Peer-reviewed veterinary case report
Clonal T and B cell receptor changes in dogs with acute myeloid
By Stokol, Tracy et al.·Published in Frontiers in veterinary science·2017·Department of Population Medicine and Diagnostic Sciences, United States·View original on PubMed →
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Original publication title: Dogs with Acute Myeloid Leukemia Have Clonal Rearrangements in T and B Cell Receptors.
- Species:
- dog
Plain-English summary
A group of dogs diagnosed with acute myeloid leukemia (AML) showed signs like swollen lymph nodes and enlarged organs. Most of these dogs were around 8 years old and had low blood cell counts, with many having immature blood cells called blasts. Testing revealed that a significant number of these dogs had rearrangements in their immune cell receptors, which can complicate the diagnosis. This study suggests that these receptor changes are common in dogs with AML, indicating that further testing may be needed to differentiate between types of leukemia.
People also search for: dog leukemia symptoms · swollen lymph nodes in dogs · dog blood test results · acute myeloid leukemia in dogs
Abstract
Clonality testing for rearrangements in the complementarity-determining region 3 of the immunoglobulin heavy chain of B lymphocytes (B cell receptor) and the T cell receptor of T lymphocytes helps distinguish between clonal and non-clonal expansions of lymphocytes. There are rare reports of clonally rearranged T and B cell receptors in dogs with acute myeloid leukemia (AML). Our objective was to determine the frequency of clonally rearranged T and B cell receptors in dogs with AML. Archived slides from historical cases of AML (from January 2010 to June 2013) and slides or liquid specimens [blood, bone marrow (BM), body cavity fluid, or tissue aspirates] from cases of AML diagnosed between June 2013 and February 2017 were used in the study. A diagnosis of AML was made on the basis of more than 20% immature neoplastic cells ("blasts") in blood, BM, or extramedullary tissues, displaying features of myeloid differentiation. Myeloid differentiation was based on a combination of morphologic criteria, positive flow cytometric labeling for surface antigens typical of myeloid origin (e.g., CD11b, CD11c, CD14 with a general lack of expression of T or B cell markers), or positive cytochemical staining reactions for myeloid-associated enzymes (e.g., alkaline phosphatase, chloroacetate esterase). There were 63 cases of AML diagnosed during this period; however, slides or liquid specimens with sufficient DNA for testing were only obtained from 25 dogs. Affected dogs represented various breeds and were a median of 8 years old, with more male (64%) than female (36%) dogs. Common clinical signs were peripheral or internal lymphadenopathy (10/25 dogs, 40%) and hepatomegaly or splenomegaly (10/25 dogs combined, 40%). Typical hematologic findings were bi- or pancytopenia (23/25 dogs, 92%), with circulating blasts (21/25, 84%). Solitary clonal (4 B cell, 6 T cell) and biclonal (6 B and T cell) rearrangements in B or T cell receptors were found in 16 dogs (64%). Our results indicate that dogs with AML can have a high frequency of clonally rearranged T or B cell receptors, including biclonality, and clonality testing should not be used as a tool to distinguish between acute leukemia of myeloid or lymphoid origin.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28620611/