Blood transfusion and immunomodulation: a possible mechanism
M S Mincheff1, H T Meryman, V Kapoor
1Holland Laboratory, American Red Cross, Rockville, MD 20855.
Older stored blood may not trigger immune responses due to diminished accessory signals. Blood over 2 weeks old might cause immunosuppression rather than alloimmunization, impacting transfusion safety.
Area of Science:
- Immunology
- Transfusion Medicine
- Cellular Biology
Background:
- Immune responses require antigen-presenting cells to provide both specific antigen and accessory signals to T cells.
- Lack of accessory signals in vitro induces T cell anergy (unresponsiveness).
- Stimulator cells in stored blood express MHC class II but may lose accessory signaling capacity.
Purpose of the Study:
- To investigate the impact of refrigerated storage on the accessory signaling function of blood stimulator cells.
- To determine the implications of diminished accessory signaling on alloimmunization and immunosuppression.
- To assess the effect of irradiation on stimulator cell accessory signaling.
Main Methods:
- Monitoring of class II MHC expression on stimulator cells during refrigerated storage.
- Assessing the accessory signal presentation capacity of stored blood.
- Evaluating the effects of UV-B and gamma irradiation on accessory signal expression.
Main Results:
- Stimulator cells retain class II MHC expression during storage, but accessory signal presentation diminishes over time.
- Accessory signal presentation capacity reaches zero by approximately 13 days of storage.
- UV-B and gamma irradiation inhibit the expression of the accessory signal by stimulator cells.
Conclusions:
- Stored blood exceeding 2 weeks may not induce alloimmunization but could potentially cause immunosuppression.
- Irradiation of blood can impair the accessory signaling function of stimulator cells.
- Findings have implications for transfusion practices and understanding immune modulation by stored blood products.
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