Login / Signup

Single-cell profiling reveals a memory B cell-like subtype of follicular lymphoma with increased transformation risk.

Xuehai WangMichael NissenDeanne GraciasManabu KusakabeGuillermo SimkinAixiang JiangGerben DunsClementine SarkozyLaura K HiltonElizabeth A ChavezGabriela C SegatRachel WongJubin KimTomohiro AokiRashedul IslamChristina MayStacy HungKate TyshchenkoRyan R BrinkmanMartin HirstAly KarsanCiara FreemanLaurie H SehnRyan D MorinAndrew J RothKerry J SavageJeffrey W CraigSohrab P ShahChristian SteidlDavid W ScottAndrew P Weng
Published in: Nature communications (2022)
Follicular lymphoma (FL) is an indolent cancer of mature B-cells but with ongoing risk of transformation to more aggressive histology over time. Recurrent mutations associated with transformation have been identified; however, prognostic features that can be discerned at diagnosis could be clinically useful. We present here comprehensive profiling of both tumor and immune compartments in 155 diagnostic FL biopsies at single-cell resolution by mass cytometry. This revealed a diversity of phenotypes but included two recurrent patterns, one which closely resembles germinal center B-cells (GCB) and another which appears more related to memory B-cells (MB). GCB-type tumors are enriched for EZH2, TNFRSF14, and MEF2B mutations, while MB-type tumors contain increased follicular helper T-cells. MB-type and intratumoral phenotypic diversity are independently associated with increased risk of transformation, supporting biological relevance of these features. Notably, a reduced 26-marker panel retains sufficient information to allow phenotypic profiling of future cohorts by conventional flow cytometry.
Keyphrases
  • single cell
  • rna seq
  • flow cytometry
  • high throughput
  • working memory
  • regulatory t cells
  • young adults
  • papillary thyroid
  • drug induced
  • childhood cancer