[PDF] Association of hypothyroid disease in Doberman Pinscher dogs with a rare major histocompatibility complex DLA class II haplotype. | Semantic Scholar (2024)

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@article{Kennedy2006AssociationOH, title={Association of hypothyroid disease in Doberman Pinscher dogs with a rare major histocompatibility complex DLA class II haplotype.}, author={Lorna J. Kennedy and Heather J. Huson and Jacob Leonard and John M Angles and Leslie E. Fox and Jerzy Wojciechowski and Christine Yuncker and George M. Happ}, journal={Tissue antigens}, year={2006}, volume={67 1}, pages={ 53-6 }, url={https://api.semanticscholar.org/CorpusID:15180138}}
  • Lorna J. Kennedy, Heather J. Huson, G. Happ
  • Published in Tissue Antigens 2006
  • Biology, Medicine

Three dog-leucocyte antigen (DLA) genes, DLA-DRB1, DQA1 and DQB1, were characterized by sequence-based typing and assigned to haplotypes for each dog and one rare haplotype was found at an increased frequency in the affected dogs compared to the unaffected dogs.

61 Citations

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61 Citations

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A further series of 173 hypothyroid dogs in a range of breeds where a significant association with DLA-DQA1*00101 is shown are reported.

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The disease shows a complex pattern of inheritance, but the observed DLA class II association with DH suggests a role for the immune system in the development of the disease.

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A limited MHC diversity in North American NSDTRs is indicated and it is suggested that the MHC may play a role in the development of hypoadrenocorticism in the N SDTR, supporting the autoimmune origin of the disease.

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Routine screening of Alaskan husky dogs, as part of the state outreach science programme, identified a new DLA-DQA1 allele, DQA 1*01801, in one animal, and data suggest that husky alleles share as much similarity to wolf alleles as to dog alleles.

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    M. Wilbe

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Results show that Giant Schnauzers carrying the haplotype DRB1*01201DQA1*00101DQB1*0020 have an increased risk to develop CLT, with an odds ratio of 6.0667 and with a p value of 0.015401 which shows that the increased risk of developing CLT is statistically significant.

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DLA class II risk haplotypes for autoimmune diseases in the bearded collie offer insight to autoimmunity signatures across dog breeds
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This study assessed the relationship between particular MHC (dog leukocyte antigen, DLA) class II haplotypes and the two autoimmune diseases most common in bearded collies and suggested this two-locus (DQ) model serves as a good indicator for susceptibility to multiple organ-specific autoimmune diseases in the canine population.

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Increased genetic risk or protection for canine autoimmune lymphocytic thyroiditis in Giant Schnauzers depends on DLA class II genotype.
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Evidence is obtained that dog leukocyte antigen (DLA) class II genotype function as either genetic risk factor that predisposes for CLT or as protective factor against the disease.

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Given the reported role of NF-κB in many human autoimmune diseases, the results suggest CLT as an excellent genetic model for human thyroiditis.

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Association of canine juvenile generalized demodicosis with the dog leukocyte antigen system.

It is suggested that an underlying DLA association exists with demodicosis in dogs and that this may represent an important immunological risk factor in the aetiology of this condition.

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Analysis of DLA-DQB1 and polymorphisms in CTLA4 in co*cker spaniels affected with immune-mediated haemolytic anaemia
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DLA-DQB1 allele and CTLA4 promoter haplotype were not found to be significantly associated with IMHA in co*cker spaniels, with other genetic and environmental factors involved in disease expression and progression.

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    [PDF] Association of hypothyroid disease in Doberman Pinscher dogs with a rare major histocompatibility complex DLA class II haplotype. | Semantic Scholar (2024)
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