Zdenek Vrozina Profile picture
Aug 26 8 tweets 2 min read Read on X
COVID-19 and the brain: a new study.
What the study looked at -
Researchers examined autopsies of 13 people who died with COVID-19 vs 23 controls.
Goal: to uncover what exactly happens inside the brain during COVID-19.🧵
The central player - microglia.
Microglia = immune cells of the brain. Normally they protect, repair, and keep things in balance.
In COVID-19, they flip - from guardians to drivers of damage.
The worst effects were seen in the medulla oblongata - the brainstem region that controls breathing and circulation.
Step by step, what happens
Loss of P2Y12 receptors - microglia can’t sense danger signals.
Activation of P2X7R + TLR3 - NLRP3 inflammasome - release of IL-1 and IL-6.
Blood–brain barrier (BBB) breaks down - immune cells infiltrate the brain.
Mitochondria in microglia collapse - leaking cytochrome c, triggering apoptosis.
Neurons and axons suffer - synapses are lost, myelin sheaths are destroyed.
Molecular findings
RNA-seq - shifts in microglial activation, oligodendrocyte differentiation, synapse organization.
Proteomics - altered proteins that regulate core microglial signatures.
Growth factors VEGF and PDGF also implicated.
Sum:
COVID-19 in the brain is not just inflammation.
It’s a chain reaction:
Microglial dysfunction.
Breakdown of blood vessels and BBB.
Cytokine storm (IL-1, IL-6).
Mitochondrial failure.
Loss of synapses and myelin.
All this hits hardest in the medulla oblongata - the area that keeps us alive
Illes at al., Focal neuropathologies in the brain of COVID-19-infected humans: inflammation, primary gliovascular failure and microglial dysfunction. nature.com/articles/s4139…
The hidden logic = viral proteins at work.
Spike (S) - activates TLRs, makes the BBB leaky - immune cell infiltration.
Nucleocapsid (N) - keeps NLRP3 + IL-1/IL-6 running - chronic neuroinflammation.
Envelope (E) - acts as a viroporin - ion imbalance - inflammasome + mitochondrial injury.
Mpro (main protease) - sabotages mitochondria & antiviral defenses - metabolic collapse, apoptosis.
Exactly matching the study’s cascade: microglia - BBB - cytokines - mitochondria - synapses/myelin - fatal failure of brainstem centers.
Plain language.
S (Spike) = the key that opens cells and inflammatory gates.
N (Nucleocapsid) = the engine of inflammation, keeping the fire burning.
E (Envelope) = the ion saboteur, wrecking balance inside cells and mitochondria.
Mpro (protease) = the enzyme manipulator, shutting down defenses and killing mitochondria.
Together they form a neurotoxic cocktail - explaining why COVID-19 can hit the brain so deeply and leave lasting scars.

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More from @ZdenekVrozina

Aug 26
Not just injections. Mucosal vaccines once promised better protection against transmission of COVID-19.
Today? Only two made it to phase III - and both are outside the West.🧵
Wantai (China) - intranasal vaccine dNS1-RBD (Pneucolin)
First mucosal vaccine to reach phase III
Tested in multi-country trials
Result: Emergency approval in China (2022)
Bharat Biotech (India) - intranasal BBV154 (iNCOVACC)
Advanced to phase III as a heterologous booster
Induced both antibody and mucosal responses
Approved in India (2022), now in use
Read 12 tweets
Aug 25
The title says it all:
“Expert consensus on combination antiviral therapy for high-risk COVID-19 patients: A timely call to action”
Translation: China experts are calling for a new HIV-inspired consensus.🧵
China already has an official consensus (2024) on oral antivirals.
But it focuses on monotherapy - one drug at a time.
That’s not enough for high-risk patients.
Why not enough?
Some remain PCR-positive after treatment,
Viral rebound occurs,
Resistance is a real risk.
For elderly, immunosuppressed, cancer patients - this can be fatal.
Read 10 tweets
Aug 24
A new preprint study shatters the idea that pediatric long COVID is just a mild or different version of the adult form.
It shows that children share the same core immune patterns - and, strikingly, some resemble those seen in chronic infections like HIV.🧵
The paper message is clear - pediatric LC is biologically defined immune dysfunction.

Children display
shifts in monocytes (↑ non-classical, ↓ CCR6),
T cell changes (↑ Tregs, ↓ central memory CD4, exhausted CD8),
exhausted B cells.
At the root lies a failure of antigen-presenting cells (monocytes & dendritic cells).
Normally, they carry viral information to T and B cells. But in LC, they express less CCR6/CCR7 - they can’t migrate properly to lymph nodes or activate adaptive immunity.
“Suppressed expression of CCR6 and CCR7… could impair antigen presentation and adaptive immunity.”
Read 13 tweets
Aug 23
How COVID-19 Might Be Accelerating HPV-Related Cancer - with lessons from HIV🧵
COVID-19 isn’t just a lung infection. A new study of over 1.2 million women found something alarming - women who had COVID later developed more HPV-linked cancers. Cervical cancer risk up 67%, anal 92%, vulvar 98%, oropharyngeal 78%.
A real case shows how fast it can happen. One woman had a precancerous lesion on her cervix (CIN2). Normally, these take years to evolve. After COVID? It turned into early cancer in just 3 months. The virus wasn’t in her cervix. The culprit? Her immune system was wrecked - T cells & NK cells had collapsed. ?pubmed.ncbi.nlm.nih.gov/36399874/
Read 14 tweets
Aug 22
Why do men with severe COVID-19 often show low testosterone and cholesterol? For years, we knew ACE2 was abundant in testicular tissue.
Now we have direct evidence - SARS-CoV-2 hijacks Leydig cells, diverting cholesterol away from hormones and into viral particles.🧵
For the first time, SARS-CoV-2 particles were found inside lipid inclusions and organelles of Leydig cells - the testicular cells that produce testosterone.
This discovery helps explain why men with severe COVID-19 often show low testosterone and cholesterol.
Already since 2020, studies had pointed out that ACE2 is highly expressed in testicular tissue, especially in Leydig and Sertoli cells.
Histopathological studies in deceased patients showed testicular damage - inflammation, degeneration, reduced spermatogenesis.
Read 12 tweets
Aug 20
COVID-19 leaves DNA scars.
A new study in BMC Infectious Diseases shows COVID-19 can leave lasting DNA damage in immune cells - even weeks after infection.
Here’s what the researchers actually found🧵
Researchers took white blood cells from
patients with mild COVID,
hospitalized patients with severe COVID (some ICU),
and healthy controls.
Simply put - they took white blood cells and used an electrophysical test (single cell gel electrophoresis - alkaline comet assay) to see how much their DNA broke into pieces. The longer the “tail moment” in the test, the more DNA damage.
Read 14 tweets

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