B3 Non-refereed article in a conference publication
The response of phagocytes to indoor air toxicity
Authors: L. Vilén, J. Atosuo, E. Suominen, E.-M. Lilius
Editors: Pedro M. Arezes, João Santos Baptista, Monica P. Barroso, Paula Carneiro, Patrício Cordeiro, Nelson Costa, Rui B. Melo, A. Sergio Miguel, Gonçalo Perestrelo
Conference name: International Symposium on Occupation Safety and Hygiene
Publisher: CRC PRESS-BALKEMA, PO BOX 11320, LEIDEN, 2301 EH, NETHERLANDS
Publication year: 2018
Book title : Occupational Safety and Hygiene VI
Journal name in source: OCCUPATIONAL SAFETY AND HYGIENE VI
First page : 341
Last page: 345
Number of pages: 5
ISBN: 978-1-138-54203-7
eISBN: 978-1-351-00888-4
DOI: https://doi.org/10.1201/9781351008884(external)
Abstract
This Perspective presents a viewpoint on potential methods assessing toxicity of indoor air. Until recently, the major techniques to document mouldy environment have been microbial isolation using conventional culture techniques for fungi and bacteria as well as in some instances polymerase chain reaction to detect microbial genetic components. It has become increasingly evident that bacterial and fungal toxins, their metabolic products and volatile organic substances emitted from corrupted constructions are the major health risks. Here, we illustrate how phagocytes, especially neutrophils can be used either in vitro as probe cells, directly exposed to the toxic agent studied, or they can act as in vivo indicators of the whole biological system exposed to the agent. There are two convenient methods assessing the responses: to measure chemiluminescence emission from activated phagocytes and to measure quantitatively by flow cytometry the expression of complement and immunoglobulin receptors on the phagocyte surface.
This Perspective presents a viewpoint on potential methods assessing toxicity of indoor air. Until recently, the major techniques to document mouldy environment have been microbial isolation using conventional culture techniques for fungi and bacteria as well as in some instances polymerase chain reaction to detect microbial genetic components. It has become increasingly evident that bacterial and fungal toxins, their metabolic products and volatile organic substances emitted from corrupted constructions are the major health risks. Here, we illustrate how phagocytes, especially neutrophils can be used either in vitro as probe cells, directly exposed to the toxic agent studied, or they can act as in vivo indicators of the whole biological system exposed to the agent. There are two convenient methods assessing the responses: to measure chemiluminescence emission from activated phagocytes and to measure quantitatively by flow cytometry the expression of complement and immunoglobulin receptors on the phagocyte surface.