
JS
5.6K posts

JS
@js4k13
Keep climbing. Help others to do the same #Fosterkids. Ms. I trade #stocks. Don't aspire to make a living, aspire to make a difference. - D. Washington






@espn From breaking barriers to inspiring millions, Jason Collins left a legacy far bigger than basketball. Heartbreaking loss. RIP.💐

Every solid tumor cancer fight should start with #DCVAX. At this point, it is well accepted that cancer is an evasion of immune cell growth modulation. #DCVAX trains the immune system that it missed some critical markers in regulating cellular growth.



A major setback for mRNA cancer vaccine technology. A closely watched phase 2/3 trial of Moderna's product to treat cutaneous squamous cell carcinoma was prematurely terminated, without revealing the reasons for aborting the trial. trialsitenews.com/a/moderna-and-…

I started my due diligence in 2017. Met Dr. Ashkan and company management at ASCO in 2019. Everything about immune biology points to a #DCVAX oncology revolution. GBM is just the start. $NWBO

The press release frames #Alzheimer’s as a BBB delivery problem. The book makes a different case. The cascade ending in Alzheimer’s begins in the periphery, in senescent cells across the dermis, subcutaneous fat, vasculature, and bone marrow whose inflammatory output reaches the brain through circulation. Microglial IL-12 in the brain drives Alzheimer’s. Peripheral IL-12 from a working dendritic cell layer prevents it. Same molecule, opposite compartments, opposite effects. IRF8 is the shared upstream regulator of both cDC1 lineage and microglial homeostasis: the peripheral cascade and the microglial cascade are the same cascade running in two compartments. The architecture: intradermal partially matured α-DC1 builds a permanent immune outpost in the dermis (a tertiary lymphoid structure) that samples senescent cells locally. Educated dendritic cells traffic through the cervical lymph node and meningeal lymphatic routes the body uses for ongoing CNS surveillance. Systemic γδ T cells clear the senescent burden across every tissue. The signal to the brain falls. The microglia, no longer under chronic peripheral STAT3 drive, begin recovering their own IRF8-dependent homeostatic programs. The BBB stops being a problem because the architecture works with the immune system the brain already permits. The APOE4 carriers at highest ARIA risk under anti-amyloid antibodies are exactly who this architecture was designed for, because no antibody is being forced through cerebral vasculature. $NWBO owns the only platform that can build it. Reprogramming Alzheimer’s Disease With a Tolerogenic #DCVax Cassette: x.com/andrewcaravell… The Biological Reboot 📕 a.co/d/0hiZWGNS
























