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Updated: May 24, 2026

Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 23, 2014
Should we be screening for anti-Js(a)?
Nancy M Nikolis1, Fouad Boctor, William Andrew Heaton
1Transfusion Service and Donor Services, North Shore University Hospital, Manhasset, NY 11030, USA.
Insights
The anti-Js(a) antibody may be missed in 30-40% of patients. Current red blood cell (RBC) screening methods may not detect Js(a) when it is the only antibody present.
Area of Science:
- Transfusion Medicine
- Immunology
- Hematology
Background:
- The Js(a) antigen is a significant red blood cell (RBC) antigen.
- Alloantibodies to RBC antigens can cause transfusion reactions.
- Current screening methods may not detect all clinically significant antibodies.
Purpose of the Study:
- To determine the frequency of anti-Js(a) alloantibodies in a patient database.
- To evaluate the detection rate of anti-Js(a) when present alone or with other antibodies.
- To assess the need for Js(a) inclusion in routine antibody screening.
Main Methods:
- Analysis of a historic patient database from North Shore University Hospital.
- Review of alloantibody screening results, focusing on anti-Js(a).
- Calculation of the frequency of anti-Js(a) and its co-occurrence with other antibodies.
Main Results:
- Anti-Js(a) was not detected in 30-40% of patients when it was the sole antibody.
- Since 1996, anti-Js(a) has only been detected in conjunction with other antibodies.
- Approximately 1.7% of patients (90 patients/year) are exposed to the Js(a) antigen.
Conclusions:
- Current antibody screening methods may fail to detect anti-Js(a) as a sole antibody.
- The clinical significance of anti-Js(a) warrants further investigation.
- Additional studies are needed to determine if Js(a) should be incorporated into antibody screening cells.
Abstract:
We analyzed our historic patient database at North Shore University Hospital and determined both the overall frequency of anti-Js(a) and the frequency at which it was detected in combination with other alloantibodies to red blood cell (RBC) antigens. Screening cells used currently are negative for Js(a). Our data suggest that anti-Js(a) would not be detected in 30 to 40 percent of patients in which it is the sole antibody present. Since 1996 the antibody was only detected when other antibodies were found in the screening process. We are exposing 1.7 percent of our patients (90 patients/year) to Js(a). The clinical significance of anti-Js(a) is apparent with previous literature, and our conclusion is that additional studies should be performed to determine whether Js(a) should be included in current antibody screening cells.
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