Agammaglobulinemia in a horse with evidence of functional T lymphocytes.
Abstract: Agammaglobulinemia was diagnosed in a 1-year-old Thoroughbred horse on the basis of the following observations: (1) absence of serum immunoglobulins M, A, and G(T); (2) small amounts of serum immunoglobulin G (16 mg/100 ml); (3) absence of specific antibody in the serum of the horse following immunization and challenge exposure to 2 antigens; (4) absence of plasma cells, primary follicles, and germinal centers in a lymph node removed after antigenic stimulation; (5) absence of "natural" serum antibodies to rabbit-erythrocytes which were easily detectable in age-matched control horse serums; and (6) increased susceptibility to infections. There was evidence of functional cell-mediated immunity which included a skin response to injected phytolectins, skin response to antigen challenge following sensitization, and in vitro proliferative response of lymph node cells to phytohemagglutinin. An intact cell-mediated immune response was also supported by the observation that the horse lived to 17 months of age without antibody production, whereas horses with an absence of both antibody production and cell-mediated immunity (combined immunodeficiency) die by 4 months of age without immunologic intervention. The known features of agammaglobulinemia in this horse are similar to those in sex-linked agammaglobulinemia in persons and are unique among the immunodeficiences described in other animals.
Publication Date: 1976-01-01 PubMed ID: 1082280
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- Journal Article
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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The study focuses on diagnosing agammaglobulinemia, a rare immune disorder, in a one-year-old Thoroughbred horse based on a series of clinical observations and tests. The study suggests that the immune disorder observed in the horse is similar to the condition in humans and unlike other immuno-deficiencies found in animals.
Diagnosis of Agammaglobulinemia
- The diagnosis of agammaglobulinemia in the horse was based on several observations. These included a lack of serum immunoglobulins M, A, and G(T), as well as scant quantities of serum immunoglobulin G measured at 16 mg/100 ml. Serum immunoglobulins are antibodies that play a crucial role in the body’s immune response.
- Further, the horse’s serum did not show the presence of specific antibodies following immunization and exposure to two antigens. The absence of specific antibodies implies that the immune system did not respond effectively to the administered vaccines.
- The horse also showed no plasma cells, primary follicles, or germinal centers in a lymph node that was removed after antigenic stimulation. These elements are significant for an immune response, their absence indicative of a compromised immune system.
- The horse lacked naturally occurring serum antibodies to rabbit erythrocytes. Age-matched control horses showed easily detectable levels of these antibodies. The absence of these antibodies signals a deficient immune response.
- Lastly, the horse was found to be more susceptible to infections – a common characteristic of agammaglobulinemia due to the compromised immune functionality.
Evidence of Functional Cell-Mediated Immunity
- Despite the agammaglobulinemia diagnosis, the horse showed signs of functional cell-mediated immunity. This included skin responses to injected phytolectins, skin response to antigen challenge after sensitization, and an in vitro proliferative response of lymph node cells to phytohemagglutinin.
- The horse’s cell-mediated immunity was intact, as indicated by its survival to 17 months of age without antibody production. As a comparison, horses lacking both antibody production and cell-mediated immunity typically die by 4 months of age without immunologic intervention.
Comparison with Human Agammaglobulinemia
- The researchers concluded that the documented features of agammaglobulinemia in this horse are similar to those in sex-linked agammaglobulinemia in humans. This is a significant finding as it links the immune disorder in this particular horse to a similar condition in humans.
- The study also underscores how the horse’s version of the disorder is unique among immuno-deficiencies in animals, thus marking it as a potential area of further study on animal immune disorders.
Cite This Article
APA
McGuire TC, Banks KL, Evans DR, Poppie MJ.
(1976).
Agammaglobulinemia in a horse with evidence of functional T lymphocytes.
Am J Vet Res, 37(1), 41-46.
Publication
Researcher Affiliations
MeSH Terms
- Agammaglobulinemia / immunology
- Agammaglobulinemia / pathology
- Agammaglobulinemia / veterinary
- Animals
- Antibody Formation
- Arthritis / veterinary
- Colostrum / immunology
- Complement C3 / analysis
- Horse Diseases / immunology
- Horse Diseases / pathology
- Horses
- Immunoglobulin A / analysis
- Immunoglobulin G / analysis
- Immunoglobulin M / analysis
- Lymph Nodes / pathology
- Lymphocyte Activation
- Male
- Skin Tests
- Spleen / pathology
- T-Lymphocytes / immunology
Citations
This article has been cited 2 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.
- McGuire TC, Banks KL, Davis WC. Alterations of the thymus and other lymphoid tissue in young horses with combined immunodeficiency.. Am J Pathol 1976 Jul;84(1):39-54.
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