Transfusion science · Blood-group conversion · Technology analysis

Enzyme-Converted Type O Whole Blood

A major compatibility advance, but does it preserve oxygen delivery?

Conceptual enzyme removal of selected A-antigen structures from red-cell surfaces while other surface markers remain

What the study tested

Nowadly and colleagues tested an enzyme process designed to remove A-antigen structures from type A swine whole blood and produce an O-like blood-group profile. The experiment used blood from 16 type A and four type O swine.

16 + 4Type A and type O swine in the experimental model.
15 minIncubation period reported for the highest enzyme concentration.
0.6%Residual A-antigen signal at the highest concentration, compared with 0.45% in the type O control.

The investigators also assessed complete blood counts, blood gases, rotational thromboelastometry, osmotic fragility and free haemoglobin.

What the result may solve

The approach may reduce ABO-mediated incompatibility by removing selected terminal A-antigen structures. If it can be translated, validated and manufactured reliably, it could make existing donor blood more flexible across blood groups.

Important boundary: this is not pig-to-human blood and it does not remove “pig immunogenicity” broadly. Swine were the experimental model. The process targets the A blood-group antigen and does not erase the full red-cell antigen profile.

What it does not yet solve

  • Non-ABO antigens, including Rh, Kell, Duffy, Kidd and other clinically important systems.
  • Dependence on donor collection, testing, storage, cold chain and inventory rotation.
  • Long-term storage stability after enzyme treatment.
  • In vivo red-cell recovery, circulation time and survival after processing.
  • Proven tissue oxygen delivery after conversion.

Reducing one compatibility barrier is scientifically important. It is not the same as demonstrating preserved therapeutic function.

The oxygen-delivery questions

  • Does enzyme treatment change P50, the Hill coefficient or the Bohr effect?
  • Are ATP and 2,3-DPG preserved through processing and storage?
  • Does red-cell deformability remain adequate under microvascular flow?
  • How do oxygen unloading, tissue extraction and organ-level oxygenation compare with untreated blood?
  • What is the usable shelf life after conversion, and does function deteriorate during storage?

These endpoints are necessary before a compatibility conversion can also be described as a successful oxygen-delivery technology.

Primary publication

Nowadly CD, et al. Enzymatic conversion of type A to type O whole blood in a swine model. Transfusion. 2026;66(3):568–578. DOI · PubMed

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