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Article
October 1981

Management of Recurrent Invasive Haemophilus influenzae Infection

Author Affiliations

From the Division of Pediatric Allergy and Immunology, Department of Pediatrics, Long Island Jewish-Hillside Medical Center, New Hyde Park, NY (Dr Fruchter); Department of Pediatrics, School of Medicine, Health Sciences Center, State University of New York at Stony Brook (Dr Fruchter); and Division of Infectious Diseases and Immunology, Department of Pediatrics, University of Rochester (NY) School of Medicine and Dentistry (Dr Insel).

Am J Dis Child. 1981;135(10):927-929. doi:10.1001/archpedi.1981.02130340033012
Abstract

• A 4½-month-old infant had three separate episodes of invasive Haemophilus influenzae type b infection and did not produce antibody to the capsular polysaccharide of H influenzae b. Immunologic evaluation disclosed normal immunoglobulin and complement concentrations and normal T-cell number and function. In view of the persistent presence of type-specific capsular polysaccharide of H influenzae b (polyribophosphate [PRP]) in blood serum without any detectable anti-PRP antibody for 30 days following H influenzae b meningitis, monthly treatment with immune human serum globulin was undertaken until spontaneous production of anti-PRP antibody occurred. The patient's 4-year-old sibling was found to be a nasopharyngeal carrier and may have been a source for reinfection. A search for possible family carriers should be conducted in evaluating the conditions of patients with recurrent invasive H influenzae b infection. In addition, temporary treatment with immune human serum globulin should be considered.

(Am J Dis Child 1981;135:927-929)

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