Chronic myeloproliferative neoplasms carrying the somatic JAK2
V617F mutation ( JAK2
V617F MPN) are characterized by the expansion of neoplastic clones and high immunogenicity. Expression of programmed cell death ligand-1 (PD-L1) in JAK2
V617F MPNs is mainly induced in megakaryocytes, platelets, and monocytes. The JAK2
V617F allele burden indicates the size of clonal hematopoiesis from hematopoietic progenitor cells. Although the importance of T cell-mediated anti-tumor immunity and JAK2
V617F allele burden in the pathogenesis of MPN progression has previously been documented, little is known about the relationship between these factors.
We therefore analyzed the phenotype and frequency of PD-1+ CD8+ T cells and the expression levels of PD-L1 in platelets in 26 patients with JAK2
V617F MPN. We found that the frequency of PD-1+ CD8+ T cells inversely correlated with the JAK2
V617F allelic burden. However, the PD-L1 expression levels on platelets had no correlation with JAK2
V617F allele burden or the CD8+ T cell subpopulations.
These data indicate that the expansion of clonal hematopoiesis restrains antitumor immunity, resulting in reduced frequency of PD1+ CD8+ T cells, and that the expression level of PD-L1 on platelets may not reflect the JAK2
V617F allele burden or antitumor immunity.
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