@adytum_official: A central question in long COVID has been whether autoantibodies (immune proteins that target the body’s own tissues) actually cause symptoms or are just bystanders. New research provides some of the strongest causal evidence yet, in a subset of patients. A Yale and Mount Sinai team (Iwasaki, Putrino, and colleagues) purified antibodies from long COVID patients and transferred them into healthy mice, which then developed symptoms including pain and sensory changes. Mice receiving antibodies from patients with new-onset chronic pain most reliably developed pain behaviors. This was press-released in May 2026. A peer-reviewed study using the same passive-transfer approach was published in Cell Reports Medicine in March 2026, identifying 134 elevated autoantibodies in long COVID and demonstrating persistent mechanical hypersensitivity in mice. This mirrors the approach that established an autoimmune basis for fibromyalgia (Goebel et al., 2021). This applies to a subset of long COVID, not all cases. The causal evidence is in animal models; the human data is associational. These findings support testing antibody-targeted therapies (such as IVIG or plasma exchange) in research settings but do not establish an approved treatment. Talk to a specialist about your own care. I’m not a doctor, just sharing research I find interesting. Sources: Santos Guedes de Sá, Iwasaki, Putrino et al. (2026). Yale/Mount Sinai (press release, May 2026). Transfer of IgG from long COVID patients induces symptomology in mice (2026). Cell Reports Medicine. DOI: 10.1016/j.xcrm.2026.00110-2 #longcovid #chronicillness #autoimmunedisease #chronicpain #medicalgaslighting
Adytum
Region: US
Tuesday 02 June 2026 15:22:20 GMT
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fragileteeth :
What does this mean for blood transfusions?
2026-06-02 18:05:36
1305
ᴀʟᴄʜᴇᴍ :
FIBROMYALGIA CAN BE DRIVEN BY ANTIBODIES?
2026-06-03 20:19:58
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Julia :
I'm really hoping that all the long COVID research will lead to treatments for people with other similar chronic illnesses, like fibromyalgia and hEDS.
2026-06-02 23:55:57
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likesewserious :
I have long covid. Low dose naltrexone helped a little, with recovering from crashes. But recently I started tirzepatide and it’s been a TOTAL GAME CHANGER
2026-06-02 23:32:02
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Madeline Faye :
Long Covid made me get PEM and sick a lot. Then I got mono again. After that I got ME/CFS. It’s like I just keep getting worse and I want to get better
2026-06-03 01:51:17
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Emily | Booktok Homesteader📚 :
I’ve been dealing with long covid since 2020, before it was even a known thing. I’ve been saying that it acts like an autoimmune disease. I literally have flare-ups. It’s been 6 years.
2026-06-03 13:32:59
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phoebe :
I remember reading about MECFS in 2016 and crying bc I felt so bad that the patients suffering weren’t being researched for treatment options. I’m happy that now doctors are looking into what’s going on so those suffering can be helped!!
2026-06-03 02:42:28
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Disabled and Proud :
Do we know if this would apply to ME/CFS patients who do not have LC?
2026-06-02 17:55:52
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ray 👤 :
ive been getting migraines since i was a kid. after i got covid in 2022 i am now debilitated by them. was diagnosed with 24/7 migraines w/ vestibular issues. i have to sit down while doing the dishes.
2026-06-03 00:09:06
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Jae 🪶 :
I've had MECFS for 27 years. I need relief. I need my life back.
2026-06-03 09:55:40
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K :
"but it's just a little cold!"
2026-06-04 20:02:02
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Kate :
I have always been sick but after getting covid my physical symptoms have been astronomically worse. I just attributed it to my condition worsening but my levels are all still the same as before. Curious to see if I have long covid too, would explain a whole lot.
2026-06-02 17:06:19
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Fixit :
I thought it was just activating MCAS..
2026-06-03 01:07:02
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jo :
i've had MECFS for a little over a year now. it has been hell on earth. this is huge, groundbreaking discovery. thank you for sharing
2026-06-03 04:37:26
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KushNBoots :
i have not felt the same since getting COVID a few years ago.
2026-06-04 18:04:03
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buzz :
I have had POTs for 20 years. 5 years ago when I got COVID, my POTs symptoms got worse. Then I got it a second time in 2022. I get vestibular migraines and I am not sure if they just happen to be similar to what consider a POTs episode, or I have those in addition to POTs, but that aspect has definitely gotten worse for me.
2026-06-03 03:38:47
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Mattnemite🧲Gaming/UGC/Jokes🥳 :
I love public health
2026-06-03 06:19:58
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Lisa Marriott :
l was diagnosed in the mid 1990s with CFS, l wish they put the level of research on all of this before covid.
2026-06-03 05:43:33
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tracee_annee 🍉 :
amazing
2026-06-02 23:22:53
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Abigail Rebecca Levy :
It is real...
2026-06-03 04:44:24
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Ivy📚🔮🎨 :
I have RA and had long covid symptoms for at least two years. I noticed they would improve around the days I took my RA med. I have to wonder if it helped me recover eventually too.
2026-06-02 23:59:02
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Feral and Chaotic✨ :
honestly this is also so important to know in terms of blood and organ donating too.
2026-06-03 17:17:29
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Acorn Baden :
What is the subset of long covid? Is it similar to Myalgic Encephalomyelitis (ME)
2026-06-02 17:14:13
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Babuska :
How are ME/CFS & Long Covid related?
2026-06-02 15:57:03
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Entei :
Posted this to my story and got a CGV 🤨
2026-06-05 01:28:22
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