Difference between revisions of "Equine Severe Combined Immune Deficiency"
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(Equine SCID) | (Equine SCID) | ||
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| + | ==Description== | ||
| + | Severe combined immunodeficiency disease (SCID) of horses is an autosomal, recessive hereditary disease occurring in 2-3% of Arab or cross-bred Arab foals. It is characterised by a complete absence of functional B and T lymphocytes and affected (homozygous) foals fail to produce antigen-specific immune responses. | ||
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| + | ==Signalment== | ||
| + | Only Arab or cross-bred Arabs are affected. | ||
*Defect in DNA-dependent protein kinase gene | *Defect in DNA-dependent protein kinase gene | ||
**Gene codes for a DNA repair enzyme involved in V(D)J recombination for antigen receptors of [[Lymphocytes - Introduction|lymphocytes]] (e.g. Ig and TCR) | **Gene codes for a DNA repair enzyme involved in V(D)J recombination for antigen receptors of [[Lymphocytes - Introduction|lymphocytes]] (e.g. Ig and TCR) | ||
Revision as of 22:15, 23 August 2010
(Equine SCID)
| This article is still under construction. |
Description
Severe combined immunodeficiency disease (SCID) of horses is an autosomal, recessive hereditary disease occurring in 2-3% of Arab or cross-bred Arab foals. It is characterised by a complete absence of functional B and T lymphocytes and affected (homozygous) foals fail to produce antigen-specific immune responses.
Signalment
Only Arab or cross-bred Arabs are affected.
- Defect in DNA-dependent protein kinase gene
- Gene codes for a DNA repair enzyme involved in V(D)J recombination for antigen receptors of lymphocytes (e.g. Ig and TCR)
- No functional B cells or T cells
- Foals develop infections (usually around 8 weeks of age as maternal antibody in colostrum wanes around this time)
- Foals usually die from bronchopneumonia