RNA Sequencing Reveals Unique Transcriptomic Signatures of the Thyroid in a Murine Lung Cancer Model Treated with PD-1 and PD-L1 Antibodies

Immune checkpoint inhibitors (ICI) are commonly associated with thyroid immune-related adverse events, yet the mechanism has not been fully elucidated. We aimed to further explore the mechanism of ICI-induced thyroid dysfunction by assessing changes induced in the thyroid transcriptome by ICI treatment (& alpha;PD-1/& alpha;PD-L1) in a lung cancer murine model. RNA-sequencing of thyroid tissues revealed 952 differentially expressed genes (DEGs) with & alpha;PD-1 treatment (|fold-change| & GE;1.8, FDR < 0.05). Only 35 DEG were identified with & alpha;PD-L1, and we therefore focused on the & alpha;PD-1 group alone. Ingenuity Pathway Analysis revealed that of 952 DEGs with & alpha;PD-1 treatment, 362 were associated with functions of cell death and survival, with predicated activation of pathways for apoptosis and necrosis (Z = 2.89 and Z = 3.21, respectively) and negative activation of pathways for cell viability and cell survival (Z = -6.22 and Z = -6.45, respectively). Compared to previously published datasets of interleukin-1 & beta; and interferon & gamma;-treated human thyroid cells, apoptosis pathways were similarly activated. However, unique changes related to organ inflammation and upstream regulation by cytokines were observed. Our data suggest that there are unique changes in gene expression in the thyroid associated with & alpha;PD-1 therapy. ICI-induced thyroid dysfunction may be mediated by increased tissue apoptosis resulting in destructive thyroiditis.

Automated summary

Immune checkpoint inhibitors (ICI) commonly lead to adverse events in the thyroid, but the mechanism is not fully understood. Through RNA-sequencing, we found 952 differentially expressed genes (DEGs) in the thyroid tissues of a lung cancer murine model treated with αPD-1. Pathway analysis revealed that apoptosis and necrosis pathways were activated, leading to tissue destruction and thyroiditis. Our study suggests unique gene expression changes in the thyroid associated with αPD-1 therapy.