Evidence map›Paper›PMID 35195152›Full record

ArticleJournal of applied oral science : revista FOB2022

Immunoexpression of PD-L1, CD4+ and CD8+ cell infiltrates and tumor-infiltrating lymphocytes (TILs) in the microenvironment of actinic cheilitis and lower lip squamous cell carcinoma.

Vinícius Gonçalves de Souza, Damilys Joelly Souza Santos, Ana Gabriela Silva, Rosy Iara Maciel de Azambuja Ribeiro, Adriano Mota Loyola, Sérgio Vitorino Cardoso, Carla Silva Siqueira Miranda, Ludimila Paula Vaz Cardoso

Open access · diamondAbstract read
In one paragraph

Article in Journal of applied oral science : revista FOB, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Vinícius Gonçalves de SouzaUniversidade Federal de Jataí, Curso de Medicina, Jataí, Goiás, Brasil.ORCID http://orcid.org/0000-0002-1656-6928
Damilys Joelly Souza SantosUniversidade Federal de Jataí, Ambulatório de Diagnóstico Estomatológico do Sudoeste Goiano (ADESGO), Jataí, Goiás, Brasil.ORCID http://orcid.org/0000-0002-1214-9369
Ana Gabriela SilvaUniversidade Federal de São João del-Rei, Curso de Medicina, Laboratório de Patologia Experimental, Minas Gerais, Brasil.ORCID http://orcid.org/0000-0002-6438-6577
Rosy Iara Maciel de Azambuja RibeiroUniversidade Federal de São João del-Rei, Curso de Medicina, Laboratório de Patologia Experimental, Minas Gerais, Brasil.ORCID http://orcid.org/0000-0002-7374-4743
Adriano Mota LoyolaUniversidade Federal de Uberlândia, Faculdade de Odontologia, Patologia Oral, Uberlândia, Minas Gerais, Brasil.ORCID http://orcid.org/0000-0001-9707-9365
Sérgio Vitorino CardosoUniversidade Federal de Uberlândia, Faculdade de Odontologia, Patologia Oral, Uberlândia, Minas Gerais, Brasil.ORCID http://orcid.org/0000-0003-1809-0617
Carla Silva Siqueira MirandaUniversidade Federal de Jataí, Curso de Medicina, Jataí, Goiás, Brasil.ORCID http://orcid.org/0000-0002-8749-2284
Ludimila Paula Vaz CardosoUniversidade Federal de Jataí, Curso de Medicina, Jataí, Goiás, Brasil.ORCID http://orcid.org/0000-0002-9373-6273
Universidade Federal de Jataí · BRFederal University of São João del-Rei · BRUniversidade Federal de Uberlândia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLower lip squamous cell carcinomas (LLSCC) could be associated with a previous history of potentially malignant oral diseases (PMOD), especially actinic cheilitis (AC), with high sun exposure being a well-described risk factor. Immune evasion mechanisms, such as the PD-1/PD-L1 (programmed cell death protein 1/programmed death-ligand 1) pathway has been gaining prominence since immunotherapy with immune checkpoint inhibitors showed a positive effect on the survival of patients with different types of neoplasms. Concomitant with the characterization of the tumor microenvironment, the expression of either or both PD-1 and PD-L1 molecules may estimate mutual relations of progression or regression of the carcinoma and prognostic values of the patient.Considering the importance of tumor microenvironment characterization, this study aims to determine the immunoexpression of PD-L1 and correlate with the frequency of CD4+ and CD8+ cells in AC and LLSCC lesions and with tumor-infiltrating lymphocytes (TILs) in LLSCC and its relationship with histopathological characteristics. METHODOLOGY: This sample includes 33 cases of AC and 17 cases of LLSCC. The cases were submitted to histopathological analysis and to CD4+, CD8+, and PD-L1+ cell determination by immunohistochemistry.

resultsThere was a significant difference among the frequencies of CD4+, CD8+, and PD-L1+ cells between AC and LSCC cases, higher in the last group. Moreover, histopathological and atypical changes in AC and LLSCC were correlated with the frequencies of PD-L1+, CD4+, and CD8+ cells. In AC, PD-L1+ cases had a low frequency of CD4+ cells, but on the other hand, PD-L1+ cases of LLSCC had a higher frequency of CD4+ and CD8+ cells.

conclusionTherefore, the PD-L1 molecule may be a potential escape route for the immune response in oral lesions, but the mechanisms differ between AC and LLSCC. Future studies related to immune evasion and immunotherapy in oral lesions should consider the analysis of inflammatory infiltrate and TILs.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsB7-H1 AntigenCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCheilitisHumansLipLymphocytes, Tumor-InfiltratingPrognosisTumor MicroenvironmentB7-H1 Antigen

Identifiers

PMID35195152
PMCPMC8860405
OpenAlexW4212843420

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.