Site icon BioInformant

Takara Bio Establishes Foothold in the Pluripotent Stem Cell Market

Takara Bio

A few years back, Takara Bio announced that the Medical Products Agency (“MPA”), the Swedish national authority responsible for regulation of drug and medical products, had granted the company a manufacturing license for derivation and banking of human embryonic stem (hES) cells to be produced under GMP conditions. The cells were to be produced at Takara Bio’s manufacturing laboratory located in Göteborg, Sweden, within Takara Bio Europe’s facility.

This announcement made Takara Bio the first company worldwide to offer this service for human ESCs.

Takara Bio’s Role with Human Pluripotent Stem Cells

The significance of this event is that Takara Bio is capable of providing a predictable and reliable source of hES cells for future cellular therapeutic development by sourcing starting material from FDA-compliant facilities, according to FDA guidelines and leveraging its proprietary, feeder-free hES cell establishment method, which is animal- and human-component free.

Historically, Takara Bio has had long-standing experience in human embryonic stem cell derivation, and under this MPA license, it can offer this as a contract manufacturing service for customers who are focused on clinical cell therapy applications.

As summarized by Hiroki Tomohisa, CEO of Takara Bio Europe AB: “Takara Bio Europe’s long-standing experience in hES cell derivation is offered as a contract manufacturing service under the MPA license. We have a proprietary feeder-free hES cell establishment method which is animal- and human-component free. Starting material is retrieved from FDA-compliant sources according to FDA guidelines.”

Takara Bio’s Cell and Gene Therapy CDMO Business

Put simply, Takara Bio’s basic strategy for the Gene Therapy segment is to develop and commercialize cutting edge technologies that are essential to gene therapy, by applying the technologies developed in their Bioindustry segment. In addition to their involvement in clinical trials, Takara Bio has been offering cell and gene therapy manufacturing and operational support as a Contract Development and Manufacturing Organization (CDMO) business at the Center for Gene and Cell Processing since the fall of 2014. This center is located in Kusatsu, Japan.

For readers who are unfamiliar with this term, a CDMO is a company that serves cell therapy companies on a contract basis. Common cell therapy CDMO services include cell therapy product development, manufacturing, clinical trial support, and commercial supply.

Although cell therapy manufacturing is becoming of mounting importance as growing numbers of cell therapeutics make their way through clinical trials, one of the major issues with moving cell therapy products from “bench to bedside” has been manufacturing bottlenecks. The heterogeneous nature of cell therapy products has introduced manufacturing complexity and regulatory concerns, as well as scale-up complexities that are not present within traditional pharmaceutical manufacturing.

Among cell therapy companies, the pressure for manufacturing innovation and optimization can incentivize them to seek third-party partners who possess technical, manufacturing, and regulatory expertise, such Takara Bio. According to Elizabeth Quinn, Associate Director, Stem Cell Marketing at Takara Bio USA, the goal of the Takara Bio is to provide “custom solutions that can address any stage of the gene and cell therapy development process.”

Clearly, Takara Bio’s Göteborg facility for derivation and banking of human embryonic stem (hES) cells to be produced under GMP conditions complements its global efforts to meet the needs of clients within the gene and cellular therapy industries.

Takara Bio’s Expertise in CAR-T

Takara Bio also has expertise in the “hot” and “up-and-coming” field of CAR-T. At first the trend was subtle, but CAR-T funding has been rapidly expanding as CAR-T therapies have reached the marketplace and created a CAR-T funding craze. In particular, CAR-T start-ups have been richly funded by investors eager to get into this trending area of regenerative medicine and IPO raises have also been aggressive.

For over 20 years, Takara Bio has developed novel products with important gene therapy applications, positioning it to ride this wave of CAR-T enthusiasm. In 1995, Takara Bio and Indiana University developed the RetroNectin method, which involves using a plate-coating substance to increase the physical interactions of cells and viruses, greatly increasing transduction efficiency.

Since that time, the company has developed additional ways of using the RetroNectin method and viral vector technology for new therapeutic applications, such as in boosting naïve T-cell expansion for CAR-T therapy.

RetroNectin reagent, now available as a GMP-grade version, has been used in over 60 clinical studies around the world. In addition to integrating this product into its T-cell immunotherapy manufacturing service, Takara has also developed RetroNectin GMP Grade to support the needs of the clinical research community.

Takara Bio’s Relationship with Shinya Yamanaka and Kyoto University’s CiRA

A project at Takara Bio that captured my attention is the development of a quality-control system for maintaining a large stock of induced pluripotent stem (iPS) cells needed for clinical trials.

Kyoto University’s Center for iPS Cell Research and Application (CiRA), headed by Shinya Yamanaka, is collaborating with Takara Bio to ensure that the needs of iPS cell clinical research and therapeutic use are met.

The relationship with Shinya Yamanaka is significant, because he discovered iPS cells in mice in 2006 and derived them from humans in 2007. The partnership with CiRA is even more substantial, because CiRA is one of the premier institutions promoting clinical research and studies with human iPS cells.

Takara Bio Group and the Cellartis Brand

The Takara Bio Group of companies has three primary sub-brands, which are: Takara, Clontech, and Cellartis. The Cellartis brand is of particular interest, because it is focused on stem cell-derived products and services for drug discovery, disease modeling, and regenerative medicine applications.

Historically, a key focus of the brand has been developing and distributing pluripotent stem cell lines, including both human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs).

Logically, Takara Bio’s recently launched clinical-grade hES cell production service is being offered under the Cellartis brand.

In recent years, the Cellartis brand has been expanding its range of stem cell product applications. In one interesting example, it launched an iPS Cell to Hepatocyte Differentiation System, which allows researchers to easily generate hepatocytes from iPSCs on demand. In another intriguing example, it launched the Cellartis DEF-CS Culture System, a unique approach to culturing stem cells that offers significant advantages relative to other methods.

Takara Bio’s iPS Cell Differentiation Expertise

While Takara Bio has traditionally been viewed as a diversified provider of research tools, the company is increasingly starting to focus on stem cell research and clinical-grade solutions. Takara Bio now offers research use only (RUO) products and services for hepatocyte, definitive endoderm (DE), beta cell, and cardiomyocyte differentiation.

For hepatocytes, it has a complete portfolio including:

It also offers Cellartis Human iPS and ES KnockIn and KnockOut Gene Editing Services. These services allow Takara Bio to combine its expertise in precise, footprint-free gene editing using CRISPR/Cas9 with its expertise in human pluripotent stem cell culturing and directed differentiation into hepatocytes, DE cells, beta cells and cardiomyocytes.

This enables the generation of disease models that are essential for advancing the understanding of disease mechanisms and the development of novel therapeutics.

Takara Bio’s Experience in Hepatocyte Differentiation

Furthermore, Takara Bio has developed a standardized differentiation protocol for industrial scale production of iPS-derived hepatocytes that mimics embryonic development to yield pure cells that exhibit the functionality and characteristics of mature hepatocytes.

Its protocol results in pure, functional hepatocytes that are functionally mature and give low variability from batch-to-batch. To the best of my knowledge, Takara Bio is the first company offering a a standardized hepatic differentiation procedure that is generally applicable across a large panel of hPSC (iPS and ES) lines without any adaptations to individual lines.

By applying this “universal” protocol across hPSC-heps derived from different donor lines, one can mirror the metabolic diversity typically observed in human primary hepatocytes from different donors. Based on recent advances in iPSC technology, iPSC lines can now be derived from individuals with specific genotypes or phenotypes.

Combining this progress with Takara Bio’s DEF-CS culture system and robust hepatic differentiation protocol allows for the generation of homogenous hepatocyte cultures from customized panels of hiPSC lines at a large scale. It also opens up new possibilities for drug discovery, toxicology studies, and regenerative medicine applications.

Because of the universal nature of Takara Bio’s differentiation protocol, it commercialized a kit to allow researchers to differentiate their own iPS lines into DE cells or hepatocytes. For those who prefer the easy route, Takara will also do this as an outsourced service.

Finally, Takara Bio now provides batches of terminally differentiated hiPS-HEP cells from multiple donors to be used in drug screening and disease model applications.

Takara Bio’s Growing Role as a Stem Cell Solution Provider

If you deeper even deeper into the company’s catalogue, you will also find that Takara Bio offers:

This hepatocyte long-term maintenance medium allows for more advanced functional studies to be performed, such as long-term toxicity studies.

A search of PubMed.gov revealed that several researchers are investigating the use of the Power medium for HBV infection studies that require hepatocytes to remain in culture for long periods of time.

Finally, Takara Bio offers:

Clearly, Takara Bio is establishing a growing foothold in the stem cell space, including the development of diverse capabilities around both human iPS cells and ESCs.

Do you have questions about Takara Bio’s products or services? Ask them in the comments below.

Source/Sponsor: Takara Bio

4.9/5 - (36 votes)
Exit mobile version