Uncovering the mechanisms underlying lack of response to immunotherapy

Immune cells surrounding a tumour with clonal neoantigens
Credit: Karen Arnott/EMBL-EBI

New research improves understanding of the molecular mechanisms behind why some cancers respond to immunotherapy and others don’t.

A new study has shed light on why immunotherapy does not always work in certain types of cancer. Led by researchers at EMBL’s European Bioinformatics Institute (EMBL-EBI), Cold Spring Harbor Laboratory (CSHL), and the Massachusetts Institute of Technology (MIT), the work focuses on understanding why some tumours fail to respond to immune checkpoint blockade (ICB) therapy, an approved immunotherapy that harnesses the power of the patient’s immune system to target and destroy cancer cells.

ICB has transformed the treatment landscape for cancer patients. Response rates range between 15% and 60%, but it is still unclear why some patients do not respond. Understanding what happens at the cellular level could help clinicians predict which patients are more likely to respond and guide treatment decisions. ICB is known to be most effective in DNA mismatch repair deficient (MMRd) tumours, but still only half of the MMRd tumours respond to ICB, and among responders, many will unfortunately relapse. This study looks at the complex mechanisms underlying response to ICB in patients with MMRd tumours.

ICB functions by obstructing an immune checkpoint – a signal exploited by cancer cells to stop the immune system from detecting the tumour through the high number of mutations found within these cancer cells. Such mutations can serve as cues that enable the immune system to identify and combat the tumour. In the context of ICB, weaker mutation signals lead to a diminished response to treatment because the immune system has a harder time finding and recognising the cancer cells.

The findings of this study, published in the journal Nature Genetics, highlight the pivotal role played in this process by intratumoral heterogeneity.

“This is an important body of work that provides new insights into the factors that control immune responses against cancer and why some tumours fail to respond to immune-stimulating therapies,” said Tyler Jacks, Professor at the Koch Institute at MIT.

“One way to picture this is to imagine a crowd, where each person is holding a yellow flashlight,” explained Isidro Cortes-Ciriano, Research Group Leader at EMBL-EBI. “If everyone turns on their flashlight, the beam of yellow light can be seen from far away. Similarly, the more cells with the same mutations in a tumour, the stronger the signal and the more likely to trigger an immune response. However, if each person in the crowd has a different coloured flashlight, the light emanating from the crowd is less clear, and the signal becomes jumbled. Similarly, if cancer cells have different mutations, the signal is harder to make out and the immune system is not triggered, so ICB doesn’t work.”

Understanding immunotherapy response 

ICB has shown remarkable efficacy in tumours with a high number of mutations, In particular, this applies to tumours with clonal neoantigens. Clonal neoantigens occur when identical mutations are present across all cells of a tumour. Despite this, less than half of MMRd tumours show long-lasting response to ICB, posing a significant challenge in optimising treatment.

This study dissects the molecular mechanisms causing resistance to ICB in MMRd tumours and shows that intratumoral heterogeneity – a wide variety of mutations spread across the tumour – dampens the immune response, leading to diminished effectiveness of the ICB treatment.

“Our goal was to unravel the mystery of why certain tumours, which should respond to immunotherapy, do not,” said Peter Westcott, Assistant Professor at Cold Spring Harbor Laboratory, former Postdoctoral Researcher at MIT. Regarding the tumours in their study, Westcott said, “There’s no question these tumours are MMRd, yet they’re not responding. That is a profoundly interesting negative result. By studying the mechanisms behind this resistance, we can pave the way for the development of more effective and personalised treatment strategies.”

Improving clinical practices

The findings of this study provide a means to identify which patients are more likely to benefit from ICB treatment, highlighting the need for personalised treatment approaches. In their investigation, the researchers used mouse models to demonstrate that inactivation of MMR is not enough to improve patient responsiveness to ICB.

“Our understanding of cancer is improving all the time, and this translates into better patient outcomes,” added Cortes-Ciriano. “Survival rates following a cancer diagnosis have significantly improved in the past twenty years, thanks to advanced research and clinical studies. We know that each patient’s cancer is different and will require a tailored approach. Personalised medicine must take into account new research that is helping us understand why cancer treatments work for some patients but not all.”

Access to clinical data

The study used preclinical models, including mouse models and cell lines, as well as clinical trial data from colon and gastric cancer patients, to study and analyse tumour responses to ICB.

Using clinical data, the researchers observed that colon and stomach tumours with a diluted mutational signal caused by intratumoral heterogeneity displayed reduced sensitivity to ICB treatment. This finding also suggests that identifying the level of signal strength in individual tumours could help predict a patient’s response to ICB in the clinic.

“One of the major challenges of the study was getting access to clinical trial data,” explained Isidro Cortes-Ciriano. “This highlights once again how important it is for research data to be accessible via secure mechanisms so it can be reused to uncover new insights and improve our understanding of disease.”

Journal: Nature Genetics
DOI: 10.1038/s41588-023-01499-4
Method of Research: Meta-analysis
Subject of Research: People
Article Title: Mismatch repair deficiency is not sufficient to elicit tumor immunogenicity
Article Publication Date: 14-Sep-2023

Media Contact

Victoria Hatch
European Molecular Biology Laboratory
Cell: 07411495115


Media Contact

Victoria Hatch
European Molecular Biology Laboratory

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