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EpitoGenesis, Inc. is a biotechnology company, which was established in November of 2008, to design and develop all natural efficacious immune enhancing adjuvants and delivery systems for prophylactic and therapeutic vaccines with strong emphasis on safety. Our goal is to eliminate vaccination side effects such as site of injection pain and swelling, fever, etc.

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Who We Are

Our passion for creating meaningful change for clients is what sets us apart. The Startup Savvy staff believes in the potential of our great idea, and it truly shows in all of our work. Our team works tirelessly in order to bring you a better tomorrow. To learn about our super stars individually, please have a look below.


Co-Founder & Partner

Entrepreneur with several years of experience from the financial industry, and over ten years of experience in the biotech arena. Her creative mindset challenged the traditional approaches to vaccine design. Through her leadership the NIDS technology was validated through non-dilutive competitive government grants and awards.



Dr. Houghton was formerly CSO of Epiphany Biosciences and head of Virology at Chiron Corporation. He is currently Canada Excellence Research Chair in Virology, and Professor at the Department of Medical Microbiology and Immunology at the University of Alberta, Canada.
Dr. Houghton and his Chiron colleagues were the first to identify the hepatitis C virus (HCV) in collaboration with the CDC. Their discovery led to a series of HCV tests that are now used globally to screen the blood supply to prevent infection. Their work also led to the identification of important new anti-HCV drug targets. For this work, Dr. Houghton received the Albert Lasker Prize in 2000 as well as numerous other awards from various countries and organizations throughout the world. More recently, Dr. Houghton has focused on vaccine approaches to hepatitis C, including strategies for immunotherapy of this viral disease.
In addition to HCV, Dr. Houghton's group was the first to characterize the hepatitis D virus (delta virus). He has published over 200 articles in the fields of gene regulation, human beta interferon and hepatitis C and D viruses. He also holds numerous patents issued in the fields of recombinant human interferons, bacterial expression vectors, and hepatitis C and D viruses.



Dr. Jan Holmgren, MD, PhD is Professor of Medical microbiology and immunology at University of Gothenburg, Sweden, a chair he took over in 1980 after Prof. Örjan Ouchterlony; he is also Director of the Göteborg University Vaccine Research Institute (GUVAX). JH has published more than 500 papers in the fields of microbiology, immunology and vaccinology, and he is an elected member of various societies and academies including e.g. the Swedish Royal Academy of Science and the Swedish Royal Academy of Engineering. He has also served on many national and international boards, e.g. on the Board of Directors of the Knut and Alice Wallenberg Foundation (Sweden), the International Vaccine Institute (IVI), and the Global Alliance for Vaccines and Immunization (GAVI), and he is a member of several international vaccine-related technical task forces or steering committees. After completing his PhD thesis on urinary tract infection immunology in 1969, a large part of JH´s research has been focused on the mechanisms of disease and immunity in cholera and other mucosal infections and on the development of mucosal vaccines. In his early work on cholera, JH discovered, for instance, both the AB subunit structure and function of cholera toxin and the GM1 ganglioside as the cholera toxin receptor. JH and his coworkers have also made many important contributions in mucosal immunology and in the development of mucosal vaccines and adjuvants. They have developed and taken the oral B subunit-whole cell cholera vaccine all the way from basic concept to an internationally widely registered product, they have developed and taken an oral ETEC vaccine from concept to phase 3 trials, and they have pioneered the development of methods for assessment of mucosal vaccine immunogenicity in humans. In more basic aspects of mucosal vaccinology, JH´s laboratory has made important contributions in mucosal adjuvant construction, in defining basic mechanisms of mucosal immune regulation, and in developing promising mucosal immunomodulating/tolerogenic vaccine therapies against autoimmune and allergic diseases, the latter based on JH´s and Cecil Czerkinsky´s discovery of cholera toxin B subunit as a uniquely efficient combined carrier and immunomodulator for inducing peripheral T cell tolerance to chemically or genetically conjugated tissue antigens or allergens. JH has received numerous major scientific prizes and other distinctions for his research contributions, e g The Royal Swedish Academy of Science Prize in Medicine for 1977 (“Hilda and Alfred Erikssons pris”); The Anders Jahre Prize II (young scientists) in Medicine for 1982 (Norway); “Söderbergska Priset” (biggest Prize of The Swedish Medical Society) for 1994 ; The Louis Jeantet Prize for Medicine for 1994 (Switzerland); The Eric K. Fernström Big Nordic Prize in Medicine 2004 (Lund University, Sweden); and The International Society for Mucosal Immunology “Distinguished Science Achievement Award 2007 “ . JH and his laboratory are extensively involved in collaborations with many international research institutions and programs, e.g. IVI, WHO, GAVI, and ICDDR,B (Bangladesh) and EU´s MUVAPRED program for mucosal vaccines



A French immunologist, Dr. Czerkinsky joined the International Vaccine Institute as the Deputy Director-General for Laboratory Sciences in October 2005. Before joining the IVI, Dr. Czerkinsky has been serving as the Director of the Division of Mucosal Immunology and Vaccinology at INSERM (French National Institute of Health and Medical Research) since 1997, focusing on vaccine research and discovery of the basic mechanisms governing induction of immunity in mucosal organs. Dr. Czerkinsky received doctoral degrees from the University of Lyon Odontology Faculty in France, and the University of Gothenburg in Sweden where he served as a professor of the immunology. He has more than 130 scientific peer-reviewed publications in immunology and vaccinology. Dr. Czerkinsky invented the ELISPOT, a method for monitoring immune responses in humans and animals, which is used in laboratories world-wide. His work has been focused on basic immunological mechanisms pertaining to vaccine development against infections, auto-immune disorders and allergies. Dr. Czerkinsky holds several patents in these areas. 

He is a co-founder of several biotechnology companies, including Maxim Pharmaceuticals Inc., a U.S. biopharmaceutical firm devoted to the development of therapeutic drugs for cancer and liver diseases.

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Advanced Solutions

For every simple solution released into the market, there’s a great amount of technology that must be either invented or adapted for that purpose, and Epitogenesis is no exception. Continue reading and learn all there is to know about the smart tech behind our successful Biotechnology Startup.

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Vaccines are the single most cost-effective medical interventions. Vaccines have eliminated many infectious diseases completely which only decades ago caused serious morbidity and mortality.

Since the days of Luis Pasteur, over a century ago, vaccine developers have continued to focus on live attenuated viruses and bacteria and chemical structures that induce strong pro-inflammatory immune responses. However, these very same responses are responsible for unwanted side effects.

To make safe vaccines using non-living, non-replicating vaccines, parts of a pathogen, e.g. a surface protein, can be engineered by recombinant technology. However, most such proteins cannot be used as standalone vaccines and need to be mixed with vaccine adjuvants (helpers) and delivery systems to enhance the immune responses against them.

Our patented Nutritive Immune-enhancing Delivery System (NIDS), is based on the surprising immunomodulatory synergy between select vitamins (e.g. A and E) and a class of naturally-occurring polyphenols, i.e. flavonoids that are found in vegetables, herbs and fruits.  The NIDS formulation contains these active ingredients which are produced as an oil in water nano-emulsion, using either natural seed oils or fatty acid blends. All the NIDS compounds are natural are chemically well-defined and can be cGMP-manufactured.  Moreover, the manufacturing process is simple and inexpensive.

We have demonstrated in preclinical studies that our NIDS-based vaccines against HIV-1 induced strong immune responses with significantly lower early innate pro-inflammatory responses compared to licensed and competitor vaccine adjuvants and delivery systems, while being more efficacious. Please see our peer-eviewed publications under the NEWS page.

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