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June 10 in Longevity and AI

Gathered globally: 5, selected: 5.

The News Aggregator is an artificial intelligence system that gathers and filters global news on longevity and artificial intelligence, and provides tailored multilingual content of varying sophistication to help users understand what's happening in the world of longevity and AI.


A team at Shift Bioscience employs a novel single-cell transcriptomic clock (AC3) to screen 1,500 genes, discovering SB000 as a single-factor intervention that reverses transcriptomic and epigenetic aging in fibroblasts and keratinocytes without activating pluripotency, paving the way for safe rejuvenation therapies.

Key points

  • AC3 single-cell transcriptomic clock screens 1,500 ORFs to identify rejuvenation factors.
  • SB000 expression reduces transcriptomic age by ~4.5 years in fibroblasts and keratinocytes without pluripotency.
  • SB000 reverses multiple epigenetic clocks and increases global CpG methylation by ~3%, preserving cell identity.

Why it matters: SB000 decouples cell rejuvenation from pluripotency, offering a safer, single-gene route to reverse aging across diverse tissues.

Q&A

  • What is SB000?
  • How does the AC3 transcriptomic clock work?
  • Why avoid pluripotency for rejuvenation?
  • What evidence shows SB000 reverses epigenetic aging?
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A single factor for safer cellular rejuvenation

In a Nature Aging study with over 10,000 participants, researchers used metabolic profiling and randomized trials to evaluate taurine levels as an aging biomarker. They found that declining taurine corresponds to existing health issues, not to the aging process itself, and that supplementation yielded no significant lifespan or healthspan improvements.

Key points

  • Large-scale Nature Aging study with 10,000 participants uses metabolomic profiling and RCTs to assess taurine’s role
  • Researchers find age-associated taurine decline correlates with comorbidities rather than causal aging factors
  • Randomized taurine supplementation shows no significant impact on lifespan or healthspan outcomes

Why it matters: Clarifying taurine’s non-causal link to aging shifts focus toward evidence-based interventions and refines biomarker selection for longevity research.

Q&A

  • What is taurine?
  • How is taurine measured in studies?
  • What is the difference between a biomarker and an aging driver?
  • Why did taurine supplementation fail to extend lifespan?
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Klotho Neurosciences has demonstrated that their adeno-associated virus (AAV9) platform delivers the secreted form of the Klotho protein (s-KL) to increase circulating levels, resulting in a 20% extension of healthy lifespan in mice. Building on foundational work linking Klotho to aging, this approach targets multiple age-associated pathologies—including cognitive decline, neuroinflammation, sarcopenia, and osteoporosis—offering a unified therapeutic strategy.

Key points

  • AAV9-mediated delivery of secreted Klotho (s-KL) increases mouse lifespan by 20%.
  • Overexpression of full-length Klotho gene extends murine lifespan by 30–40%.
  • s-KL therapy mitigates cognitive decline, neuroinflammation, sarcopenia, and osteoporosis.

Why it matters: Demonstrating a single protein-based therapy that extends healthy lifespan and ameliorates multiple age-related diseases marks a paradigm shift in anti-aging therapeutics.

Q&A

  • What is the secreted form of Klotho (s-KL)?
  • How does AAV9 delivery work in this context?
  • Which age-related conditions might benefit from s-KL therapy?
  • Why is Klotho considered a master regulator of aging?
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KLOTHO NEUROSCIENCE, INC. ANNOUNCES AN APPROACH TO INCREASE LONGEVITY AND HEALTHY LIFE SPAN - REPLACE A SILENCED GENE CALLED ALPHA-KLOTHO ("α-KLOTHO") | KLTO Stock News

Immortal Dragons, a Singapore-based longevity fund founded by Boyang Wang, strategically funds high-risk, high–impact projects. The fund prioritizes replacement-focused approaches—such as xenotransplantation, cryopreservation, and 3D bioprinting—over purely economic returns, aiming to catalyze breakthroughs in healthspan extension and inspire broader sector investment.

Key points

  • Immortal Dragons deploys a $40M AUM fund via a flexible CVC model with a single LP, enabling rapid, independent investments free of rigid mandates.
  • The fund targets replacement-driven interventions—xenotransplantation, cryopreservation, ex vivo 3D bioprinting of organs and tissues, and neural tissue augmentation—to pursue high-impact anti-aging strategies.
  • By emphasizing underfunded, moonshot projects and role-model outliers over blockbuster pharma ventures, the fund seeks to demonstrate lifespan extension potential and catalyze broader capital inflows.

Why it matters: By focusing on replacement-based, high-risk longevity interventions, Immortal Dragons aims to break translational bottlenecks and redefine investment incentives in anti-aging research.

Q&A

  • What is a replacement strategy in longevity science?
  • How does xenotransplantation differ from organ repair?
  • Why prioritize impact over economic returns in fund investments?
  • What role does 3D bioprinting play in replacement therapies?
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Boyang Wang on Targeting Underfunded Longevity Projects

IMR Solutions research demonstrates that integrating AI into ERP systems—via predictive analytics, NLP, and machine learning—yields a 65% reduction in manual processes and anticipates Generation Alpha’s demand for adaptive, context-aware enterprise tools.

Key points

  • AI-native ERP in SAP HANA reduces manual processing tasks by 65%
  • Predictive analytics, NLP, and machine learning drive adaptive, context-aware workflows
  • Implementation delivers a 45% improvement in operational efficiency

Why it matters: AI-enhanced ERP represents a paradigm shift, transforming enterprise software into collaborative partners and giving companies a competitive edge in talent acquisition.

Q&A

  • What defines an AI-native ERP?
  • Why focus on Generation Alpha?
  • How does predictive analytics work in ERP?
  • What role does NLP play in user interaction?
  • Are existing ERP implementations obsolete?
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