The state of stem cell research in Canada

Stem cell research is no stranger to Canada, which has always been at the forefront of biomedical research. Since the first implications in the 1990s to the cutting-edge clinical tests of today, Canadian researchers have also played an important role in contributing to our knowledge on stem cell biology and the therapeutic potential of the cells.

This article deliberates on the history of stem cell research in Canada, analyses the present situation, demonstrates its major developments, looks at regulation and ethical issues, at present use in clinics, and prospects.

Stem Cell Research

Historical Context of Stem Cell Research in Canada

If you are searching for where to get stem cell therapy in Canada, you should first understand the wealth of history and research. Canadian research in Stem cell research began in the early 1990s with the isolation and characterisation of hematopoietic (blood‑forming) stem cells.

  • 1991: The Terry Fox Laboratory (Vancouver) is founded, which is mandated to research stem cells in cancer and regenerative medicine.
  • 1998: The U.S. research of human embryonic stem cells led even the Canadian labs to start examining pluripotent cells with tight restrictions.
  • 2001: The Canadian Institutes of Health Research (CIHR) established the Stem Cell Network, a pan-Canadian consortium to finance and organize stem cell science.
  • 2004 06: ViaCyte and STEMCELL Technologies are examples of early academia-private sector partnerships that lead to the commercialization of stem cell tools and reagents.

These milestones herald the strong research infrastructure in Canada that has the collaboration of the universities, hospital-based research centres, and biotechnology enterprises.

Current State of Stem Cell Research

Canada is a leader in stem cells and has an ecosystem today consisting of:

  • Academic institutions
  • Industry Partnerships
  • Collaborative Networks

Research belongs to many fields:

  • Basic Science: The processes of pluripotency, differentiation, and (tissue) regeneration.
  • Disease Modeling: Modeling neurodegenerative diseases, heart disease, and rare genetic diseases by using induced pluripotent stem cells (iPSCs).
  • 3D bioprinting of organoids and Tissue Engineering: Organoids could be used to perform 3D bioprinting of organoids used in drug screening and organoid-derived xenografts in transplantation.
  • Immunotherapy: The transgenic expression of CAR‑T cells through the hematopoietic stem cells, with the help of blood cancer.

Key Advancements and Breakthroughs

The field has been developed to some degree by a number of Canadian breakthroughs:

Organoid Models

Based on organoids of iPSCs derived from patients, researchers at the University of Toronto developed mini‑brain and mini‑lung organoids, which allow personalised drug testing of neurological and respiratory disorders.

Cardiac Regeneration

The team at the McEwen Centre showed transplantation of the cardiac progenitor cells in an animal model after myocardial infarction, which will enhance heart performance and minimise scarring.

Manufacturing of Stem Cells

STEMCELL Technologies increased the manufacture of stem cells to Good Manufacturing Practice (GMP) grade at lower costs and higher access to clinical trials.

Gene-edited stem cells

In their study at McGill University, scientists used CRISPR genome editing to fix defects in models of the sickle cell disease by introducing corrective antibodies into models and transplanting them with stem cells to bring sick patients back to normal hemoglobin production.

Regulatory Framework and Ethical Considerations

The stem cell research in Canada is regulated by the pristine regulatory and ethical environment:

Assisted Human Reproduction Act (AHRA)

AHRA came into being in 2004 and bans reproductive cloning as well as governs the utilisation of human gametes and embryos, and the generation of embryos for research.

Health Canada

Classifies cell therapy products as drugs under the Food and Drugs Act, and Clinical Trial Applications (CTAs) are required whenever investigational stem cell coloration is the mode of treatment.

Tri-Council Policy Statement (TCPS2)

All research involving humans mandates that the research be ethically reviewed by the Research Ethics Boards.

Committees On Oversight of Stem Cells

Most institutions, including Swiss Medica, have special committees to monitor stem cell projects to see whether they meet the guiding provisions in the country and the optimal practices in other countries.

There are controversies regarding ethical aspects:

  • Embryonic stem cells: the Pros and cons of Embryonic Stem Cells.
  • Consent to iPSC Derivation: Meaning that donors should be aware of how their cells will be used in the future.
  • Equitable Access: It levels the playing field of disparate access to expensive cell therapies when they enter the healthcare setting.

Stem Cell Therapy in Canada

Canada is also one of the world’s leaders in bringing stem cell research into translational medicine. Among outstanding trials, one should mention:

  • Parkinson’s Disease
  • Diabetes Type 1
  • Ophthamology

Safety and efficacy of patients involved in such trials are closely followed, and the results are tightly controlled by oversight provided by Health Canada according to high-ranking standards on quality and reporting.

Future Prospects

The future of stem cell research in Canada is very bright, and several trends are destined to dominate the next 10 years. For example, AI could accelerate stem cell research by 60% in the coming years. Some of the future prospects include:

  • Bioengineering Advances
  • Artificial Intelligence (AI) and Machine Learning (ML)
  • Indications: The efficacy of these drugs is extended in clinical uses
  • Commercial Scale-Up
  • Regulatory Adaptation

Continued development/modifications of Health Canada policies to adopt and keep up with fast-changing technology, and at the same time ensure patient safety.

Stem cell studies in Canada are an example of synergy between scientific quality, ethical accountability, and regulatory stringency. The next years will be of decisive importance because initial victories will be converted to approved treatments, converting Canada into a source of hope to patients all over the world.

 

 

About Joel Levy 2707 Articles
Publisher at Toronto Guardian. Photographer and Writer for Toronto Guardian and Joel Levy Photography