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DOI: 10.1055/a-1275-7759
Primäre Immundefekte und Autoimmunität
Rheumatologische Manifestationen bei pädiatrischen Patienten mit primären Immundefekten – was gibt es Neues?Primary immunodeficiencies and autoimmunityRheumatological manifestations in pediatric patients with primary immunodeficiency – an updateZUSAMMENFASSUNG
Primäre Immundefekte sind seltene angeborene Erkrankungen, die lange Zeit vor allem durch eine erhöhte Infektanfälligkeit und das Auftreten schwerer und opportunistischer Infektionen charakterisiert waren. In den letzten Jahren wurden aber zunehmend primäre Immundefekte identifiziert, bei denen die Immundysregulation im Vordergrund steht und die durch Autoimmunität und Autoinflammation gekennzeichnet sind. Chronische Arthritiden und andere rheumatologische Symptome können dabei nicht nur als Komplikation der Immundefekte auftreten, sondern auch eines der charakteristischen Krankheits-definierenden Symptome darstellen. Gerade im Kindes- und Jugendalter kann die rheumatologische Manifestation zudem als erstes klinisches Symptom des zugrunde liegenden Immundefekts auftreten. Daher ist in der Kinder- und Jugendrheumatologie ein grundlegendes Wissen über primäre Immundefekte unabdingbar. Im folgenden Übersichtsartikel soll ein Überblick über primäre Immundefekte, die mit rheumatologischen Symptomen einhergehen können, gegeben werden. Ein besonderer Fokus liegt dabei auf kürzlich charakterisierten neuen Immundefekten, bei denen die Autoimmunität häufig im Vordergrund steht.
SUMMARY
Primary immunodeficiencies are rare diseases generally characterized by increased susceptibility to infections. In contrast to this definition, over the last years several primary immunodeficiency syndromes were identified that mainly present with immune dysregulation, namely autoimmunity and autoinflammation, as major manifestations. In some cases, chronic arthritis and other rheumatological phenomena might be the most important symptom in these immunodeficiencies. Especially in children and teenagers, rheumatological symptoms can also be the first and, at time of diagnosis, only symptom of the underlying immune dysregulation. Therefore, pediatric rheumatologists should provide a basic knowledge about primary immunodeficiencies. This review comprises recent updates on primary immunodeficiencies with immune dysregulation and rheumatological manifestations.
Publikationsverlauf
Artikel online veröffentlicht:
10. Dezember 2020
© 2020. Thieme. All rights reserved.
Georg Thieme Verlag KG
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Literatur
- 1 Picard C. et al International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity. J Clin Immunol 2018; 38 (01) 96-128
- 2 Walter JE, Ayala IA, Milojevic D. Curr Opin Pediatr. 2019; 31 (06) 851-862 DOI: doi: 10.1097.
- 3 Fischer A, Provot J, Jais JP. et al members of the CEREDIH French PID study group. J Allergy Clin Immunol 2017; 140 (05) 1388-1393.e8 DOI: doi: 10.1016/j.jaci.2016.12.978. Epub 2017 Feb 10. PMID: 28192146.
- 4 Bruton OC. et al Absence of serum gamma globulins. AMA Am J Dis Child 1952; 84 (05) 632-636
- 5 Jesus AA., Duarte AJ, Oliveira JB. Autoimmunity in hyper-IgM syndrome. J Clin Immunol 2008; 28 (Suppl. 01) S62-S66
- 6 Fu JL. et al X-linked agammaglobulinemia presenting as juvenile chronic arthritis: report of one case. Acta Paediatr Taiwan 1999; 40 (04) 280-283
- 7 Sukumaran S. et al A child with x-linked agammaglobulinemia and enthesitis-related arthritis. Int J Rheumatol 2011; 2011: 175973
- 8 Verbruggen G. et al X linked agammaglobulinaemia and rheumatoid arthritis. Ann Rheum Dis 2005; 64 (07) 1075-1078
- 9 Levy J. et al Clinical spectrum of X-linked hyper-IgM syndrome. J Pediatr 1997; 131 1 Pt 1 47-54
- 10 Webster EA. et al An aggressive form of polyarticular arthritis in a man with CD154 mutation (X-linked hyper-IgM syndrome). Arthritis Rheum 1999; 42 (06) 1291-1296
- 11 Sibilia J. et al Hyper-IgM syndrome associated with rheumatoid arthritis: report of RA in a patient with primary impaired CD40 pathway. Br J Rheumatol 1996; 35 (03) 282-284
- 12 Melegari A. et al Immunodeficiency and autoimmune phenomena in female hyper-IgM syndrome. Ann N Y Acad Sci 2007; 1109: 106-108
- 13 Jorgensen GH. et al Familial aggregation of IgAD and autoimmunity. Clin Immunol 2009; 131 (02) 233-239
- 14 Cassidy JT, Pettym RE, Sullivan DB. Abnormalities in the distribution of serum immunoglobulin concentrations in juvenile rheumatoid arthritis. J Clin Invest 1973; 52 (08) 1931-1936
- 15 Odnoletkova I. et al The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data. Orphanet J Rare Dis 2018; 13 (01) 201
- 16 Kuijpers TW. et al CD20 deficiency in humans results in impaired T cell-independent antibody responses. J Clin Invest 2010; 120 (01) 214-222
- 17 van Zelm MC. et al An antibody-deficiency syndrome due to mutations in the CD19 gene. N Engl J Med 2006; 354 (18) 1901-1912
- 18 van Zelm MC. et al CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency. J Clin Invest 2010; 120 (04) 1265-1274
- 19 Wentink MW. et al CD21 and CD19 deficiency: Two defects in the same complex leading to different disease modalities. Clin Immunol 2015; 161 (02) 120-127
- 20 Grimbacher B. et al Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency. Nat Immunol 2003; 4 (03) 261-268
- 21 Castigli E. et al TACI is mutant in common variable immunodeficiency and IgA deficiency. Nat Genet 2005; 37 (08) 829-834
- 22 Warnatz K. et al B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans. Proc Natl Acad Sci U S A 2009; 106 (33) 13945-13950
- 23 Tuijnenburg P. et al Loss-of-function nuclear factor kappaB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans. J Allergy Clin Immunol 2018; 142 (04) 1285-1296
- 24 Chen K. et al Germline mutations in NFKB2 implicate the noncanonical NF-kappaB pathway in the pathogenesis of common variable immunodeficiency. Am J Hum Genet 2013; 93 (05) 812-824
- 25 Conley ME, Notarangelo LD, Etzioni A. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol 1999; 93 (03) 190-197
- 26 Elkaim E. et al Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase delta syndrome 2: A cohort study. J Allergy Clin Immunol 2016; 138 (01) 210-218 e9
- 27 Jamee M. et al Clinical, Immunological, and Genetic Features in Patients with Activated PI3Kdelta Syndrome (APDS): a Systematic Review. Clin Rev Allergy Immunol 2019 DOI: May 21. doi: 10.1007/s12016-019-08738-9
- 28 Coulter TI. et al Clinical spectrum and features of activated phosphoinositide 3-kinase delta syndrome: A large patient cohort study. J Allergy Clin Immunol 2017; 139 (02) 597-606 e4
- 29 Barzaghi F. et al Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study. J Allergy Clin Immunol 2018; 141 (03) 1036-1049 e5
- 30 Gambineri E. et al Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome. Front Immunol 2018; 9: 2411
- 31 Cepika AM. et al Tregopathies: Monogenic diseases resulting in regulatory T-cell deficiency. J Allergy Clin Immunol 2018; 142 (06) 1679-1695
- 32 Mitsuiki N, Schwab C, Grimbacher B. What did we learn from CTLA-4 insufficiency on the human immune system?. Immunol Rev 2019; 287 (01) 33-49
- 33 Schwab C. et al Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects. J Allergy Clin Immunol 2018; 142 (06) 1932-1946
- 34 Lopez-Herrera G. et al Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. Am J Hum Genet 2012; 90 (06) 986-1001
- 35 Gámez-Díaz L, August D, Stepensky P. et al J Allergy Clin Immunol. 2016; 137 (01) 223-230 DOI: doi: 10.1016/j.jaci.2015.09.025.
- 36 Oz RS, Gluth M, Tesher MS. Pediatric Autoimmune Inner Ear Disease: A Rare, But Treatable Condition. Pediatr Ann 2019; 48 (10) e391-e394
- 37 Mogensen TH. IRF and STAT Transcription Factors – From Basic Biology to Roles in Infection, Protective Immunity, and Primary Immunodeficiencies. Front Immunol 2018; 9: 3047
- 38 Gadina M. et al Translational and clinical advances in JAK-STAT biology: The present and future of jakinibs. J Leukoc Biol 2018; 104 (03) 499-514
- 39 Holland SM. et al STAT3 mutations in the hyper-IgE syndrome. N Engl J Med 2007; 357 (16) 1608-1619
- 40 Haapaniemi EM. et al Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3. Blood 2015; 125 (04) 639-648
- 41 Milner JD. et al Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations. Blood 2015; 125 (04) 591-599
- 42 Toubiana J. et al Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. Blood 2016; 127 (25) 3154-3164
- 43 Pelkonen P. et al Chronic arthritis associated with chromosome deletion 22q11.2 syndrome. J Rheumatol 2002; 29 (12) 2648-2650
- 44 Sullivan KE. et al Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome). Arthritis Rheum 1997; 40 (03) 430-436
- 45 Crestani E. et al Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. J Allergy Clin Immunol 2015; 136 (05) 1401-1404 e1–3
- 46 Lee BW, Yap HK. Polyarthritis resembling juvenile rheumatoid arthritis in a girl with chronic granulomatous disease. Arthritis Rheum 1994; 37 (05) 773-776
- 47 Winkelstein JA. et al Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000; 79 (03) 155-169
- 48 Schroder-Braunstein J, Kirschfink M. Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management. Mol Immunol 2019; 114: 299-311
- 49 Meyer-Bahlburg A, Dressler F, Baumann U. Chronic arthritis in a boy with Cernunnos immunodeficiency. Clin Immunol 2014; 154 (01) 47-48