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| *Primary immunodeficiencies may affect either the [[Innate Immune System - WikiBlood|innate immune system]] or the [[Adaptive Immune System - WikiBlood|adaptive immune system]] | | *Primary immunodeficiencies may affect either the [[Innate Immune System - WikiBlood|innate immune system]] or the [[Adaptive Immune System - WikiBlood|adaptive immune system]] |
| *They are categorised by either the type or the developmental stage of the cells involved | | *They are categorised by either the type or the developmental stage of the cells involved |
− | *Lymphoid cell disorders affect [[Lymphocytes - WikiBlood#T cells|T cells]] or [[Lymphocytes - WikiBlood#B cells|B cells]] (or both) | + | *Lymphoid cell disorders affect [[Lymphocytes#T cells|T cells]] or [[Lymphocytes#B cells|B cells]] (or both) |
| *Myeloid cell disorders affect phagocytic function | | *Myeloid cell disorders affect phagocytic function |
| *The severity of the immunodeficiency depends on at which stage in development the problem occurs | | *The severity of the immunodeficiency depends on at which stage in development the problem occurs |
| **E.g. Defects early on in development will affect the entire immune system | | **E.g. Defects early on in development will affect the entire immune system |
− | *[[Lymphocytes - WikiBlood#T cells|T cell]] deficiencies can affect both the cell-mediated and humoral response as [[Lymphocytes - WikiBlood#T cells|T cells]] play a central role in the immune system | + | *[[Lymphocytes#T cells|T cell]] deficiencies can affect both the cell-mediated and humoral response as [[Lymphocytes#T cells|T cells]] play a central role in the immune system |
| | | |
| ===Deficiencies of Innate Immunity=== | | ===Deficiencies of Innate Immunity=== |
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| *Occurs in 2-3% of Arabian foals | | *Occurs in 2-3% of Arabian foals |
| *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 - WikiBlood|lymphocytes]] (e.g. Ig and TCR) | + | **Gene codes for a DNA repair enzyme involved in V(D)J recombination for antigen receptors of [[Lymphocytes|lymphocytes]] (e.g. Ig and TCR) |
− | *No functional [[Lymphocytes - WikiBlood#B cells|B cells]] or [[Lymphocytes - WikiBlood#T cells|T cells]] | + | *No functional [[Lymphocytes#B cells|B cells]] or [[Lymphocytes#T cells|T cells]] |
| *Foals develop infections (usually around 8 weeks of age as maternal [[Immunoglobulins - WikiBlood|antibody]] in [[Materno-fetal immunity - WikiBlood#Passive transfer via colostrum|colostrum]] wanes around this time) | | *Foals develop infections (usually around 8 weeks of age as maternal [[Immunoglobulins - WikiBlood|antibody]] in [[Materno-fetal immunity - WikiBlood#Passive transfer via colostrum|colostrum]] wanes around this time) |
| *Foals usually die from bronchopneumonia | | *Foals usually die from bronchopneumonia |
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| *Affects Basset Hounds and Corgis | | *Affects Basset Hounds and Corgis |
| *X-linked recessive defect in the gene coding for the IL-2 receptor | | *X-linked recessive defect in the gene coding for the IL-2 receptor |
− | **IL-2 receptor is a receptor for the cytokine IL-2 which causes [[Lymphocytes - WikiBlood#T cells|T cells]] to proliferate | + | **IL-2 receptor is a receptor for the cytokine IL-2 which causes [[Lymphocytes#T cells|T cells]] to proliferate |
| *Causes lymphoid hypoplasia, stunted growth and increases the animal's susceptibility to infection | | *Causes lymphoid hypoplasia, stunted growth and increases the animal's susceptibility to infection |
| *Animal usually dies from pneumonia or sepsis as the level of maternal [[Immunoglobulins - WikiBlood|antibody]] decreases | | *Animal usually dies from pneumonia or sepsis as the level of maternal [[Immunoglobulins - WikiBlood|antibody]] decreases |
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| [[Image:Nude Mouse.jpg|right|thumb|150px|Nude Mouse - Copyright Michigan State University- Carcinogenesis Laboratory]] | | [[Image:Nude Mouse.jpg|right|thumb|150px|Nude Mouse - Copyright Michigan State University- Carcinogenesis Laboratory]] |
| *Severe Combined Immune Deficiency(SCID) | | *Severe Combined Immune Deficiency(SCID) |
− | **No functional [[Lymphocytes - WikiBlood#B cells|B cells]] or [[Lymphocytes - WikiBlood#T cells|T cells]] | + | **No functional [[Lymphocytes#B cells|B cells]] or [[Lymphocytes#T cells|T cells]] |
| | | |
| *Athymic nude mice (no [[Thymus - Anatomy & Physiology|thymus]]) | | *Athymic nude mice (no [[Thymus - Anatomy & Physiology|thymus]]) |
− | **No functional [[Lymphocytes - WikiBlood#T cells|T cells]] | + | **No functional [[Lymphocytes#T cells|T cells]] |
| **Cell-mediated immunodeficiency | | **Cell-mediated immunodeficiency |
| | | |
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| [[Image:Kinetics of FeLV 2.jpg|thumb|right|150px|Kinetics of FeLV - Copyright Dr Brian Catchpole BVetMed PhD MRCVS]] | | [[Image:Kinetics of FeLV 2.jpg|thumb|right|150px|Kinetics of FeLV - Copyright Dr Brian Catchpole BVetMed PhD MRCVS]] |
| *Oncogenic retrovirus | | *Oncogenic retrovirus |
− | *Causes neoplasia (lymphoma), myelosuppression (anaemia) and immunosuppression (of [[Lymphocytes - WikiBlood#T cells|T cells]]) | + | *Causes neoplasia (lymphoma), myelosuppression (anaemia) and immunosuppression (of [[Lymphocytes#T cells|T cells]]) |
| *2 strains: | | *2 strains: |
| **FeLV-A | | **FeLV-A |
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| *Subtypes A, B and D | | *Subtypes A, B and D |
| *Causes increased susceptibility to infections and neoplasia | | *Causes increased susceptibility to infections and neoplasia |
− | *Specifically destroys [[Lymphocytes - WikiBlood#Helper CD4+|CD4+ T cells]] | + | *Specifically destroys [[Lymphocytes#Helper CD4+|CD4+ T cells]] |
| *Virus is present in saliva, blood and other bodily fluids | | *Virus is present in saliva, blood and other bodily fluids |
| *Feral and outdoor cats (mostly tom cats) are most at risk | | *Feral and outdoor cats (mostly tom cats) are most at risk |