Irreversible loss of donor blood leucocyte activation may explain a paucity of transfusion-associated graft-versus-host disease from stored blood

被引:14
作者
Chang, H
Voralia, M
Bali, M
Sher, GD
Branch, DR
机构
[1] Canadian Blood Serv, Toronto, ON M5G 2M1, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Univ Hlth Network, Toronto Gen Hosp, Toronto, ON, Canada
[4] Univ Hlth Network, Princess Margaret Hosp, Toronto, ON, Canada
关键词
TA-GVHD; donor leucocytes; blood-storage lesion; T-cell activation;
D O I
10.1046/j.1365-2141.2000.02330.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transfusion-associated graft-versus-host disease (TA-GVHD) is usually a fatal outcome of blood transfusion therapy, caused by viable leucocytes contained in the donor blood. Most cases of TA-GVHD occur when less than 4-d-old brood is transfused. We therefore examined the molecular changes that occur during storage that may account for the paucity of TA-GVHD following infusion of older blood. Leucocyte number and viability were essentially unchanged from freshly obtained brood, but the expression of cell-surface lymphocyte activation antigens (CD3, CD4, CD28, CD2, CD45) decreased rapidly within the first 24 h and continued to fall to less than 20% of original levels by d 9 of storage at 4 degreesC. The decrease in CD antigen expression directly correlated with a decreasing ability to induce activation of the T-lymphocyte cellular signal transduction pathway As a result, cells became less responsive in a mixed lymphocyte culture(MLC) by d 3, with abrogation of the MLC responsiveness by d 5, Donor leucocytes stored for 4 d or less at 4 degreesC were able to partially re-express CD antigens and reconstitute their signalling pathway when placed at 37 degreesC, whereas those stored for more than 4 d were not. These irreversible changes result from a permanent downregulation of donor cell protein synthesis. These findings provide a mechanism to explain the paucity of TA-GVHD following transfusion of blood that is more than 4 d-old. Further study may show that aged blood provides additional assurances for the prevention of TA-GVHD; however, use of aged blood should not replace current protocols using irradiation.
引用
收藏
页码:146 / 156
页数:11
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