Human data.
In a cohort of 44M+ people, those hospitalized with severe COVID-19 had a 19% higher risk of being diagnosed with lung cancer compared to uninfected controls!
Mild infections didn’t carry this risk - it’s the severity that matters.
Animal models.
Mice that had recovered from severe COVID-19 or flu showed faster tumor growth and worse survival after tumor initiation.
The effect persisted for weeks to months after the virus was cleared.
What’s happening in the lungs?
Severe viral pneumonia doesn’t just leave scar tissue. It rewires the lung environment.
Special neutrophils (SiglecFhi) accumulate and promote tumor growth.
CD8⁺ T cells - the cancer-killing army - become exhausted.
Lung epithelial cells get stuck in a risky in-between state, more prone to transformation.
Epigenetic memory of inflammation.
After infection, DNA in lung cells stays more open at cytokine genes (IL-6, G-CSF, TNF).
That keeps the lung in a pro-tumor mode - easier recruitment of harmful neutrophils, weaker immune surveillance.
How long does this last?
The study doesn’t show a clear end point.
In mice, the effect persists for at least 2 months (equivalent to several years in humans).
Authors write this inflammatory memory may last months to years - which means survivors need long-term monitoring.
Protection.
In mice, mRNA vaccination against SARS-CoV-2 prevented the tumor-promoting effect - tumor growth looked like in uninfected animals.
Mild infections alone didn’t accelerate tumors.
Vaccination may indirectly protect against cancer by preventing severe disease.
Therapeutic angle.
Blocking neutrophils (CXCR2 inhibitor) + blocking PD-L1 worked synergistically.
Fewer harmful neutrophils, more active CD8⁺ T cells, less tumor growth.
Sum:
Severe viral pneumonia (COVID-19, flu) can prime the lungs for cancer - not immediately, but months or even years later.
That means -
Survivors of severe infection may need closer cancer surveillance
Preventing severe infections (by vacc) isn’t just about avoiding ICU…it may also be about preventing cancer.
This is a preprint, not yet peer-reviewed.
Qian at al. 2025, Respiratory viral infections prime accelerated lung cancer growth. biorxiv.org/content/10.110…
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A new preprint study shows that the SARS-CoV-2 protein ORF6 directly kills human neurons.
Not by accident, but through necroptosis - a kind of cell death where neurons burst and fuel inflammation.
This may underlie the long-term brain symptoms of Long COVID.🧵
Researchers tested 22 viral proteins. The most toxic? ORF6.
In neurons, it flipped on the necroptosis switch - RIPK3 and MLKL.
Biologically - these molecules punch holes in the cell membrane until the neuron literally ruptures.
In patient brain tissue, especially the hippocampus (memory center), they found the same pattern
dead neurons + necroptosis markers.
That’s a direct biological link between infection and symptoms like brain fog and memory loss.
A new Danish study shows what many of us feared - putting kids protection only on vaccines is a dead end.
The real failure has been ignoring clean air, filtration, transmission prevention.
That’s what harms children most.
317 000 kids, followed for 11 months.🧵
The study looked at the basic 2-dose Pfizer vaccine (BNT162b2) in adolescents 12–15.
From July 2021 to June 2022 - across the shift from Delta to Omicron.
Effectiveness was modest and faded fast.
First weeks - about 50% protection against hospitalization, less against infection
After 1 year - protection against mild infections was almost gone
Protection against hospitalization fell to 20%
That means - after one year, out of 100 vaccinated kids, about 6 fewer got infected compared to unvaccinated.
Chen et al., 2025 looked at school-age kids (6–18) and found brain changes after COVID.
What about toddlers?
This new study shows that even mild infection left detectable alterations in their developing brains.🧵
Data in Scientific Reports (2025):
Even mild COVID-19 in toddlers leaves measurable changes in the brain.
Researchers used advanced MRI to look at brain shape, connectivity, and the system that clears waste (glymphatic system).
Who was studied?
19 children who had mild COVID (avg age 3.4 yrs)
22 healthy controls (3.9 yrs)
Scans were done about 30 days after infection.
All were recruited from a hospital cohort, but none had severe disease.
New study: Omicron ≠ harmless for kids
We often hear - Omicron is just a mild flu, harmless for children.
A new study in Pediatric Neurology shows otherwise - even mild infections can leave measurable marks on the brain and cognition.🧵
Cohort: 60 children (6–18 y), infected during the 2022 Omicron wave in Taiwan.
All had mild disease (no breathing problems).
They underwent MRI brain scans, visual perception tests, and symptom tracking at 3 and 6 months.
Persistent symptoms
37% still had neuropsychiatric issues at 3 months
28% at 6 months (sic!)
Most common - headaches/dizziness, attention & memory problems, mood changes, sleep issues.
We age. So do our cells.
But what if aging isn’t just wear and tear - but a failure of our mitochondria, the tiny engines that power every heartbeat?
A new study shows:
Mitochondrial breakdown doesn’t follow aging.
It drives it - especially in the heart.🧵
In the past decade:
Global cardiovascular disease (CVD) has risen by 29%
CVD-related deaths are up 19%
Why?
Not just bad diets or lack of exercise - but an aging population and rising metabolic dysfunction.
So why is age the #1 risk factor for heart disease?
Because aging hearts are running low on cellular energy.
And the cause of that?
Failing mitochondria.
SARS-CoV-2 can break immune balance - sometimes boosting our ability to neutralize the virus, other times increasing the risk of autoimmune damage.
A new study shows how autoantibodies after COVID-19 act like a double-edged sword.🧵
Autoantibodies = antibodies that mistakenly attack the body’s own tissues (aka nuclear proteins, enzymes, or immune receptors).
They’re common in diseases like lupus.
After COVID-19, autoantibodies often appear. But what do they mean for severity and immunity?
Alone, no single autoantibody predicted hospitalization. But the combination of SSA/Ro52 (nuclear protein), Jo-1 (tRNA enzyme), and RNP (RNA-protein complex) showed up more often in hospitalized & ICU patients.