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Authors Zhao S, Sun M, Meng H, Ji H, Liu Y, Zhang M, Li H, Li P, Zhang Y, Zhang Q
Received 28 January 2019
Accepted for publication 30 April 2019
Published 23 May 2019 Volume 2019:11 Pages 4743—4756
DOI https://doi.org/10.2147/CMAR.S203156
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Cristina Weinberg
Peer reviewer comments 2
Editor who approved publication: Dr Antonella D'Anneo
Background: Toll-like
receptor 4 (TLR4), a member of the pattern recognition receptors, has been
reported to be involved in carcinogenesis. However, the clinical impact of TLR4
in peripheral T-cell lymphomas (PTCL) remains unclear.
Methods: The
current study, using immunohistochemical staining, first examined TLR4 and
programmed cell death-ligand 1 (PD-L1) expression in patients with PTCL, to
correlate TLR4 and PD-L1 expression with clinicopathological parameters.
Results: It was
found that the rates of high expression of TLR4 and PD-L1 were 41.7% and 45.8%,
respectively. TLR4 expression was closely associated with PD-L1 expression. The
expression of TLR4 was closely related to primary extranodal site involvement,
increased Ann Arbor stage, and low hemoglobin expression, while the expression
of PD-L1 was closely related to a low platelet count and multiple extranodal
organ involvements (>1). High expression of either TLR4 or PD-L1 indicated a
poor survival rate for patients with PTCL. Multivariate analyses further
confirmed that increased expression levels of TLR4 and PD-L1 are unfavorable
prognostic factors for PTCL.
Conclusion: This
study demonstrates that the expressions of TLR4 and PD-L1 are independent
predictors of survival time for patients with PTCL. Thus, TLR4 and PD-L1 may
serve as potential therapeutic targets in PTCL patients.
Keywords: TLR4,
PD-L1, peripheral T-cell lymphomas, non-Hodgkin’s lymphoma, immune checkpoint
inhibitor, survival
