Circulating Tfh1

• Published in: PloS one Vol. 13; no. 1; p. e0190468
• Main Authors: Byford, Elliot T, Carr, Matthew, Ladikou, Eleni, Ahearne, Matthew J, Wagner, Simon D
• Format: Journal Article
• Language: English
• Published: Public Library of Science 02.01.2018
• Subjects: Analysis; Cancer; Development and progression; Gene expression; Genetic aspects; Non-Hodgkin's lymphomas; Statistics; T cells; United States
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0190468

CD4.sup.+ T-cell subsets are found in the tumour microenvironment (TME) of low-grade B-cell non-Hodgkin's lymphomas such as marginal zone lymphoma (MZL) or follicular lymphoma (FL). Both numbers and architecture of activating follicular helper T-cells (Tfh) and suppressive Treg in the TME of FL are associated with clinical outcomes. There has been almost no previous work on CD4.sup.+ T-cells in MZL. It is now recognised that circulating CD4.sup.+ CXCR5.sup.+ T-cells are the memory compartment of Tfh cells. We determined differences in number of circulating Tfh (cTfh) cells and cTfh subsets between normal subjects and patients with FL or MZL. Lymphoma patients showed increased numbers of cTfh1 and reduced cTfh17 cells due to decreased expression of the subset-defining marker CCR6 in patients. PD1, a surface marker associated with Tfh cells, showed increased expression on cTfh subsets in patients. Focusing on MZL we determined expression of 96 T-cell associated genes by microfluidic qRT-PCR. Analysis of differentially expressed genes showed significant differences between normal subjects and patients both for bulk cTfh (CCL4) and the cTfh1 subset (JAK3). While our findings require confirmation in larger studies we suggest that analysis of number and gene expression of circulating T-cells might be a source of clinically useful information as is the case for T-cells within lymphoma lymph nodes.