Abstract
Monocytes are key cells of the immune system; various cell subsets have distinct phenotypic characteristics and functions. We characterized canine monocyte subsets in different hematologic disorders by analyzing peripheral blood cells for their expression of CD14 and major histocompatibility complex class II (MHCII). Flow cytometry data of canine blood samples were evaluated retrospectively. We assigned 132 total cases to one of the following categories: healthy, inflammatory, T-zone lymphoma/leukemia (TZL), T-cell chronic lymphocytic leukemia (CLL), B-cell CLL, T-cell stage V lymphoma (SVL), B-cell SVL, acute lymphoblastic or undifferentiated leukemia (ALL/AUL), or acute myeloid leukemia (AML). We analyzed age, sex, breed, light scatter properties, WBC count, CD14pos cells, CD14posMHCIIpos cells, CD14posMHCIIneg cells, and the CD14posMHCIIpos/CD14posMHCIIneg ratio. All groups were compared with the healthy group. In healthy dogs, CD14posMHCIIpos cells were larger and had a more complex internal structure than CD14posMHCIIneg cells. Absolute numbers of CD14posMHCIIneg cells were significantly increased in all groups except the TZL and B-cell SVL groups. Absolute numbers of CD14posMHCIIpos cells were significantly increased in the T-cell CLL, B-cell CLL, and T-cell SVL groups, mildly increased in the inflammatory and TZL groups, and decreased in the ALL/AUL group. The CD14posMHCIIpos/CD14posMHCIIneg ratio was markedly decreased in both acute leukemia groups, being <1 in all cases and usually close to 0. We found significant changes in canine monocyte subsets in different hematologic conditions. To our knowledge, a decreased CD14posMHCIIpos/CD14posMHCIIneg ratio has not been identified previously as a hallmark of acute leukemia in dogs.
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
