HSP and CD279 gene expression as candidate biomarkers in symptomatic LGLL patients

The clinical presentation of T-cell large granular lymphocytic leukemia (T-LGLL) is extremely variable: 30% of patients have neutropenia with no associated symptoms, others present with bacterial infections and sepsis may occur. Tools to predict patient outcome are lacking. Stemming from preliminary results obtained by single cell-RNAseq we investigated by qPCR HSP and IFIT gene families in 27 LGLL patients (23T-LGLL and 4 NK-LGLL), including 11 with neutropenia and/or thrombocytopenia and 16 asymptomatic for the disease. HSP90AA1 and HSPA1B, among HSP family and CD279 exhibited a significantly higher expression in CD3 + CD57 + sorted cells of symptomatic LGLL patients compared to asymptomatic patients and healthy controls. Also, monocytes derived from symptomatic LGLL patients expressed high levels of CCL3, CCL4 and CCL5 mRNA and of IL-1β, IL-6, TNF, and PD-L1 mRNA, thus confirming a pro-inflammatory cytokine profile reminiscent of a non-classical phenotype. Overall, these data provide a rationale for considering HSP and CD279 genes as potential biomarkers for distinguishing symptomatic LGLL patients from asymptomatic ones, emphasizing the importance of further research to explore their implications for targeted therapy development.

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Publication Details

Journal
Discover Oncology
Published
2024-12-18
DOI
https://doi.org/10.1007/s12672-024-01657-y
Citations
1
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.24

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article

HSP and CD279 gene expression as candidate biomarkers in symptomatic LGLL patients

Giuliana Gregato, Patrizia Mancuso, Federica Melle, Giovanna Motta et al.
1 citations
Discover Oncology
Immune Cell Function and Interaction
0.24
article

HSP and CD279 gene expression as candidate biomarkers in symptomatic LGLL patients

Giuliana Gregato, Patrizia Mancuso, Federica Melle, Giovanna Motta, Roberto Chiarle, Stefania Orecchioni, Giovanna Talarico, Andrea Franceschini, Annamaria Tenore, Stefano Pileri, Paolo Falvo, Saveria Mazzara, Francesco Bertolini, Claudia Poletti, Alessandro Raveane
article en
1 citations

Abstract

The clinical presentation of T-cell large granular lymphocytic leukemia (T-LGLL) is extremely variable: 30% of patients have neutropenia with no associated symptoms, others present with bacterial infections and sepsis may occur. Tools to predict patient outcome are lacking. Stemming from preliminary results obtained by single cell-RNAseq we investigated by qPCR HSP and IFIT gene families in 27 LGLL patients (23T-LGLL and 4 NK-LGLL), including 11 with neutropenia and/or thrombocytopenia and 16 asymptomatic for the disease. HSP90AA1 and HSPA1B, among HSP family and CD279 exhibited a significantly higher expression in CD3 + CD57 + sorted cells of symptomatic LGLL patients compared to asymptomatic patients and healthy controls. Also, monocytes derived from symptomatic LGLL patients expressed high levels of CCL3, CCL4 and CCL5 mRNA and of IL-1β, IL-6, TNF, and PD-L1 mRNA, thus confirming a pro-inflammatory cytokine profile reminiscent of a non-classical phenotype. Overall, these data provide a rationale for considering HSP and CD279 genes as potential biomarkers for distinguishing symptomatic LGLL patients from asymptomatic ones, emphasizing the importance of further research to explore their implications for targeted therapy development.

Discover OncologyVol. 15(1)
Human Technopole (IT), Ripamonti (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), European Institute of Oncology (IT), Politecnico di Milano (IT)
Ministero della Salute, Fondazione Umberto Veronesi, Associazione Italiana per la Ricerca sul Cancro
Openalex Percentile: Top 39%
Immune Cell Function and Interaction
0.24
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