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Lund University

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Sara Ek

Molecular investigations of mantle cell lymphoma and development of companion diagnostic tools

 

The proposed translational project address crucial, specific clinical questions for mantle cell lymphoma patients at distinct stages of the course of disease, such as diagnosis, upon treatment resistance and at relapse. Advanced technologies will be used and combined to pin-point the association between molecular, cellular and clinical parameters with the ultimate goal of developing tools for companion diagnostics.

 

B cell lymphomas are malignancies where much remains to be achieved in terms of improved treatment. While some subtypes have quite indolent features and good prognosis, others are related to an aggressive clinical course and have only a few years of median survival time. One of the subtypes with the poorest survival is mantle cell lymphoma (MCL), which constitute 6-7% of B cell lymphomas. To enable prolonged survival, early specific diagnosis followed by an aggressive treatment protocol is required. However, despite recent advances, typical MCL patients have a relative poor prognosis with 33% of younger patients surviving for less than five years. Lately, these patients have commonly been treated with combinations of regiments, most often including Rituximab (anti-CD20) in combination with chemotherapy. However, several experimental protocols include very promising new targeted therapies, such as mTOR and BTK inhibitor, and also epigenetic drugs, for example Decitabine and Valproate. The number of potentially effective drugs increases the complexity of designing and evaluating novel clinical protocols for MCL, and companion diagnostic biomarkers/tools for treatment selection in both the front-line and relapsed setting are much needed.

The specific aims of the project are to:

  1. At diagnosis: Identify, characterize and validate companion diagnostic biomarkers to allow future prospective stratification of patients into modern combinatorial treatment protocols, such as the Nordic MCL2/3 protocol.
  2. Upon treatment resistance: Investigate/address the molecular mechanisms responsible for development of resistance to the nucleoside analogues Cytarabine, and identify predictive markers.
  3. At relapse: Identify cellular and molecular markers to predict outcome of patients treated with targeted therapy, to allow optimal treatment selection (Nordic MCL6/Philemon protocol).

 

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Patient stratification through affinity-based proteomics of liquid and tissue biopsies

Patient stratification in relation to therapy in and outside clinical trials is a major challenge. Treatments are costly and associated with major side-effects. Increasing the precision in this selection of drugs is a fundamental question to solve within clinical oncology. The challenge lies in the heterogeneity of the individual tumor. Tissue-biopsies are often taken at a single site and at a single time-point and do not reflect the heterogeneity found both within the specific tumor mass, between metastatic sites and variations over time.



Project description: We aim at combining several state-of the art principles and technologies to achieve what previously has been impossible – i.e using a liquid biopsy of systemic released immune-regulatory and tumor secreted proteins, to establish a predictive biomarker signature that allow treatment selection. The four work-packages are briefly described below (1-3).

  1. Selection of antigens and development of novel bioinformatics concepts. Bioinformatic mining of previously generated data from the IMMRay platform (immunovia.com) will be used to guide antigen selection in combination with biological insight. The proposed project is further dependent on development of novel bioinformatics concept to combine data from multiple biomarkers.
  2. Capture of novel targets through antibody engineering. Antibody-engineering will be used to develop affinity reagents that can detect circulating proteins relevant for response to immune-regulatory drugs. Specifically, we will use large, in-house antibody fragment libraries and established technology to select specific binders using phage display technology focusing on development of high-affinity antibodies capable of detecting relevant molecules present in liquid biopsies.
  3. Technical development of affinity-based proteomics. Parallel antibody-based enrichment of low abundant proteins followed by exact quantification by mass spectrometry (MS) analysis will allow sensitive and exact detection. This approach is elegant in that the antibody enrichment provides unparalleled sensitivity, while the MS readout ensures an absolute specificity and allows for absolute quantification. Most importantly, this setup also allows for differential analysis of different proteoforms or post-translational modifications, as the antibody would capture all protein variants and the MS provides a specific readout of all. 

 

The project will be co-supervised by a number of experts to allow an initial and continuous integrated approach, all the way from selection of antigens based on biological knowledge and previous data from the IMMRay platform, selection of antibodies, evaluation and testing on clinical material and development of novel bioinformatics concepts All expertise is available locally in Lund, and is committed to the project.

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Page Manager:

Sara Ek

Professor

Program Director

 

Email:

sara.ek@immun.lth.se

Phone:

+46-462223824

 

Department of Immunotechnology

 

Lund University

Medicon Village

Bilding 406

Scheelevägen 2

 

223 81 Lund