Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004 Feb;44(2):197-201.
doi: 10.1111/j.1537-2995.2004.00643.x.

Clinical significance of anti-Jra: report of two cases and review of the literature

Affiliations
Review

Clinical significance of anti-Jra: report of two cases and review of the literature

MeeAe Y Kwon et al. Transfusion. 2004 Feb.

Abstract

Background: Jra is a high-frequency antigen seen in all populations, but the clinical significance of Jra antibodies is incompletely understood. Two cases are reported in which patients with anti-Jra received incompatible transfusions.

Case reports: A 69-year-old Japanese man had anti-K and anti-Jra. Despite multiple transfusions of Jr(a+), K- RBCs, his clinical course remained stable without evidence of hemolysis. A 45-year-old Japanese woman with anti-Jra was transfused with two units of Jr(a+) RBCs without clinical evidence of hemolysis. However, the same patient received an additional unit of Jr(a+) RBCs 1 week after the initial transfusions and, within 6 hours of transfusion, developed signs and symptoms of an acute hemolytic transfusion reaction.

Study design and methods: Routine serologic methods were used to study the patients' RBCs and plasma. A monocyte monolayer assay (MMA) was used to determine the potential clinical significance of the anti-Jra, where reactivity (R) greater than 5 percent indicates potential clinical significance.

Results: The anti-Jra in the first case had a pretransfusion titer of 32 with a MMA result of 3.3 percent R. No clinical or laboratory evidence of hemolysis was seen after transfusion of 4 units of Jr(a+), K- RBCs. The anti-Jra in the second case had a pretransfusion titer of 32 with a MMA result of 24.5 percent R. This patient developed an acute hemolytic reaction after transfusion of Jr(a+) RBCs.

Conclusion: Anti-Jra can be clinically significant as demonstrated by acute hemolysis in the second case. The MMA accurately predicted the clinical outcome of each case and appears to be a useful tool in predicting the biologic behavior of anti-Jra.

PubMed Disclaimer

LinkOut - more resources