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Published in: European Journal of Pediatrics 6/2015

01-06-2015 | Review

Treatment of hyperimmunoglobulinemia D syndrome with biologics in children: review of the literature and Finnish experience

Authors: Svetlana Kostjukovits, Liisa Kalliokoski, Kaisu Antila, Matti Korppi

Published in: European Journal of Pediatrics | Issue 6/2015

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Abstract

Hyperimmunoglobulinemia D syndrome (HIDS) is an autoinflammatory disorder that is caused by mevalonate kinase deficiency (MKD). Recent advances in the pathogenesis of MKD, including the proposed mechanisms of inflammasome activation, provide the basis for the development of new treatment modalities. So far, feedback on the treatment of HIDS with biological medicines has come from case reports with limited numbers of patients. In this review, we summarize the data that is currently available on the treatment of HIDS in children, with the emphasis on new therapies, and present three Finnish pediatric cases treated with anakinra. Case reports have been published on 33 pediatric HIDS patients who have been treated with biological medicines, and in some cases, they were treated with more than one drug. Of these patients, 21 were treated with anakinra and 16 with etanercept, resulting in complete or partial responses in 90 and 50 % of cases, respectively. A further five patients were treated with canakinumab, with complete or partial responses.
Conclusion: The accumulating evidence on the efficacy and safety of biological drugs in pediatric HIDS suggests that the anti-interleukin-1 agent anakinra is the drug of choice for HIDS in children.
What is Known:
Various biologic drugs have been tried for the treatment of HIDS.
What is New:
Based on the 90 % response rate, anakinra seems to be the drug of choice for HIDS in children.
Literature
1.
go back to reference Arkwright PD, McDermott MF, Houten SM, Frenkel J, Waterham HR, Aganna E et al (2002) Hyper IgD syndrome (HIDS) associated with in vitro evidence of defective monocyte TNFRSF1A shedding and partial response to TNF receptor blockade with etanercept. Clin Exp Immunol 130(3):484–488CrossRefPubMedCentralPubMed Arkwright PD, McDermott MF, Houten SM, Frenkel J, Waterham HR, Aganna E et al (2002) Hyper IgD syndrome (HIDS) associated with in vitro evidence of defective monocyte TNFRSF1A shedding and partial response to TNF receptor blockade with etanercept. Clin Exp Immunol 130(3):484–488CrossRefPubMedCentralPubMed
2.
go back to reference Bader-Meunier B, Florkin B, Sibilia J, Acquaviva C, Hachulla E, Grateau G, SOFREMIP (Société Francophone pour la Rhumatologie et les Maladies Inflammatoires en Pédiatrie), CRI (Club Rhumatismes et Inflammations) et al (2011) Mevalonate kinase deficiency: a survey of 50 patients. Pediatrics 128(1):e152–e159CrossRefPubMed Bader-Meunier B, Florkin B, Sibilia J, Acquaviva C, Hachulla E, Grateau G, SOFREMIP (Société Francophone pour la Rhumatologie et les Maladies Inflammatoires en Pédiatrie), CRI (Club Rhumatismes et Inflammations) et al (2011) Mevalonate kinase deficiency: a survey of 50 patients. Pediatrics 128(1):e152–e159CrossRefPubMed
3.
go back to reference Bianco AM, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A (2014) Mevalonate kinase deficiency and IBD: shared genetic background. Gut 63(8):1367–1368CrossRefPubMedCentralPubMed Bianco AM, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A (2014) Mevalonate kinase deficiency and IBD: shared genetic background. Gut 63(8):1367–1368CrossRefPubMedCentralPubMed
4.
go back to reference Biggs C, Dedeoglu F (2014) A81: spectrum of mevalonate kinase deficiency: is colitis more common than we think? Arthritis Rheum 66(Suppl 11):S114CrossRef Biggs C, Dedeoglu F (2014) A81: spectrum of mevalonate kinase deficiency: is colitis more common than we think? Arthritis Rheum 66(Suppl 11):S114CrossRef
5.
go back to reference Bodar EJ, Kuijk LM, Drenth JP, van der Meer JW, Simon A, Frenkel J (2011) On-demand anakinra treatment is effective in mevalonate kinase deficiency. Ann Rheum Dis 70(12):2155–2158CrossRefPubMed Bodar EJ, Kuijk LM, Drenth JP, van der Meer JW, Simon A, Frenkel J (2011) On-demand anakinra treatment is effective in mevalonate kinase deficiency. Ann Rheum Dis 70(12):2155–2158CrossRefPubMed
6.
go back to reference Breda L, Nozzi M, Di Marzio D, De Sanctis S, Gattorno M, Chiarelli F (2009) Recurrent pericarditis in hyper-IgD syndrome. Clin Exp Rheumatol 27(4):695PubMed Breda L, Nozzi M, Di Marzio D, De Sanctis S, Gattorno M, Chiarelli F (2009) Recurrent pericarditis in hyper-IgD syndrome. Clin Exp Rheumatol 27(4):695PubMed
7.
go back to reference Campanilho-Marques R, Brogan PA (2014) Mevalonate kinase deficiency in two sisters with therapeutic response to anakinra: case report and review of the literature. Clin Rheumatol 33(11):1681–1684CrossRefPubMed Campanilho-Marques R, Brogan PA (2014) Mevalonate kinase deficiency in two sisters with therapeutic response to anakinra: case report and review of the literature. Clin Rheumatol 33(11):1681–1684CrossRefPubMed
8.
go back to reference Cantarini L, Vitale A, Magnotti F, Lucherini OM, Caso F, Frediani B et al (2013) Weekly oral alendronate in mevalonate kinase deficiency. Orphanet J Rare Dis 8:196CrossRefPubMedCentralPubMed Cantarini L, Vitale A, Magnotti F, Lucherini OM, Caso F, Frediani B et al (2013) Weekly oral alendronate in mevalonate kinase deficiency. Orphanet J Rare Dis 8:196CrossRefPubMedCentralPubMed
9.
go back to reference Cerretti DP, Kozlosky CJ, Mosley B, Nelson N, Van Ness K, Greenstreet TA et al (1992) Molecular cloning of the interleukin-1 beta converting enzyme. Science 256(5053):97–100CrossRefPubMed Cerretti DP, Kozlosky CJ, Mosley B, Nelson N, Van Ness K, Greenstreet TA et al (1992) Molecular cloning of the interleukin-1 beta converting enzyme. Science 256(5053):97–100CrossRefPubMed
10.
go back to reference Cuisset L, Drenth JP, Simon A, Vincent MF, van der Velde VS, van der Meer JW et al (2001) Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome. Eur J Hum Genet 9(4):260–266CrossRefPubMed Cuisset L, Drenth JP, Simon A, Vincent MF, van der Velde VS, van der Meer JW et al (2001) Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome. Eur J Hum Genet 9(4):260–266CrossRefPubMed
11.
go back to reference Demirkaya E, Caglar MK, Waterham HR, Topaloğlu R, Ozen S (2007) A patient with hyper-IgD syndrome responding to anti-TNF treatment. Clin Rheumatol 26(10):1757–1759CrossRefPubMed Demirkaya E, Caglar MK, Waterham HR, Topaloğlu R, Ozen S (2007) A patient with hyper-IgD syndrome responding to anti-TNF treatment. Clin Rheumatol 26(10):1757–1759CrossRefPubMed
14.
go back to reference Frenkel J, Rijkers GT, Mandey SH, Buurman SW, Houten SM, Wanders RJ et al (2002) Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 46:2794–2803CrossRefPubMed Frenkel J, Rijkers GT, Mandey SH, Buurman SW, Houten SM, Wanders RJ et al (2002) Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 46:2794–2803CrossRefPubMed
15.
go back to reference Galeotti C, Meinzer U, Quartier P, Rossi-Semerano L, Bader-Meunier B, Pillet P et al (2012) Efficacy of interleukin-1-targeting drugs in mevalonate kinase deficiency. Rheumatology (Oxford) 51(10):1855–1859CrossRef Galeotti C, Meinzer U, Quartier P, Rossi-Semerano L, Bader-Meunier B, Pillet P et al (2012) Efficacy of interleukin-1-targeting drugs in mevalonate kinase deficiency. Rheumatology (Oxford) 51(10):1855–1859CrossRef
16.
go back to reference Gençpınar P, Makay BB, Gattorno M, Caroli F, Ünsal E (2012) Mevalonate kinase deficiency (hyper IgD syndrome with periodic fever)—different faces with separate treatments: two cases and review of the literature. Turk J Pediatr 54(6):641–644PubMed Gençpınar P, Makay BB, Gattorno M, Caroli F, Ünsal E (2012) Mevalonate kinase deficiency (hyper IgD syndrome with periodic fever)—different faces with separate treatments: two cases and review of the literature. Turk J Pediatr 54(6):641–644PubMed
17.
go back to reference Gül A, Tugal-Tutkun I, Dinarello CA, Reznikov L, Esen BA, Mirza A et al (2012) Interleukin-1β-regulating antibody XOMA 052 (gevokizumab) in the treatment of acute exacerbations of resistant uveitis of Behcet’s disease: an open-label pilot study. Ann Rheum Dis 71(4):563–566CrossRefPubMed Gül A, Tugal-Tutkun I, Dinarello CA, Reznikov L, Esen BA, Mirza A et al (2012) Interleukin-1β-regulating antibody XOMA 052 (gevokizumab) in the treatment of acute exacerbations of resistant uveitis of Behcet’s disease: an open-label pilot study. Ann Rheum Dis 71(4):563–566CrossRefPubMed
18.
19.
go back to reference Hashkes PJ, Spalding SJ, Giannini EH, Huang B, Johnson A, Park G et al (2012) Rilonacept for colchicine-resistant or -intolerant familial Mediterranean fever: a randomized trial. Ann Intern Med 157(8):533–541CrossRefPubMed Hashkes PJ, Spalding SJ, Giannini EH, Huang B, Johnson A, Park G et al (2012) Rilonacept for colchicine-resistant or -intolerant familial Mediterranean fever: a randomized trial. Ann Intern Med 157(8):533–541CrossRefPubMed
20.
go back to reference Hoffman HM, Throne ML, Amar NJ, Cartwright RC, Kivitz AJ, Soo Y et al (2012) Long-term efficacy and safety profile of rilonacept in the treatment of cryopyrin-associated periodic syndromes: results of a 72-week open-label extension study. Clin Ther 34(10):2091–2103CrossRefPubMed Hoffman HM, Throne ML, Amar NJ, Cartwright RC, Kivitz AJ, Soo Y et al (2012) Long-term efficacy and safety profile of rilonacept in the treatment of cryopyrin-associated periodic syndromes: results of a 72-week open-label extension study. Clin Ther 34(10):2091–2103CrossRefPubMed
21.
go back to reference Hoffmann GF, Charpentier C, Mayatepek E, Mancini J, Leichsenring M, Gibson KM et al (1993) Clinical and biochemical phenotype in 11 patients with mevalonic aciduria. Pediatrics 91(5):915–921PubMed Hoffmann GF, Charpentier C, Mayatepek E, Mancini J, Leichsenring M, Gibson KM et al (1993) Clinical and biochemical phenotype in 11 patients with mevalonic aciduria. Pediatrics 91(5):915–921PubMed
22.
go back to reference Houten SM, Kuis W, Duran M, de Koning TJ, van Royen-Kerkhof A, Romeijn GJ, Frenkel J et al (1999) Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome. Nat Genet 22(2):175–177CrossRefPubMed Houten SM, Kuis W, Duran M, de Koning TJ, van Royen-Kerkhof A, Romeijn GJ, Frenkel J et al (1999) Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome. Nat Genet 22(2):175–177CrossRefPubMed
23.
go back to reference Korppi M, Van Gijn ME, Antila K (2011) Hyperimmunoglobulinemia D and periodic fever syndrome in children. Review on therapy with biological drugs and case report. Acta Paediatr 100(1):21–25CrossRefPubMed Korppi M, Van Gijn ME, Antila K (2011) Hyperimmunoglobulinemia D and periodic fever syndrome in children. Review on therapy with biological drugs and case report. Acta Paediatr 100(1):21–25CrossRefPubMed
25.
go back to reference Kuijk LM, Mandey SH, Schellens I, Waterham HR, Rijkers GT, Coffer PJ et al (2008) Statin synergizes with LPS to induce IL-1beta release by THP-1 cells through activation of caspase-1. Mol Immunol 45:2158–2165CrossRefPubMed Kuijk LM, Mandey SH, Schellens I, Waterham HR, Rijkers GT, Coffer PJ et al (2008) Statin synergizes with LPS to induce IL-1beta release by THP-1 cells through activation of caspase-1. Mol Immunol 45:2158–2165CrossRefPubMed
26.
go back to reference Lachmann HJ, Goodman HJ, Andrews PA, Gallagher H, Marsh J, Breuer S et al (2006) AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases. Arthritis Rheum 54(6):2010–2014CrossRefPubMed Lachmann HJ, Goodman HJ, Andrews PA, Gallagher H, Marsh J, Breuer S et al (2006) AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases. Arthritis Rheum 54(6):2010–2014CrossRefPubMed
27.
go back to reference Levy M, Arion A, Berrebi D, Cuisset L, Jeanne-Pasquier C, Bader-Meunier B et al (2013) Severe early-onset colitis revealing mevalonate kinase deficiency. Pediatrics 132(3):e779–e783CrossRefPubMed Levy M, Arion A, Berrebi D, Cuisset L, Jeanne-Pasquier C, Bader-Meunier B et al (2013) Severe early-onset colitis revealing mevalonate kinase deficiency. Pediatrics 132(3):e779–e783CrossRefPubMed
28.
go back to reference Li Cavoli G, Passantino D, Tortorici C, Bono L, Ferrantelli A, Giammarresi C et al (2012) Renal amyloidosis due to hyper-IgD syndrome. Nefrologia 32(6):865–866PubMed Li Cavoli G, Passantino D, Tortorici C, Bono L, Ferrantelli A, Giammarresi C et al (2012) Renal amyloidosis due to hyper-IgD syndrome. Nefrologia 32(6):865–866PubMed
29.
go back to reference Mandey SH, Kuijk LM, Frenkel J, Waterham HR (2006) A role for geranylgeranylation in interleukin-1beta secretion. Arthritis Rheum 54:3690–3695CrossRefPubMed Mandey SH, Kuijk LM, Frenkel J, Waterham HR (2006) A role for geranylgeranylation in interleukin-1beta secretion. Arthritis Rheum 54:3690–3695CrossRefPubMed
30.
go back to reference Mansouri B, Richards L, Menter A (2014) Treatment of two patients with generalised pustular psoriasis with the interleukin-1β inhibitor gevokizumab. Br J Dermatol. doi:10.1111/bjd.13614 Mansouri B, Richards L, Menter A (2014) Treatment of two patients with generalised pustular psoriasis with the interleukin-1β inhibitor gevokizumab. Br J Dermatol. doi:10.​1111/​bjd.​13614
31.
go back to reference Marchetti F, Barbi E, Tommasini A, Oretti C, Ventura A (2004) Inefficacy of etanercept in a child with hyper-IgD syndrome and periodic fever. Clin Exp Rheumatol 22(6):791–792PubMed Marchetti F, Barbi E, Tommasini A, Oretti C, Ventura A (2004) Inefficacy of etanercept in a child with hyper-IgD syndrome and periodic fever. Clin Exp Rheumatol 22(6):791–792PubMed
32.
go back to reference Martinon F, Burns K, Tschopp J (2002) The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta. Mol Cell 10:417–426CrossRefPubMed Martinon F, Burns K, Tschopp J (2002) The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta. Mol Cell 10:417–426CrossRefPubMed
33.
go back to reference Martinon F, Mayor A, Tschopp J (2009) The inflammasomes: guardians of the body. Annu Rev Immunol 27:229–265CrossRefPubMed Martinon F, Mayor A, Tschopp J (2009) The inflammasomes: guardians of the body. Annu Rev Immunol 27:229–265CrossRefPubMed
34.
go back to reference Nevyjel M, Pontillo A, Calligaris L, Tommasini A, D’Osualdo A, Waterham HR et al (2007) Diagnostics and therapeutic insights in a severe case of mevalonate kinase deficiency. Pediatrics 119:e523–e527CrossRefPubMed Nevyjel M, Pontillo A, Calligaris L, Tommasini A, D’Osualdo A, Waterham HR et al (2007) Diagnostics and therapeutic insights in a severe case of mevalonate kinase deficiency. Pediatrics 119:e523–e527CrossRefPubMed
35.
go back to reference Normand S, Massonnet B, Delwail A, Favot L, Cuisset L, Grateau G et al (2009) Specific increase in caspase-1 activity and secretion of IL-1 family cytokines: a putative link between mevalonate kinase deficiency and inflammation. Eur Cytokine Netw 20(3):101–107PubMed Normand S, Massonnet B, Delwail A, Favot L, Cuisset L, Grateau G et al (2009) Specific increase in caspase-1 activity and secretion of IL-1 family cytokines: a putative link between mevalonate kinase deficiency and inflammation. Eur Cytokine Netw 20(3):101–107PubMed
36.
go back to reference Obici L, Manno C, Muda AO, Picco P, D’Osualdo A, Palladini G et al (2004) First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome. Arthritis Rheum 50(9):2966–2969CrossRefPubMed Obici L, Manno C, Muda AO, Picco P, D’Osualdo A, Palladini G et al (2004) First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome. Arthritis Rheum 50(9):2966–2969CrossRefPubMed
37.
go back to reference Pappu AS, Bacon SP, Illingworth DR (2003) Residual effects of lovastatin and simvastatin on urinary mevalonate excretions in patients with familial hypercholesterolemia. J Lab Clin Med 141(4):250–256CrossRefPubMed Pappu AS, Bacon SP, Illingworth DR (2003) Residual effects of lovastatin and simvastatin on urinary mevalonate excretions in patients with familial hypercholesterolemia. J Lab Clin Med 141(4):250–256CrossRefPubMed
38.
go back to reference Pontillo A, Paoluzzi E, Crovella S (2010) The inhibition of mevalonate pathway induces upregulation of NALP3 expression: new insight in the pathogenesis of mevalonate kinase deficiency. Eur J Hum Genet 18:844–847CrossRefPubMedCentralPubMed Pontillo A, Paoluzzi E, Crovella S (2010) The inhibition of mevalonate pathway induces upregulation of NALP3 expression: new insight in the pathogenesis of mevalonate kinase deficiency. Eur J Hum Genet 18:844–847CrossRefPubMedCentralPubMed
39.
go back to reference Rigante D, Ansuini V, Bertoni B, Pugliese AL, Avallone L, Federico G et al (2006) Treatment with anakinra in the hyperimmunoglobulinemia D/periodic fever syndrome. Rheumatol Int 27(1):97–100CrossRefPubMed Rigante D, Ansuini V, Bertoni B, Pugliese AL, Avallone L, Federico G et al (2006) Treatment with anakinra in the hyperimmunoglobulinemia D/periodic fever syndrome. Rheumatol Int 27(1):97–100CrossRefPubMed
40.
go back to reference Santos JA, Aróstegui JI, Brito MJ, Neves C, Conde M (2014) Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype. Gene 542(2):217–220CrossRefPubMed Santos JA, Aróstegui JI, Brito MJ, Neves C, Conde M (2014) Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype. Gene 542(2):217–220CrossRefPubMed
41.
go back to reference Shendi HM, Devlin LA, Edgar JD (2014) Interleukin 6 blockade for hyperimmunoglobulin D and periodic fever syndrome. J Clin Rheumatol 20(2):103–105PubMed Shendi HM, Devlin LA, Edgar JD (2014) Interleukin 6 blockade for hyperimmunoglobulin D and periodic fever syndrome. J Clin Rheumatol 20(2):103–105PubMed
42.
go back to reference Shendi HM, Walsh D, Edgar JD (2012) Etanercept and anakinra can prolong febrile episodes in patients with hyperimmunoglobulin D and periodic fever syndrome. Rheumatol Int 32(1):249–251CrossRefPubMed Shendi HM, Walsh D, Edgar JD (2012) Etanercept and anakinra can prolong febrile episodes in patients with hyperimmunoglobulin D and periodic fever syndrome. Rheumatol Int 32(1):249–251CrossRefPubMed
43.
go back to reference Siewert R, Ferber J, Horstmann RD, Specker C, Heering PJ, Timmann C (2006) Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease? Am J Kidney Dis 48(3):e41–e45CrossRefPubMed Siewert R, Ferber J, Horstmann RD, Specker C, Heering PJ, Timmann C (2006) Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease? Am J Kidney Dis 48(3):e41–e45CrossRefPubMed
44.
go back to reference Simon A, Drewe E, van der Meer JW, Powell RJ, Kelley RI, Stalenhoef AF et al (2004) Simvastatin treatment for inflammatory attacks of the hyperimmunoglobulinemia D and periodic fever syndrome. Clin Pharmacol Ther 75(5):476–483CrossRefPubMed Simon A, Drewe E, van der Meer JW, Powell RJ, Kelley RI, Stalenhoef AF et al (2004) Simvastatin treatment for inflammatory attacks of the hyperimmunoglobulinemia D and periodic fever syndrome. Clin Pharmacol Ther 75(5):476–483CrossRefPubMed
45.
go back to reference Stoffels M, Jongekrijg J, Remijn T, Kok N, van der Meer JW, Simon A (2014) TLR2/TLR4-dependent exaggerated cytokine production in hyperimmunoglobulinaemia D and periodic fever syndrome. Rheumatology (Oxford) 54(2):363–368 Stoffels M, Jongekrijg J, Remijn T, Kok N, van der Meer JW, Simon A (2014) TLR2/TLR4-dependent exaggerated cytokine production in hyperimmunoglobulinaemia D and periodic fever syndrome. Rheumatology (Oxford) 54(2):363–368
46.
go back to reference Takada K, Aksentijevich I, Mahadevan V, Dean JA, Kelley RI, Kastner DL (2003) Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 48(9):2645–2651CrossRefPubMed Takada K, Aksentijevich I, Mahadevan V, Dean JA, Kelley RI, Kastner DL (2003) Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 48(9):2645–2651CrossRefPubMed
47.
go back to reference Ter Haar N, Lachmann H, Özen S, Woo P, Uziel Y, Modesto C, Paediatric Rheumatology International Trials Organisation (PRINTO) and the Eurofever/Eurotraps Projects et al (2013) Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review. Ann Rheum Dis 72(5):678–685CrossRefPubMed Ter Haar N, Lachmann H, Özen S, Woo P, Uziel Y, Modesto C, Paediatric Rheumatology International Trials Organisation (PRINTO) and the Eurofever/Eurotraps Projects et al (2013) Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review. Ann Rheum Dis 72(5):678–685CrossRefPubMed
48.
go back to reference Thors VS, Vastert SJ, Wulffraat N, van Royen A, Frenkel J, de Sain-van der Velden M et al (2014) Periodic fever in MVK deficiency: a patient initially diagnosed with incomplete Kawasaki disease. Pediatrics 133(2):e461–e465CrossRefPubMed Thors VS, Vastert SJ, Wulffraat N, van Royen A, Frenkel J, de Sain-van der Velden M et al (2014) Periodic fever in MVK deficiency: a patient initially diagnosed with incomplete Kawasaki disease. Pediatrics 133(2):e461–e465CrossRefPubMed
49.
go back to reference Topaloğlu R, Ayaz NA, Waterham HR, Yüce A, Gumruk F, Sanal O (2008) Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up. Clin Rheumatol 27(10):1317–1320CrossRefPubMed Topaloğlu R, Ayaz NA, Waterham HR, Yüce A, Gumruk F, Sanal O (2008) Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up. Clin Rheumatol 27(10):1317–1320CrossRefPubMed
50.
go back to reference Tricarico PM, Kleiner G, Valencic E, Campisciano G, Girardelli M, Crovella S et al (2014) Block of the mevalonate pathway triggers oxidative and inflammatory molecular mechanisms modulated by exogenous isoprenoid compounds. Int J Mol Sci 15(4):6843–6856CrossRefPubMedCentralPubMed Tricarico PM, Kleiner G, Valencic E, Campisciano G, Girardelli M, Crovella S et al (2014) Block of the mevalonate pathway triggers oxidative and inflammatory molecular mechanisms modulated by exogenous isoprenoid compounds. Int J Mol Sci 15(4):6843–6856CrossRefPubMedCentralPubMed
51.
go back to reference van der Hilst JC, Bodar EJ, Barron KS, Frenkel J, Drenth JP, van der Meer JW, International HIDS Study Group et al (2008) Long-term follow-up, clinical features, and quality of life in a series of 103 patients with hyperimmunoglobulinemia D syndrome. Medicine (Baltimore) 87(6):301–310CrossRef van der Hilst JC, Bodar EJ, Barron KS, Frenkel J, Drenth JP, van der Meer JW, International HIDS Study Group et al (2008) Long-term follow-up, clinical features, and quality of life in a series of 103 patients with hyperimmunoglobulinemia D syndrome. Medicine (Baltimore) 87(6):301–310CrossRef
52.
go back to reference van der Hilst JC, Drenth JP, Bodar EJ, Bijzet J, van der Meer JW, Simon A, International HIDS Study Group (2005) Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in hyper-IgD syndrome. Amyloid 12(2):115–119CrossRefPubMed van der Hilst JC, Drenth JP, Bodar EJ, Bijzet J, van der Meer JW, Simon A, International HIDS Study Group (2005) Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in hyper-IgD syndrome. Amyloid 12(2):115–119CrossRefPubMed
53.
go back to reference von Linstow ML, Rosenfeldt V (2014) Neonatal hepatitis as first manifestation of hyperimmunoglobulinemia D syndrome. Case Rep Pediatr 2014:936890 von Linstow ML, Rosenfeldt V (2014) Neonatal hepatitis as first manifestation of hyperimmunoglobulinemia D syndrome. Case Rep Pediatr 2014:936890
54.
go back to reference Yel S, Gunduz Z, Bastug F, Dusunsel R, Dursun I, Poyrazoglu H et al (2013) Amyloidosis in a child with hyperimmunoglobulinemia D syndrome. Iran J Kidney Dis 7(1):70–72PubMed Yel S, Gunduz Z, Bastug F, Dusunsel R, Dursun I, Poyrazoglu H et al (2013) Amyloidosis in a child with hyperimmunoglobulinemia D syndrome. Iran J Kidney Dis 7(1):70–72PubMed
Metadata
Title
Treatment of hyperimmunoglobulinemia D syndrome with biologics in children: review of the literature and Finnish experience
Authors
Svetlana Kostjukovits
Liisa Kalliokoski
Kaisu Antila
Matti Korppi
Publication date
01-06-2015
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Pediatrics / Issue 6/2015
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-015-2505-9

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