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Erschienen in: Clinical Rheumatology 1/2021

05.07.2020 | Case Based Review

A case of cryopyrin-associated periodic fever syndrome during canakinumab administration complicated by inflammatory bowel disease

verfasst von: Yuichi Yamasaki, Tomohiro Kubota, Syuji Takei, Hiroyuki Imanaka, Yukiko Nonaka, Yoshifumi Kawano

Erschienen in: Clinical Rheumatology | Ausgabe 1/2021

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Abstract

Cryopyrin-associated periodic fever syndrome (CAPS) is a highly debilitating disorder, which is characterized by unregulated interleukin-1β production driven by autosomal dominantly inherited mutations in the NLRP3 gene. Patients with CAPS often present with early-onset episodes of fever and rash. These patients also present with variable systemic signs and symptoms, such as arthritis, sensorineural hearing loss, chronic aseptic meningitis, and skeletal abnormalities, but minimal gastrointestinal symptoms. Recently, effective therapies for CAPS targeted against interleukin-1 have become available. We report a case of a young Japanese woman with CAPS who developed inflammatory bowel disease during canakinumab therapy. The patient had colostomy after intestinal perforation and changed canakinumab to infliximab. To the best of our knowledge, this is the first report of a case of inflammatory bowel disease secondary to CAPS complicated by gastrointestinal symptoms and arthritis which canakinumab could not control. Patients with CAPS who have symptoms that cannot be controlled by canakinumab should be considered for possible co-morbidities.
Literatur
1.
Zurück zum Zitat Stojanov S, Kastner DL (2005) Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol 17:586–599CrossRef Stojanov S, Kastner DL (2005) Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol 17:586–599CrossRef
2.
Zurück zum Zitat Shinkai K, McCalmont TH, Leslie KS (2008) Cryopyrin-associated periodic syndromes and autoinflammation. Clin Exp Drmatol 33:1–9 Shinkai K, McCalmont TH, Leslie KS (2008) Cryopyrin-associated periodic syndromes and autoinflammation. Clin Exp Drmatol 33:1–9
3.
Zurück zum Zitat Aksentijevich I, Putnam CD, Remmers EF et al (2007) The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Arthritis Rheum 56:1273–1285CrossRef Aksentijevich I, Putnam CD, Remmers EF et al (2007) The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Arthritis Rheum 56:1273–1285CrossRef
4.
Zurück zum Zitat Booshehri LM, Hoffman HM (2019) CAPS and NLRP3. J Clin Immunol 39:277–286CrossRef Booshehri LM, Hoffman HM (2019) CAPS and NLRP3. J Clin Immunol 39:277–286CrossRef
5.
Zurück zum Zitat Kuemmerle-Deschner JB (2015) CAPS – pathogenesis, presentation and treatment of an autoinflammatory disease. Semin Immunopathol 37:377–385CrossRef Kuemmerle-Deschner JB (2015) CAPS – pathogenesis, presentation and treatment of an autoinflammatory disease. Semin Immunopathol 37:377–385CrossRef
6.
Zurück zum Zitat Milhavet F, Cuisset L, Hoffman HM, Slim R, el-Shanti H, Aksentijevich I, Lesage S, Waterham H, Wise C, Sarrauste de Menthiere C, Touitou I (2008) The infevers autoinflammatory mutation online registry: update with new genes and functions. Hum Mutat 29:803–808CrossRef Milhavet F, Cuisset L, Hoffman HM, Slim R, el-Shanti H, Aksentijevich I, Lesage S, Waterham H, Wise C, Sarrauste de Menthiere C, Touitou I (2008) The infevers autoinflammatory mutation online registry: update with new genes and functions. Hum Mutat 29:803–808CrossRef
7.
Zurück zum Zitat Van Gijn ME, Ceccherini I, Shinar Y et al (2018) New workflow for classification of genetic variants’ pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory Diseases (INSAID). J Med Genet 55:530–537CrossRef Van Gijn ME, Ceccherini I, Shinar Y et al (2018) New workflow for classification of genetic variants’ pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory Diseases (INSAID). J Med Genet 55:530–537CrossRef
8.
Zurück zum Zitat Touitou I, Lesage S, McDermott M, Cuisset L, Hoffman H, Dode C, Shoham N, Aganna E, Hugot JP, Wise C, Waterham H, Pugnere D, Demaille J, de Menthiere CS (2004) Infevers: an evolving mutation database for autoinflammatory syndromes. Hum Mutat 24:194–198CrossRef Touitou I, Lesage S, McDermott M, Cuisset L, Hoffman H, Dode C, Shoham N, Aganna E, Hugot JP, Wise C, Waterham H, Pugnere D, Demaille J, de Menthiere CS (2004) Infevers: an evolving mutation database for autoinflammatory syndromes. Hum Mutat 24:194–198CrossRef
9.
Zurück zum Zitat Hawkins PN, Lachmann HJ, McDermott MF (2003) Interleukin-I-receptor antagonist in the Muckle-Wells syndrome. N Engl J Med 348:2583–2584CrossRef Hawkins PN, Lachmann HJ, McDermott MF (2003) Interleukin-I-receptor antagonist in the Muckle-Wells syndrome. N Engl J Med 348:2583–2584CrossRef
10.
Zurück zum Zitat Lachmann HJ, Kone-Paut I, Kuemmerle-Deschner JB, Leslie KS, Hachulla E, Quartier P, Gitton X, Widmer A, Patel N, Hawkins PN, Canakinumab in CAPS Study Group (2009) Use of canakinumab in the cryopyrin-associated periodic syndrome. N Engl J Med 360:2416–2425CrossRef Lachmann HJ, Kone-Paut I, Kuemmerle-Deschner JB, Leslie KS, Hachulla E, Quartier P, Gitton X, Widmer A, Patel N, Hawkins PN, Canakinumab in CAPS Study Group (2009) Use of canakinumab in the cryopyrin-associated periodic syndrome. N Engl J Med 360:2416–2425CrossRef
11.
Zurück zum Zitat Hoffman HM (2009) Rilonacept for the treatment of cryopyrin-associated periodic syndromes (CAPS). Expert Opin Biol Ther 9:519–531CrossRef Hoffman HM (2009) Rilonacept for the treatment of cryopyrin-associated periodic syndromes (CAPS). Expert Opin Biol Ther 9:519–531CrossRef
12.
Zurück zum Zitat Kone-Paut I, Darce-Bello M, Shahram F, Gattorno M, Cimaz R, Ozen S, Cantarini L, Tugal-Tutktun I, Assaad-Khalil S, Hofer M, Kuemmerle-Deschner J, Benamour S, al Mayouf S, Pajot C, Anton J, Faye A, Bono W, Nielsen S, Letierce A, Tran TA, the PED-BD International Expert Committee (2011) Registries in rheumatological and musculoskeletal conditions. Paediatric Behcet’s disease: an international cohort study of 110 patients. One-year follow-up data. Rheumatology (Oxford) 50:184–188CrossRef Kone-Paut I, Darce-Bello M, Shahram F, Gattorno M, Cimaz R, Ozen S, Cantarini L, Tugal-Tutktun I, Assaad-Khalil S, Hofer M, Kuemmerle-Deschner J, Benamour S, al Mayouf S, Pajot C, Anton J, Faye A, Bono W, Nielsen S, Letierce A, Tran TA, the PED-BD International Expert Committee (2011) Registries in rheumatological and musculoskeletal conditions. Paediatric Behcet’s disease: an international cohort study of 110 patients. One-year follow-up data. Rheumatology (Oxford) 50:184–188CrossRef
13.
Zurück zum Zitat Sibley CH, Plass N, Snow J, Wiggs EA, Brewer CC, King KA, Zalewski C, Kim HJ, Bishop R, Hill S, Paul SM, Kicker P, Phillips Z, Dolan JG, Widemann B, Jayaprakash N, Pucino F, Stone DL, Chapelle D, Snyder C, Butman JA, Wesley R, Goldbach-Mansky R (2012) Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: a cohort study to determine three- and five-year outcomes. Arthritis Rheum 64:2375–2386CrossRef Sibley CH, Plass N, Snow J, Wiggs EA, Brewer CC, King KA, Zalewski C, Kim HJ, Bishop R, Hill S, Paul SM, Kicker P, Phillips Z, Dolan JG, Widemann B, Jayaprakash N, Pucino F, Stone DL, Chapelle D, Snyder C, Butman JA, Wesley R, Goldbach-Mansky R (2012) Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: a cohort study to determine three- and five-year outcomes. Arthritis Rheum 64:2375–2386CrossRef
14.
Zurück zum Zitat Kuemmerle Deschner JB, Verma D, Endres T et al (2017) Clinical and molecular phenotypes of low penetrance variants of NLRP3: diagnostic and therapeutic challenges. Arthritis Rheum 69:2233–2240CrossRef Kuemmerle Deschner JB, Verma D, Endres T et al (2017) Clinical and molecular phenotypes of low penetrance variants of NLRP3: diagnostic and therapeutic challenges. Arthritis Rheum 69:2233–2240CrossRef
15.
Zurück zum Zitat Tourkochristou E, Aggeletopoulou I, Konstantakis C, Triantos C (2019) Role of NLRP3 inflammasome in inflammatory bowel diseases. World J Gastroenterol 25:4796–4804CrossRef Tourkochristou E, Aggeletopoulou I, Konstantakis C, Triantos C (2019) Role of NLRP3 inflammasome in inflammatory bowel diseases. World J Gastroenterol 25:4796–4804CrossRef
16.
Zurück zum Zitat Villani AC, Lemire M, Fortin G, Louis E, Silverberg MS, Collette C, Baba N, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Fortin PR, Wither JE, Sarfati M, Rutgeerts P, Rioux JD, Vermeire S, Hudson TJ, Franchimont D (2009) Common variants in the NLRP3 region contribute to Crohn’s disease susceptibility. Nat Genet 41:71–76CrossRef Villani AC, Lemire M, Fortin G, Louis E, Silverberg MS, Collette C, Baba N, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Fortin PR, Wither JE, Sarfati M, Rutgeerts P, Rioux JD, Vermeire S, Hudson TJ, Franchimont D (2009) Common variants in the NLRP3 region contribute to Crohn’s disease susceptibility. Nat Genet 41:71–76CrossRef
17.
Zurück zum Zitat Mao L, Kitani A, Strober W, Fuss IJ (2018) The role of NLRP3 and IL-1β in the pathogenesis of inflammatory bowel disease. Front Immunol 9:2566CrossRef Mao L, Kitani A, Strober W, Fuss IJ (2018) The role of NLRP3 and IL-1β in the pathogenesis of inflammatory bowel disease. Front Immunol 9:2566CrossRef
18.
Zurück zum Zitat Kujundzic M (2013) The role of biologic therapy in the treatment of extraintestinal manifestations and complications of inflammatory bowel disease. Acta Med Croatica 67:195–201PubMed Kujundzic M (2013) The role of biologic therapy in the treatment of extraintestinal manifestations and complications of inflammatory bowel disease. Acta Med Croatica 67:195–201PubMed
19.
Zurück zum Zitat Barrie A, Regueiro M (2007) Biologic therapy in the management of extraintestinal manifestations of inflammatory bowel disease. Inflamm Bowl Dis 13:1424–1429CrossRef Barrie A, Regueiro M (2007) Biologic therapy in the management of extraintestinal manifestations of inflammatory bowel disease. Inflamm Bowl Dis 13:1424–1429CrossRef
20.
Zurück zum Zitat Kaufman I, Caspi D, Yeshurun D, Dotan I, Yaron M, Elkayam O (2005) The effect of infliximab on extraintestinal manifestations of Crohn’s disease. Rheumatol Int 25:406–410CrossRef Kaufman I, Caspi D, Yeshurun D, Dotan I, Yaron M, Elkayam O (2005) The effect of infliximab on extraintestinal manifestations of Crohn’s disease. Rheumatol Int 25:406–410CrossRef
21.
Zurück zum Zitat Ellman M, Hanauer S, Sitrin M, Cohen R (2001) Crohn’s disease arthritis treated with infliximab: an open trial in four patients. J Clin Rheumatol 7:67–71CrossRef Ellman M, Hanauer S, Sitrin M, Cohen R (2001) Crohn’s disease arthritis treated with infliximab: an open trial in four patients. J Clin Rheumatol 7:67–71CrossRef
22.
Zurück zum Zitat Fingerhutova S, Franova J, Hlavackova E et al (2019) Muckle-Wells syndrome across four generations in one Czech family: natural course of the disease. Front Immunol 10:802CrossRef Fingerhutova S, Franova J, Hlavackova E et al (2019) Muckle-Wells syndrome across four generations in one Czech family: natural course of the disease. Front Immunol 10:802CrossRef
23.
Zurück zum Zitat Lasiglie D, Mensa VA, Ferrera D et al (2017) Cryopyrin-associated periodic syndrome in Italian patients: evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization. J Rheumatol 44:1667–1673CrossRef Lasiglie D, Mensa VA, Ferrera D et al (2017) Cryopyrin-associated periodic syndrome in Italian patients: evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization. J Rheumatol 44:1667–1673CrossRef
24.
Zurück zum Zitat Abdulla MC, Alungal J, Hawkins PN, Mohammed S (2015) Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation. J Postgrad Med 61:120–122CrossRef Abdulla MC, Alungal J, Hawkins PN, Mohammed S (2015) Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation. J Postgrad Med 61:120–122CrossRef
25.
Zurück zum Zitat Caorsi R, Lepore L, Zulian F, Alessio M, Stabile A, Insalaco A, Finetti M, Battagliese A, Martini G, Bibalo C, Martini A, Gattorno M (2013) The schedule of administration of canakinumab in cryopyrin associated periodic syndrome is driven by the phenotype severity rather than the age. Arthritis Res Ther 15:R33CrossRef Caorsi R, Lepore L, Zulian F, Alessio M, Stabile A, Insalaco A, Finetti M, Battagliese A, Martini G, Bibalo C, Martini A, Gattorno M (2013) The schedule of administration of canakinumab in cryopyrin associated periodic syndrome is driven by the phenotype severity rather than the age. Arthritis Res Ther 15:R33CrossRef
26.
Zurück zum Zitat Aoyama K, Amano H, Takaoka Y, Nishikomori R, Ishikawa O (2012) Cryopyrin-associated periodic syndrome: a case report and review of the Japanese literature. Acta Derm Venereol 92:395–398CrossRef Aoyama K, Amano H, Takaoka Y, Nishikomori R, Ishikawa O (2012) Cryopyrin-associated periodic syndrome: a case report and review of the Japanese literature. Acta Derm Venereol 92:395–398CrossRef
27.
Zurück zum Zitat Kilic H, Sahin S, Duman C, Adrovic A, Barut K, Turanli ET, Yildirim SR, Kizilkilic O, Kasapcopur O, Saltik S (2019) Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome. Eur J Paediatr Neurol 23:466–472CrossRef Kilic H, Sahin S, Duman C, Adrovic A, Barut K, Turanli ET, Yildirim SR, Kizilkilic O, Kasapcopur O, Saltik S (2019) Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome. Eur J Paediatr Neurol 23:466–472CrossRef
28.
Zurück zum Zitat Houx L, Hachulla E, Kone-Paut I, Quartier P, Touitou I, Guennoc X, Grateau G, Hamidou M, Neven B, Berthelot JM, Lequerré T, Pillet P, Lemelle I, Fischbach M, Duquesne A, le Blay P, le Jeunne C, Stirnemann J, Bonnet C, Gaillard D, Alix L, Touraine R, Garcier F, Bedane C, Jurquet AL, Duffau P, Smail A, Frances C, Grall-Lerosey M, Cathebras P, Tran TA, Morell-Dubois S, Pagnier A, Richez C, Cuisset L, Devauchelle-Pensec V (2015) Musculoskeletal symptoms in patients with cryopyrin-associated periodic syndromes: a large database study. Arthritis Rheumatol 67:3027–3036CrossRef Houx L, Hachulla E, Kone-Paut I, Quartier P, Touitou I, Guennoc X, Grateau G, Hamidou M, Neven B, Berthelot JM, Lequerré T, Pillet P, Lemelle I, Fischbach M, Duquesne A, le Blay P, le Jeunne C, Stirnemann J, Bonnet C, Gaillard D, Alix L, Touraine R, Garcier F, Bedane C, Jurquet AL, Duffau P, Smail A, Frances C, Grall-Lerosey M, Cathebras P, Tran TA, Morell-Dubois S, Pagnier A, Richez C, Cuisset L, Devauchelle-Pensec V (2015) Musculoskeletal symptoms in patients with cryopyrin-associated periodic syndromes: a large database study. Arthritis Rheumatol 67:3027–3036CrossRef
29.
Zurück zum Zitat Marchica C, Zawawi F, Basodan D, Scuccimarri R, Daniel SJ (2018) Resolution of unilateral sensorineural hearing loss in a pediatric patient with a severe phenotype of Muckle-Wells syndrome treated with Anakinra: a case report and review of the literature. J Otolaryngol Head Neck Surg 47:9CrossRef Marchica C, Zawawi F, Basodan D, Scuccimarri R, Daniel SJ (2018) Resolution of unilateral sensorineural hearing loss in a pediatric patient with a severe phenotype of Muckle-Wells syndrome treated with Anakinra: a case report and review of the literature. J Otolaryngol Head Neck Surg 47:9CrossRef
30.
Zurück zum Zitat Mehr S, Allen R, Boros C, Adib N, Kakakios A, Turner PJ, Rogers M, Zurynski Y, Singh-Grewal D (2016) Cryopyrin-associated periodic syndrome in Australian children and adults: epidemiological, clinical and treatment characteristics. J Paediatr Child Health 52:889–895CrossRef Mehr S, Allen R, Boros C, Adib N, Kakakios A, Turner PJ, Rogers M, Zurynski Y, Singh-Grewal D (2016) Cryopyrin-associated periodic syndrome in Australian children and adults: epidemiological, clinical and treatment characteristics. J Paediatr Child Health 52:889–895CrossRef
31.
Zurück zum Zitat Naz Villalba E, Gomez de la Fuente E, Caro Gutierrez D, Pinedo Moraleda F, Yanguela Rodilla J, Mazagatos Angulo D, López Estebaranz JL (2016) Muckle-Wells syndrome: a case report with an NLRP3 T348M mutation. Pediatr Dermatol 33:e311–e314CrossRef Naz Villalba E, Gomez de la Fuente E, Caro Gutierrez D, Pinedo Moraleda F, Yanguela Rodilla J, Mazagatos Angulo D, López Estebaranz JL (2016) Muckle-Wells syndrome: a case report with an NLRP3 T348M mutation. Pediatr Dermatol 33:e311–e314CrossRef
32.
Zurück zum Zitat Posch C, Kaulfersch W, Rappersberger K (2014) Cryopyrin-associated periodic syndrome. Pediatr Dermatol 31:228–231CrossRef Posch C, Kaulfersch W, Rappersberger K (2014) Cryopyrin-associated periodic syndrome. Pediatr Dermatol 31:228–231CrossRef
33.
Zurück zum Zitat Ramos E, Arostegui JI, Campuzano S, Rius J, Bousono C, Yague J (2005) Positive clinical and biochemical responses to anakinra in a 3-yr-old patient with cryopyrin-associated periodic syndrome (CAPS). Rheumatology (Oxford) 44:1072–1073CrossRef Ramos E, Arostegui JI, Campuzano S, Rius J, Bousono C, Yague J (2005) Positive clinical and biochemical responses to anakinra in a 3-yr-old patient with cryopyrin-associated periodic syndrome (CAPS). Rheumatology (Oxford) 44:1072–1073CrossRef
34.
Zurück zum Zitat Eskola V, Pohjankoski H, Kroger L, Aalto K, Latva K, Korppi M (2018) Cryopyrin-associated periodic syndrome in early childhood can be successfully treated with interleukin-I blockades. Acta Paediatr 107:577–580CrossRef Eskola V, Pohjankoski H, Kroger L, Aalto K, Latva K, Korppi M (2018) Cryopyrin-associated periodic syndrome in early childhood can be successfully treated with interleukin-I blockades. Acta Paediatr 107:577–580CrossRef
35.
Zurück zum Zitat Iida Y, Wakiguchi H, Okazaki F, Nakamura T, Yasudo H, Kubo M, Sugahara K, Yamashita H, Suehiro Y, Okayama N, Hashimoto K, Iwamoto N, Kawakami A, Aoki Y, Takada H, Ohga S, Hasegawa S (2019) Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene. Clin Rheumatol 38:943–948CrossRef Iida Y, Wakiguchi H, Okazaki F, Nakamura T, Yasudo H, Kubo M, Sugahara K, Yamashita H, Suehiro Y, Okayama N, Hashimoto K, Iwamoto N, Kawakami A, Aoki Y, Takada H, Ohga S, Hasegawa S (2019) Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene. Clin Rheumatol 38:943–948CrossRef
36.
Zurück zum Zitat Lainka E, Neudorf U, Lohse P, Timmann C, Bielak M, Stojanov S, Huss K, Kries R, Niehues T (2010) Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics. Klin Padiatr 222:356–361CrossRef Lainka E, Neudorf U, Lohse P, Timmann C, Bielak M, Stojanov S, Huss K, Kries R, Niehues T (2010) Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics. Klin Padiatr 222:356–361CrossRef
Metadaten
Titel
A case of cryopyrin-associated periodic fever syndrome during canakinumab administration complicated by inflammatory bowel disease
verfasst von
Yuichi Yamasaki
Tomohiro Kubota
Syuji Takei
Hiroyuki Imanaka
Yukiko Nonaka
Yoshifumi Kawano
Publikationsdatum
05.07.2020
Verlag
Springer International Publishing
Erschienen in
Clinical Rheumatology / Ausgabe 1/2021
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-020-05267-1

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