Genetic and phenotypic characterization of indolent T-cell lymphoproliferative disorders of the gastrointestinal tract

Abstract

Indolent T-cell lymphoproliferative disorders of the gastrointestinal tract are rare clonal T-cell diseases that more commonly occur in the intestines and have a protracted clinical course. Different immunophenotypic subsets have been described, but the molecular pathogenesis and cell of origin of these lymphocytic proliferations is poorly understood. Hence, we performed targeted next-generation sequencing and comprehensive immunophenotypic analysis of ten indolent T-cell lymphoproliferative disorders of the gastrointestinal tract, which comprised CD4⁺ (n=4), CD8⁺ (n=4), CD4⁺/CD8⁺ (n=1) and CD4^-/CD8^- (n=1) cases. Genetic alterations, including recurrent mutations and novel rearrangements, were identified in 8/10 (80%) of these lymphoproliferative disorders. The CD4⁺, CD4⁺/CD8⁺, and CD4^-/CD8^- cases harbored frequent alterations of JAK-STAT pathway genes (5/6, 82%); <i>STAT3</i> mutations (n=3), <i>SOCS1</i> deletion (n=1) and <i>STAT3-JAK2</i> rearrangement (n=1), and 4/6 (67%) had concomitant mutations in epigenetic modifier genes (<i>TET2</i>, <i>DNMT3A</i>, <i>KMT2D</i>). Conversely, 2/4 (50%) of the CD8⁺ cases exhibited structural alterations involving the 3' untranslated region of the <i>IL2</i> gene. Longitudinal genetic analysis revealed stable mutational profiles in 4/5 (80%) cases and acquisition of mutations in one case was a harbinger of disease transformation. The CD4⁺ and CD4⁺/CD8⁺ lymphoproliferative disorders displayed heterogeneous Th1 (T-bet⁺), Th2 (GATA3⁺) or hybrid Th1/Th2 (T-bet⁺/GATA3⁺) profiles, while the majority of CD8⁺ disorders and the CD4^-/CD8^- disease showed a type-2 polarized (GATA3⁺) effector T-cell (Tc2) phenotype. Additionally, CD103 expression was noted in 2/4 CD8⁺ cases. Our findings provide insights into the pathogenetic bases of indolent T-cell lymphoproliferative disorders of the gastrointestinal tract and confirm the heterogeneous nature of these diseases. Detection of shared and distinct genetic alterations of the JAK-STAT pathway in certain immunophenotypic subsets warrants further mechanistic studies to determine whether therapeutic targeting of this signaling cascade is efficacious for a proportion of patients with these recalcitrant diseases.