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Can serological methods help distinguish between prophylactic and alloimmune anti-D?
C Irving1, M Crennan1, T Vanniasinkam2
1Haematology Department, Melbourne Pathology, Collingwood, Victoria, Australia.
Transfusion Medicine (Oxford, England)
|May 17, 2017
Summary
The enzyme indirect antiglobulin test (EIAT) can confirm alloimmune anti-D in pregnant women but cannot exclude it. This aids in differentiating antibody sources, which is crucial for managing RhD alloimmunisation.
Area of Science:
- Immunohaematology
- Transfusion Medicine
- Serology
Background:
- Distinguishing prophylactic from alloimmune anti-D is vital for RhD-negative pregnant women.
- Current methods rely on patient history and serological scoring.
- A specific test for alloimmune anti-D can improve diagnostic accuracy.
Purpose of the Study:
- To evaluate the enzyme indirect antiglobulin test (EIAT) and polyethylene glycol IAT (PIAT) for differentiating anti-D sources.
- To compare EIAT and PIAT against the standard low ionic strength solution-IAT (LISS-IAT).
Main Methods:
- Tested 273 plasma samples from antenatal, preoperative, and postmenopausal individuals.
- Utilized column agglutination testing (CAT) for initial anti-D identification.
- Compared tube LISS-IAT, EIAT, and PIAT, calculating agglutination score differences.
Main Results:
- EIAT showed a significant increase in agglutination score for alloimmune anti-D samples compared to LISS-IAT.
- EIAT demonstrated 59% sensitivity, 100% positive predictive value, and 100% specificity for alloimmune anti-D.
- 32% of alloimmune anti-D samples showed a +2 or +3 score increase with EIAT.
Conclusions:
- EIAT can confirm the presence of alloimmune anti-D when detected in routine screening.
- EIAT is not sufficient to exclude alloimmune anti-D.
- Further development may enhance EIAT's utility in differentiating anti-D antibody origins.

