With the advancement in technology, changes have also come in the way of detection and treatment of diseases. Researchers in Sweden have developed computer models or "digital twins" with a goal to improve diagnosis and treatment. One such model was used to identify the most important disease protein in hay fever.
In studies it was observed that with common diseases, medication is ineffective in 40-70% of the patients. The conclusion was made that one reason for this is that diseases are seldom caused by s single "fault", which can easily be treated. In most diseases, the symptoms are the result of altered interaction between thousands of genes in many different cell types. It was added that the timing from evolution of the disease till the period taken for the symptoms to turn up plays an important role. In some cases, as the symptoms evolve late, the diagnosis becomes late, contributing to the insufficient medical efficacy.
In recent study, an international research team aimed to bridge the gap between the complexity and modern health care by constructing computational disease model of the altered gene interactions across many cell types at different time points. In a recent study, an international research team aimed to bridge the gap between this complexity and modern health care by constructing computational disease models of the altered gene interactions across many cell types at different time points.
The researchers' long-term goal is to develop such computational models into "digital twins" of individual patients' diseases. Such medical digital twins might be used to tailor medication so that each patient could be treated with the right drug at the right time. Ideally, each twin could be matched with and treated with thousands of drugs in the computer, before actual treatment on the patient begins.
The researchers started by developing methods to construct digital twins of patients with hay fever. They used a technique, single-cell RNA sequencing, to determine all gene activity in each of thousands of individual immune cells " more specifically white blood cells. Since these interactions between genes and cell types may differ between different time points in the same patient, the researchers measured gene activity at different time points before and after stimulating white blood cells with pollen.
The researchers started by developing methods to construct digital twins of patients with hay fever.In order to construct computer models of all the data, the researchers used network analyses. Networks can be used to describe and analyse complex systems. For example, a football team could be analysed as a network based on the passes between the players. The player that passes most to other players during the whole match may be most important in that network. Similar principles were applied to construct the computer models, or "twins", as well as to identify the most important disease protein. In the current study, the researchers found that multiple proteins and signalling cascades were important in seasonal allergies, and that these varied greatly across cell types and at different stages of the disease.
"We can see that these are extremely complicated changes that occur in different phases of a disease. The variation between different times points means that you have to treat the patient with the right medicine at the right time", says Dr Mikael Benson, professor at Linköping University, Sweden, who led the study.
At the end, the researchers identified the most important protein in the twin model of hay fever. They show that inhibiting this protein, called PDGF-BB, in experiments with cells was more effective than using a known allergy drug directed against another protein, called IL-4.
The study demonstrates that the methods could potentially be applied to give the right treatment at the right time in other immunological diseases, like rheumatism or inflammatory bowel diseases. Clinical implementation will require international collaborations between universities, hospitals and companies.
The study is based on an interdisciplinary collaboration between 15 researchers in Sweden, the US, Korea and China. The research has received financial support from the EU, NIH, the Swedish and Nordic Research Councils, and the Swedish Cancer Society.