Faculty, Staff and Student Publications
Language
English
Publication Date
11-1-2024
Journal
Laboratory Investigation
DOI
10.1016/j.labinv.2024.102147
PMID
39389311
Abstract
Angioimmunoblastic T-cell lymphoma (AITL), the most common form of peripheral T-cell lymphoma, originates from follicular helper T (Tfh) cells and is notably resistant to current treatments. The disease progression and maintenance, at least in early stages, are driven by a complex interplay between neoplastic Tfh and clusters of B-cells within the tumor microenvironment, mirroring the functional crosstalk observed inside germinal centers. This interaction is further complicated by recurrent mutations, such as TET2 and DNMT3A, which are present in both Tfh cells and B-cells. These findings suggest that the symbiotic relationship between these 2 cell types could represent a therapeutic vulnerability. This review examines the key components and signaling mechanisms involved in the synapses between B-cells and Tfh cells, emphasizing their significant role in the pathobiology of AITL and potential as therapeutic targets.
Keywords
Animals, Humans, B-Lymphocytes, Signal Transduction, T Follicular Helper Cells, Tumor Microenvironment, Lymphoma, T-Cell, Peripheral, Angioimmunoblastic T-cell lymphoma, B-cells, BCL-6, CD40-CD40L, CXCR5, ICOS, T follicular helper cells
Published Open-Access
no
Recommended Citation
Sainz, Tania P; Sahu, Vishal; Gomez, Javier A; et al., "Role of the Crosstalk B:Neoplastic T Follicular Helper Cells in the Pathobiology of Nodal T Follicular Helper Cell Lymphomas" (2024). Faculty, Staff and Student Publications. 6476.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/6476
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