NK cells (Natural Killer cells) are part of the immune system's surveillance function. At Cellforce One, NK-related consultation begins with medical history, cancer history, current treatment status, screening results, and physician explanation. If appropriate, the route is intravenous infusion under the filed Category III plan PB3250244.
Filed / notified under Japan's Act on Safety of Regenerative Medicine — Category III plan PB3250244. Out-of-pocket / private treatment. Diagnosis, prescription, and treatment decisions are made through physician consultation.
NK cells are discussed in immune-surveillance research. This is used as background for physician explanation, not as a standalone treatment decision.
Research discusses senescent-cell biology, SASP, inflammation, and aging-related changes. Individual relevance must be reviewed medically.
If considered after screening, NK cell therapy is explained as an intravenous route within the filed provision framework. Individual results vary.
The following mechanisms are discussed in immune-surveillance research. They are not presented as proof of an individual effect.
Research discusses NKG2D ligands such as MICA/B and ULBP as immune-surveillance signals.
Activating receptor recognizing PVR / Nectin-2. Research suggests a complementary role to NKG2D in senescent cell recognition.
A natural cytotoxicity receptor (NCR). Research suggests NKp46 recognizes specific ligands on senescent cell surfaces and contributes to immune surveillance.
Perforin forms pores in target cell membranes; granzyme B enters and induces apoptosis. Research suggests selective targeting with limited impact on healthy cells.
The mechanisms above describe pathways suggested by basic research. Clinical effects vary by individual; a specific outcome is not promised.
CFO delivers autologous NK cell therapy by combining the CANK protocol, partner cell-processing infrastructure, and physician-led indication review.
All NK cells used are derived from the patient. Allogeneic (donor) NK cells are not used. Research suggests autologous-derived therapy carries lower immune rejection risk.
Activation culture using IL-2 and autologous plasma — designed to enhance expression of NKG2D, DNAM-1, and NKp46 receptors. Performed under partner CPC quality controls.
CANK protocol supervised by Dr. Tsutomu Nakazawa (Grandsoul Research Institute; author, Frontiers in Immunology 2025). Culture design reflects basic research and clinical experience.
Filed / notified under Japan's Act on Safety of Regenerative Medicine — Category III, plan number PB3250244. Filing represents the provider framework, not national endorsement of treatment effect.
NK cell senotherapy is the "Review" step in the DDR protocol. Before infusion, screening (Detect) is essential to confirm indication.
Precision diagnostics (MRI, blood, biomarkers) establish your baseline. Indication and priority for NK infusion are determined in physician consultation.
Activated autologous NK cells (CANK protocol) are administered intravenously. Research suggests reinforced immune surveillance against senescent and abnormal cells.
Where appropriate, MSC (mesenchymal stem cells) and autologous EVs (extracellular vesicles) support tissue repair. Sequencing is designed individually in physician consultation.
Six peer-reviewed papers covering NK-related immune surveillance and senescent-cell research. Citations are research background and do not promise individual outcomes.
Research discusses how activated NK cells recognize senescent-cell-related signals via NKG2D and DNAM-1 receptor pathways.
Read on Frontiers →Research suggests molecular mechanisms by which senescent cells evade NK-mediated immune surveillance with age, framing the rationale for reinforcing NK function.
Read on Nature Aging →Research suggests immune system aging is associated with accelerated aging across organ systems, framing immune function as a systemic health indicator.
Read on Nature →Research describes how NK cells recognize specific ligands on senescent cell surfaces as part of immune surveillance pathways.
Read on Nature →Research suggests an association between NKG2D and DNAM-1 receptor expression on activated NK cells and senescent cell recognition performance.
Read on Frontiers →Research describes apoptosis induced by perforin and granzyme B released by NK cells as a mechanism of senescent cell elimination.
Read on Cell Death & Disease →Goals, history, cancer history, current care, and prior assessment results are shared in physician consultation. Suitability and alternatives are reviewed individually.
Approximately 30 mL of peripheral blood is collected and transported to the CPC the same day for PBMC isolation.
Cell-processing details, timing, quality documents, and route are explained individually when NK therapy is selected after physician review.
Activated NK cells are administered as an intravenous infusion (typically 60–90 minutes), followed by brief observation.
Biomarkers and self-reported indicators are reassessed 1–3 months post-infusion. Continued tracking is supported via Monthly Longevity Review.
Follow-up may include inflammation markers, biomarkers, self-reported indicators, and medical-record organization when the physician considers them useful.
The CFO Monthly Longevity Review is a member program that organizes your health data monthly during your stay in Japan and after you return home, with periodic review by Japanese physicians. We offer enrollment as a post-treatment follow-up option.
A filed Category III regenerative-medicine option in which NK cells may be prepared from the patient's blood and administered by intravenous infusion when appropriate after physician review.
A portmanteau of "senescent" + "therapy" — therapeutic strategies targeting senescent cells. NK-based senotherapy uses immune cells rather than small molecules.
When NK therapy is considered, the physician explains the preparation method, cell-processing route, risks, costs, and alternatives. Public information does not replace individual medical judgment.
Individual results vary. Research findings are background information and do not promise a specific outcome.
Determined per individual through physician consultation. Options range from a single infusion to multi-session protocols based on goals, condition, and assessment results.
Transient reactions such as fever or fatigue may occur with infusion-based procedures, and other risks can differ by condition. The physician explains possible risks and alternatives before any treatment decision.
No. NK therapy is not a substitute for standard cancer care. Research suggests potential support for the immune environment, but it is offered as concurrent or complementary support to standard care, with diagnosis and treatment decisions made by physicians on an individual basis.
Yes. Pre-arrival consultation via WhatsApp or email, followed by blood draw → culture → infusion scheduled around your Japan visit. You may return home during the culture period and come back for infusion.
Biomarker follow-up (NK activity, CRP, etc.) is recommended. For ongoing monitoring, we offer enrollment in the CFO Monthly Longevity Review.
The NK provision plan is filed / notified as a Category III regenerative medicine provision plan (PB3250244) under Japan's Act on Safety of Regenerative Medicine. Filing represents the provider framework, not national treatment-effect endorsement.
A physician consultation reviews your current health status, records, screening needs, risks, costs, and whether NK-related consultation is appropriate.
Domestic patients prefer LINE; international patients typically use WhatsApp.
These links point to Japan's public registry pages for filed regenerative-medicine provision plans and to the clinic's official YouTube / Instagram channels. Registry publication is a reference for filed provision-plan information; it is not evidence of individual treatment outcomes or absence of risk.