Dynamic changes in clinicopathological variables and gene expression in dogs with immune-mediated hemolytic anemia

BACKGROUND: Immune-mediated hemolytic anemia (IMHA) is a common autoimmune disease of dogs that is difficult to treat effectively. Little is known about how clinicopathological and immune variables change with time in dogs with IMHA, and whether these changes could guide therapeutic interventions. AIMS: To investigate dynamic changes in clinicopathological variables as well as immune and glucocorticoid-regulated gene expression in dogs with IMHA, and to determine whether these changes are associated with recovery from anemia and severity of treatment-related adverse effects. ANIMALS: 29 client-owned dogs with non-associative IMHA. METHODS: Dogs with IMHA underwent clinical monitoring, with collection of residual blood samples at serial time points. Expression of immune and glucocorticoid-regulated genes was quantified using real time quantitative polymerase chain reactions, with serum cytokine concentrations measured using multiplex arrays. RESULTS: Several clinical and gene expression variables changed with time in dogs with IMHA undergoing treatment, and we identified 6 major clusters representing different patterns of temporal change. No candidate dynamic variables were associated with more rapid recovery from anemia, but early increases in serum alkaline phosphatase (ALP) activity were associated with severity of later polydipsia. CONCLUSIONS: Immune and clinicopathological variables are highly changeable after onset of treatment in dogs with IMHA, with early increases in serum ALP activity being associated with later severity of polydipsia. This parameter is therefore a key candidate for further investigations of individualization of immunosuppressive therapy for dogs with IMHA.

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Publication Details

Journal
PLoS ONE
Published
2026-10-28
DOI
https://doi.org/10.1371/journal.pone.0359710
Primary Topic
Veterinary Medicine and Surgery
Type
article
Field-Weighted Citation Impact
0.00

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article

Dynamic changes in clinicopathological variables and gene expression in dogs with immune-mediated hemolytic anemia

Barbara Glanemann, Briän Catchpole, Gina Parkes, Sivert Nerhagen et al.
PLoS ONE
Veterinary Medicine and Surgery
article

Dynamic changes in clinicopathological variables and gene expression in dogs with immune-mediated hemolytic anemia

Barbara Glanemann, Briän Catchpole, Gina Parkes, Sivert Nerhagen, James W. Swann, Balázs Szladovits, Yu-Mei Chang, Anna Riddle, Samantha Mason
article en

Abstract

BACKGROUND: Immune-mediated hemolytic anemia (IMHA) is a common autoimmune disease of dogs that is difficult to treat effectively. Little is known about how clinicopathological and immune variables change with time in dogs with IMHA, and whether these changes could guide therapeutic interventions. AIMS: To investigate dynamic changes in clinicopathological variables as well as immune and glucocorticoid-regulated gene expression in dogs with IMHA, and to determine whether these changes are associated with recovery from anemia and severity of treatment-related adverse effects. ANIMALS: 29 client-owned dogs with non-associative IMHA. METHODS: Dogs with IMHA underwent clinical monitoring, with collection of residual blood samples at serial time points. Expression of immune and glucocorticoid-regulated genes was quantified using real time quantitative polymerase chain reactions, with serum cytokine concentrations measured using multiplex arrays. RESULTS: Several clinical and gene expression variables changed with time in dogs with IMHA undergoing treatment, and we identified 6 major clusters representing different patterns of temporal change. No candidate dynamic variables were associated with more rapid recovery from anemia, but early increases in serum alkaline phosphatase (ALP) activity were associated with severity of later polydipsia. CONCLUSIONS: Immune and clinicopathological variables are highly changeable after onset of treatment in dogs with IMHA, with early increases in serum ALP activity being associated with later severity of polydipsia. This parameter is therefore a key candidate for further investigations of individualization of immunosuppressive therapy for dogs with IMHA.

PLoS ONEVol. 21(10)
Royal Veterinary College (GB), Columbia University (US)
University of Oxford, Royal Veterinary College, Kennel Club Charitable Trust
Good health and well-being
Openalex Percentile: Top 10%
Veterinary Medicine and Surgery
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