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Review

Nanomaterials and the Serosal Immune System in the Thoracic and Peritoneal Cavities

by
C. Frieke Kuper
1,*,
Raymond H. H. Pieters
2,3 and
Jolanda H. M. van Bilsen
4,*
1
Consultant, Haagstraat 13, 3581 SW Utrecht, The Netherlands
2
Immunotoxicology, Institute for Risk Assessment Sciences, Utrecht University, Yalelaan 1, 3584 CL Utrecht, The Netherlands
3
Innovative Testing in Life Sciences & Chemistry, Research Centre for Healthy and Sustainable Living, University of Applied Sciences Utrecht, Padualaan 97, 3584 CH Utrecht, The Netherlands
4
Department for Risk Analysis for Products in Development, Netherlands Organization for Applied Scientific Research (TNO), Princetonlaan 6, 3584 CB Utrecht, The Netherlands
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2021, 22(5), 2610; https://doi.org/10.3390/ijms22052610
Submission received: 8 February 2021 / Revised: 23 February 2021 / Accepted: 27 February 2021 / Published: 5 March 2021
(This article belongs to the Special Issue Interaction of Nanomaterials with the Immune System)

Abstract

The thoracic and peritoneal cavities are lined by serous membranes and are home of the serosal immune system. This immune system fuses innate and adaptive immunity, to maintain local homeostasis and repair local tissue damage, and to cooperate closely with the mucosal immune system. Innate lymphoid cells (ILCs) are found abundantly in the thoracic and peritoneal cavities, and they are crucial in first defense against pathogenic viruses and bacteria. Nanomaterials (NMs) can enter the cavities intentionally for medical purposes, or unintentionally following environmental exposure; subsequent serosal inflammation and cancer (mesothelioma) has gained significant interest. However, reports on adverse effects of NM on ILCs and other components of the serosal immune system are scarce or even lacking. As ILCs are crucial in the first defense against pathogenic viruses and bacteria, it is possible that serosal exposure to NM may lead to a reduced resistance against pathogens. Additionally, affected serosal lymphoid tissues and cells may disturb adipose tissue homeostasis. This review aims to provide insight into key effects of NM on the serosal immune system.
Keywords: innate lymphocytes; FALC; MS; pericardium; peritoneum; pleura; SALC; serosa innate lymphocytes; FALC; MS; pericardium; peritoneum; pleura; SALC; serosa
Graphical Abstract

Share and Cite

MDPI and ACS Style

Kuper, C.F.; Pieters, R.H.H.; van Bilsen, J.H.M. Nanomaterials and the Serosal Immune System in the Thoracic and Peritoneal Cavities. Int. J. Mol. Sci. 2021, 22, 2610. https://doi.org/10.3390/ijms22052610

AMA Style

Kuper CF, Pieters RHH, van Bilsen JHM. Nanomaterials and the Serosal Immune System in the Thoracic and Peritoneal Cavities. International Journal of Molecular Sciences. 2021; 22(5):2610. https://doi.org/10.3390/ijms22052610

Chicago/Turabian Style

Kuper, C. Frieke, Raymond H. H. Pieters, and Jolanda H. M. van Bilsen. 2021. "Nanomaterials and the Serosal Immune System in the Thoracic and Peritoneal Cavities" International Journal of Molecular Sciences 22, no. 5: 2610. https://doi.org/10.3390/ijms22052610

APA Style

Kuper, C. F., Pieters, R. H. H., & van Bilsen, J. H. M. (2021). Nanomaterials and the Serosal Immune System in the Thoracic and Peritoneal Cavities. International Journal of Molecular Sciences, 22(5), 2610. https://doi.org/10.3390/ijms22052610

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