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Chuck Darwin
Chuck Darwin
@cdarwin@c.im  ·  activity timestamp 6 days ago

Much of cancer’s biological power comes from the fact that to the body, it doesn’t always seem like a pathogen.

Because cancer arises from mutations in each patient’s own DNA, the disease complicates our immune system’s central task of differentiating between body and foreign object,
host and invader,
“self” and “not self.”

Physicians long hypothesized that there was a link between cancer and swelling
—a critical sign that the immune system “sees” an enemy to ward off.

In the 1890s #William #Coley,
now known as the father of #immunotherapy,

successfully spurred remission in patients with inoperable tumors by injecting them with bacteria like those that cause strep throat.

But the mechanisms behind Coley’s treatments were poorly understood,
and for decades after his discovery, researchers weren’t sure our immune systems could detect cancer at all.

Because doctors didn’t know exactly how the body perceives and responds to cancer,
early treatments were highly invasive and highly toxic:

The first tactic was major surgery on the organs where cancer was taking root.

That was followed in the 20th century by the development of systemic radiation and chemotherapy to attack cancer cells throughout the body.

Over time oncologists narrowed and refined these approaches incrementally,
using more precise surgery,
more focused radiation
and chemo that killed fewer normal cells as collateral.

Still, the dream was to harness immunotherapy,
which represented a dramatic departure from the usual tactics in seeking to use the human body’s own systems to go after cancer in a more targeted way.

As demand for COVID vaccines has slackened,
there has been a rush to apply mRNA technology to a long list of illnesses.

The first real proof that immune cells are capable of recognizing tumors didn’t come until the 1950s and 1960s.

Gradually, researchers came to understand that cancer deploys a host of tricks to suppress the immune response to growing tumors.

Some forms of cancer use fibrous tissue called #stroma to construct shields that make it difficult for immune cells to penetrate or attack tumors.

Other cancers take advantage of the balancing act our immune systems are always performing when they decide how heavily to invest the body’s defenses in warding off a given threat.

Some tumors produce proteins that can shut down key immune cells.

Tumors may even recruit immune cells to promote the growth of blood vessels that will supply them with oxygen and nutrients.

As scientists learned more about how cancer manipulates the immune system,
they started identifying ways to thwart it.

Inside our cells, proteins are constantly being chopped up into smaller sequences of amino acids,
some of which are then presented on the cell surface as part of what’s collectively known as
the major histocompatibility complex, or #MHC
—essentially the immune system’s tool for differentiating self and foreign molecules.

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Chuck Darwin
Chuck Darwin
@cdarwin@c.im  ·  activity timestamp 6 days ago

Vaccines based on mRNA can be tailored to target a cancer patient’s unique tumor mutations.

But crumbling support for cancer and mRNA vaccine research has endangered this promising therapy

The results of Brigham’s trial were an early sign that mRNA vaccines may be effective for a wide variety of cancers:

Whereas pancreatic cancer is known for its low rate of mutations,
the earliest data on personalized mRNA vaccines came from studies of melanoma,
which researchers had targeted specifically because it tends to mutate so frequently.

An earlier phase 2 trial in patients with advanced melanoma found that for those who received both a personalized mRNA vaccine and so-called immune checkpoint inhibitors,
the risk of death or recurrence decreased by almost half compared with those who got only checkpoint inhibitors.

Ongoing companion trials are targeting kidney and bladder carcinomas
and lung cancer.

. In each case, the vaccine is additive:

administered after surgery and with standard drugs.

The shot’s job is to prime the immune system to recognize abnormal proteins arising from mutations
and attack any lingering malignancy that escaped conventional treatments
—or stamp out future recurrence.

Seeing promising results in fundamentally different kinds of tumors has motivated researchers to pursue personalized mRNA vaccines much more broadly.

In doing so, they’ve developed an approach at the nexus of several important trends,
pairing insights about our immune system’s response
to cancer
with advances in vaccine production spurred by the COVID pandemic,
the rise of algorithms powered by artificial intelligence,
and the plummeting cost of genetic sequencing.

Today there are at least 50 active clinical trials in the U.S., Europe and Asia
targeting more than 20 types of cancer.

A melanoma trial led by pharmaceutical companies Moderna and Merck has now reached phase 3,
the last step before a medicine can be approved for public consumption.

Personalized melanoma vaccines could be available as early as 2028,
with mRNA vaccines for other cancers to follow.

But the promise of this novel approach couldn’t have come at a more perilous time for the field.

🆘 In the first weeks of the second Trump administration,
U.S. cancer research was thrown into unprecedented turmoil as federal grants were terminated en masse.

According to one Senate analysis, funding from the National Cancer Institute was cut by 31 percent in just the first three months of 2025.

By March cancer researchers worried that mRNA vaccines were facing particular scrutiny.

⚠️KFF Health News reported that
#MichaelMemoli ,
acting director of the National Institutes of Health,
had asked that any grants, contracts or collaborations involving mRNA be flagged for Health and Human Services Secretary Robert F. Kennedy, Jr., best known prior to assuming that role as one of the nation’s most prominent anti-vaccine campaigners.

🔥Suddenly, the optimism around personalized mRNA vaccines was overshadowed by a sense that the public investment that sustained cancer research was being dismantled piece by piece.
https://www.scientificamerican.com/article/personalized-mrna-vaccines-will-revolutionize-cancer-treatment-if-federal/

Scientific American

Personalized Cancer Vaccines Are Almost Here—But Federal Funding Cuts Could Derail Them

Vaccines based on mRNA can be tailored to target a cancer patient’s unique tumor mutations. But crumbling support for cancer and mRNA vaccine research has endangered this promising therapy
Chuck Darwin
Chuck Darwin
@cdarwin@c.im replied  ·  activity timestamp 6 days ago

Much of cancer’s biological power comes from the fact that to the body, it doesn’t always seem like a pathogen.

Because cancer arises from mutations in each patient’s own DNA, the disease complicates our immune system’s central task of differentiating between body and foreign object,
host and invader,
“self” and “not self.”

Physicians long hypothesized that there was a link between cancer and swelling
—a critical sign that the immune system “sees” an enemy to ward off.

In the 1890s #William #Coley,
now known as the father of #immunotherapy,

successfully spurred remission in patients with inoperable tumors by injecting them with bacteria like those that cause strep throat.

But the mechanisms behind Coley’s treatments were poorly understood,
and for decades after his discovery, researchers weren’t sure our immune systems could detect cancer at all.

Because doctors didn’t know exactly how the body perceives and responds to cancer,
early treatments were highly invasive and highly toxic:

The first tactic was major surgery on the organs where cancer was taking root.

That was followed in the 20th century by the development of systemic radiation and chemotherapy to attack cancer cells throughout the body.

Over time oncologists narrowed and refined these approaches incrementally,
using more precise surgery,
more focused radiation
and chemo that killed fewer normal cells as collateral.

Still, the dream was to harness immunotherapy,
which represented a dramatic departure from the usual tactics in seeking to use the human body’s own systems to go after cancer in a more targeted way.

As demand for COVID vaccines has slackened,
there has been a rush to apply mRNA technology to a long list of illnesses.

The first real proof that immune cells are capable of recognizing tumors didn’t come until the 1950s and 1960s.

Gradually, researchers came to understand that cancer deploys a host of tricks to suppress the immune response to growing tumors.

Some forms of cancer use fibrous tissue called #stroma to construct shields that make it difficult for immune cells to penetrate or attack tumors.

Other cancers take advantage of the balancing act our immune systems are always performing when they decide how heavily to invest the body’s defenses in warding off a given threat.

Some tumors produce proteins that can shut down key immune cells.

Tumors may even recruit immune cells to promote the growth of blood vessels that will supply them with oxygen and nutrients.

As scientists learned more about how cancer manipulates the immune system,
they started identifying ways to thwart it.

Inside our cells, proteins are constantly being chopped up into smaller sequences of amino acids,
some of which are then presented on the cell surface as part of what’s collectively known as
the major histocompatibility complex, or #MHC
—essentially the immune system’s tool for differentiating self and foreign molecules.

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