Supercell Acquires Exclusive Licensing from Japanese Immunotherapy Leader for Advanced NK Cell Treatment Technology

Supercell Biotechnology Corporation commemorates the first anniversary of rebranding from previously-called SinoCell Technologies, due to the company’s capital increase by RMT Holding Group. Demonstrating the strategic move at the Healthcare+ Expo Taiwan, their theme “Hope Begins from Now”, encapsulates their global expansion and transformation in healthcare.

Supercell, through partnerships in regenerative medicine, has secured an exclusive license for a Japanese-developed natural killer (NK) cell culture technique. The technique, pivotal in cancer cell elimination and immune system enhancement, will be showcased at the expo, highlighting their latest experimental advancements[1].

The majority of NK cells administered on day 14 are CD56brightCD16NK cells, which primarily enhance immune function but show reduced expression of the CD16 membrane protein, crucial for tumor cell destruction. Dr. Hiroshi Terunuma’s methodology indicates that by day 21, CD56brightCD16+NK cells become the dominant cell type. These cells demonstrate increased expression of both CD56 and CD16 membrane proteins, enabling both cytotoxic and immunomodulatory effects. The results showed both qualitative and quantitative enhancements, as evidenced by the presence of more than 60 x 108 NK cells, a purity level greater than 80%, and an amplification rate exceeding 1,500-fold.

Dr. Hiroshi Terunuma, a distinguished international authority in cancer treatment based in Japan and a long-standing partner of Supercell, has successfully administered NK cell therapy in over 40,000 cases. In a clinical study, 63 patients diagnosed with terminal malignant pancreatic cancer received conventional cancer therapy supplemented by NK cell infusion. Results showed a significant improvement in survival rates, with 41 patients doubling their expected lifespan from 6 to 13 months[2]. Moreover, a British patient with terminal colon cancer achieved a complete remission, showcasing the effectiveness and progressive potential of NK cell therapy.[3]

If adopted as a standard practice in future healthcare, this approach could enhance cellular immunity, potentially leading to increased resilience in the face of a progressively complex disease environment.

Sean Ishihara, Chairman of RMT Group, parent company of Supercell Biotechnology Corporation, emphasizes, “medical care is a universal right.” Unlike typical biotech companies focused on going public, Supercell prioritizes researching and developing safe, effective biotech applications. The company actively collaborates with international experts to realize this mission. Through these partnerships, Supercell aims to deliver top-quality solutions worldwide.

[1] Terunuma, H. Autologous Immune Enhancement Therapy for Cancer—Our experience since 2004. J. Stem Cells Regen. Med. 2012, 8, 205–206.

[2] Terunuma H, Deng X, Nishino N, Watanabe K. NK cell-based autologous immune enhancement therapy (AIET) for cancer. J Stem Cells Regen Med. 2013 Apr 30;9(1):9-13. doi: 10.46582/jsrm.0901003. PMID: 24693203; PMCID: PMC3908307.

[3] https://inews.co.uk/news/health/colon-cancer-patient-turned-away-nhs-disease-free-months-live-1845098 (Colon cancer patient who turned away from NHS ‘disease free’ 6 years after being told he had months to live, By Paul Gallagher, September 10, 2022 6:00 am (Updated at September 13, 2022 11:05 am))

Hot this week

Spartan Medical Broadens Single-Use Sterile Instrument Portfolio to Improve Outcomes, Increase Efficiency, and Generate Cost Savings

Spartan Medical products portfolio of single-use, sterile med tech includes micro and minor surgical convenience kits, kerrison rongeurs, spinal and general surgical retractors, dural repair kits, synthetic biologics, and a wide range of orthopedic pre-sterilized implants and devices.

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

The ACURATE Prime aortic valve system is designed with several features to build upon the clinical performance of the ACURATE neo2™ platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

Noctrix Health Announces New CMS Reimbursement Codes and Payment for Nidra Tonic Motor Activation Therapy for Restless Legs Syndrome

Nidra TOMAC Tonic Motor Activation Therapy, which was authorized for marketing in the United States last year following its designation as a "Breakthrough Device" by the US Food & Drug Administration (FDA), remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS.