Targeting NK cells may mean more effective immunotherapy in resistant tumours

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CD45 immune cells (green) are unable to penetrate the tumour bed (red). Photo: VIB.

Researchers at the VIB-KU Leuven Center for Cancer Biology have uncovered that ‘natural killer’ cells (NK), a type of immune cell, may actually be hindering the immune system’s ability to attack tumours in patients who don’t respond to immune checkpoint blockade therapies (ICB), a form of immune therapy.

The findings of the study have been published in Cancer Discovery, a journal of the American Association for Cancer Research.

Melanoma, one of the deadliest forms of skin cancer, affects an estimated 330,000 people worldwide each year and causes nearly 60,000 deaths annually. While early-stage melanoma is one of the most curable cancers, later-stage melanomas can present significant difficulties in treatment due to therapy resistance. Even though immune therapy treatments such as immune checkpoint blockade (ICB) therapies have transformed cancer treatment, around half of patients with advanced melanoma do not respond to these therapies.

Now, a study conducted by researchers from the VIB-KU Leuven Center for Cancer Biology uncovered that ‘natural killer’ (NK) cells may actually be contributing to tumor resistance in patients who don’t respond to ICB.

In the study, led by Jean-Christophe Marine, researchers collected tumor biopsies from melanoma patients both before and shortly after initiating ICB therapy. Using advanced spatial omics technology, they precisely mapped the location of different immune cells within the tumor microenvironment. Strikingly, they found that in patients who did not respond to treatment, there was a significant early increase in cytotoxic NK cells. However, these cells were positioned at the tumor’s periphery rather than infiltrating its core. In contrast, tumors that responded to ICB therapy showed a different immune landscape, with NK cells located inside the tumor bed alongside CD8 T cells, the immune system’s primary tumour-attacking cells.

“We were surprised to find that NK cells, traditionally seen as allies in the fight against cancer, can, in certain contexts, actually prevent T cells from doing their job,” said Joanna Pozniak, first author of the study.

“It challenges how we think about the immune landscape of tumors and points to new, actionable targets for patients who currently have few options.”

To further investigate why NK cells were acting in this manner, the team developed a mouse model in which immune cells were unable to infiltrate melanoma tumours – just like seen in many patients resistant to ICB immunotherapy – and where they could pharmacologically deplete NK cells. The result: CD8 T cells were suddenly able to infiltrate the tumour core and the tumour was cleared once ICB was administered. Additionally, further analysis revealed that NK cells are actively recruited to block access to the tumor via the CX3CR1 chemokine receptor.

“We did not expect to find that NK cells were acting like gatekeepers for T cells,” said Jean-Christophe Marine, director of the VIB-KU Leuven Center for Cancer Biology.

“Blocking their ‘key’, the CX3CR1 signal, may offer a new therapeutic avenue to sensitize tumours to ICB treatment.”

The study, which was published in the journal Cancer Discovery, is a direct result of the Pointillism project, an initiative under the umbrella of VIB’s Grand Challenges Program. The goal of the project was to apply single-cell multi‑omics and spatial profiling to dissect the cellular and molecular landscape of tumours with high precision. In its first phase, the project identified candidate biomarkers that may predict which melanoma and breast cancer patients respond to immune‑checkpoint blockade (ICB) therapy.

In a next phase, the newly launched Pointillism 2.0 project will look at validating and combining biomarkers to develop a high-performance biomarker panel, potentially in the form of a blood test, to quickly and accurately determine a patient’s likelihood of responding to ICB.

“We hope that our work will unlock ICB treatment for more patients in the future,” Marine said.

“While cancer treatments have advanced significantly over the past decades, many challenges remain. That’s why we keep on looking for new ways to help patients overcome their cancer.”

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Jim Cornall is editor of Deeptech Digest and publisher at Ayr Coastal Media. He is an award-winning writer, editor, photographer, broadcaster, designer and author. Contact Jim here.