Page 9 - N&V Winter 2019
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We found that patients with thickened  cancer are over-active and actually cause  that change the fats in the body.
       arteries had changes in the types of fat in  disease. From our previous research we  Following on from this discovery, we
       their blood and increased numbers of iNKT  know that an important factor that controls  thought that diet could be an important
       cells compared to patients with normal  immune cell behaviour is the amount of fat  therapeutic option for patients in order to
       arteries. Our results suggested that very  they have on their surface (the cell  control their risk of heart disease. We
       detailed analysis of blood fats and iNKT  membrane). We also know that the  therefore asked 300 patients about their
       cells could be used to predict the early  pathways controlling how much fat is  opinions on diet using an online survey
       signs of heart disease in lupus patients. This  produced by immune cells are disrupted in  promoted through social media. This data is
       work has been published in scientific  people with lupus. In this project we wanted  now published in Lupus (Robinson et al
       journals (Smith et al, Science Immunology,  to find out whether the defects identified in  2019) and the results highlighted a huge
       2016) and presented at scientific meetings  adult patients were also seen in patients  gap in dietary education for patients.
       as talks (5 national/international meetings)  with JSLE.               Patients feel it is important to know how
       and as posters (4 national/international  In the last 3 to 4 years we have been  diet can help their disease symptoms
       meetings).
                                           investigating a group of 65 young patients  however few patients receive clinical
       We are now continuing this work in a  with JSLE compared to age and sex  counselling regarding diet.
       number of ways: we are working to try to  matched teenage healthy controls. We
       identify a blood fat profile (unique to lupus  have performed a very thorough investi-  We now want to identify potential drugs or
       patients) that can be used in the clinic to  gation of over 44 different types of  dietary/life-style interventions for future
       predict increased risk of heart disease in  immune cells in the blood of patients and  clinical studies - tailored for patients
       adult patients. This will allow us to identify  controls. In particular, because JSLE is often  stratified for their cardiovascular disease
       patients that need specific advice and  diagnosed during puberty, we have been  risk that have different fat profiles. We will
       treatment in order to reduce their risk of  investigating the differences between  involve young people with JSLE with the
       heart disease. We are also investigating  immune cells from males versus females.  design of such studies and are already
       the causes of altered blood fats and how  We have identified several important  doing so through collection of food
       this can influence defects in the immune  differences and are still working to  frequency questionnaires in lupus clinics
       system in lupus patients. To carry out this  pinpoint the relationship between sex  and engagement events, including the
       work we have obtained grants from other  hormones, immune cells defects and fat  involvement of professional nutritionists.
       charities; including the University College  defects in JSLE patients. In particular we  Once we can understand the link between
       London Hospital Biomedical Research  are developing complex ways to analyse  fat levels in the blood and different
       Centre and from the pharmaceutical  the data in order to combine all the  disease features we can identify and
       company UCB Pharma. We now have a   detailed information that we have to  propose potential new treatments for JSLE
       research assistant and a new PhD student  improve our understanding of what goes  patients. This includes using drugs that
       working on this project.            wrong in patients and in the long term help  reduce fat levels such as statins, dietary
                                                                              supplements or life-style counselling. We
       In the second project, ‘Understanding  to improve treatments.          plan to use blood fat levels to match
       Immunopathogenesis of Juvenile onset SLE:  We know that heart disease is also a major  patients with the most appropriate therapy.
       could targeting lipids control disease  serious complication for patients with JSLE  We are already discussing ways to set up
       progression’ we collaborated with Dr John  (more so than in patients with adult onset  a clinical study to do this.
       Ioannou and Dr Coziana Ciurtin – Principal  disease). Therefore we have also  Understanding these differences could help
       Investigators in the Adolescent Centre for  performed a very detailed investigation of  develop more appropriate treatment
       Rheumatology Versus Arthritis at UCL.   over 200 different types of blood fat (as  options for JSLE patients, such as using
       This project was focused on investigating  described above for adult patients). We  drugs or diet to change the type of
       the immune cells and blood fats in lupus  identified that JSLE patients can be divided  particular fats that are contributing to
       patients diagnosed when they were   into three groups:                 immune cell defects in patients. We have
       children or adolescents (juvenile-onset SLE  Group 1: High bad fat;    presented this work as talks at a number of
       or JSLE). In young people the immune  Group 2: High good fat and       national and international scientific
       system is still developing; very little is  Group 3: low good and bad fat.   meetings, including the British Society for
       known about what goes wrong in patients  JSLE patients in each group had different  Rheumatology, the American College for
       that develop JSLE, whether the defects are  clinical and immune cell features. In  Rheumatology annual meetings and the
       the same as seen in adult disease and  particular, JSLE patients in Group 1 had  forthcoming EULAR 2019 meeting. Further
       whether the same treatments are relevant  markers associated with increased risk of  funding has been obtained from The
       for this group of young patients.                                      Rosetrees Trust and LUPUS UK to support
                                          cardiovascular disease (heart disease). Our
       In adult patients with SLE we know that  results suggest that we can use detailed  George Robinson to continue this work.
       many of the immune cells involved in  blood fat measurements to pinpoint JSLE                   Dr Liz Jury
       protecting the body from infections or  patients that would benefit from therapies
                                         OcTObER




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       luPus uK NEWS & VIEWS SUMMER 2019
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