Mechanisms and pathologic significances in increase in serum interleukin-6 (IL-6) and soluble IL-6 receptor after administration of an anti-IL-6 receptor antibody, tocilizumab, in patients with…
By N. Nishimoto, K. Terao, T. Mima, H. Nakahara, N. Takagi, Takahiro Kakehi. Blood, 2008
767 citations recorded by the source corpus.
Subfields: Genetics, Pathology and Forensic Medicine, Rheumatology
View Paper: https://www.semanticscholar.org/paper/e89b09f26725be8c4ee66dd266eebe06baec9c55
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In Genetics
In Pathology and Forensic Medicine
In Rheumatology
- Martina Anzaghe
- S. Rose‐John
- Simon A. Jones
- J. Scheller
- Yen-Ju Lin
- Toshio Tanaka
- T. Kishimoto
- M. Narazaki
Citations in the corpus
- Clinical and Biologic Correlates of Neurotoxicity Associated with CAR T Cell Therapy in Patients with B-cell Acute Lymphoblastic Leukemia (B-ALL) (2018, background): “Suboptimal response of neurotoxicity to tocilizumab may be due to elevation of multiple cytokines in addition to IL6 in patients with severe neurotoxicity, or because tocilizumab induces a transient increase of serum IL6 which might increase CNS levels (27).”
- IL-6 in inflammation, immunity, and disease. (2014, background): “It was found that if free serum concentration of tocilizumab is maintained at more than 1 mg/ml, CRP remains negative (Nishimoto et al. 2008), indicating that IL-6 plays a major role in the induction of CRP expression and that IL-6 may be involved in the development of almost all chronic inflammator”
- Identification of Predictive Biomarkers for Cytokine Release Syndrome after Chimeric Antigen Receptor T cell Therapy for Acute Lymphoblastic Leukemia (2016, background): “In other IL6-mediated diseases, IL6 levels often go up and sIL6R levels either increase or decrease after treatment as the interaction between IL6R and IL6 is blocked (21, 23, 24).”
- Tocilizumab for the treatment of severe COVID-19 pneumonia with hyperinflammatory syndrome and acute respiratory failure: A single center study of 100 patients in Brescia, Italy (2020, unknown): “IL-6 serum levels increased, similarly to what was reported after TCZ administration in patients with Rheumatoid Arthritis and Castleman disease [22].”
- Tocilizumab treatment in COVID‐19: A single center experience (2020, background): “Actually, IL‐6 is mainly eliminated via IL‐6R‐mediated clearance.(8) Binding of TCZ to IL‐6R inhibits receptor‐mediated clearance of IL‐6, leading to its accumulation in serum.”
- Therapeutic strategies for the clinical blockade of IL-6/gp130 signaling. (2011, background): “Patients treated with tocilizumab show only a mild accumulation of IL-6, due to blockade of IL-6R– dependent internalization, which regulates IL-6 clearance (118).”
- Endothelial activation and blood-brain barrier disruption in neurotoxicity after adoptive immunotherapy with CD19 CAR-T cells (2017, background): “094 40–60 years 42 (66) 8 (13) 14 (22) 64 >60 years 27 (64) 7 (17) 8 (19) 42 Sex, n (%) Male 59 (63) 17 (18) 17 (18) 93 0.”
- Targeting interleukin-6 in inflammatory autoimmune diseases and cancers. (2014, background): “Serum levels of CRP remain suppressed whenever free tocilizumab levels are above 1 μg/mL, suggesting that CRP is a downstream biomarker that allow to estimate the duration and magnitude of IL-6 suppression in vivo (Nishimoto et al., 2008).”
- Update on the Pathomechanism, Diagnosis, and Treatment Options for Rheumatoid Arthritis (2020, background): “Clinical research suggests that tocilizumab does not inhibit IL-6 production directly, instead, as long as free tocilizumab is detectable, the sIL-6R is saturated with tocilizumab [250].”