure this out. Every week there is a new theory, a new presentation with a bunch nonsense. In two months this presentation will be invalidated when another study finds something completely unrelated. You can find hundreds of “hopeful” articles and videos which all point to a different root cause, and they come out every week. It’s been like this for years! Are you better? No. Will you be better in 5 years? I doubt it. I hope you are better. But guess what? The solution won’t come from these dummies at Solve Nothing. Some brilliant person from Sweden, the UK or China will figure it out. We just need to pay that person a lot of money and he/she could figure this out in a week. Think about it…these dopes won’t be able to make videos if there is a cure. Then what will they do to pass the time? Actually do work? C’mon!

@jakeclarke8706 Месяц назад

Thank you for all your hard work

@HarryJensen-kr4qz Месяц назад

Was 68, now 71. Had covid in 2020 & 2021. Had brain fog/vertigo, had what I believed to be shingles in right arm. Was several years ago, seem fine now. Best luck to anyone still struggling.

@Swansue Месяц назад

What’s the treatment?

@polyrhythmnix9723 Месяц назад

Thank you for your work. I wish I could participate in one of these studies, but I don't live in America, lel :/

@valerielord1088 17 дней назад

I need to share this with a family member. In place of the usual icons, there is ink a link to an ad by the CDC, stating that the vaccine is safe and effective.

@ashantimatthewson1702 Месяц назад

Is there any hope for muscle wasting after cv and vac? 39 and recliner bound from mysterious wasting. Every test comes back fine

@janisedmondson7132 Месяц назад

Could treatment with immunology intravenous help?

@jianhan3538 21 день назад

Have you done TCR/BCR sequencing? Still have peripheral blood samples to gather that info? We may collaborate.

@omygod9062 14 дней назад

The Ugg in mice says it all….balance, pain extremities…yahoo……get on it everyone……we are desperate….xxx

@justcees Месяц назад

Sadly, dr. Putrinos efforts maybe thwarted due to staffing issues. I waited more than 2 mos. For a scheduled APPT. only TO BE cancelled 1 week before the visit. The group running these studies don't respond to emails or telephine calls. It is atrocious how ME/CFS/LC people are being treated STILL. @Dr. Putrino, IF he is truly interested should look into what is going on with this study n STAFF.