Tandem Grants 2025-2026

The Tandem grant scheme aims to strengthen and support high-quality translational/clinical research at an international level. StratRegen invites collaborative project applications from a fundamental/pre-clinical researcher and a clinical researcher, with the goal of fostering the transition from basic research to clinical translation and vice versa.

The steering committee for SFO stem cells and regenerative medicine has decided to award 2 tandem grants for 2025 and 2026. 

Each grant has a value of 2 million SEK per year. 

 

Konstantinos Meletis & Per Svenningsson

Early diagnosis and gene therapy in Parkinson’s disease targeting a vulnerable dopamine neuron type.

 

Close-up portrait of Dinos Meletis
Dinos Meletis, Photo: Erik Flyg

 

This collaborative project aims to develop innovative diagnostics and gene therapies for Parkinson’s disease (PD) by targeting the most vulnerable dopamine neurons. The project will use adeno-associated virus (AAV)-based gene therapy to protect vulnerable Anxa1+ dopamine neurons from early degeneration and establish new biomarker assays from cerebrospinal fluid (CSF) and blood for diagnosis of prodromal PD.

Per Svenningsson
Per Svenningsson, Photo: Andreas Andersson

 

By integrating basic neuroscience and clinical neurology, this collaboration will bridge molecular and circuit discoveries with patient applications, with the potential to establish new diagnostic tools and cellular strategies to prevent disease progression.

Image from the mouse brain showing genetically labeled sensitive dopamine neurons (yellow signal) epressing the Anxa1 marker (purple signal), compared to all dopamine neurons (blue signal).
Image from the mouse brain showing genetically labeled sensitive dopamine neurons (yellow signal) epressing the Anxa1 marker (purple signal), compared to all dopamine neurons (blue signal). Photo: Dr. Ioannis Mantas

 

More research is performed in Konstantinos Meletis´s and Per Svenningsson´s groups. 

 

 

Andrea Ponzetta & Magnus Tobiasson

Investigating Post-Transplant Relapse Mechanisms in Myelodysplastic Syndrome

 

Andrea Ponzetta
Andrea Ponzetta Photo: N/A

 

Our research explores the cellular and molecular dynamics underlying relapse in myelodysplastic syndrome (MDS) patients following allogeneic hematopoietic stem cell transplantation (HSCT). Using single-cell RNA sequencing (scRNA-seq), CITE-seq, and T-cell receptor sequencing (scTCR-seq), we characterize the reconstitution of hematopoietic stem and progenitor cells (HSPCs) and immune subsets. 

Portrait of Magnus Tobiasson
Magnus Tobiassion Photo: N/A

 

Our prospective clinical trial evaluates preemptive treatment of molecular relapse with Azacitidine to mitigate disease progression while assessing its impact on the graft-versus-leukemia (GvL) effect. In addition, we study the combined effect of Azacitidine and Venetoclax in patients with clinical relapse. By leveraging a unique biobank of serial patient samples, we aim to refine relapse intervention strategies and improve post-HSCT therapeutic outcomes.

Project description Tandem grant Ponzetta Tobiasson
Project description Photo: N/A

 

More research is performed in Andrea Ponzetta´s and Magnus Tobiasson´s groups

Content reviewer:
Daniel Holl
09-02-2025