Subscribe to RSS
DOI: 10.1055/s-2007-985877
© Georg Thieme Verlag KG Stuttgart · New York
Severe Combined Immunodeficiency Signalized by Eosinophilia and Lymphopenia in Rotavirus Infected Infants
Hinweis auf schweren kombinierten Immundefekt durch Eosinophilie und Lymphopenie bei Säuglingen mit RotavirusinfektionPublication History
Publication Date:
30 November 2007 (online)
Abstract
Background: Severe combined immunodeficiency (SCID) is a heterogeneous disease consisting of several different subtypes. Most subtypes present during infancy and without treatment, infections usually lead to early death. Diagnosis of SCID can be difficult as new subtypes are expected to be discovered soon. Late diagnosis is associated with a poorer outcome. Infections like rotavirus enteritis cannot be cleared in children with SCID due to impaired immunity. The aim of our study was to identify clues in children with rotavirus enteritis that aid to diagnose SCID early.
Patients and Methods: Total white blood counts in a cohort of SCID patients with persistent rotavirus infection at diagnosis (n = 18) were compared to total white blood counts in matched control patients without SCID but with rotavirus infection.
Results: Relative and absolute lymphopenia and eosinophilia were more common in SCID patients (p<0.005).
Conclusion: In infants with rotavirus infection, a full blood count should be performed: Eosinophilia and/or lymphopenia raise a high suspicion of SCID.
Zusammenfassung
Hintergrund: Der schwere kombinierte Immundefekt (SCID) ist eine heterogene Gruppe von Erkrankungen mit unterschiedlichen Subtypen. Die meisten Subtypen manifestieren sich in der Säuglingszeit und führen ohne Therapie in der Regel zum frühen Tod. Die Diagnose eines SCID kann schwierig sein, da ständig neue Subtypen entdeckt werden. Eine Verzögerung der Diagnose ist mit einer schlechteren Prognose assoziiert. Infektionen wie die Rotavirus-Enteritis können von Kindern mit SCID nicht bewältigt werden. Ziel der Studie war die Identifikation von klinischen Merkmalen, die bei Kindern mit Rotavirus-Enteritis eine frühe Diagnosestellung des schweren kombinierten Immundefektes (SCID) ermöglichen.
Patienten und Methoden: Differentialblutbilder einer Kohorte von Patienten mit SCID und chronischer Rotavirusinfektion bei Diagnose (n = 18) und von gematchten Kontrollpatienten mit Rotavirusinfektion ohne SCID wurden verglichen.
Ergebnisse: Relative und absolute Lymphopenie und Eosinophilie traten bei SCID-Patienten deutlich häufiger auf (p<0.005).
Schlussfolgerung: Bei Säuglingen mit Rotavirusinfektion ist ein Differentialblutbild anzufertigen: Eosinophilie und/oder Lymphopenie sind hoch verdächtig auf das Vorliegen eines SCID.
Key words
severe combined immunodeficiency - persistent rotavirus infection - lymphopenia - eosinophilia
Schlüsselwörter
schwerer kombinierter Immundefekt - chronische Rotavirusinfektion - Lymphopenie - Eosinophilie
References
-
1 Behrman RE, Kliegman RM, Jenson HB.
Nelson Textbook of Pediatrics . 16th edition Saunders, New York 2000 -
2 Buckley RH, Fischer A.
Bone marrow transplantation for primary immunodeficiency diseases. In: Ochs HD, Smith CIE, Puck JM, (Eds). Primary immunodeficiency diseases: a molecular and genetic approach. Oxford University Press, New York, NY 1999 - 3 Buckley RH, Schiff RI, Schiff SE, Markert ML, Williams LW, Harville TO Roberts JL, Puck JM. Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants. J Pediatr. 1997; 130 143-149
- 4 Centers for Disease Control and Prevention . Applying public health strategies, to primary immunodeficiency diseases: a potential approach to genetic disorders. MMWR. 2004; 52 11-63
- 5 Chan K, Puck JM. Development of population - based newborn screening for severe combined immunodeficiency. J Allergy Clin Immunol. 2005; 115 391-398
- 6 Comans-Bitter WM, Groot R de, Beemd R van den, Neijens HJ, Hop WC, Groeneveld K Hooijkaas H, Dongen JJ vsn. Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulation. J Pediatrics. 1997; 130 388-393
- 7 Haertel C, Strunk T, Bucsky P, Schultz C. Failure to thrive in a 14-month-old boy with lymphopenia and eosinophilia. Klin Padiatr. 2004; 216 24-25
- 8 Kalman L, Lindegren ML, Kobrynski L, Vogt R, Hannon H, Howard JT Buckley R. Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review. Gent Med. 2004; 6 16-26
- 9 Lang P, Schumm M, Greil J, Bader P, Klingebiel T, Müller I, Feuchtinger T, Pfeiffer M, Schlegel P-G, Niethammer D, Handgretinger R. A comparison between three graft manipulation methods for haploidentical stem cell transplantation in pediatric patients: preliminary results of a pilot study. Klin Padiatr. 2005; 217 334-338
- 10 Meisel R, Enczmann J, Balzer S, Bernbeck B, Kramm C, Schönberger S, Sinha K, Tröger A, Wernet P, Göbel U, Laws H-J, Dilloo D. Similar survival following HLA-identical sibling transplantation for standard indication in children with haematologic malignancies: a single center comparison of mobilized peripheral blood stem cell with bone marrow transplantation. Klin Padiatr. 2005; 217 135-141
- 11 Myers LA, Dhavalkumar DP, Puck JM, Buckley RH. Hematopoetic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improves survival. Blood. 2002; 99 872-878
- 12 Ochs HD, Smith CIE, Puck JM. Primary immunodeficiency disease: a molecular and genetic approach. Oxford University Press, New York, NY 1999
- 13 Pickering LK, Bartlett AV, Reves RR, Morrow A. Asymptomatic excretion of rotavirus before and after rotavirus diarrhea in children in day care centers. J Pediatr. 1988; 112 361-365
- 14 Rodriguez WJ, Kim HW, Brandt CD, Schwartz RH, Gardner MK, Jeffries B, Parrott RH, Kaslow RA, Smith JI, Kapikian AZ. Longitudinal study of rotavirus infection and gastroenteritis in families served by a pediatric medical practice: clinical and epidemiologic observations. Pediatr Infect Dis J.. 1987; 6 170-176
- 15 Ryser O, Morell A, Hitzig WH. Primary immunodeficiencies in Switzerland: first report of the national registry in adults and children. J Clin Immunol. 1988; 8 479-488
-
16 SAS Institute Inc .
SAS/STAT User's Guide . Version 9.1. Cary NC:SAS Institute Inc. 2004 - 17 Staat MA, Azimi PH, Berke T, Roberts N, Bernstein DI, Ward RL, Pickering LK, Matson DO. Clinical presentations of rotavirus infection among hospitalized children. Pediatr Infect Dis J. 2002; 21 221-227
- 18 Stephan JL, Vlekova V, Deist F Le, Blanche S, Donadieu J, Saint-Basile G De, Durandy A, Griscelli C, Fischer A. Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients. J Pediatr. 1993; 123 564-572
- 19 Villa A, Sobacchi C, Notarangelo LD, Bozzi F, Abinun M, Abrahamsen TG, Arkwright PD, Baniyash M, Brooks EG, Conley ME, Cortes P, Duse M, Fasth A, Filipovich AM, Infante AJ, Jones A, Mazzolari E, Muller SM, Pasic S, Rechavi G, Sacco MG, Santagata S, Schroeder ML, Seger R, Strina D, Ugazio A, Valiaho J, Vihinen M, Vogler LB, Ochs H, Vezzoni P, Friedrich W, Schwarz K. V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. Blood. 2001; 97 81-88
- 20 Ward RL, Clemens JD, Sack DA, Knowlton DR, MacNeal MM, Huda N, Ahmed F, Rao M, Schiff GM. Culture adaptation and characterization of group A rotaviruses causing diarrheal illnesses in Bangladesh from 1985-1986. J Clin Microbiol. 1991; 29 1915-1923
Correspondence
PD Dr. T. Niehues
Abteilung für Pädiatrische Onkologie
Hämatologie und Klinische Immunologie
Heinrich-Heine-Universität
Moorenstr. 5
40225 Düsseldorf
Phone: +49/211/811 76 80
Fax: +49/211/811 62 06
Email: niehues@uni-duesseldorf.de
URL: http://www.helferzelle.eu