Tocilizumab does not block interleukin-6 (IL-6) signaling in murine cells
PLoS ONE, ISSN: 1932-6203, Vol: 15, Issue: 5, Page: e0232612
2020
- 23Citations
- 49Captures
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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.
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Metrics Details
- Citations23
- Citation Indexes23
- 23
- CrossRef2
- Captures49
- Readers49
- 49
Article Description
Tocilizumab is a humanized monoclonal antibody that is approved for the treatment of different human inflammatory diseases, including rheumatoid arthritis and cytokine release syndrome. Tocilizumab binds to the interleukin-6 receptor (IL-6R) and thereby blocks signaling of the pro-inflammatory cytokine IL-6. Initial studies and all authority assessment reports state that tocilizumab is effective in humans, but cannot bind to the murine or rat IL-6R and thus not block IL-6 signaling in the mouse. However, several recent studies described the use of tocilizumab in mice and reported biological effects that were attributed to IL-6 blockade. In this study, we investigate the capability of tocilizumab to block IL-6 signaling using different human and murine cell lines. Our results unequivocally confirm the original state of the art that tocilizumab blocks signaling via the human IL-6R, but does not block IL-6 signaling in murine cells.
Bibliographic Details
10.1371/journal.pone.0232612; 10.1371/journal.pone.0232612.g001; 10.1371/journal.pone.0232612.g004; 10.1371/journal.pone.0232612.g003; 10.1371/journal.pone.0232612.g002
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85084277426&origin=inward; http://dx.doi.org/10.1371/journal.pone.0232612; http://www.ncbi.nlm.nih.gov/pubmed/32365119; https://dx.plos.org/10.1371/journal.pone.0232612; https://dx.plos.org/10.1371/journal.pone.0232612.g001; http://dx.doi.org/10.1371/journal.pone.0232612.g001; https://dx.plos.org/10.1371/journal.pone.0232612.g004; http://dx.doi.org/10.1371/journal.pone.0232612.g004; https://dx.plos.org/10.1371/journal.pone.0232612.g003; http://dx.doi.org/10.1371/journal.pone.0232612.g003; https://dx.plos.org/10.1371/journal.pone.0232612.g002; http://dx.doi.org/10.1371/journal.pone.0232612.g002; https://dx.doi.org/10.1371/journal.pone.0232612.g001; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0232612.g001; https://dx.doi.org/10.1371/journal.pone.0232612.g002; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0232612.g002; https://dx.doi.org/10.1371/journal.pone.0232612.g003; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0232612.g003; https://dx.doi.org/10.1371/journal.pone.0232612; https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0232612; https://dx.doi.org/10.1371/journal.pone.0232612.g004; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0232612.g004; https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0232612&type=printable
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