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Journal article

FOXP3 infiltrating lymphocyte density and PD-L1 expression in operable non-small cell lung carcinoma

Abstract:

Purpose/Aim: Regulatory FOXP3+ T-cells control the cytotoxic activity of effector cells and may have an essential role in the development of immune tolerance in cancer patients. Programed death ligand 1 PD-L1, expressed on cancer cell membranes also blocks the cytotoxic activity of PD1+ cytotoxic lymphocytes.

Materials and Methods: We assessed the immunohistochemical detection of these immune-tolerance related markers in a series of 98 non-small cell lung carcinomas (NSCLC) treated with surgery. The Tumor Infiltration Lymphocyte TIL density (mean number per x400 optical field) and the percentage of FOXP3+ TILs were assessed.

Results: PD-L1 expression was directly linked with the TIL density (p = 0.01) and with the extent of infiltration with FOXP3+ TILs, named as the FIL-score (p = 0.01). FIL-score was significantly higher in stage I disease (p = 0.04). IL6 expression was linked with high TIL-score. A low TIL-score, characterizing immune deficient tumors defined a significantly poorer prognosis subgroup of patients (p = 0.03). Stratification of these tumors according to the FIL-score showed that FOXP3 expression by TILs correlated with an even a poorer prognosis in univariate (p = 0.007; median survival 14 vs. 44 months, respectively) and in multivariate analysis (p = 0.01, hazard ratio 4.3).

Conclusion: Tumor stroma infiltration by FOXP3+ Tregs is an early event in the progression of NSCLC. Low lymphocytic infiltration defines poor prognosis, which becomes worse when the small numbers of infiltrating lymphocytes characterizing these tumors contain FOXP3 + Tregs. Furthermore, the direct association of FOXP3+ Treg infiltration density with PD-L1 expression by cancer cells implies a co-ordinated immune-suppressive activity in NSCLC.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1080/01902148.2019.1617371

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Clinical Laboratory Sciences
Role:
Author
ORCID:
0000-0002-3197-273X
More by this author
Institution:
University of Oxford
Department:
RDM
Sub department:
RDM Clinical Laboratory Sciences
Role:
Author


Publisher:
Taylor and Francis
Journal:
Experimental Lung Research More from this journal
Volume:
45
Issue:
3-4
Pages:
76-83
Publication date:
2019-05-28
Acceptance date:
2019-05-07
DOI:
EISSN:
1521-0499
ISSN:
0190-2148


Pubs id:
pubs:999022
UUID:
uuid:2b4a023f-597f-447d-9279-6ddc072c7a40
Local pid:
pubs:999022
Source identifiers:
999022
Deposit date:
2019-05-17

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