RNA performs a number of biological duties, from delivering genetic information to manufacturing proteins. But RNA is also expelled from cells via cell death or active release, and can then find its way into blood plasma.
A Cornell-led collaboration developed machine-learning models that use these cell-free molecular RNA dregs to diagnose pediatric inflammatory conditions that are difficult to differentiate. The diagnostic tool can accurately determine if a patient has Kawasaki disease (KD), Multisystem Inflammatory Syndrome in Children (MIS-C), a viral infection or a bacterial infection, while simultaneously monitoring the patient’s organ health.
Inflammatory diseases are a particular threat to children because the symptoms – such as fever and rash – are generic, and the patients often get misdiagnosed. If not properly treated, MIS-C can cause swelling in the heart, lungs, brain and other organs. Similarly, KD – the primary cause of acquired heart disease in children – can lead to cardiac aneurysms and heart attack. A cell-free RNA-based test would be the first molecular diagnostic tool that clinicians can use to catch these inflammatory conditions at the crucial early stage in children.
The team’s paper, “,” published Sept. 6 in Proceedings of the ³Ô¹ÏÍøÕ¾ Academy of Sciences. The lead author is Conor Loy, Ph.D. ’24, who is currently an .
The Cornell team was led by , associate professor of biomedical engineering in Cornell Engineering, in collaboration with researchers led by Dr. Charles Chiu, a specialist in precision medicine for infectious disease with University of California, San Francisco, and Dr. Jane Burns, a expert on KD, with University of California, San Diego, the paper’s co-senior authors with De Vlaminck.
Their partnership grew out of a previous collaboration, supported by the ³Ô¹ÏÍøÕ¾ Institutes of Health (NIH), that began four years ago and used next-generation sequencing to characterize the severe cases of in children that spiked during the pandemic. Initially, De Vlaminck and Loy were focused on the potential of using cell-free DNA to investigate the diseases, but they found themselves increasingly interested in cell-free RNA, because of the rich information content it provides. While cell-free RNA has been shown to be an effective biomarker for pregnancy and cancer, it’s not as well studied as cell-free DNA.
“When you analyze RNA in plasma, what you’re looking at is RNA from dying cells, and also RNA that’s been released from cells anywhere in the body,” Loy said. “This gives you a huge advantage. In inflammatory conditions, there’s lots of cell death. Cells are, in some cases, exploding and their RNA gets released into plasma. By isolating that RNA and sequencing it, we can discover biomarkers for disease and backtrack where the RNA is coming from to measure cell death.”
The collaborators provided 370 plasma samples from pediatric patients with a range of inflammatory conditions. The team converted the RNA to DNA, then conducted DNA sequencing that analyzed the protein-coding regions of the genome. Loy spent a year experimenting with machine-learning algorithms to find disease signatures in the samples, basically creating a pipeline of different tools to make sense of cell-free RNA.
Beyond developing an accurate model for diagnosis, the researchers also demonstrated that cell-free RNA sequencing can be used to quantify injury to specific tissues and organs, including the liver, heart, endothelium, nervous system and the upper respiratory tract.
“I think a lot of the novelty and the technical innovation, the engineering, is in the data analysis,” De Vlaminck said. “We’re able to quantify how much of the RNA is coming from different organs. How much is coming from the liver, or epithelial cells in the vascular system. By quantifying the sources, we can also learn about injury processes that are likely immune-related but happening in vascularized tissues.”
At the same time, much about cell-free RNA is still unknown.
“We show that cell-free RNA is useful, but now we feel obligated to also understand a bit more about the biology of where the molecules come from, and perhaps more importantly, why you can reproducibly isolate them from plasma, and why they’re stable in plasma,” De Vlaminck said. “It’s because they’re protected. We think we’ve started to get a handle on that as well.”
Co-authors include Andrew Bliss ’24, research scientist Joan Lenz, research technician Emma Belcher; and researchers from University of California, San Francisco; University of California, San Diego; Children’s ³Ô¹ÏÍøÕ¾ Hospital, Washington D.C.; Rady Children’s Hospital-San Diego; Yale School of Medicine; and Emory University.
The research was supported by the NIH’s ³Ô¹ÏÍøÕ¾ Institute of Child Health and Human Development.
