AI Article Synopsis

  • Blood transfusions are crucial for saving lives, but compatibility issues with blood types can pose challenges in emergencies.
  • A new nanoplatform has been developed that uses a polymer core coated with red blood cell (RBC) membranes to capture harmful antibodies, allowing for safer transfusions between incompatible blood types.
  • This innovative solution not only neutralizes specific antibodies without causing inflammation or other complications but also effectively uses expired RBCs, demonstrating its potential for improving transfusion outcomes.

Article Abstract

Blood transfusions save lives and improve health every day. Despite the matching of blood types being stricter than it ever has been, emergency transfusions among incompatible blood types are still inevitable in the clinic when there is a lack of acceptable blood types for recipients. Here to overcome this, a counter measure nanoplatform consisting of a polymeric core coated by a red blood cell (RBC) membrane is developed. With A-type or B-type RBC membrane camouflaging, the nanoplatform is capable of specifically capturing anti-A or anti-B IgM antibodies within B-type or A-type whole blood, thereby decreasing the corresponding IgM antibody levels and then allowing the incompatible blood transfusions. In addition to IgM, the anti-RBC IgG antibody in a passive immunization murine model can likewise be neutralized by this nanoplatform, leading to prolonged circulation time of incompatible donor RBCs. Noteworthily, nanoplatform made by expired RBCs (>42 days stored hypothermically) and then subjected to lyophilization does not impair their effect on antibody neutralization. Most importantly, antibody-captured RBC-NP do not exacerbate the risk of inflammation, complement activation, and coagulopathy in an acute hemorrhagic shock murine model. Overall, this biomimetic nanoplatform can safely neutralize the antibody to enable incompatible blood transfusion.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11304279PMC
http://dx.doi.org/10.1002/advs.202310230DOI Listing

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