Center for Vaccine Research 2017

Center for Vaccine Research 2017

Center for Vaccine Research

Center for Vaccine Research consists of Department of Infectious Disease Immunology and Vaccine Development. The Center is unique in its composition as it includes not only a basic and translational research department but also GMP facilities, animal testing facilities and has expertise that enables accelerated development of new vaccines. 

Center for Vaccine Research

The program in CVR currently has two TB vaccines in late stage clinical testing and different liposomal adjuvant formulations and a novel Chlamydia trachomatis vaccine in phase 1 trials. In collaboration with industrial partners, CVR as developed novel TB diagnostic tests (the IGRA assays) that are in widespread worldwide clinical use today and has recently completed developing a novel specific skin test reagent (C-TB) to substitute for tuberculin. 

Research Consortia

POR TB Consortium

Title: POR TB Consortium; Phase 2 trial to determine efficacy of the multistage vaccine H56:IC31 for Prevention of Recurrent TB disease

Objective: The project aims 1) to accelerate the clinical development of the leading TB vaccine candidate (H56:IC31) by conducting a phase 2 prevention of recurrent TB vaccine trial 2) to support capacity Development to expand TB vaccine clinical trial and Laboratory expertise in Sub-saharan Africa 3) to advance understanding of mechanisms of reactogenisity, immunogenicity and efficacy

Participants: The Aurum Institute, South Africa; Ospedale San Raffaele, Italy; University of Cape Town, SATVI, South Africa; Task Foundation NPC, South Africa; University of Cape Town, Lung Institute, South Africa; National Institute of Medical Research - Tanzania (NIMR); Areas Global Tuberculosis Foundation NPC, South Africa and Statens Serum Institut (SSI), Denmark

Funded by: The European & Developing Countries Clinical Trials Partnership (EDCTP)

EDCTP logoPOR TB Consortium logo

Contact: Rasmus Skaarup Mortensen, rjm@ssi.dk

A dual function TB subunit vaccine

Title: A dual function TB subunit vaccine designed for non-interference with BCG and post-exposure activity

Objective: The project aims to perform molecular modifications of a family of new vaccine candidates in order to enhance immunogenicity in vivo in preventive and post-exposure settings. Further the project will evaluate the modified vaccines in multiple novel advanced animal models of post-Mtb exposure and develop a GMP product towards clinical trial progression of the best vaccine candidate.

Participants: Staten Serum Institut (SSI,Denmark), Center for Infectious Disease Research (CIDR, USA), Public Health England (PHE)

Funded by: National Institutes of Health (NIH), USA

National Institutes of Health logo

Contact: Rasmus Skaarup Morten, rjm@ssi.dk

NeoPepVac

Title: Personalized cancer immunotherapy using adjuvanted Neo-epitope Peptide based Vaccines

Objective: The overall aim of the project is to generate personalized immune therapy vaccines that are likely to be highly efficacious in a large fraction of cancer patients and strengthen the effect of check-point inhibitors. The four specific objectives are: to develop personalized cancer vaccines based on peptides in combination with the CAF09b adjuvant designed to provide optimal immunotherapy through CTL induction to complete a phase l trial with neoepitope based immunotherapy in cancer patients and provide PoC for the overall strategy, safety and clinical feasibility improve prediction algorithms, through identification of neoepitopes using syngenic mouse models and in-depth analyses of immune reactivity in vaccinated patients to develop vaccine delivery strategies to broaden the neoepitope repertoire and increase the response and efficacy of the vaccine.

Participants: NeoPepVac is a Danish consortium comprising 4 partners, Statens Serum Institut, Evaxion Biotech, Technical University of Denmark and Herlev Hospital

Funded by: Innovation Fund Denmark

Innovation Fund Denmark Logo

Contact: Gabriel Pedersen, gakp@ssi.dk

TransVac2

Title: European Vaccine Research and Development Infrastructure

Objective: The objective of the Transvac2 consortium is to further advance the establishment of a fully operational and sustainable European vaccine R&D infrastructure. TransVac2 will support innovation for both prophylactic and therapeutic vaccine development based on a disease-overarching and one-health approach, thereby optimizing the knowledge and expertise gained during the development of both human and animal vaccines. Read more at www.transvac.org

Participants: TransVac2 is a European consortium comprising a comprehensive collection of 26 leading European institutions.

Funded by:European Union H2020

EU logo    TransVac2 logo

Contact: Gabriel Pedersen, gakp@ssi.dk Ida Svahn Rasmussen, idsr@ssi.dk

TBVAC2020

Title: Advancing novel and promising TB vaccine candidates from discovery to preclinical and early clinical development

Objective: TBVAC2020 aims to innovate and diversify the current TB vaccine and biomarker pipeline while at the same time develop new tools that allow us to select as early as possible the most promising TB vaccine candidates, and accelerate their development. TBVAC2020 proposes to achieve this by combining research activities e.g. vaccine discovery, new preclinical models addressing clinical challenges and identification and characterisation of correlates of protection with head-to-head comparative preclinical and clinical evaluation. Read more at www.tbvi.eu/for-partners/tbvac2020/

Participants: TBVAC2020 is an international consortium consisting 40 partners from Europa, Asia, Africa and Australia

Funded by: European Union H2020

EU logo TBVAC2020 logo

Contact: Rasmus Skaarup Mortensen, rjm@ssi.dk Gabriel Pedersen, gakp@ssi.dk

Eliciting lung-localized CD4 T cell responses against Mtb

Title: Eliciting lung-localized CD4 T cell responses against Mycobacterium tuberculosis in preventive and post-exposure settings

Objective: The project aims to elucidate basic mechanisms for how CD4 T cells can migrate into the lung tissue, how they are positioned relative to the infected areas (granulomas) and how they can be retained once there as well as be refractory to functional exhaustion during the chronic / latent phase of the infection. In addition, the project aims to develop vaccination strategies that optimally prime such protective CD4 T cells, regardless of previous exposure status to Mtb.

Participants: Center for Infectious Disease Research (CIDR) USA, Statens Serum Institut (SSI) Denmark University of Cape Town/SATVI, South Africa

Funded by: National Institutes of Health (NIH), USA

National Institutes of Health logo

Contact: Thomas Lindenstrøm, thi@ssi.dk