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Revolutionizing cellular sorting to treat diseases: next generation of therapies become “magnetic” to the core

Revolutionizing cellular sorting

Scientists have developed a potentially transformative new technique that could aid in the discovery and development of new therapeutics for a number of globally prevalent autoimmune diseases. Conditions such as lupus, rheumatoid arthritis and Crohn disease are all caused by altered cytokine secretion of immune cells. To find treatments for such diseases, experts need to identify the genetic regulators of the secretion so they can explore the most effective ways of inhibiting them. An international team of researchers has developed a new method, referred to as Secretion-Enabled Cell Ranking and Enrichment (SECRE) and detailed in a paper published in Nature Biomedical Engineering. They have demonstrated the method is accurate in sorting hundreds of millions of CRISPR-edited cells based on their secretion patterns, and identifying the genetic regulators of cytokine secretion in an autoimmune condition.

In addition to this, the method takes into account the detailed profiles of approved treatments, and those under development, to establish if therapies already in existence can be reapplied in new ways. Writing in the study, the researchers detail how they have validated their approach on the cells known to play an essential role in the development and severity of IBD, and proved it has the potential of finding new ways of treating conditions that impact millions of people globally. The research is the result of a project lasting around four years between scientists in the UK, United States and Canada, world-leading experts in engineering new tools for the diagnosis and treatment of disease, led by Professor Shana Kelley, President of the Chan-Zuckerberg Institute and Professor at Northwestern University.

Dr Mahmoud Labib, Lecturer in the University of Plymouth’s Peninsula Medical School, and the main inventor of the approach, stated: This is an incredibly novel approach that can potentially deliver huge benefits for patients, clinicians and the drug companies working to establish new treatments. It gives us the ability to sort large number of cells based on their secretion patterns and identify therapeutic targets that could be applied to help those with conditions for which there are currently few therapeutic options. Through our existing work, we have demonstrated there is the potential for it to help identify ways of treating various autoimmune conditions, but my work is also now extending to types of cancer including some of the most aggressive types of brain tumors.”

How the SECRE technique works

The Secretion-Enabled Cell Ranking and Enrichment (SECRE) technique captures the secreted cytokine on the surface of the cell. These cytokines are then labelled with magnetic nanoparticles and sorted at high resolution within a microfluidic device, fabricated using scaled three-dimensional printing. The SECRE technique enables rapid and high-throughput sorting of cells based on their secretion patterns, which makes it amenable to large-scale functional genetic screens. This approach also links the functional signature of the cell with its phenotype, allowing for selective sorting of specific subsets of immune cells on the basis of specific cell-surface markers as well as the secretion specific factors.

A potential treatment for bowel diseases?

Inflammatory bowel disease (IBD) is a long-term health condition that has been estimated to affect around 7 million people worldwide. It is characterised by chronic inflammation of the digestive tract, which can result in severe pain and diarrhoea and, despite several medications, there is presently no known resolutive aid. As part of work to validate their approach, the researchers examined the effect of several kinase inhibitors on CD4+ T cells, which are known to produce IFN-gamma, a cytokine widely implicated in several autoimmune diseases including IBD. The inhibitors looked at included XMU-MP1, a small molecule that has previously been explored as a treatment for heart failure, hair loss and some other medical conditions.

In this instance, the researchers used XMU-MP1 to treat mice with a form of colitis that has a similar cell secretion profile to that found in humans with IBD. They found the mice experience significantly less weight loss and reduced colitis symptoms, while their colons remained virtually normal in appearance and did not show any significant loss of intestinal stem cells. Based on these findings, the researchers say their results suggest that using XMU-MP1 as a means to inhibit IFN-gamma production in the gut may represent an ideal means to control IBD. They also say it provides a promising future strategy for the therapeutic molecular targeting of the condition, although extensive clinical trials would be required before it could be considered as a treatment.

  • Edited by Dr. Gianfrancesco Cormaci, PhD; specialist in Clinical Biochemistry.

Scientific references

Labib M et al. Nat Biomed Engineer 2023 Nov 27; in press.

Chen K, Duong BTV et al. Nat Commun. 2023; 14(1):5576.

Wang Z et al. Nat Biomed Eng. 2023 Sep; 7(9):1188-1203.

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Dott. Gianfrancesco Cormaci
Dott. Gianfrancesco Cormaci
Laurea in Medicina e Chirurgia nel 1998; specialista in Biochimica Clinica dal 2002; dottorato in Neurobiologia nel 2006; Ex-ricercatore, ha trascorso 5 anni negli USA (2004-2008) alle dipendenze dell' NIH/NIDA e poi della Johns Hopkins University. Guardia medica presso la casa di Cura Sant'Agata a Catania. Medico penitenziario presso CC.SR. Cavadonna (SR) Si occupa di Medicina Preventiva personalizzata e intolleranze alimentari. Detentore di un brevetto per la fabbricazione di sfarinati gluten-free a partire da regolare farina di grano. Responsabile della sezione R&D della CoFood s.r.l. per la ricerca e sviluppo di nuovi prodotti alimentari, inclusi quelli a fini medici speciali.

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