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Leukocyte and plasma activation profiles in chronically transfused patients with a history of allergic reactions.

作者信息

Fontaine Magali J, Shih Hank, Schubert Richard, Wong Wendy, Andrews Jennifer, Jeng Michael, Tirouvanziam Rabindra

机构信息

Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland.

Department of Pathology, Stanford School of Medicine, Stanford, Callifornia.

出版信息

Transfusion. 2017 Nov;57(11):2639-2648. doi: 10.1111/trf.14275. Epub 2017 Sep 6.

DOI:10.1111/trf.14275
PMID:28880378
Abstract

BACKGROUND

Allergic transfusion reactions are drawbacks to the benefits of transfusion. Classically, allergic transfusion reactions depend on histamine release from mast cells or basophils, but other leukocyte subsets may also be important. Thus, we propose to better define the exact leukocyte subsets involved in allergic transfusion reactions.

STUDY DESIGN AND METHODS

The overall objective of the current study was to compare the activation of specific peripheral blood leukocyte subsets (monocytes, neutrophils, eosinophils, and basophils) in a cohort of 13 patients who received chronic transfusions and had a history of allergic transfusion reactions compared with a control group of patients who received chronic transfusions and had no history of allergic transfusion reactions. Leukocyte subsets were analyzed by flow cytometry at baseline and after red blood cell transfusion, and cytokine levels in platelet-free plasma collected at the same time points were measured by Luminex assay.

RESULTS

Flow cytometry and cytokine profiles before and after transfusion did not differ significantly between patients who did and did not have a history of allergic transfusion reactions (p > 0.05). However, post-transfusion samples from both groups showed a decrease in CD63 expression in basophils, monocytes, and eosinophils and a decrease in CD45 expression in all leukocyte subsets compared with pretransfusion samples. Interleukin 10 levels increased after transfusion in the group with a history of allergic transfusion reactions (p = 0.0469), and RANTES (regulated upon activation, normal T-cell expressed and secreted) was significantly decreased post-transfusion in all patients (p = 0.0122).

CONCLUSION

None of the leukocyte subsets from patients who had a history of allergic transfusion reactions significantly increased in activation either before or after transfusion. All leukocyte subsets from patients who did and did not have a history of allergic transfusion reactions decreased in their activation profile upon transfusion challenge.

摘要

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