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Identification of Neutrophil Extracellular Traps in Paraffin-Embedded Feline Arterial Thrombi using Immunofluorescence Microscopy
Published on: March 29, 2020
Flow cytometric detection of alpha-1-acid glycoprotein on feline circulating leucocytes
S Paltrinieri1, I Marchini, M E Gelain
1Department of Veterinary Pathology, Hygiene and Public Health, Unit of Veterinary General Pathology and Parasitology, University of Milan, Italy. saverio.paltrinieri@unimi.it
Insights
Alpha-1-acid glycoprotein (AGP) can be detected on feline white blood cells, particularly during inflammation. This study found no link between AGP-positive leucocytes and feline infectious peritonitis (FIP).
Area of Science:
- Veterinary Immunology
- Clinical Pathology
Background:
- Alpha-1-acid glycoprotein (AGP) is an acute-phase protein with a known role in inflammation.
- The presence and significance of AGP on feline leucocytes, particularly in relation to specific diseases, remain largely unexplored.
Purpose of the Study:
- To determine if alpha-1-acid glycoprotein (AGP) is detectable on the surface of circulating leucocytes in cats.
- To investigate the association between AGP-positive leucocytes and various feline diseases, including feline coronavirus (FCoV) infection and feline infectious peritonitis (FIP).
Main Methods:
- Flow cytometry was employed to detect AGP on feline leucocytes using an anti-feline AGP antibody.
- Serum protein electrophoresis, routine haematology, and serum AGP concentration measurements were conducted.
- Statistical analysis (Chi-square test) was used to compare the proportion of cats with AGP-positive leucocytes across different groups.
Main Results:
- AGP-positive leucocytes were identified in 23% of the cats studied.
- A higher proportion of AGP-positive granulocytes and monocytes was observed in sick cats, especially those with non-FIP diseases, and in cats with elevated serum AGP concentrations.
- No significant association was found between AGP-positive leucocytes and feline coronavirus (FCoV) seropositivity or leucocytosis.
Conclusions:
- The study confirms the presence of AGP on feline leucocytes, particularly in inflammatory conditions.
- No correlation was established between AGP-positive leucocytes and feline infectious peritonitis (FIP).
- Further research is warranted to understand the underlying mechanisms and potential diagnostic utility of AGP-positive leucocytes in feline inflammatory diseases.
Objective:
To assess whether alpha-1-acid glycoprotein (AGP) can be detected on the membrane of feline circulating leucocytes.
Design:
The presence of AGP on circulating leucocytes was investigated in both clinically healthy cats and cats with different diseases. A group of feline coronavirus (FCoV)-positive cats, comprising cats with feline infectious peritonitis (FIP) and cats not affected by FIP but seropositive for FCoV, were included in this study because the serum concentration of AGP increases during FCoV infection.
Procedure:
Flow cytometry (using an anti-feline AGP antibody), serum protein electrophoresis, routine haematology and measurement of the serum AGP concentration were performed using blood samples from 32 healthy cats (19 FCoV-seropositive), 13 cats with FIP and 12 with other diseases (6 FCoV-seropositive). The proportion of cats with AGP-positive leucocytes in the different groups (e.g. controls vs sick; FIP vs other diseases, etc.) or in cats with different intensities of inflammatory response was compared using a Chi-square test.
Results:
AGP-positive leucocytes were found in 23% of cats. Compared with controls, the proportion of patients with positive granulocytes and monocytes was higher among sick cats (especially cats with diseases other than FIP) and cats with high serum AGP concentration, but not in cats with leucocytosis or that were FCoV-seropositive.
Conclusion:
AGP-positive leucocytes can be found in feline blood, especially during inflammation. Conversely, no association between AGP-positive leucocytes and FIP was found. Further studies are needed to elucidate the mechanism responsible for this finding and its diagnostic role in cats with inflammation.

