CO44 | First interlaboratory validation workshop of immunofluorescence microscopy on the peripheral blood smear for recognizing patients with inherited platelet disorders
Background and Aims: Recognizing patients with inherited platelet disorders (IPD) still represents a challenge, and a multidisciplinary approach is routinely required. We have established a method for phenotyping platelets on the peripheral blood smear using immunofluorescence- and light microscopy...
Saved in:
| Format: | Article |
|---|---|
| Language: | English |
| Published: |
PAGEPress Publications
2025-08-01
|
| Series: | Bleeding, Thrombosis and Vascular Biology |
| Subjects: | |
| Online Access: | https://www.btvb.org/btvb/article/view/250 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Background and Aims: Recognizing patients with inherited platelet disorders (IPD) still represents a challenge, and a multidisciplinary approach is routinely required. We have established a method for phenotyping platelets on the peripheral blood smear using immunofluorescence- and light microscopy, which we have proposed as a screening-tool for IPD. The method has been validated by blinded comparison with molecular testing for 9 different disorders, for which typical changes of platelet structure can be identified. However, an interlaboratory validation of this approach has not been performed so far. To test the reproducibility of the technique and to implement its use in different Countries, we promoted a first, interlaboratory validation workshop of immunofluorescence microscopy on the blood smear for recognizing IPD.
Methods: Unstained and unfixed, native air-dried blood smears were prepared and shipped by regular mail to each participating Center, where they were fixed and stored at -20°C upon delivery. Subsequently, the slides were stained using a standard panel of 13 mouse or rabbit anti-human primary antibodies against different platelet structures (alpha- and dense granule, surface glycoproteins (GP) Ib/IX and IIb/IIIa, cytoskeleton, and the stem-cell antigen CD34) and 2 fluorescence-labelled goat anti-mouse or -rabbit secondary antibodies. Each participating Laboratory performed the investigation independently, reported results according to a defined evaluation-grid, and eventually formulated a possible diagnosis documenting the suspicion with pictures.
Results: Six European and one Australian Institution performing diagnosis of bleeding disorders participated in the project. By investigating blood films obtained from healthy controls, the reproducibility of preanalytical conditions, as well as of the staining- and observation method was initially ensured. Subsequently, blood smears from healthy controls or patients with IPD confirmed at molecular level were blindly shipped to each Center, which independently performed the investigation. Seven out of seven Laboratories correctly predicted the diagnosis of MYH9-related thrombocytopenia, Glanzmann thrombasthenia, and GFI1B-related thrombocytopenia; 6/7 of Bernard-Soulier syndrome, delta-storage pool disorder, and TUBB1-related thrombocytopenia; 5/7 of GATA1-related thrombocytopenia. Moreover, most of the participating groups correctly recognized the healthy controls, which only in five cases were wrongly reported as possible pathological samples.
Conclusions: The validation workshop confirmed the technical reproducibility of immunofluorescence microscopy on the blood smear - even when performed by some Laboratories for the first time. Even in this multicenter setting, the technique provided reproducible results. Additional training is expected to further increase the sensitivity and specificity of this approach.
|
|---|---|
| ISSN: | 2785-5309 |