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A Global Standard for Immune Compatibility

               Tolerogenic platforms can become the backbone of a new
               biologic commons—shared technologies that nations can
               adapt, manufacture, and distribute based on their own needs
               and population profiles.

               But for that to happen:


                   •  Global regulators and procurement agencies
                       (like WHO, Gavi, and PAHO) must begin
                       evaluating biologics by durability and delivery
                       independence.
                   •  Philanthropic capital must prioritize shelf-stable,
                       low-cost, tolerogenic therapies as a global public
                       good.
                   •  Clinical trials in diverse geographies must track
                       ADA rates and SLOR across different HLA
                       haplotypes, nutrition baselines, and microbiomes.


               Because if immune rejection is preventable—and we do
               nothing to prevent it—we are not just failing scientifically.


               We are failing ethically.




               Durability as a Tool of Justice


               In the world’s most fragile healthcare systems, the biologic
               that works once and fades is not just ineffective—it’s cruel.
               It gives hope, then withdraws it. It invites reliance, then
               punishes it.






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