Klin Padiatr 2011; 223(06): 378-385
DOI: 10.1055/s-0031-1287835
Bericht
© Georg Thieme Verlag KG Stuttgart · New York

Interdisziplinäre AWMF-Leitlinie zur Diagnostik von primären Immundefekten (S2k)

Interdisciplinary AWMF Guideline for the Diagnostics of Primary Immunodeficiency
S. Farmand
1   Zentrum für Kinder- und Jugendmedizin, Universitätsklinikum Freiburg
2   Zentrum für Chronische Immundefizienz, Universitätsklinikum Freiburg
,
U. Baumann
3   Pädiatrische Pneumologie, Allergologie und Neonatologie, Medizinische Hochschule Hannover
,
H. von Bernuth
4   Klinik für Kinderheilkunde mit Schwerpunkt Pneumologie und Immunologie, Universitätskinderklinik der Charité Berlin
,
M. Borte
5   Klinik für Kinder- und Jugendmedizin, Fachbereich Pädiatrische Rheumatologie, Immunologie und Infektiologie, Klinikum St. Georg gGmbH, Leipzig
,
E. Foerster-Waldl
6   Universitätsklinik für Kinder- und Jugendheilkunde, Ambulanz für Störungen der Immunabwehr, Medizinische Universität Wien
,
K. Franke
7   St. Marien-Krankenhaus gemGmbH, Siegen
,
P. Habermehl
8   Kinderarztpraxis, Mainz-Hechtsheim
,
P. Kapaun
9   Kinderarztpraxis, Hamburg
,
G. Klock
10   dsai, Regionalgruppe Frankfurt, Fachbereich Chemie, Technische Universität Kaiserslautern
,
J. Liese
11   Pädiatrische Infektiologie und Immunologie, Universitätskinderklinik Würzburg
,
R. Marks
12   Kompetenzzentrum Leukämien und Präleukämien, Universitätsklinikum Freiburg
,
R. Müller
13   Klinik und Poliklinik für HNO-Heilkunde, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden
,
T. Nebe
14   Hämatologisches Speziallabor, MVZ Onkologikum, Frankfurt/Main
,
T. Niehues
15   Zentrum für Kinder- und Jugendmedizin, HELIOS Klinikum Krefeld
,
V. Schuster
16   Universitätsklinik für Kinder- und Jugendliche, Universitätsklinikum Leipzig
,
K. Warnatz
2   Zentrum für Chronische Immundefizienz, Universitätsklinikum Freiburg
,
T. Witte
17   Klinik für Immunologie und Rheumatologie, Medizinische Hochschule Hannover
,
S. Ehl
1   Zentrum für Kinder- und Jugendmedizin, Universitätsklinikum Freiburg
,
I. Schulze
1   Zentrum für Kinder- und Jugendmedizin, Universitätsklinikum Freiburg
› Author Affiliations
Further Information

Publication History

Publication Date:
03 November 2011 (online)

Zusammenfassung

Hintergrund:

Primäre Immundefekte sind potenziell lebensbedrohliche Erkrankungen. Auch wenn in den letzten Jahren zunehmend mehr immunologische Defekte klinisch und molekulargenetisch charakterisiert wurden, so werden primäre Immundefekt in der täglichen Praxis oftmals noch zu spät erkannt. Vor dem Hintergrund, dass eine frühe Diagnosestellung die Morbidität und Mortalität der betroffenen Patienten senken kann, wurde daher im Auftrag der Arbeitsgemeinschaft Pädiatrische Immunologie (API) und der Deutschen Gesellschaft für Immunologie (DGfI) eine interdisziplinäre S2-Leitlinie zur Diagnostik von Primären Immundefekten erstellt.

Methodik:

Grundlage der Leitlinie sind im Wesentlichen Expertenmeinungen auf der Basis bereits verfügbarer Leitlinien und Empfehlungen aus Deutschland und anderen Ländern, ergänzt durch Daten aus Studien, die die getroffenen Kernaussagen unterstützen (Evidenzgrad III). Unter Beteiligung von 20 Vertretern aus 14 Fachgesellschaften, Verbänden und Vereinigungen entstand eine konsensbasierte Leitlinie mit repräsentativer Entwicklergruppe und strukturierter Konsensusfindung (S2k). Der nominale Gruppenprozess zur Konsensusfindung fand unter Moderation einer Vertreterin der Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften (e.V.) (AWMF) im April 2011 statt.

Ergebnisse:

Die aufgestellten Kernaussagen wurden diskutiert und im strukturierten Konsensverfahren abgestimmt. Insbesondere wurden modifizierte Warnzeichen für primäre Immundefekte formuliert und immunologische Notfallsituationen definiert.

Abstract

Background:

Primary immunodeficiencies are potentially life-threatening diseases. Over the last years, the clinical phenotype and the molecular basis of an increasing number of immunological defects have been characterized. However, in daily practice primary immunodeficiencies are still often diagnosed too late. Considering that an early diagnosis may reduce morbidity and mortality of affected patients, an interdisciplinary guideline for the diagnosis of primary immunodeficiencies was developed on behalf of the Arbeitsgemeinschaft Pädiatrische Immunologie (API) and the Deutsche Gesellschaft für Immunologie (DGfI).

Methods:

The guideline is based on expert opinion and on knowledge from other guidelines and recommendations from Germany and other countries, supplemented by data from studies that support the postulated key messages (level of evidence III). With the contribution of 20 representatives, belonging to 14 different medical societies and associations, a consensus-based guideline with a representative group of developers and a structured consensus process was created (S2k). Under the moderation of a representative of the Association of the Scientific Medical Societies in Germany (AWMF) the nominal group process took place in April 2011.

Results:

The postulated key messages were discussed and voted on following a structured consensus procedure. In particular, modified warning signs for primary immunodeficiencies were formulated and immunological emergency situations were defined.

 
  • Literatur

  • 1 Aghamohammadi A, Moin M, Karimi A et al. Immunologic evaluation of patients with recurrent ear, nose, and throat infections. Am J Otolaryngol 2008; 29: 385-392
  • 2 Arason GJ, Jorgensen GH, Ludviksson BR. Primary immunodeficiency and autoimmunity: Lessons from human diseases. Scand J Immunol 2010; 71: 317-328
  • 3 Ardeniz O, Cunningham-Rundles C. Granulomatous disease in common variable immunodeficiency. Clin Immunol 2009; 133: 198-207
  • 4 Azar AE, Ballas ZK. Evaluation of the adult with suspected immunodeficiency. Am J Med 2007; 120: 764-768
  • 5 Baumann U, Belohradsky B, vBernuth H et al. Primäre Immundefekte – Warnzeichen und Algorithmen zur Diagnosefindung. 1. Auflage: UNI-MED Verlag AG Bremen; 2010
  • 6 Berrington JE, Flood TJ, Abinun M et al. Unsuspected pneumocystis carinii pneumonia at presentation of severe primary immunodeficiency. Arch dis child 2000; 82: 144-147
  • 7 Berron-Ruiz A, Berron-Perez R, Ruiz-Maldonado R. Cutaneous markers of primary immunodeficiency diseases in children. Pediatr Dermatol 2000; 17: 91-96
  • 8 Björkander J, Björkqvist M, Brodszki N et al. Riktlinjer för utredning, diagnostik och behandling av primär immunbrist: CVID, IgG-subklassbrist, IgA-brist, XLA, SCID och CGD. In: http://www.slipi.nu Version II, 2009
  • 9 Boyle JM, Buckley RH. Population prevalence of diagnosed primary immunodeficiency diseases in the United States. J Clin Immunol 2007; 27: 497-502
  • 10 Buckley RH, Ballow M, Berger M et al. Immune deficiency foundation diagnostic & clinical care guidelines for primary immunodeficiency diseases. In: Immune deficiency foundation. Second edition 2009
  • 11 Bustamante J, Boisson-Dupuis S, Jouanguy E et al. Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases. Curr Opin Immunol 2008; 20: 39-48
  • 12 Casanova JL, Jouanguy E, Lamhamedi S et al. Immunological conditions of children with BCG disseminated infection. Lancet 1995; 346: 581-
  • 13 Chapel H, Lucas M, Lee M et al. Common variable immunodeficiency disorders: Division into distinct clinical phenotypes. Blood 2008; 112: 277-286
  • 14 Cheraghi M, Salvi S. Environmental tobacco smoke (ETS), respiratory health in children. Eur J Pediatr 2009; 168: 897-905
  • 15 Cunningham-Rundles C. Hematologic complications of primary immune deficiencies. Blood Rev 2002; 16: 61-64
  • 16 Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: Clinical and immunological features of 248 patients. Clin Immunol 1999; 92: 34-48
  • 17 Dale D. ELANE-related neutropenia. In: GeneReviews [Internet]. Seattle 1993–2002 updated 2011 Jul 14
  • 18 de Vries E. Patient-centred screening for primary immunodeficiency: A multi-stage diagnostic protocol designed for non-immunologists. Clin exp immunol 2006; 145: 204-214
  • 19 de Vries E, Driessen G. Educational paper: Primary immunodeficiencies in children: A diagnostic challenge. Eur J Pediatr 2011; 170: 169-177
  • 20 Feigin RCJ, Demmler G, Kaplan S. Immunological and phagocytic responses to infection. In: Textbook of pediatric infectious disease. 5th Edition Volume 1. Saunders Elsevier; 2004
  • 21 Felgentreff K, Perez-Becker R, Speckmann C et al. Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency. Clin Immunol 2011;
  • 22 Furst DE. Serum immunoglobulins and risk of infection: How low can you go?. Semin Arthritis Rheum 2009; 39: 18-29
  • 23 Guerrerio AL, Frischmeyer-Guerrerio PA, Lederman HM et al. Recognizing gastrointestinal and hepatic manifestations of primary immunodeficiency diseases. J Pediatr Gastroenterol Nutr 2010; 51: 548-555
  • 24 Hague RA, Rassam S, Morgan G et al. Early diagnosis of severe combined immunodeficiency syndrome. Arch dis child 1994; 70: 260-263
  • 25 Hayward AR, Harvey BAM, Leonard J et al. Delayed separation of the umbilical-cord, widespread infections, and defective neutrophil mobility. Lancet 1979; 1: 1099-1101
  • 26 Herriot R, Sewell WA. Antibody deficiency. J Clin Pathol 2008; 61: 994-1000
  • 27 Hoffmann JC, Fischer I, Hohne W et al. Methodological basis for the development of consensus recommendations. Z Gastroenterol 2004; 42: 984-986
  • 28 Janka G. Hemophagocytic lymphohistiocytosis: When the immune system runs amok. Klin Padiatr 2009; 221: 278-285
  • 29 Jedrychowski W, Maugeri U, Flak E et al. Predisposition to acute respiratory infections among overweight preadolescent children: An epidemiologic study in Poland. Public Health 1998; 112: 189-195
  • 30 Joshi AY, Iyer VN, Hagan JB et al. Incidence and temporal trends of primary immunodeficiency: A population-based cohort study. Mayo Clin Proc 2009; 84: 16-22
  • 31 Lierl M. Periodic fever syndromes: A diagnostic challenge for the allergist. Allergy 2007; 62: 1349-1358
  • 32 Malphettes M, Gerard L, Carmagnat M et al. Late-onset combined immune deficiency: A subset of common variable immunodeficiency with severe T cell defect. Clin Infect Dis 2009; 49: 1329-1338
  • 33 Modell V. The impact of physician education and public awareness on early diagnosis of primary immunodeficiencies – Robert A. Good immunology symposium. Immunol Res 2007; 38: 43-47
  • 34 Monto AS, Sullivan KM. Acute respiratory illness in the community – frequency of illness and the agents involved. Epidemiol Infect 1993; 110: 145-160
  • 35 Nafstad P, Hagen JA, Oie L et al. Day care centers and respiratory health. Pediatrics 1999; 103: 753-758
  • 36 Nelson KS, Lewis DB. Adult-onset presentations of genetic immunodeficiencies: genes can throw slow curves. Curr Opin Infect Dis 2010; 23: 359-364
  • 37 Noroski LM, Shearer WT. Screening for primary immunodeficiencies in the clinical immunology laboratory. Clin Immunol Immunopathol 1998; 86: 237-245
  • 38 Notarangelo LD, Fischer A, Geha RS et al. Primary immunodeficiencies: 2009 update. J Allergy Clin Immunol 2009; 124: 1161-1178
  • 39 Oliveira JB, Fleisher TA. Laboratory evaluation of primary immunodeficiencies. J Allergy Clin Immunol 2010; 125: S297-S305
  • 40 Oudesluysmurphy AM, Eilers GAM, Degroot CJ. The time of separation of the umbilical-cord. Eur J Pediatr 1987; 146: 387-389
  • 41 Pachlopnik Schmid J, Canioni D, Moshous D et al. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency). Blood 2011; 117: 1522-1529
  • 42 Paller AS, Massey RB, Curtis MA et al. Cutaneous granulomatous lesions in patients with ataxia-telangiectasia. J Pediatr 1991; 119: 917-922
  • 43 Park MA, Li JT, Hagan JB et al. Common variable immunodeficiency: a new look at an old disease. Lancet 2008; 372: 489-502
  • 44 Patiroglu T, Unal E, Yikilmaz A et al. Atypical presentation of chronic granulomatous disease in an adolescent boy with frontal lobe located Aspergillus abscess mimicking intracranial tumor. Childs Nerv Syst 2010; 26: 149-154
  • 45 Reda SM, Afifi HM, Amine MM. Primary immunodeficiency diseases in Egyptian children: A single-center study. J Clin Immunol 2009; 29: 343-351
  • 46 Schimke LF, Sawalle-Belohradsky J, Roesler J et al. Diagnostic approach to the hyper-IgE syndromes: Immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis. J Allergy Clin Immunol 2010; 126: 611-U350
  • 47 Schutze GE, Mason Jr EO, Barson WJ et al. Invasive pneumococcal infections in children with asplenia. Pediatr Infect Dis J 2002; 21: 278-282
  • 48 Shapiro RS. Malignancies in the setting of primary immunodeficiency: Implications for hematologists/oncologists. Am J Hematol 2011; 86: 48-55
  • 49 Shovlin CL, Simmonds HA, Fairbanks LD et al. Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency. J Immunol 1994; 153: 2331-2339
  • 50 Slatter MA, Gennery AR. Clinical immunology review series: An approach to the patient with recurrent infections in childhood. Clin Exp Immunol 2008; 152: 389-396
  • 51 Stark D, Barratt JLN, van Hal S et al. Clinical significance of enteric protozoa in the immunosuppressed human population. Clin Microbiol Rev 2009; 22: 634-650
  • 52 Subbarayan A, Colarusso G, Hughes SM et al. Clinical features that identify children with primary immunodeficiency diseases. Pediatrics 2011; 127: 810-816
  • 53 Takada H, Yoshikawa H, Imaizumi M et al. Delayed separation of the umbilical cord in two siblings with interleukin-1 receptor-associated kinase 4 deficiency: Rapid screening by flow cytometer. J Pediatr 2006; 148: 546-548
  • 54 Teachey DT, Seif AE, Grupp SA. Advances in the management and understanding of autoimmune lymphoproliferative syndrome (ALPS). Br J Haematol 2010; 148: 205-216
  • 55 Teepe J, Grigoryan L, Verheij TJM. Determinants of community-acquired pneumonia in children and young adults in primary care. Eur Respir J 2010; 35: 1113-1117
  • 56 Thomsen RW, Hundborg HH, Lervang HH et al. Diabetes mellitus as a risk and prognostic factor for community-acquired bacteremia due to enterobacteria: A 10-year, population-based study among adults. Clin Infect Dis 2005; 40: 628-631
  • 57 Uffelman JA, Engelhar WE, Jolliff CR. Quantitation of immunoglobulins in normal children. Clin Chim Acta 1970; 28: 185-192
  • 58 Westerberg LS, Klein C, Snapper SB. Breakdown of T cell tolerance and autoimmunity in primary immunodeficiency – lessons learned from monogenic disorders in mice and men. Curr Opin Immunol 2008; 20: 646-654
  • 59 Winkelstein JA, Marino MC, Ochs H et al. The X-linked hyper-IgM syndrome – clinical and immunologic features of 79 patients. Medicine 2003; 82: 373-384
  • 60 Wood P. Primary antibody deficiencies: Recognition, clinical diagnosis and referral of patients. Clin Med 2009; 9: 595-599
  • 61 Yarmohammadi H, Estrella L, Doucette J et al. Recognizing primary immune deficiency in clinical practice. Clin Vaccine Immunol 2006; 13: 329-332