Your browser doesn't support javascript.
loading
Smith-Magenis Syndrome Patients Often Display Antibody Deficiency but Not Other Immune Pathologies.
Perkins, Tiffany; Rosenberg, Jacob M; Le Coz, Carole; Alaimo, Joseph T; Trofa, Melissa; Mullegama, Sureni V; Antaya, Richard J; Jyonouchi, Soma; Elsea, Sarah H; Utz, Paul J; Meffre, Eric; Romberg, Neil.
Afiliação
  • Perkins T; Department of Pediatrics, Yale University School of Medicine, New Haven, Conn.
  • Rosenberg JM; Division of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, Calif.
  • Le Coz C; Division of Allergy Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Penn.
  • Alaimo JT; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Tex.
  • Trofa M; Division of Allergy Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Penn.
  • Mullegama SV; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Tex.
  • Antaya RJ; Department of Pediatrics, Yale University School of Medicine, New Haven, Conn; Department of Dermatology, Yale University School of Medicine, New Haven, Conn.
  • Jyonouchi S; Division of Allergy Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Penn.
  • Elsea SH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Tex.
  • Utz PJ; Division of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, Calif; Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, Calif.
  • Meffre E; Department of Immunobiology, Yale University School of Medicine, New Haven, Conn; Department of Internal Medicine, Yale University School of Medicine, New Haven, Conn.
  • Romberg N; Division of Allergy Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Penn. Electronic address: rombergn@email.chop.edu.
J Allergy Clin Immunol Pract ; 5(5): 1344-1350.e3, 2017.
Article em En | MEDLINE | ID: mdl-28286158
BACKGROUND: Smith-Magenis syndrome (SMS) is a complex neurobehavioral disorder associated with recurrent otitis. Most SMS cases result from heterozygous interstitial chromosome 17p11.2 deletions that encompass not only the intellectual disability gene retinoic acid-induced 1 but also other genes associated with immunodeficiency, autoimmunity, and/or malignancy. OBJECTIVES: The goals of this study were to describe the immunological consequence of 17p11.2 deletions by determining the prevalence of immunological diseases in subjects with SMS and by assessing their immune systems via laboratory methods. METHODS: We assessed clinical histories of 76 subjects with SMS with heterozygous 17p11.2 deletions and performed in-depth immunological testing on 25 representative cohort members. Laboratory testing included determination of serum antibody concentrations, vaccine titers, and lymphocyte subset frequencies. Detailed reactivity profiles of SMS serum antibodies were performed using custom-made antigen microarrays. RESULTS: Of 76 subjects with SMS, 74 reported recurrent infections including otitis (88%), pneumonia (47%), sinusitis (42%), and gastroenteritis (34%). Infections were associated with worsening SMS-related neurobehavioral symptoms. The prevalence of autoimmune and atopic diseases was not increased. Malignancy was not reported. Laboratory evaluation revealed most subjects with SMS to be deficient of isotype-switched memory B cells and many to lack protective antipneumococcal antibodies. SMS antibodies were not more reactive than control antibodies to self-antigens. CONCLUSIONS: Patients with SMS with heterozygous 17p.11.2 deletions display an increased susceptibility to sinopulmonary infections, but not to autoimmune, allergic, or malignant diseases. SMS sera display an antibody reactivity profile favoring neither recognition of pathogen-associated antigens nor self-antigens. Prophylactic strategies to prevent infections may also provide neurobehavioral benefits to selected patients with SMS.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Síndrome de Smith-Magenis / Síndromes de Imunodeficiência Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Síndrome de Smith-Magenis / Síndromes de Imunodeficiência Idioma: En Ano de publicação: 2017 Tipo de documento: Article