The effects of HIV and oncogenic human papillomavirus on the tumor immune microenvironment of penile squamous cell carcinoma.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 22 12 2023
accepted: 02 03 2024
medline: 1 5 2024
pubmed: 1 5 2024
entrez: 1 5 2024
Statut: epublish

Résumé

Penile squamous cell carcinoma (PSCC) occurs more frequently in some developing countries compared to developed countries. Infection with HIV and/or high-risk human papillomavirus (hrHPV) are risk factors for penile cancer development. The tumor microenvironment of PSCC may predict prognosis and may inform on the best targets for immunotherapy. We evaluated the immune microenvironment of penile tumors histologically, and determined whether and/or how HIV and/or hrHPV infections affect this tumor microenvironment. We conducted a prospective analytical cross-sectional study in which penile cancer tumors from 35 patients presenting at the University Teaching Hospital in Lusaka, Zambia were histologically staged and assessed for presence of tumor infiltrating immune cells and expression of immune checkpoints. Immunohistochemistry was used to evaluate immune checkpoints and infiltrating immune cells, while multiplex real-time polymerase chain reaction was used for hrHPV genotyping. The median age of all participants was 55 years. About 24% had advanced histological stage, 83% were HIV+, and 63% had hrHPV detected in their tumors using multiplex real-time polymerase chain reaction. PDL1 expression was significantly higher in HIV- participants than HIV+ participants (p = 0.02). Tumors with multiple hrHPV infections had a significantly higher number of cells expressing TIM3 than those with one hrHPV (p = 0.04). High grade tumors had a significantly higher infiltrate of FoxP3+ cells (p = 0.02), CD68+ cells (p = 0.01), CD163+ cells (p = 0.01), LAG3+ cells (p = 0.01), PD1+ cells (p = 0.01) and TIM3+ cells (p = 0.03) when compared with low grade tumours. There was significant moderate to strong positive correlation of cells expressing PD1 and LAG3 (⍴ = 0.69; p = 0.0001), PD1 and TIM3 (⍴ = 0.49; p = 0.017) and TIM3 and LAG3 PDL1 (⍴ = 0.61; p = 0.001). In conclusion, the tumor microenvironment of penile squamous cell carcinoma seems to be affected by both HIV and HPV infections. TIM3 appears to be a potential therapeutic target in PSCC patients with hrHPV infections.

Identifiants

pubmed: 38691575
doi: 10.1371/journal.pone.0300729
pii: PONE-D-23-42111
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0300729

Informations de copyright

Copyright: © 2024 Mumba et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Chibamba Mumba (C)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Zoran Muhimbe (Z)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Victor Mapulanga (V)

Department of Surgery, School of Medicine, University of Zambia, Lusaka, Zambia.

Musonda Kawimbe (M)

HHV8 Research Molecular Virology Laboratory, University Teaching Hospital, Lusaka, Zambia.

Keagan Mutale (K)

HHV8 Research Molecular Virology Laboratory, University Teaching Hospital, Lusaka, Zambia.

Anglin Hamasuku (A)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Jane Musumali (J)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Nicholas K Mwale (NK)

Department of Physiological Sciences, School of Medicine, University of Zambia, Lusaka, Zambia.

Owen Ngalamika (O)

HHV8 Research Molecular Virology Laboratory, University Teaching Hospital, Lusaka, Zambia.
Dermatology and Venerology Division, School of Medicine, University of Zambia, Lusaka, Zambia.

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Classifications MeSH