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Test Name:
Neutrophil Antibodies, by IFA
- SBMF No:
42250 - Performance Lab Name:
Mayo Medical Laboratories - Test Mnemonic:
LAGG/TT - ABN:
Required – Not FDA-Approved - CPT Code:
86021 - LOINC Code:
19146-0 - Ref Lab Test No:
LAGGT | 8976 - Also Known As:
Anti-Leukocyte Antibodies
Anti-Granulocyte Antibodies
Anti-Neutrophil Antibodies
Granulocyte Antibodies
Granulocyte Binding IgG
Leukoagglutinin - Also See:
44427 Neutrophil-Associated Antibodies, by Flow Cytometry - Spec Type:
Serum - Spec Container:
Red top (serum) tube - Pref Vol:
1.5 mL - Min Vol:
0.3 mL - Fasting:
No - Spec Collect:
Do not use gel-barrier tubes for specimen collection
Routine venipuncture
Note: Only pretransfusion reaction specimen is acceptable - Spec Process:
Clot 30 minutes
Promptly centrifuge 15 minutes
Immediately transfer serum to separate plastic tube - Spec Store Transport:
Refrigerated - Spec Reject:
Specimen collected in gel-barrier tube
Specimen collected after transfusion reaction - Methodology:
Indirect Immunofluorescence Assay (IFA) - Use:
The work-up of individuals having febrile, nonhemolytic transfusion reactions
The detection of individuals with autoimmune neutropenia - Clinical Significance:
Granulocyte antibodies are induced by pregnancy or prior transfusion and are associated with febrile, nonhemolytic transfusion reactions. Patients who have been immunized by previous transfusions, pregnancies, or allografts frequently experience febrile, nonhemolytic transfusion reactions which must be distinguished from hemolysis before further transfusions can be safely administered. Granulocyte antibodies may also be present in autoimmune neutropenia. - Reference Range:
Reference values not applicable
Interpretation:
A positive result in an individual being worked up for a febrile transfusion reaction indicates the need for leukocyte-poor (filtered) red blood cells.This test cannot distinguish between allo- and autoantibodies
Cautions:
Not useful for diagnosis of neutropenia caused by marrow suppression by drugs or tumorsReference:
"Granulocyte Antibodies, Serum." 2011 Online Test Catalog, Mayo Medical Laboratories, 2011. Web. 18 November 2011 <http://www.mayomedicallaboratories.com/test-catalog/Overview/8976> - Additional Test Info:
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration. - Day Run:
Mon, Wed, Fri - Time Run:
7:30 am - 5:00 pm - Time Reported:
8-15 days - Test Type:
IMMUNOLOGY