PD-1 and PD-L1 expression in mycosis fungoides and Sézary Syndrome.


Journal

Italian journal of dermatology and venereology
ISSN: 2784-8450
Titre abrégé: Ital J Dermatol Venerol
Pays: Italy
ID NLM: 101778002

Informations de publication

Date de publication:
Aug 2022
Historique:
pubmed: 5 4 2022
medline: 4 8 2022
entrez: 4 4 2022
Statut: ppublish

Résumé

The mechanisms involved in mycosis fungoides, and Sezary Syndrome progression are largely unknown. Over the last decade the interest in immune system contrast of neoplasm has grown owing to the introduction of immunotherapy. PD-1 and its ligand (PD-L1) are the target of several immunotherapy treatment. In the literature reports on the expression of PD-1 and PD-L1 have provided contrasting results. In our analysis we investigated PD-1 expression in neoplastic cells and in tumor infiltrating lymphocytes (TILs) as well as PD-L1 expression in tumor cells and in tumor associated macrophages (TAMs). PD-L1 and PD-1 positive cells were counted in 5 high-power fields (HPF) and scored as the average number of positive neoplastic cells/TILs/TAMs per HPF. From databases of two institutions (Bologna and Florence) thirty-five patients corresponding to 43 biopsies were retrieved. In seven instances sequential biopsies were present. No statistically significant expression was observed comparing early to advanced stages by analysing PD-1 by tumor cells and TILs and of PD-L1 by tumor cells and TAMs. Our results corroborate that PD-1 and PD-L1 expression is not stage-dependent in mycosis fungoides and Sezary syndrome. However, PD-1 and PD-L1 expression in affected patients provides a rationale to schedule anti PD-1/PD-L1 drugs.

Sections du résumé

BACKGROUND BACKGROUND
The mechanisms involved in mycosis fungoides, and Sezary Syndrome progression are largely unknown. Over the last decade the interest in immune system contrast of neoplasm has grown owing to the introduction of immunotherapy. PD-1 and its ligand (PD-L1) are the target of several immunotherapy treatment. In the literature reports on the expression of PD-1 and PD-L1 have provided contrasting results.
METHODS METHODS
In our analysis we investigated PD-1 expression in neoplastic cells and in tumor infiltrating lymphocytes (TILs) as well as PD-L1 expression in tumor cells and in tumor associated macrophages (TAMs). PD-L1 and PD-1 positive cells were counted in 5 high-power fields (HPF) and scored as the average number of positive neoplastic cells/TILs/TAMs per HPF.
RESULTS RESULTS
From databases of two institutions (Bologna and Florence) thirty-five patients corresponding to 43 biopsies were retrieved. In seven instances sequential biopsies were present. No statistically significant expression was observed comparing early to advanced stages by analysing PD-1 by tumor cells and TILs and of PD-L1 by tumor cells and TAMs.
CONCLUSIONS CONCLUSIONS
Our results corroborate that PD-1 and PD-L1 expression is not stage-dependent in mycosis fungoides and Sezary syndrome. However, PD-1 and PD-L1 expression in affected patients provides a rationale to schedule anti PD-1/PD-L1 drugs.

Identifiants

pubmed: 35373781
pii: S2784-8671.22.07275-9
doi: 10.23736/S2784-8671.22.07275-9
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

355-362

Auteurs

Alessandro Pileri (A)

Unit of Dermatology, IRCCS Sant'Orsola Polyclinic, Bologna, Italy - alessandro.pileri2@unibo.it.
Unit of Dermatology, Department of Experimental Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy - alessandro.pileri2@unibo.it.

Valentina Tabanelli (V)

Division of Hematopathology, IRCCS European Institute of Oncology (IEO), Milan, Italy.

Fabio Fuligni (F)

Department of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.

Claudio Agostinelli (C)

Unit of Hematopathology, Department of Experimental Diagnostic and Specialty Medicine, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Unit of Hematopathology, IRCCS Sant'Orsola Polyclinic, Bologna, Italy.

Alba Guglielmo (A)

Unit of Dermatology, IRCCS Sant'Orsola Polyclinic, Bologna, Italy.
Unit of Dermatology, Department of Experimental Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.

Elena Sabattini (E)

Unit of Hematopathology, Department of Experimental Diagnostic and Specialty Medicine, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

Vieri Grandi (V)

Division of Dermatology, Department of Health Sciences, University of Florence, Florence, Italy.

Stefano A Pileri (SA)

Division of Hematopathology, IRCCS European Institute of Oncology (IEO), Milan, Italy.

Nicola Pimpinelli (N)

Division of Dermatology, Department of Health Sciences, University of Florence, Florence, Italy.

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Classifications MeSH