Volume 29, Issue 1 404069 pp. 47-53
Article
Open Access

Diagnostic and Prognostic Utility of PD-1 In B Cell Lymphomas

S. Muenst

S. Muenst

Institute of Pathology University Hospital Basel, Switzerland

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S. Hoeller

S. Hoeller

Institute of Pathology University Hospital Basel, Switzerland

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N. Willi

N. Willi

Institute of Pathology Cantonal Hospital Liestal, Switzerland

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S. Dirnhofer

S. Dirnhofer

Institute of Pathology University Hospital Basel, Switzerland

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A. Tzankov

Corresponding Author

A. Tzankov

Institute of Pathology University Hospital Basel, Switzerland

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First published: 29 May 2013

Abstract

Aims: Programmed death-1 (PD-1) is expressed by germinal center-associated helper T-cells and acts as a negative regulator of the immune system. PD-1 is encountered on tumor cells of angioimmunoblastic T-cell lymphoma and is a postulated diagnostic marker in chronic lymphocytic leukemia (CLL/SLL). Recent data suggest prognostic importance of PD-1 in follicular lymphoma (FL). We assessed the diagnostic potential and the prognostic importance of PD-1 in B-cell lymphomas.

Methods: Distribution of PD-1+ lymphocytes in B-cell lymphomas was studied on 403 cases. Correlation with known biologic and clinical key data was performed. Prognostic cut-off scores were determined by receiver operating curve analysis. Results: PD-1+ tumor-infiltrating lymphocytes were numerous in extranodal marginal zone lymphomas and FL. Their amount decreased from FL grade 1 to grade 3 and to FL with transformation to diffuse large B-cell lymphoma. An increased amount of PD-1 tumor-infiltrating lymphocytes above the prognostic cut-off score (> 2.8%) was a positive prognostic factor of disease-specific survival (DSS) in FL-patients. Five percent of the studied 66 CLL/SLL cases showed unequivocal PD-1 positivity of neoplastic cells.

Conclusions: Increased number of PD-1+ tumor-infiltrating lymphocytes is associated with significantly improved DSS in FL and may be useful to predict its heterogeneous clinical behavior. PD-1 has probably limited diagnostic value for primary histopathological CLL/SLL diagnostics.

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