Scientists find a new way to reverse immune suppression in tumors

Date:
September 20, 2021
Source:
Weill Cornell Medicine
Summary:
Malignant tumors can enhance their ability to survive and spread by
suppressing anti-tumor immune cells in their vicinity, but a new
study has uncovered a new way to counter this immunosuppressive
effect.



FULL STORY ========================================================================== Malignant tumors can enhance their ability to survive and spread by
suppressing antitumor immune cells in their vicinity, but a study led
by researchers at Weill Cornell Medicine and NewYork-Presbyterian has
uncovered a new way to counter this immunosuppressive effect.


==========================================================================
In the study, published Sept. 20 in Nature Cancer, the researchers
identified a set of anti-immunosuppressive factors that can be secreted
by cells called club cells that line airways in the lungs. They showed
in a mouse model of lung cancer that these club cell factors inhibit
highly potent immunosuppressive cells called myeloid-derived suppressor
cells (MDSCs), which tumors often recruit to help them evade antitumor
immune responses.

The inhibition of the MDSCs led to an increase in the number of antitumor
T cells at the tumor site, and greatly improved the effectiveness of
FDA approved PD1 immunotherapy.

"These club cell-secreted factors are able to nullify immune suppressor
cells that otherwise help tumors escape an effective antitumor response,"
said co- senior author Dr. Vivek Mittal, director of research at the
Neuberger Berman Lung Cancer Center and the Ford-Isom Research Professor
of Cardiothoracic Surgery at Weill Cornell Medicine. "We're excited
by the possibility of developing these club cell factors into a cancer treatment." The research is part of a broad scientific effort in recent decades to find ways to harness the immune system against cancers. That
effort has yielded treatments such as "immune checkpoint inhibitors"
(ICIs) which partly undo tumors' immunosuppressive effects. In recent
years, oncologists also have observed that ionizing radiation, long
a standard treatment for many cancers, can further undo this immune
suppression and thereby enhance the effectiveness of ICI treatments.

In the new study, Dr. Mittal and co-senior authors Dr. Nasser Altorki,
chief of the Division of Thoracic Surgery at Weill Cornell Medicine and NewYork- Presbyterian/Weill Cornell Medical Center, and Dr. Dingcheng Gao, associate professor of cell and developmental biology at Weill Cornell Medicine, teamed up to determine how radiation has this immune-enhancing effect.



========================================================================== Using a mouse model of non-small-cell lung carcinoma, the most common
form of lung cancer, they first established that this effect peaked at a moderate dose of radiation, and caused the quadrupling, to 40 percent,
of the proportion of ICI-treated mice who survived tumor-free to the
end of the two-month observation period.

The researchers then found that radiation has this effect by activating
and stimulating the proliferation of lung-resident club cells, which
are known to help protect and repair sensitive airway linings, in part
by reducing inflammation.

"It's possible that we see a peak stimulation of these cells at a
particular radiation dose because a lower dose doesn't stress the cells
enough, whereas a higher dose kills them," said Dr. Altorki, who is also director of the Neuberger Berman Lung Cancer Research Center, the David
B. Skinner, M.D.

Professor of Thoracic Surgery and leader of the Experimental Therapeutics Program of the Sandra and Edward Meyer Cancer Center at Weill Cornell
Medicine.

The activated club cells secrete various molecules, and the researchers
found that they could replace the radiation with a "club cocktail"
of eight of these molecules and get essentially the same ICI-enhancing
result.

They also determined that this immune-restoring effect of the club cell molecules stems from their inhibition of MDSCs -- which have long been
seen as an obstacle to the improved efficacy of cancer immunotherapies.

To confirm the relevance of these laboratory findings to human cancers,
the researchers looked at blood serum sampled from lung cancer patients
in a clinical trial of radiotherapy plus ICI, conducted recently by
Dr. Altorki and colleagues at Weill Cornell Medicine. They observed that
levels of a key club cocktail molecule, CC10, were significantly elevated
in most (5 of 8) of the patients who improved following the treatment,
but in none (0 of 9) of the patients who failed to improve -- hinting
that CC10 can help patients improve.

The researchers now are working to determine which of the molecules in
their club cocktail are most important for inhibiting MDSCs and enhancing cancer treatments. They also plan to investigate whether these club cell molecules can inhibit MDSCs in other tumor contexts.

"We hope that these secreted molecules will be able to enhance treatments
not just for non-small cell lung cancer patients but for patients
with other cancers as well," said Dr. Gao, who is also a member of the
Meyer Cancer Center. "These molecules may also be useful as biomarkers predicting the response to combined radiotherapy and immunotherapy." ========================================================================== Story Source: Materials provided by Weill_Cornell_Medicine. Note:
Content may be edited for style and length.


========================================================================== Journal Reference:
1. Ban, Y., Markowitz, G.J., Zou, Y. et al. Radiation-activated
secretory
proteins of Scgb1a1 club cells increase the efficacy of immune
checkpoint blockade in lung cancer. Nat Cancer, 2021 DOI:
10.1038/s43018-021-00245-1 ==========================================================================

Link to news story: https://www.sciencedaily.com/releases/2021/09/210920113021.htm

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