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Updated: Jul 13, 2026

Induction of Alloantigen-specific Anergy in Human Peripheral Blood Mononuclear Cells by Alloantigen Stimulation with Co-stimulatory Signal Blockade
Published on: March 14, 2011
Alloimmunization in preterm infants after repeated transfusions of WBC-reduced RBCs from the same donor
R G Strauss1, K Johnson, G Cress
1Department of Pathology, University of Iowa College of Medicine, Iowa City 52242-1182, USA. ronald-strauss@uiowa.edu
Preterm infants receiving limited donor exposure rarely develop red blood cell (RBC) antibodies. While white blood cell (WBC) antibodies are uncommon, the benefit of WBC-reduced blood components remains uncertain for these infants.
Area of Science:
- Neonatal Medicine
- Transfusion Medicine
- Immunology
Background:
- Preterm infants are a heavily transfused patient group.
- Alloimmunization against RBC and WBC antigens is rare in multiply transfused infants.
- The impact of limited donor exposure and WBC-reduced RBCs on alloimmunization risk is unknown.
Purpose of the Study:
- To investigate alloimmunization rates in preterm infants exposed to limited donors.
- To assess the potential benefit of WBC-reduced RBC components in preventing alloimmunization.
Main Methods:
- Preterm infants (0.6-1.3 kg birth weight) received prestorage WBC-reduced RBCs from dedicated donors.
- Serial blood samples were collected and tested for RBC and WBC antibodies (HLA class I or neutrophil-specific).
Main Results:
- No infants developed RBC antibodies.
- 13% of infants produced WBC antibodies (excluding passive maternal antibodies).
- WBC antibodies identified were against HLA class I or neutrophil-specific antigens, with no adverse effects.
Conclusions:
- Limited donor exposure programs do not necessitate changes in blood banking practices due to rare RBC antibody production.
- The benefits of WBC reduction are uncertain due to the uncommon occurrence of infant WBC antibody production.
- Further research is required to justify changes in transfusion practices for preterm infants.
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