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Published on: October 14, 2021
Expression of HECA-452 in parapsoriasis and mycosis fungoides
R Di Trolio1, G Di Lorenzo, E Barbiero
1Dipartimento di Patologia Sistematica-Clinica Dermatologica, Università degli Studi di Napoli Federico II, Via Pansini 5, 80131 Naples, Italy.
Abstract:
We have investigated the HECA-452 expression in large plaque parapsoriasis (PP) and mycosis fungoides (MF) patients, evaluating the potential role of this biomarker in both cutaneous disorders. Skin specimens from 72 PP and 61 MF patients were selected in this study. We compared their actual histological diagnosis with their previous diagnosis and we found that all 72 PP patients had the same diagnosis as before (stable PP), while 26 out of 61 MF had a previous PP histological diagnosis (evolving PP). Our results show an increased expression of HECA-452 in MF compared to PP (p<0.01). Furthermore, evolving PP showed a significantly higher level of HECA-452 than stable PP (p<0.05). We conclude that HECA-452 expression increases during the natural history of Mycosis Fungoides. HECA-452 could be used as a biomarker for MF and predict which PP evolves to MF.
Insights
HECA-452 expression increases as parapsoriasis (PP) evolves into mycosis fungoides (MF). This biomarker may help differentiate between stable PP, evolving PP, and MF, aiding in diagnosis and prognosis.
Area of Science:
- Dermatology
- Immunohistochemistry
- Cutaneous Lymphoma Research
Background:
- Parapsoriasis (PP) and mycosis fungoides (MF) are distinct but related cutaneous T-cell lymphomas.
- Distinguishing between stable PP and evolving PP that may progress to MF can be challenging.
- Identifying reliable biomarkers is crucial for accurate diagnosis and patient management.
Purpose of the Study:
- To investigate the expression of HECA-452 in patients with large plaque parapsoriasis (PP) and mycosis fungoides (MF).
- To evaluate the potential role of HECA-452 as a biomarker in the progression of PP to MF.
- To correlate HECA-452 levels with disease status (stable PP, evolving PP, MF).
Main Methods:
- Histological analysis of skin specimens from 72 PP and 61 MF patients.
- Immunohistochemical assessment of HECA-452 expression.
- Comparison of HECA-452 levels between PP and MF groups, and between stable and evolving PP subgroups.
Main Results:
- HECA-452 expression was significantly increased in MF compared to PP (p<0.01).
- Evolving PP demonstrated significantly higher HECA-452 levels than stable PP (p<0.05).
- A subset of MF patients (26/61) had a prior histological diagnosis of PP, indicating disease evolution.
Conclusions:
- HECA-452 expression increases during the natural progression of mycosis fungoides.
- HECA-452 serves as a potential biomarker for differentiating MF from PP.
- Elevated HECA-452 levels may predict the evolution of PP to MF, aiding in early detection and intervention.
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