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Peer Reviewed Publication: World's first demonstration of cross species epigenetic transfer that significantly reverses biological age by Scientists at Yuvan Research. MOUNTAIN VIEW, Calif., Nov. 1, 2023 /PRNewswire/ -- In a groundbreaking research paper titled "Reversal of Biological Age in Multiple Rat Organs by Young Porcine Plasma Fraction" published in GeroScience, scientists have unveiled a remarkable breakthrough in the field of aging biology. A therapeutic called E5 developed by Harold Katcher PhD and his colleagues was injected into old rats making them significantly younger within days. E5 consists of nanoparticles of complex structure, including exosomes, from young plasma sourced from another species. Steve Horvath, PhD, formerly a Professor of Genetics and Biostatistics at UCLA played an instrumental role in this study with his invention of epigenetic clocks, which determine biological age using DNA samples. Horvath remarked, "Initially, I could hardly believe the profound epigenetic rejuvenation effects of E5. However, our findings are robustly supported by parallel rodent studies from different labs." Upon final analysis by Horvath and his team, there was a remarkable 67.4% average reversal in the epigenetic age of treated elderly rats. If these results translate similarly to humans, it could equate to an 80-year-old reverting to the age of 26. Two unlikely co-founders Harold Katcher and Akshay Sanghavi embarked on an impossible quest 5 years ago to 'cure' aging. Sanghavi, having lost his mother to diabetes, was researching aging from 12 years and had set up trials to upregulate repair pathways that go down with age. He came across Katcher's 2013 paper on Heterochronic Plasma Exchange and reached out to him to join his small team. The rest, as they say, is history. Their venture Yuvan Research is in Mountain View, California. Another aging clock confirmed Horvath results, GlycanAge developed by Professor Gordan Lauc also showed age reversal of around 50%. Lauc said, "Human studies clearly demonstrated that glycans are very responsive to different interventions, but changes are usually relatively slow and not too extensive. Dramatic reduction in glycan age of rats treated with E5 is fascinating." Michael Snyder, Chair of the Department of Genetics and Professor of Genetics at Stanford University who did not participate in this study but sits on the Scientific Advisory Board of Yuvan Research said, "The results are stunning and have enormous potential, not just for humans, but also for animals including pets." SOURCE Yuvan Research Inc.

DECODE Platform Identifies Immunodominant Epitopes From E1 and E2 HPV Antigens That Drive Cytotoxic Response in Early and Relapsed/Refractory Cases of HPV 16-Positive Oropharyngeal Squamous Cell Carcinoma (OPSCC) Increased Prevalence of Difficult to Treat HPV 33-Positive Oropharyngeal Squamous Cell Carcinoma Was Observed and Characterized by Fewer Cytotoxic CD8+ T cells and Deficient Epitope Presentation, Potentially Contributing to Inferior Outcomes with Current Treatments CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Repertoire® Immune Medicines presented research today conducted with the company’s proprietary DECODE™ platform, which characterizes the cellular response to disease, identifying novel therapeutic targets in human papillomavirus (HPV) 16 and HPV 33-positive tumors. This research is part of Repertoire’s collaboration with Dana-Farber Cancer Institute to advance discovery and development of treatments for HPV-positive oropharyngeal (head and neck) cancers and was presented at the Society for Immunotherapy of Cancer (SITC 2022) 37th Annual Meeting, in Boston. “One of the growing challenges in HPV-positive cancer treatment is that we are observing an increase in the prevalence of HPV high-risk genotypes associated with worse outcomes,” said Glenn J. Hanna, M.D., director of the Center for Salivary and Rare Head and Neck Cancers at Dana-Farber Cancer Institute.1 “The research we conducted with the DECODE platform suggests that current treatments may not be targeting some key antigens active in these genotypes, which has significant implications for patient treatment. Importantly, we now have data that point to antigens active in driving these malignancies, which we can use to develop novel targeted medicines.” The DECODE platform is a suite of integrated experimental and computational technologies designed to decipher the immune synapse, the complex interface between T cells and the epitopes they recognize. DECODE is being used to assess the immunogenicity pro HPV 16 and HPV 33-positive tumors in oropharyngeal squamous cell carcinoma (OPSCC). By characterizing the cellular response to these cancers, it is possible to identify the specific epitopes eliciting the strongest T cell activity in tumors and the associated T cell receptors (TCRs) binding those epitopes, identifying what may be ideal targets for immunotherapies. “Using the DECODE platform, we have a window into the mechanisms involved in the immune surveillance of cancer, which offers us the ability to develop highly selective immune-based medicines,” said Anthony Coyle, Ph.D., President, Research and Development, Repertoire Immune Medicines. “The data we presented today from our DECODE platform illustrate the immunogenic pro HPV 16 and HPV 33-positive tumors, providing us with insights into the specific epitopes that are drivers of these cancers and are targets for new immunotherapies.” HPV infection is a risk factor for several cancers, including OPSCC. Many therapeutic approaches for OPSCC target the epitopes from E6 and E7 antigens of HPV; however, these treatments are not successful for every patient and new approaches based on highly prevalent immunodominant epitopes in both early-stage and relapsed/refractory patients may offer more effective treatment for certain genotypes of HPV-positive OPSCC. DECODE Discovery in HPV 16 and HPV 33-Positive Oropharyngeal Squamous Cell Carcinoma In order to better characterize the cellular response to HPV-positive OPSCC across common human leukocyte antigen (HLA) haplotypes, biopsies were collected from patients with HPV 16-positive or HPV 33-positive OPSCC. All samples were assessed using the DECODE platform. In patients with HPV 16-positive tumors, effective cytotoxic responses were induced by antigens E1 and E2 of HPV, which were substantially greater than the response driven by E5, E6 and E7. These findings suggest HPV 16 E1 and E2-directed immunotherapy may be effective among patients with HPV 16-positive OPSCC expressing these antigens. HPV 33-positive OPSCC is characterized with an inferior survival rate compared to HPV 16-positive head and neck cancers. To better understand the potential reasons for this difference in outcomes, a comparison of the immunogenic pro HPV 16 and HPV 33-positive tumors was conducted with DECODE. HPV 33-positive tumors in this research had fewer cytotoxic CD8+ T cells and fewer activated antibody-secreting B cells compared to HPV 16-positive tumors. In addition, the HPV 33-positive tumors had poor antigen presentation and deficient HPV E7 recognition by T cells. Both genotypes of OPSCC are typically treated with the same standard of care, but the differences observed in the HPV 33-positive tumor composition and cellular phenotype would be expected to lead to a poor immune response and may be the cause of the inferior treatment outcomes observed in the population of patients with this tumor genotype. Additional detail from this ongoing research is included in Poster #86, HPV16 E1 and E2 elicit a robust cytotoxic immune response in virally driven Oropharyngeal Squamous Cell Carcinoma, and in Poster #1404, HPV33-driven Oropharyngeal Squamous Cell Carcinomas are increasing in prevalence and are characterized by low CD8 infiltration and epitope presentation deficiencies. These data, as well as the company’s early research in targeting interleukin-2 (IL-2) to solid tumors, will be presented during the poster session at the SITC congress on Thursday, November 10, through Friday, November 11, 2022, 9:00 a.m. – 9:00 p.m. EST. About the DECODE™ Platform The DECODE platform is a powerful discovery engine that characterizes essential elements of the immune synapse. In particular, the platform identifies T cell receptor-antigen pairs in the context of other important features of the immune synapse, such as T cell function and how antigens are presented by molecules on antigen-presenting cells, known as major human leukocyte antigen, or HLA, molecules. Repertoire intends to utilize these insights into key drivers that govern immune function to design and develop novel immune product candidates. About Repertoire® Immune Medicines Repertoire Immune Medicines is a biotechnology company dedicated to creating treatments for diseases based on the power of the human T cell repertoire to eliminate cancer cells, target pathogens and regulate immune function in autoimmune disease. Our proprietary DECODETM platform is designed to provide a comprehensive understanding of the full repertoire of interactions between T cell receptors and their antigen targets that take place when diseased cells are present. This complex and intricate biological process is known as the immune synapse. We believe the ability to decipher these interactions represents one of the greatest opportunities for innovation in medical science. Utilizing our DECODE platform, our goal is to identify the specific T cell-antigen pairs that provide immune surveillance in cancer, generate memory responses to pathogens, and those that cause tissue damage in autoimmune disease. Repertoire was founded in 2019 by Flagship Pioneering. Its team operates from sites in Cambridge, Massachusetts and Zurich, Switzerland and uses its DECODE technology to rationally design treatments for cancers, autoimmune disorders and infectious diseases. To learn more about Repertoire, please visit our website: and follow us on LinkedIn and Twitter. 1. Dr. Glenn Hanna receives research support from Repertoire Immune Medicines through Dana-Farber Cancer Institute.