Landscape of tumor and immune system cells-derived exosomes in lung cancer: mediators of antitumor immunity regulation

Front Immunol. 2023 Oct 17:14:1279495. doi: 10.3389/fimmu.2023.1279495. eCollection 2023.

Abstract

The immune system plays a critical role in cancer, including lung cancer, which is the leading cause of cancer-related deaths worldwide. Immunotherapy, particularly immune checkpoint blockade, has revolutionized the treatment of lung cancer, but a large subset of patients either do not respond or develop resistance. Exosomes, essential mediators of cell-to-cell communication, exert a profound influence on the tumor microenvironment and the interplay between cancer and the immune system. This review focuses on the role of tumor-derived exosomes and immune cells-derived exosomes in the crosstalk between these cell types, influencing the initiation and progression of lung cancer. Depending on their cell of origin and microenvironment, exosomes can contain immunosuppressive or immunostimulatory molecules that can either promote or inhibit tumor growth, thus playing a dual role in the disease. Furthermore, the use of exosomes in lung cancer immunotherapy is discussed. Their potential applications as cell-free vaccines and drug delivery systems make them an attractive option for lung cancer treatment. Additionally, exosomal proteins and RNAs emerge as promising biomarkers that could be employed for the prediction, diagnosis, prognosis and monitoring of the disease. In summary, this review assesses the relationship between exosomes, lung cancer, and the immune system, shedding light on their potential clinical applications and future perspectives.

Keywords: exosome; immune cell; immunotherapy; lung cancer; tumor microenvironment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Communication
  • Exosomes* / metabolism
  • Humans
  • Immune System / metabolism
  • Immunotherapy
  • Lung Neoplasms* / metabolism
  • Lung Neoplasms* / therapy
  • Tumor Microenvironment

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The authors acknowledge funding from ISCIII (PI20/01109) and co-funded by FEDER from Regional Development European Funds (European Union), the Ministry of Health and Social Welfare of the Junta de Andalucía (Nicolas Monardes Program RC-0004-2020, and PECART-0091-2020), Andalusian Research, Development and Innovation Plan (PY20_00992), and Andalusia-Roche Network Mixed Alliance in Precision Medical Oncology, resources of which are composed of financial contribution from Andalusian Public Health System though of grant entitled “ALIANZA MIXTA EN RED ANDALUCÍA - ROCHE EN ON ONCOLOGÍA MÉDICA DE PRECISIÓN (INVESTIGACIÓN BÁSICA/TRASLACIONAL)” financed by Regional Ministry of Health and Families (PIP-0044-2020) through a competitive public call for proposals and by Roche Farma S. A. with private funds. Roche Farma S.A had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.