Beyond bacterial killing: NADPH oxidase 2 is an immunomodulator
Immunology Letters, ISSN: 0165-2478, Vol: 221, Page: 39-48
2020
- 39Citations
- 38Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations39
- Citation Indexes39
- 39
- CrossRef23
- Captures38
- Readers38
- 38
Review Description
NADPH oxidase 2 is a superoxide-generating enzymatic complex based on the catalytic subunit gp91phox that is also known as Nox2. Initially identified in neutrophils, NADPH oxidase 2 was long considered responsible only for the killing of phagocytized microorganisms. However, advances in knowledge about redox signalling and the discovery of Nox2 expression in different cell types, including macrophages, endothelial cells (ECs), dendritic cells (DCs), B and T lymphocytes, have changed this paradigm. For instance, Nox2 expressed in macrophages and neutrophils limits the transcription of cytokines and toll-like receptors (TLRs) induced by lipopolysaccharide (LPS), whereas DC Nox2 facilitates antigen cross-presentation to T cells. More recently, our group observed that Nox2 inhibits the suppressive ability of regulatory T cells (Tregs) by limiting NF-κB and FoxP3 activation. In this review, we discuss non-canonical microbicidal functions and redox-signalling-associated roles of Nox2 in different cell types, emphasizing its roles in the innate and adaptive immune system.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0165247819306005; http://dx.doi.org/10.1016/j.imlet.2020.02.009; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85080050559&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32092360; https://linkinghub.elsevier.com/retrieve/pii/S0165247819306005; https://dx.doi.org/10.1016/j.imlet.2020.02.009
Elsevier BV
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