Abstract | BACKGROUND: STUDY DESIGN AND METHODS: In a Phase 1 study, fathers of selected NAIT cases not resolved by serologic testing but thought to have a high likelihood of NAIT on clinical and serologic grounds were typed for LFHPAs by DNA sequencing. In a Phase 2 study, high-throughput methods were used to type fathers of 1067 consecutive unresolved NAIT cases for LFHPAs. Mothers of 1338 unresolved cases were also typed to assess the prevalence of LFHPAs in a population racially/ethnically similar to the fathers. RESULTS: In Phase 1, LFHPAs were identified in 16 of 244 fathers (6.55%). In Phase 2, LFPAs were found in only 28 of 1067 fathers (2.62%). LFHPAs were identified in 27 of 1338 maternal samples (2.01%). HPA-9bw was by far the most common LFHPA identified in the populations studied and was the only LFHPA that was significantly more common in fathers than in mothers of affected infants (p = 0.02). CONCLUSIONS: Maternal immunization against recognized LFHPAs accounts for only a small fraction of the cases of apparent NAIT not resolved by standard serologic testing. Typing of the fathers of such cases for LFHPAs is likely to be rewarding only when a maternal antibody specific for a paternal platelet glycoprotein is demonstrated and/or there is compelling clinical evidence for NAIT.
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Authors | Julie A Peterson, Maria Gitter, Daniel W Bougie, Shannon Pechauer, Kathleen A Hopp, Brad Pietz, Aniko Szabo, Brian R Curtis, Janice McFarland, Richard H Aster |
Journal | Transfusion
(Transfusion)
Vol. 54
Issue 5
Pg. 1286-93
(May 2014)
ISSN: 1537-2995 [Electronic] United States |
PMID | 24128174
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | © 2013 American Association of Blood Banks. |
Chemical References |
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Topics |
- Alleles
- Antigens, Human Platelet
(genetics)
- Female
- High-Throughput Screening Assays
- Humans
- Male
- Polymorphism, Single Nucleotide
- Thrombocytopenia, Neonatal Alloimmune
(etiology)
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