Environmental Chemical-Induced Reactive Oxygen Species Generation and Immunotoxicity: A Comprehensive Review

• Published in: Antioxidants & redox signaling Vol. 40; no. 10-12; p. 691
• Main Authors: D'Souza, Leonard Clinton, Paithankar, Jagdish Gopal, Stopper, Helga, Pandey, Ashutosh, Sharma, Anurag
• Format: Journal Article
• Language: English
• Published: United States 01-04-2024
• Subjects: Humans; Oxidative Stress; Reactive Oxygen Species; Signal Transduction; Toll-Like Receptors; Xenobiotics - toxicity; immunotoxicity; redox signaling; immunity; xenobiotics; oxidative stress; ROS
• ISSN: 1557-7716
• DOI: 10.1089/ars.2022.0117

Reactive oxygen species (ROS), the reactive oxygen-carrying chemicals moieties, act as pleiotropic signal transducers to maintain various biological processes/functions, including immune response. Increased ROS production leads to oxidative stress, which is implicated in xenobiotic-induced adverse effects. Understanding the immunoregulatory mechanisms and immunotoxicity is of interest to developing therapeutics against xenobiotic insults.
While developmental studies have established the essential roles of ROS in the establishment and proper functioning of the immune system, toxicological studies have demonstrated high ROS generation as one of the potential mechanisms of immunotoxicity induced by environmental chemicals, including heavy metals, pesticides, aromatic hydrocarbons (benzene and derivatives), plastics, and nanoparticles. Mitochondrial electron transport and various signaling components, including NADH oxidase, toll-like receptors (TLRs), NF-κB, JNK, NRF2, p53, and STAT3, are involved in xenobiotic-induced ROS generation and immunotoxicity.
With many studies demonstrating the role of ROS and oxidative stress in xenobiotic-induced immunotoxicity, rigorous and orthogonal approaches are needed to achieve in-depth and precise understanding. The association of xenobiotic-induced immunotoxicity with disease susceptibility and progression needs more data acquisition. Furthermore, the general methodology needs to be possibly replaced with high-throughput precise techniques.
The progression of xenobiotic-induced immunotoxicity into disease manifestation is not well documented. Immunotoxicological studies about the combination of xenobiotics, age-related sensitivity, and their involvement in human disease incidence and pathogenesis are warranted.
40, 691-714.