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A family of selective immunodeficiency with normal immunoglobulins: possible autosomal dominant inheritance.

作者信息

Higuchi S, Awata H, Nunoi H, Tsuchiya H, Naoe H, Igarashi H, Matsuda I

机构信息

Department of Paediatrics, Kumamoto University Medical School, Japan.

出版信息

Eur J Pediatr. 1994 May;153(5):328-32. doi: 10.1007/BF01956412.

DOI:10.1007/BF01956412
PMID:8033920
Abstract

We report here our findings in two Japanese siblings who experienced recurrent bacterial and viral infections since early infancy. Recent symptoms included diarrhoea, conjunctivitis, rashes, headache, sore throat, joint pain, vomiting and vertigo, all similar to those seen in toxic shock syndrome, except for shock. These symptoms improved following gammaglobulin treatment. Staphylococcus aureus with coagulase type IV was continuously isolated from nasal smears producing toxic shock syndrome toxin-1 (TSST-1). Serum antibodies did not or only poorly responded to TSST-1, diphtheria toxoid, varicella virus and rubella virus, whereas total and subclass levels of serum immunoglobulin and in vitro DNA synthesis of lymphocytes stimulated by TSST-1, Staph. aureus, varicella vaccine and mitogens were normal. In the family, ten other members in three generations (five males: five females) including the mother had similar clinical symptoms. Thus, the disease may be inherited in an autosomal dominant fashion.

摘要

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J Clin Immunol. 2007 May;27(3):327-38. doi: 10.1007/s10875-007-9072-4. Epub 2007 Mar 6.
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