Active Infection & Immunity Cancer

The Nanoscale Phenotype of Immune Responses in Health and Disease

In plain English

AI plain-English summary

A single immune cell’s surface is a crowded, nanoscale landscape of receptors and protrusions that determines whether it kills a cancer cell or leaves it alone—and that landscape may look radically different in a sick person versus a healthy one. This matters because current models of immunity focus mostly on which receptors are present, not how they are arranged or how the cell moves. The team will compare Natural Killer (NK) cells from healthy donors and cancer patients, tracking every step of the kill process: initial contact, synapse assembly, release of lethal proteins, detachment, and re-engagement with a new target. They will use super-resolution microscopy to map receptor organisation and secretion patterns at the single-cell level. If successful, this fundamental science could reveal entirely new mechanisms of immune failure in cancer—for example, that a receptor is present but mis-clustered, or that a cell cannot detach to attack again. Such insights would open new avenues for drug design, beyond simply blocking or activating receptors. The work is curiosity-driven, but past discoveries about NK cell biology have already spawned cancer immunotherapies now in clinical trials.

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Familiarity with the body's response to a cut or an infection - redness, tenderness and inflammation - belies the wonders taking place, where swarms of different cells move in to fight off germs, as well as repair the damage and deal with the debris. Far from conscious control, this reflex is essential for our survival. A simple view of this is that the immune system attacks germs which invade the body opportunistically. But over the last few decades, a painstaking, game-changing scientific adventure unfolded in which the world of immunity has opened up for what it really is: not simply a few types of immune cells which attack germs, but a multi-layered, dynamic lattice of interlocking sub-systems, one of the most complex and important frontiers of scientific enquiry we know of. Advances in technology are helping us understand the immune system as never before, and to develop medicines which boost the system to fight cancer better, to dampen it to combat the symptoms of auto-immune disease, and to help develop better vaccines. Activating and inhibitory receptors on the surface of immune cells are critical determinants of immune activity. The level of each receptor and its ligand, and how well they bind, are primary determinants of disease outcomes. However, advances in microscopy are now revealing a host of other factors which control immune responses. This includes protrusions from immune cells which contact other cells, a complex nanoscale organisation of activating and inhibitory receptors, clusters of proteins secreted by immune cells to kill diseased cells, and novel mechanisms by which immune cells can detach from one target cell to attack again. Understanding immunity on a nanoscale is a major new frontier and will lead to completely new ideas for medicine. My own research laboratory has decades of experience studying human immune cells called Natural Killer (NK) cells. These immune cells are able to directly kill cancer cells, and are a hot topic in developing new cancer therapies. NK cells are also important in viral defence, microbial pathogens, autoimmune diseases, reproductive complications and transplantation. Their activation is regulated by many activating and inhibitory receptors at their surface. However, the central tenet of this proposal is that their activity is also influenced by nanoscale processes, beyond simple ligation of receptors. For example, the presence of a receptor may remain similar in health and disease, but its nanoscale organisation can be altered to affect its activity. Also, it is entirely unexplored whether or not disease impacts NK cell protrusion density or the capacity of NK cells for serial killing, and so on. Indeed, nanoscale processes which regulate NK cells (and other immune cells) may be a major factor missing in our understanding of health and disease. Here, we will compare NK cells from healthy donors and cancer patients, assessing every stage of their interaction with a cancer cell on a nanoscale - from an initial cell-cell contact to the assembly of a synapse, release of effector particles, subsequent detachment and serial engagement. Activating and inhibitory receptors will be mapped to understand signal integration and immune response thresholds, the structure and function of immune cell secretions will be analysed, and determinants of cell detachment and serial killing will be determined, and then compared in health and disease. Single cell secretions, visualised by super-resolution microscopy, will lead to a new approach to characterising immune responses. We will also compare types of NK cell. For example, it is entirely unexplored if memory-like NK cells exhibit faster interaction dynamics and greater serial killing. A large consortium of collaborators will facilitate this complex interdisciplinary endeavour, from using new instrumentation, developing image analysis and access to clinical samples. Strong links to industry will translate these new ideas to medicines.

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Researchers

Daniel Davis (Principal Investigator)

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Peptide-Specific Natural Killer Cell Receptors in Health and Disease
The supramolecular dynamics of human immune cell recognition and communication
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Original classification

Research Grant

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