logo
Artificial Blood: Sci-Fi Breakthrough or False Hope?

Artificial Blood: Sci-Fi Breakthrough or False Hope?

Medscape2 days ago

Japanese researchers have developed artificial blood, marking a significant step in this long-standing scientific pursuit. However, large-scale production remains a challenge. In France, the national blood service Établissement français du sang regularly raises alarms over critically low blood supplies, with daily donations falling short of the 10,000 units needed to meet transfusion demands. This challenge is further complicated by ABO/Rh compatibility issues, prompting targeted appeals for rare blood-type donors. This shortage is not unique to France. It is a global concern, often even more severe elsewhere, driving continued efforts to create viable artificial alternatives.
Vesicle Trials
Researchers at Nara University in Nara, Japan have created 'hemoglobin vesicles' (HbVs): Haemoglobin encapsulated within a lipid shell that mimics red blood cells. In a 2022 trial, investigators injected 100 mL of HbVs into 12 healthy volunteers, with no serious adverse events reported.
The team plans to administer up to 400 mL to a larger cohort. If safety is confirmed, future studies will assess haemodynamic and respiratory effectiveness. Investigators hope to achieve industrial production and clinical use by 2030.
Storage Benefits
Artificial blood offers two key advantages over donor blood. First, it can be stored at room temperature for up to 2 years or up to 5 years if frozen, whereas donated blood expires after 6 weeks. Second, HbVs lack ABO and Rh antigens, making them theoretically compatible with all recipients. Notably, the solution turned purple.
Failed Attempts
The quest for artificial blood holds great promise, as tens of thousands die annually from blood shortages, particularly in low-income countries. However, previous efforts have been repeatedly stalled. In 2011, Luc Douay, MD, PhD, senior study author and Professor of Haematology at Université Pierre et Marie Curie in Paris, France, performed France's first transfusion using stem cell-derived red cells. In Japan, military physicians transfused experimental blood into rabbits in 2019 and reported encouraging results from stem cell-derived erythrocyte injections in the United Kingdom in 2022.
'All attempts have failed so far,' Douay said in 2017. While the latest Japanese trials offer renewed hope, experts emphasise the need to expand natural blood donation programs.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Submarines Are Hard to Detect. Climate Change Might Make It Even Harder.
Submarines Are Hard to Detect. Climate Change Might Make It Even Harder.

New York Times

timean hour ago

  • New York Times

Submarines Are Hard to Detect. Climate Change Might Make It Even Harder.

Submarines are among the most advanced and deadly weapons systems in the world. Armed with torpedoes, cruise missiles and sometimes intercontinental ballistic missiles, they're capable of operating deep below the surface for months at a time and are notoriously hard to detect. Now, their ability to hide in the vast oceans may be getting a boost from an unlikely source: climate change. The waters where many submarines lurk have been quickly warming, as humans pump out greenhouse gasses and oceans absorb the excess heat that gets trapped in the atmosphere. And that warming, according to a recent paper produced by the NATO Defense College in Rome, can have a powerful effect on how sound, the primary means of detecting submarines, behaves underwater. It could make large areas of the oceans impenetrable to submarine hunters. 'We observed, in most areas that we looked at, a reduction in the range of detection,' said Mauro Gilli, a researcher who studies military technology. His team modeled the way sound waves moved through the depths from 1970 to 1999. And they compared it with the way current climate modeling predicts they will move between 2070 and 2099. There were significant differences. The researchers found that in the North Atlantic, where Russian submarines play cat and mouse with NATO forces, the distances at which they can be heard will shrink significantly. This could be by almost half in the Bay of Biscay, off the coasts of France and Spain. There were similar dynamics in play in the western Pacific, where Chinese and American submarines operate and where detection ranges could shrink by up to 20 percent. The underlying science has been well understood since before World War II, when scientists discovered that sound, which travels faster through warmer water, tends to bend toward cooler layers, where it moves more slowly. Want all of The Times? Subscribe.

Moon Surgical Discusses Maestro at NVIDIA GTC Paris, Celebrating 1,300+ Procedures in the Past Year and the Power of Physical AI
Moon Surgical Discusses Maestro at NVIDIA GTC Paris, Celebrating 1,300+ Procedures in the Past Year and the Power of Physical AI

Yahoo

time3 hours ago

  • Yahoo

Moon Surgical Discusses Maestro at NVIDIA GTC Paris, Celebrating 1,300+ Procedures in the Past Year and the Power of Physical AI

PARIS and SAN FRANCISCO, June 12, 2025 /PRNewswire/ -- Moon Surgical, the French-American leader in Physical AI for the operating room, today announced its participation at NVIDIA GTC Paris during VivaTech2025. In collaboration with NVIDIA, Moon Surgical is highlighting the Maestro System as a pioneering example of Physical AI in action—empowering surgical teams across the globe. As of today, the Maestro System has supported over 1,500 procedures worldwide, with more than 1,300 of those performed in the past year alone. With the integration of Physical AI—merging perceptive robotics and real-time computing—Maestro has proven its adaptability across 60 different minimally invasive procedures and its growing role in high-volume outpatient care. Physical AI is the integration of perceptive hardware with powerful local computing, enabling software-defined systems to understand and interact with the physical world in real time. From system deployment to procedural subtasks, physical AI combines the forces of robotic devices and agentic AI, it is the infrastructure layer to the operating room. Maestro uses ambient sensing, and robotics powered by NVIDIA Holoscan and NVIDIA IGX technologies to bring this type of capability to the clinical edge — empowering surgical teams to deliver consistent, efficient care. Anne Osdoit, CEO of Moon Surgical, will present a session titled "Reimagining Surgical Robotics as Physical AI Agents for Global Reach" at GTC Paris, spotlighting how generative Physical AI is redefining the role of surgical robotics through simulation and human collaboration. Maestro is designed to enhance—not replace—human expertise, acting as an extension of the surgical team to facilitate coordination, communication, and refined technique during minimally invasive surgery. About Moon Surgical (AI / MIS focused)Moon Surgical is transforming the operating room with Physical AI, seamlessly integrating intelligence and robotics to elevate the capabilities of surgical teams. The Maestro System represents a new category of minimally invasive surgery—expanding the scale at which robotics are delivered into the operating rooms. Instinctive, collaborative, and cost-effective, Maestro empowers teams to deliver exceptional care with greater adaptability and control. Moon Surgical. Inspiring and Innovating the Art of Surgery. For investor and media inquiries, please email us at info@ Check us out at or follow us on LinkedIn. View original content to download multimedia: SOURCE Moon Surgical

Enterome raises $19 million to fund clinical development of its OncoMimics™ immunotherapy to treat Follicular Lymphoma
Enterome raises $19 million to fund clinical development of its OncoMimics™ immunotherapy to treat Follicular Lymphoma

Yahoo

time3 hours ago

  • Yahoo

Enterome raises $19 million to fund clinical development of its OncoMimics™ immunotherapy to treat Follicular Lymphoma

Proceeds to fund Phase 1/2 trial of EO2463 OncoMimics™, as a monotherapy or in combination, to treat multiple forms of indolent non-Hodgkin lymphoma (iNHL) $9 million from new investor The Institute for Follicular Lymphoma Innovation (IFLI) $10 million from existing specialist investors, including The Leukemia & Lymphoma Society Therapy Acceleration Program® (LLS TAP) Paris, France – June 12, 2025Enterome SA, a clinical-stage company developing first-in-class OncoMimics™ immunotherapies to treat cancer, has raised $19 million in a new private financing to advance its lead clinical program EO2463 OncoMimics™ immunotherapy to treat indolent non-Hodgkin lymphoma (iNHL). The new funds will be used to expand and finalize the ongoing Phase 1/2 SIDNEY clinical trial of EO2463 and prepare the candidate for a registrational trial. New U.S. investor The Institute for Follicular Lymphoma Innovation (IFLI), a global non-profit foundation dedicated to advancing research and treatment for follicular lymphoma, invested $9 million in the round, of which $5 million will be allocated to Enterome upon closing and an additional $4 million in conditional tranched funding. Existing shareholders invested an additional $10 million including: SymBiosis, a U.S. venture capital firm; Seventure Partners, based in France; Lundbeckfonden BioCapital from Denmark; Primo Capital, an Italian venture capital and private equity firm; and The U.S. Leukemia & Lymphoma Society Therapy Acceleration Program® (LLS TAP). 'Attracting highly specialized blood cancer investor IFLI to this financing demonstrates the conviction of our new and existing investors in the potential of OncoMimics™ for blood and solid tumor cancers,' said Pierre Bélichard, Enterome's Chief Executive Officer. 'We currently are generating exciting clinical proof of concept data for EO2463 monotherapy in several iNHL patient populations included in the Phase 1/2 SIDNEY clinical trial. Most importantly, EO2463 has shown robust clinical efficacy and exceptional safety and tolerability – which is especially impressive for such a potent immunotherapy. This offers a new hope for these patients and a rare opportunity to create an entirely new market segment for an impactful therapeutic. This financing will enable us to continue the SIDNEY trial of EO2463 and prepare to launch a first pivotal Phase 3 trial of this candidate for the 'watch-and-wait' iNHL population.' The company presented interim SIDNEY dataat the American Society of Hematology (ASH) conference in December 2024, showing highly encouraging responses in the Cohort 2 of 'watch and wait' iNHL patients in the ongoing SIDNEY study. This population, as the name suggests, is generally not eligible to receive other treatments due to the unacceptable risk-benefit ratio (in this iNHL sub-population) of the most commonly used blood cancer therapies. The company also recently disclosed having held positive meetings with both FDA (Type C meeting) and EMA (Scientific Advice), outlining a clear regulatory path registration for marketing authorizations in 'watch-and-wait' iNHL. 'This investment aligns with IFLI's mission to accelerate the development of innovative therapies and precision biomarkers for follicular lymphoma,' said Michel Azoulay, MD, Chief Medical Officer at IFLI. 'EO2463 represents a novel class of synthetic, off-the-shelf Immunotherapeutics with a unique mechanism of action that selectively targets malignant B cells. We are particularly interested in supporting Enterome's efforts to demonstrate EO2463's clinical efficacy across multiple lines of therapy, including in relapsed and refractory settings.' Enterome recently announced that it will present new data showing EO2463 also has a meaningful impact when tested in combination with standard of care in relapsed and refractory iNHL patients at the International Conference on Malignant Lymphoma (ICML) in Lugano on June 21. Previous findings presented at ASCO in 2024 in the relapsed and refractory patient population further suggested the potential to identify individuals most likely to benefit from EO2463 treatment, supported by biomarker analyses. Lore Gruenbaum, Chief Scientific Officer at LLS, said, 'It is important for us to continue to support Enterome, a company working to develop novel therapeutics based on our shared commitment to create better therapies for blood cancers. LLS has invested over $1.8 billion in groundbreaking research since our inception in 1949. Our active partnership with Enterome, through our Therapy Acceleration Program, will continue to advance the clinical development of the OncoMimics™ family of novel immunotherapeutics for the benefit of blood cancer patients. We are particularly excited to help advance EO2463 which has shown promising signs of efficacy as monotherapy with excellent safety and tolerability in 'watch-and-wait' iNHL patients, who currently have no approved treatment options.' EO2463 is an innovative, off-the-shelf immunotherapy candidate that combines four synthetic OncoMimics™ peptides. These non-self, microbial-derived peptides correspond to CD8 HLA-A2 epitopes that mimic the B lymphocyte-specific lineage markers CD20, CD22, CD37, and CD268 (BAFF receptor). EO2463 also includes the helper peptide (CD4+ epitope) universal cancer peptide 2 (UCP2). The unique ability of EO2463 immunotherapy to selectively target multiple B cell markers enables the destruction of malignant B lymphocytes. By ensuring broad target coverage across malignant B cells, this novel approach aims to simultaneously improve safety and maximize efficacy, reducing the tumor cells' capacity to develop immune-resistance mechanisms such as antigen escape. SIDNEY is an ongoing 12-month open label Phase 1/2 study that aims to assess safety, tolerability, immunogenicity, and preliminary efficacy of EO2463 monotherapy and combination therapy in up to about 55 patients with follicular lymphoma and marginal zone lymphoma including divided into three cohorts: newly diagnosed patients eligible to watch-and-wait (monotherapy); newly diagnosed patients in need of therapy / first line (combo with rituximab); patients with relapsed/refractory disease (combo with R2). In addition to safety, survival, response rates and other measures of efficacy are being collected. OncoMimics™ were inspired by the microbial origin of certain autoimmune diseases. The Company uses AI and machine learning to identify microbial proteins that closely mimic the structure, effect or actions of specific cancer antigens (as well as hormones or cytokines). Memory T cells against microbial antigen are created during early development, sometimes leading to autoimmune disorders. In the case of OncoMimics™, however, this means that the immune system can mount a rapid, robust and durable immune response that is highly targeted and specific for the OncoMimics™ and the cancer antigens they closely resemble. This is possible because, unlike cancer antigens, OncoMimics™ bypass the biological process, known as thymic deletion, that prevents the immune system from mounting an attack against the 'self' proteins (e.g. antigen) on tumor and blood cancer cells. Once activated, the immune system attacks with high specificity and potency the cancer antigens targeted by the OncoMimics™, killing the cancer cells that carry them. OncoMimics™ are synthetic peptides that are easy to manufacture, store, distribute and administer as an off-the-shelf subcutaneous injection. In clinical testing to date they have been shown to be extremely well tolerated, especially compared to other potent immunotherapies. Enterome SA ( is a privately held clinical-stage biopharmaceutical company developing OncoMimics™, a new proprietary immunotherapeutic modality inspired by the microbial origin of certain autoimmune diseases, to treat cancer. The Company's wholly-owned OncoMimics™ pipeline includes three distinct clinical-stage drug candidates: EO2463 to treat indolent non-Hodgkin lymphomas; EO4010 to treat third-line colorectal cancer; and EO2401 to treat glioblastoma and adrenal tumors. Each of these candidates has shown positive early clinical efficacy and exceptional safety and tolerability. For more information, please contact: ENTEROME INVESTOR & MEDIA RELATIONS Pierre BélichardChief Executive Officer +33 (0)1 75 77 27 85 Cohesion BureauChris Maggos / Giovanni Ca' Zorzi +41 (0)79 367 6254 / +33 (0)7 84 67 07 27enterome@ Attachment 20250612_Enterome _PR_Funding_Round_finalError in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store