| Literature DB >> 308999 |
F C Schmalstieg, G C Mills, J A Nelson, L T May, A S Goldman, R M Goldblum.
Abstract
A 10-month-old child with a profound deficiency of adenosine deaminase and severe combined immunodeficiency was treated for a period of 17 months with red cell and plasma transfusions containing normal amounts of the deficient enzyme. Following each transfusion, the plasma adenosine, red cell and lymphocyte ATP, urinary adenine, and urinary deoxyadenosine decreased transiently. During this period, the absolute blood lymphocyte count rose and a limited increased in the response of the lymphocytes to PHA-P was observed. Delayed hypersensitivity skin tests remained negative during the transfusion periods. A quantitative elevation of serum immunoglobulins occurred, but specific antibody formation was not elicited. In contrast to a previous report of successful therapy of ADA deficiency with red cell and plasma infusions, this patient responded poorly to enzyme replacement therapy. The difference may be related to a more profound enzyme deficiency in our patient.Entities:
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Year: 1978 PMID: 308999 DOI: 10.1016/s0022-3476(78)80894-4
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406