High PD-L1 expression is associated with unfavorable clinical features in myelodysplastic neoplasms

Leticia Rodrigues Sampaio; Mateus de Aguiar Viana; Vanessa Silva de Oliveira; Bruna Vitoriano Ferreira; Mayara Magna Lima Melo; Roberta Taiane Germano de Oliveira; Daniela de Paula Borges; Silvia Maria Meira Magalhãesa; Ronald F Pinheiro

doi:10.1016/j.htct.2023.05.002

High PD-L1 expression is associated with unfavorable clinical features in myelodysplastic neoplasms

Hematol Transfus Cell Ther. 2023 Jun 5:S2531-1379(23)00100-1. doi: 10.1016/j.htct.2023.05.002. Online ahead of print.

Authors

Leticia Rodrigues Sampaio¹, Mateus de Aguiar Viana¹, Vanessa Silva de Oliveira¹, Bruna Vitoriano Ferreira¹, Mayara Magna Lima Melo¹, Roberta Taiane Germano de Oliveira¹, Daniela de Paula Borges¹, Silvia Maria Meira Magalhãesa¹, Ronald F Pinheiro²

Affiliations

¹ Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Fortaleza, CE, Brazil.
² Universidade Federal do Ceará (UFC), Fortaleza, CE, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Fortaleza, CE, Brazil. Electronic address: ronaldpinheiro@pq.cnpq.br.

PMID: 37543491
DOI: 10.1016/j.htct.2023.05.002

Abstract

Introduction: Immune checkpoints are regulators of the immune system response that allow self-tolerance. Molecules such as Programmed Cell Death Protein 1 (PD-1) and its Ligand (PD-L1) participate in the immune checkpoint by signaling co-inhibition of lymphocyte responses. In cancers, PD-L1 expression is associated with the immune evasion mechanism, which favors tumor growth. The use of anti-PD-1/PD-L1 drugs is already well described in solid tumors, but still not fully understood in hematologic malignancies. Myelodysplastic neoplasms (MDSs) are heterogeneous bone marrow disorders with an increased risk of progression to Acute Myeloid Leukemia (AML). The MDS affects hematopoietic stem cells and its pathogenesis is linked to genetic and epigenetic defects, in addition to immune dysregulation. The influence of the PD-L1 on the MDS remains unknown.

Methods: In this study, we evaluated the mRNA expression of the PD-L1 in 53 patients with MDS, classified according to the WHO 2016 Classification.

Results: Patients with dyserythropoiesis presented significantly higher PD-L1 expression than patients without dyserythropoiesis (p = 0.050). Patients classified as having MDS with an excess of blasts 2 (MDS-EB2) presented a significant upregulation in the mRNA expression of the PD-L1 compared to the MDS with an excess of blasts 1 (MDS-EB1) (p = 0.050). Furthermore, we detected three patients with very high levels of PD-L1 expression, being statistically classified as outliers.

Conclusion: We suggested that the high expression of the PD-L1 is associated with a worse prognosis in the MDS and functional studies are necessary to evaluate the possible use of anti-PD-L1 therapies for high-risk MDS, such as the MDS-EBs.

Keywords: Dyserythropoiesis; Immune evasion; Myelodysplastic syndrome; Protein death ligand 1.