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Cited by 108Immunodeficiency and Autoimmune DisordersAnimal health and immunologyBiochemical and Molecular Research

The DOI matches its Crossref record, with a small difference in title or year; 37 of the 37 references it cites were found in a registry or an index.

Hypercatabolism of IgG, IgA, IgM, and albumin in the Wiskott-Aldrich syndrome

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Blaese, R. Michael, Strober, Warren, Levy, Arthur L., Waldmann, Thomas A.·1971·Journal of Clinical Investigation
DOI 10.1172/jci106731PMC PMC292175
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Abstract

The Wiskott-Aldrich syndrome is an immune deficiency disorder with an impairment of both humoral and cellular immune responses. Metabolic turnover studies of IgG, IgA, IgM, and albumin were conducted in seven patients with the Wiskott-Aldrich syndrome using purified radioiodinated proteins. The survival of each of the proteins studied was significantly shortened with a half-time of 7.5 days for IgG (normal 22.9 +/-4 SD), 3.0 days for IgA (normal 5.8 +/-1), 5.0 days for IgM (normal 10.1 +/-2.1), and 8.6 days for albumin (normal 17, range 13-20); the fractional catabolic rates were correspondingly elevated and the distribution of protein among the body compartments was normal. For three of the four proteins. IgG, IgA, and albumin, the steady-state synthetic rates were generally elevated leading to normal or even elevated serum proteins levels. Thus, in the case of IgA, the synthetic rate averaged five times normal while the fractional degradative rate was twice normal. The resulting serum concentration was, therefore, significantly elevated, IgM represented an exception to this pattern in that the increased rate of degradation was not counterbalanced by an increased synthetic rate and, therefore, the serum levels were low. Albumin clearance studies using albumin-(51)Cr showed gastrointestinal protein loss in these patients to be slightly greater than normal, but this could account for only a small fraction of the hypercatabolism observed. There was no proteinuria or abnormalities of thyroid, adrenal, renal, or liver function. Thus, none of the previously recognized causes of increased serum protein catabolism were present. Patients with the Wiskott-Aldrich syndrome, therefore, have a unique disorder of serum protein metabolism characterized by endogenous hypercatabolism of at least four major serum proteins. This phenomenon may be related to reticuloendothelial hyperfunction since the Wiskott-Aldrich syndrome is associated with reticuloendothelial hyperplasia and accelerated clearance of colloidal materials from the plasma.

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Metadata

Authors
Blaese, R. M., Strober, W., Levy, A. L., & Waldmann, T. A.
Affiliations
National Institutes of Health (US)
ORCID
Venue
Journal of Clinical Investigation
Publisher
American Society for Clinical Investigation
Published
1971-11-01
Volume
50
Issue
11
Pages
2331-2338
ISSN
0021-9738 (ISSN-L)
DOI
10.1172/jci106731
PMC
PMC292175
OpenAlex
W81571208
Cited by
108
References
37
Citations by year
2026: 1 · 2025: 4 · 2024: 1 · 2023: 3 · 2021: 3 · 2020: 3 · 2019: 3 · 2018: 2 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 3
FWCI
4.45
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Investigation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal health and immunology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
Keywords
Wiskott-Aldrich syndrome, hypercatabolism, IgG, immunoglobulin A, immunoglobulin M, albumin, protein turnover, fractional catabolic rate, protein synthesis, immunodeficiency, proteinuria
MeSH terms
Adolescent, Child, Child, Preschool, Chromium Isotopes, Humans, Immunoglobulin A, Immunoglobulin G, Immunoglobulins, Immunologic Deficiency Syndromes, Infant, Lymphatic Diseases, Male, Metabolic Clearance Rate, Protein-Losing Enteropathies, Mononuclear Phagocyte System, Serum Albumin, Wiskott-Aldrich Syndrome

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