In vivo neutralization of anti-A and successful transfusion of A antigen-incompatible red blood cells in an animal model

Transfusion. 2011 Dec;51(12):2664-75. doi: 10.1111/j.1537-2995.2011.03184.x. Epub 2011 May 20.

Abstract

Background: Our aim was to determine if the historical principle of Lewis glycolipid neutralization of antibody and subsequent Lewis-incompatible transfusion could be extended and applied to the ABO blood group system using synthetic glycolipid-like constructs.

Study design and methods: In vitro experiments with human blood and blood group A function-spacer-lipid constructs (FSL-A) were used to determine rates and concentrations that caused antigen transformation and anti-A neutralization. FSL-A constructs were intravenously infused into naive and anti-A-immunized mice to determine in vivo antigen transformation, anti-A inhibition, and tolerance to A antigen-incompatible transfusions (A+biotin kodecytes).

Results: FSL-A was able to cause in vivo transformation of circulating mouse cells into A antigen-positive cells (in vivo A kodecytes) without consequence in animals either with or without circulating anti-A. FSL-A was able to neutralize circulating anti-A and allow for successful transfusion of incompatible A kodecytes. In the absence of FSL-A neutralization incompatible cells were rapidly destroyed.

Conclusions: FSL constructs have the potential to neutralize circulating antibodies and allow for, or mitigate, the consequences of ABO-incompatible red blood cell transfusion.

MeSH terms

  • ABO Blood-Group System / immunology*
  • Animals
  • Blood Component Removal / instrumentation
  • Blood Component Removal / methods*
  • Blood Group Incompatibility / immunology
  • Blood Group Incompatibility / prevention & control*
  • Erythrocyte Transfusion* / instrumentation
  • Erythrocyte Transfusion* / methods
  • Female
  • Humans
  • Isoantibodies / immunology*
  • Male
  • Mice

Substances

  • ABO Blood-Group System
  • Isoantibodies