The rapid sequence 51Chromium red cell survival test is now a widely accepted laboratory procedure used primarily in situations when compatible blood cannot be found by usual in vitro serologic techniques. The project, therefore, now concentrates on those patients and blood donors who have poorly understood and incompletely characterized red cell antibodies detected in their serum. Characterization of the in vivo significance of these antibodies will allow more rational selection of blood for these people should transfusion be necessary in the future. Several rare or unusual antibodies have been studied (e.g. anti-Yta, anti-H, anti-A1I, """"""""enzyme-reactive"""""""" antibodies, etc.). Collaborative studies have been completed with the American Red Cross to compare the 51Cr test with an in-vitro macrophage effector assay. Three distinct patterns of immune red cell destruction have been confirmed using 51Cr labelled cells. These patterns can be identified when the test is carried to 24 hrs, allowing more appropriate transfusion decisions to be made.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL002001-11
Application #
3963121
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code
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