Immunodeficiency disease in animals.
Abstract: Significant contributions to understanding the role of lymphocyte subpopulations in the immune response and to the characterization of immunodeficiencies in children have been achieved through study of animal models of immunodeficiency. Additional contributions can be made in two important areas. One is through identification of relevant, naturally-occurring models of adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency. The second, and potentially more important contribution, would be the identification of the metabolic basis for existing immune deficiencies. The necessary collaborative working arrangements should be established to achieve this objective. Demonstration of the metabolic basis for immune deficiencies in animals may enable the identification of similar defects in people, and eventually lead to enzyme or metabolite delivery schemes for treatment of affected children.
Publication Date: 1982-01-01 PubMed ID: 6750648
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Review
Summary
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This research article discusses the significant contributions gained from studying animal models of immunodeficiency, and suggests two potential ways to deepen this understanding: identification of naturally occurring models of specific deficiencies, and uncovering the metabolic basis for these immune deficiencies. Such studies may lead to new treatments for affected children.
Understanding Immunodeficiency Through Animal Models
- The article begins by acknowledging the significant contributions already achieved through studying animal models of immunodeficiency. This research has advanced our understanding of the role of lymphocyte subpopulations in the immune response and has aided in characterising immunodeficiencies in children.
Identifying Relevant Naturally Occurring Models
- The authors suggest that further contributions could be made by identifying naturally-occurring animal models of specific deficiencies such as adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency. Understanding these diseases in animals can aid in developing treatments and preventive strategies for similar conditions in humans.
Discovering the Metabolic Basis of Immune Deficiencies
- The second potential area of contribution stated by the authors is the identification of the metabolic basis of immune deficiencies. This could provide valuable insight into how these diseases manifest and progress and could potentially lead to the development of novel treatments.
Collaborative Working Arrangements and Potential Outcomes
- To achieve these objectives, the authors encourage the establishment of necessary collaborative working arrangements. They believe that the demonstration of the metabolic basis for immune deficiencies in animals could eventually enable the identification of similar defects in people.
- This understanding could, in turn, lead to the development of enzyme or metabolite delivery schemes for the treatment of affected children, offering a promising research direction for improving human health.
Cite This Article
APA
Perryman LE, Magnuson NS.
(1982).
Immunodeficiency disease in animals.
Prog Clin Biol Res, 94, 271-307.
Publication
Researcher Affiliations
MeSH Terms
- Adenosine Deaminase / deficiency
- Animals
- B-Lymphocytes / immunology
- Cattle
- Cattle Diseases / immunology
- Chickens
- Disease Models, Animal
- Dysgammaglobulinemia / veterinary
- Guinea Pigs
- Horse Diseases / immunology
- Horses
- Humans
- Immunologic Deficiency Syndromes / metabolism
- Immunologic Deficiency Syndromes / veterinary
- Lymphocytes / metabolism
- Mice
- Mice, Nude
- Purines / metabolism
- T-Lymphocytes / immunology
Citations
This article has been cited 1 times.- Perryman LE, McGuire TC, Banks KL. Animal model of human disease. Infantile X-linked agammaglobulinemia. Agammaglobulinemia in horses.. Am J Pathol 1983 Apr;111(1):125-7.
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