212
Views
21
CrossRef citations to date
0
Altmetric
Drug Profile

Tocilizumab: molecular intervention therapy in children with systemic juvenile idiopathic arthritis

&
Pages 735-743 | Published online: 10 Jan 2014

References

  • Cassidy JT, Petty RE. Juvenile idiopathic arthritis. In: Textbook of Pediatric Rheumatology (5th Edition). Cassidy JT, Petty RE (Eds). WB Saunders, PA, USA, 291–303 (2005).
  • Billiau AD, Roskams T, Van Damme-Lombaerts R, Matthys P, Wouters C. Macrophage activation syndrome: characteristic findings on liver biopsy illustrating the key role of activated IFN-γ-producing lymphocytes and IL-6- and TNF-α-producing macrophages. Blood105, 1648–1651 (2005).
  • Packham JC, Hall MA, Pimm TJ. Long-term follow-up of 246 adults with juvenile idiopathic arthritis: predictive factors for mood and pain. Rheumatology (Oxford)41, 1444–1449 (2002).
  • Pascual V, Allantaz F, Patel P et al. How the study of children with rheumatic diseases identified interferon α and interleukin 1 as novel therapeutic targets. Immunol. Rev.223, 39–59 (2008).
  • Vastert SJ, van Wijk R, D’Urbano LE et al. Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset juvenile idiopathic arthritis. Rheumatology49, 441–449 (2010).
  • de Jager W, Vastert SJ, Beekman JM et al. Defective phosphorylation of interleukin-18 receptor b causes impaired natural killer cell function in systemic-onset juvenile idiopathic arthritis. Arthritis Rheum.60, 2782–2793 (2009).
  • de Benedetti F, Massa M, Robbioni P. Correlation of interleukin-6 levels with joint involvement and thrombocytosis in patients with systemic juvenile rheumatoid arthritis. Arthritis Rheum.34, 1158–1163 (1991).
  • Lieskovska J, Guo D, Derman E. Growth impairment in IL-6-overexpressing transgenic mice is associated with induction of SOCS3 mRNA. Growth Horm. IGF Res.13, 26–35 (2003).
  • Vastert SJ, Kuis W, Grom AA. Systemic JIA: new development in the understanding of the pathophysiology and therapy. Best Pract. Res. Clin. Rheumatol.23, 655–664 (2009).
  • Harden LM, du Plessis I, Poole S et al. Interleukin (IL)-6 and IL-1β act synergistically within the brain to induce sickness behavior and fever in rats. Brain Behav. Immun.22, 838–849 (2008).
  • Raj DSC. Role of interleukin-6 in the anemia of chronic disease. Semin. Arthritis Rheum.38, 382–388 (2009).
  • Fournier T, Medjoubi-N N, Porquet D. α-1-acid glycoprotein. Biochim. Biophys. Acta1482, 157–171 (2000).
  • Hagihara K, Nishikawa T, Sugamata Y et al. Essential role of STAT3 in cytokine-driven NF-κB-mediated serum amyloid A gene expression. Genes Cells10, 1051–1063 (2005).
  • Nishikawa T, Hagihara K, Serada S et al. Transcriptional complex formation of c-Fos, STAT3, and hepatocyte NF-1α is essential for cytokine-driven C-reactive protein gene expression. J. Immunol.180, 3492–3501 (2008).
  • Houssiau FA, Devogelaer JP, Van Damme J, de Deuxchaisnes CN, Van Snick J. Interleukin-6 in synovial fluid and serum of patients with rheumatoid arthritis and other inflammatory arthritides. Arthritis Rheum.31, 784–788 (1988).
  • Yoshizaki K, Matsuda T, Nishimoto N et al. Pathogenic significance of interleukin-6 (IL-6/BSF-2) in Castleman’s disease. Blood74, 1360–1367 (1989).
  • Iwamoto M, Nara H, Hirata D, Minota S, Nishimoto N, Yoshizaki K. Humanized monoclonal anti-interleukin-6 receptor antibody for treatment of intractable adult-onset Still’s disease. Arthritis Rheum.46, 3388–3389 (2002).
  • Sato K, Tsuchiya, Saldanha J et al. Reshaping a human antibody to inhibit the interleukin-6-dependent tumor cell growth. Cancer Res.53, 851–856 (1993).
  • Yokota S, Miyame T, Imagawa T et al. Therapeutic efficacy of humanized recombinant anti-interleukin-6 receptor antibody in children with systemic-onset juvenile idiopathic arthritis. Arthritis Rheum.52, 818–825 (2005).
  • Yokota S, Imagawa T, Mori M et al. Efficacy and safety of tocilizumab in patients with systemic-onset juvenile idiopathic arthritis: a randomized, double-blind, placebo-controlled, withdrawal Phase III trial. Lancet371, 998–1006 (2008).
  • de Benedetti F, Martini A. Targeting the interleukin-6 receptor: a new treatment for systemic juvenile idiopathic arthritis? Arthritis Rheum.52, 687–693 (2005).
  • Pascual V, Allantaz F, Arce E et al. Role of interleukin-1 (IL-1) in the pathogenesis of systemic onset juvenile idiopathic arthritis and clinical aspect to IL-1 blockade. J. Exp. Med.201, 1479–1486 (2005).
  • Lurati A, Teruzzi B, Salmaso A et al. Macrophage activation syndrome during anti-IL1 receptor therapy (anakinra) in a patient affected by systemic-onset idiopathic juvenile arthritis. Paed. Rheumatol. Online3, 79–85 (2005).
  • Lequerre T, Quarties F, Rosellini D et al. Interleukin-1 receptor antagonist (anakinra) treatment in patients with systemic-onset juvenile idiopathic arthritis or adult onset Still disease: preliminary experience in France. Ann. Rheum. Dis.67, 302–308 (2008).
  • Petty RE, Southwood TR, Manners P et al. International League of Association for Rheumatology. International League Association for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001. J. Rheumatol.31, 390–392 (2004).
  • Zak M, Muller J, Karup Pedersen F. Final height, armspan, subischial leg length and body proportion in juvenile chronic arthritis: a long-term follow-up study. Horm. Res.52, 80–85 (1999).
  • Nakajima S, Naruto T, Miyamae T, Imagawa T, Mori M, Nishimaki S, Yokota S. Interleukin-6 inhibits early differentiation of ATDC5 chondrogenic progenitor cells. Cytokine47, 91–97 (2009).
  • Immonen K, Savolainen A, Kautiainen H, Hakala M. Longterm outcome of amyloidosis associated with juvenile idiopathic arthritis. J. Rheumatol.35, 907–912 (2008).
  • Cortis E, Insalaco A. Macrophage activation syndrome in juvenile idiopathic arthritis. Acta Pediatr. Suppl.95, 38–41 (2005).
  • Grom AA. Natural killer cell dysfunction: a common pathway in systemic-onset juvenile rheumatoid arthritis, macrophage activation syndrome, and hemophagocytic lymphohistiocytosis? Arthritis Rheum.50, 689–698 (2004).
  • Janka G. Hemophagocytic lymphohistiocytosis: when the immune system runs amok. Klin. Padiatr.221, 278–285 (2009).
  • Kishimoto T, Hirano T. Molecular regulation of B lymphocyte response. Annu. Rev. Immunol.6, 485–512 (1988).
  • Hirano T. Interleukin-6 and its receptor: ten years later. Int. Rev. Immunol.16, 249–284 (1998).
  • Taga T, Kishimoto T. Gp130 and the interleukin-6 family of cytokines. Annu. Rev. Immunol.15, 797–819 (1997).
  • Leaman DW, Leung S, Li X, Stark GR. Regulation of STAT-dependent pathway by growth factors and cytokines. FASEB J.10, 1578–1588 (1996).
  • Taga T, Kishimoto T. Gp130 and the interleukin-6 family of cytokines. Ann. Rev. Immunol.15, 797–819 (1997).
  • De Benedetti F, Pignati P, Gerloni V et al. Differences in synovial fluid cytokine levels between juvenile and adult rheumatoid arthritis. J. Rheumatol.24, 1403–1409 (1997).
  • Romanovsky AA, Almeida MC, Aronoff DM et al. Fever and hypothermia in systemic inflammation: recent discoveries and revisions. Front. Biosci.10, 2193–2216 (2005).
  • Pignatti P, Vivarelli M, Meazza C, Rizzolo MG, Martini A, De Benedetti F. Abnormal regulation of interleukin 6 in systemic juvenile idiopathic arthritis. J. Rheumatol.28, 1670–1676 (2001).
  • Grom AA. Macrophage activation syndrome and reactive hemophagocytic lymphohistiocytosis: the same entities? Curr. Opin Rheumatol.15, 587–590 (2003).
  • Ravelli A, Caria MC, Buratti S et al. Methotrexate as a possible trigger of macrophage activation syndrome in systemic juvenile idiopathic arthritis. J. Rheumatol.28, 865–867 (2001).
  • Bihl F, Emmenegger U, Reichen J et al. Macrophage activation syndrome is associated with lobular hepatitis and severe duct injury with cholestasis. J. Hepatol.44, 1208–1212 (2006).
  • Stabile A, Bertoni B, Ansuini V, La Torraca I, Salli A, Rigante D. The clinical spectrum and treatment options of macrophage activation syndrome in the pediatric age. Eur. Rev. Med. Pharmacol. Sci.10, 53–59 (2006).
  • Miller LL, Miller SC, Torti SV, Tsuji Y, Torti FM. Iron-independent induction of ferritin H chain by tumor necrosis factor. Proc. Natl Acad. Sci. USA88, 4946–4950 (1991).
  • Aulitzky WE, Tilg H, Herold M, Berger M, Vogel W, Judmaier G. Enhanced serum levels of β-2-microglobulin, neopterin, and interferon-γ in patients treated with recombinant tumor necrosis factor-α. J. Interferon Res.8, 655–664 (1988).
  • Pucci B, Bertani F, Karpinich NO et al. Detailing the role of Bax translocation, cytochrome c release, and perinuclear clustering of the mitochondria in the killing of HeLa cells by TNF. J. Cell. Physiol.217, 442–449 (2008).
  • Soriano ME, Nicolosi L, Bernardi P. Desensitization of the permeability transition pore by cyclosporin a prevents activation of the mitochondrial apoptotic pathway and liver damage by tumor necrosis factor-α. J. Biol. Chem.279, 36803–36808 (2004).
  • Semb H, Peterson J, Tavernier J, Olivecrona T. Multiple effects of tumor necrosis factor on lipoprotein lipase in vivo. J. Biol. Chem.262(17), 8390–8394 (1987).
  • Romanovsky AA, Simons CT, Kulchitsky VA. ‘Biphasic’ fever often consist of more than two phases. Am. J. Physiol. Regul. Integr. Comp. Physiol.275, R323–R331 (1998).
  • Takeuchi O, Hoshino K, Kawai T et al. Differential roles of TLR2 and TLR4 in recognition of Gram-negative and Gram-positive bacterial cell wall components. Immunity11, 443–451 (1999).
  • Harden LM, du Plessis I, Poole S, Laburn HP. Interleukin-6 and leptin mediate lipopolysaccharide-induced fever and sickness behavior. Physiol. Behav.89, 146–155 (2006).
  • Oka T, Oka K, Kobayashi T et al. Charcteristics of thermoregulatory and febrile responses in mice defiant in prostaglandin EP1 and EP3 receptors. J. Physiol.551, 945–954 (2003).
  • Jones SA, Richards PJ, Scheller J, Rose-John S. IL-6 transsignaling: the in vivo consequences. J. Interferon Cytokine Res.25, 241–253 (2005).
  • Jacober ML, Mamoni RL, Lima CS, Dos Anjos BL, Grotto HZ. Anaemia in patients with cancer: role of inflammatory activity on iron metabolism and severity of anaemia. Med. Oncol.24, 323–329 (2007).
  • Veldhuis GJ, Willemse PH, Mulder NH, Limburg PC, De Vries EG. Potential use of recombinant human interleukin-6 in clinical oncology. Leuk. Lymphoma20, 373–379 (1996).
  • Nemeth E, Ganz T. The role of hepcidin in iron metabolism. Acta Haematol.122, 78–86 (2009).
  • Mima T, Nishimoto N. Clinical value of blocking IL-6 receptor. Curr. Opin Rheumatol.21, 224–230 (2009).
  • Nemeth E, Rivera S, Gabayan V, Keller C, Taudorf S, Pedersen BK. IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin. J. Clin. Invest.113, 1271–1276 (2004).
  • Novick D, Engelmann H, Revel M, Leitner O, Rubinstein M. Monoclonal antibodies to the soluble human IL-6 receptor: affinity purification, ELISA, and inhibition of ligand binding. Hybridoma10, 137–146 (1999).
  • Nishimoto N, Yoshizaki K, Miyasaka N, Yamamoto K, Kawai S, Takeuchi T. Treatment of rheumatoid arthritis with humanized anti-interleukin-6 receptor antibody: a multicenter, double-blind, placebo-controlled trial. Arthritis Rheum.50, 1761–1769 (2004).
  • Giannini EH, Ruperto N, Ravelli A, Lovell DJ, Felson DT, Martini A. Preliminary definition of improvement in juvenile arthritis. Arthritis Rheum.40, 1202–1209 (1997).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.