Congenital Tuftsin Deficiency
- 16 December 1983
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 419 (1) , 214-219
- https://doi.org/10.1111/j.1749-6632.1983.tb37106.x
Abstract
The serum tuftsin activity in four different pediatric groups has been studied: (a) 20 premature infants, (b) 20 full-term infants, (c) 20 normal children (controls), and (d) 5 patients with recurrent and severe infections of the respiratory system, skin, and lymph nodes. The normal children as well as the premature and full-term infants had normal tuftsin activity. Tuftsin activity in the serum of the 5 patients in group (d) was absent. Cellular and humoral immunity in these patients was normal. All patients have been shown to have a mutant peptide that is strongly inhibitory to the normal tetrapeptide tuftsin. The clinical response of these patients to gamma-globulin was excellent.Keywords
This publication has 8 references indexed in Scilit:
- Sepsis NeonatorumNew England Journal of Medicine, 1981
- Tuftsin deficiency: A new syndrome with defective phagocytosisThe Journal of Pediatrics, 1972
- DISORDERS OF NEUTROPHIL AND MONOCYTE FUNCTIONBritish Journal of Haematology, 1971
- A Familial Deficiency of the Phagocytosis-Enhancing Activity of Serum Related to a Dysfunction of the Fifth Component of Complement (C5)New England Journal of Medicine, 1970
- Increased Susceptibility to Infection Associated with Abnormalities of Complement-Mediated Functions and of the Third Component of Complement (C3)New England Journal of Medicine, 1970
- Immunoglobulin Levels and Gestational AgeNeonatology, 1969
- The Physiological Role of the Lymphoid System. IV. The Separation of γ-Globulin into Physiologically Active Components by Cellulose Phosphate Chromatography*Biochemistry, 1967
- In Vitro Bactericidal Capacity of Human Polymorphonuclear Leukocytes: Diminished Activity in Chronic Granulomatous Disease of Childhood *Journal of Clinical Investigation, 1967