| Literature DB >> 53333 |
R G Keightley, A R Lawton, M D Cooper, E J Yunis.
Abstract
Following transplantation with allogeneic fetal liver, a boy with a severe combined immunodeficiency and adenosine-deaminase (A.D.A.) deficiency developed immunocompetent T and B cells in an orderly manner. Engraftment was indicated by appearance of A.D.A. activity and donor-lymphocyte and red-cell antigens. The child remained free of major infections until one year later when he developed an ultimately fatal nephrotic syndrome associated with immune-complex glomerulonephritis.Entities:
Mesh:
Substances:
Year: 1975 PMID: 53333 DOI: 10.1016/s0140-6736(75)90238-x
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321