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Mass Cytometry Analysis Reveals that Specific Intratumoral CD4(+) T Cell Subsets Correlate with Patient Survival in Follicular Lymphoma

Follicular lymphoma (FL) is an indolent B cell malignancy characterized by an extensive but poorly functional T cell infiltrate in the tumor microenvironment. Using mass cytometry, we identified at least 12 subsets of intratumoral CD4(+) T cells, 3 of which were unique to FL biopsies versus control...

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Detalles Bibliográficos
Autores principales: Yang, Zhi-Zhang, Jin Kim, Hyo, Villasboas, Jose C., Price-Troska, Tammy, Jalali, Shahrzad, Wu, Hongyan, Luchtel, Rebecca A., Polley, Mei-Yin C., Novak, Anne J., Ansell, Stephen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402596/
https://www.ncbi.nlm.nih.gov/pubmed/30784598
http://dx.doi.org/10.1016/j.celrep.2019.01.085
Descripción
Sumario:Follicular lymphoma (FL) is an indolent B cell malignancy characterized by an extensive but poorly functional T cell infiltrate in the tumor microenvironment. Using mass cytometry, we identified at least 12 subsets of intratumoral CD4(+) T cells, 3 of which were unique to FL biopsies versus control tissues. Of these subsets, the frequency of naive T cells correlated with improved patient survival. Although total PD-1(+) T cell numbers were not associated with patient outcome, specific PD-1(+) T cell subpopulations were associated with poor survival. Intratumoral T cells lacking CD27 and CD28 co-stimulatory receptor expression were enriched in FL and correlated with inferior patient outcomes. In vitro models revealed that CD70(+) lymphoma cells played an important role in expanding this population. Taken together, our mass cytometry results identified CD4(+) memory T cell populations that are poorly functional due to loss of co-stimulatory receptor expression and are associated with an inferior survival in FL.