Ki‐67/CD3 ratio in the diagnosis of chronic inflammatory enteropathy in dogs
Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE. Objective T...
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Published in | Journal of veterinary internal medicine Vol. 34; no. 1; pp. 92 - 97 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Hoboken, USA
John Wiley & Sons, Inc
01.01.2020
Wiley |
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Abstract | Background
T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE.
Objective
To investigate Ki‐67 in relation to T cells as a marker for CIE in dogs.
Animals
Eleven dogs with CIE and 6 healthy beagle controls (CO).
Methods
Retrospective case‐control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double‐labeled immunofluorescence was used to investigate colocalization of Ki‐67 and CD3 in epithelium and lamina propria (LP) of villi and crypts.
Results
Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3‐7) compared to CO (all 0; P < .001). The Ki‐67/CD3 double‐positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm2; IQR, 0‐0.54) versus CO (0.08 cells/mm2; IQR, 0‐0.26; P = .044). A significant correlation was found between CCECAI and the Ki‐67/CD3 ratio in the LP of the crypt region (r = 0.670; P = .012) in dogs with CIE.
Conclusions and Clinical Importance
The Ki‐67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki‐67/CD3 could be a useful tool for detection of CIE. |
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AbstractList | T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki-67 is an indicator for cell growth but there are only a few studies in dogs with CIE.
To investigate Ki-67 in relation to T cells as a marker for CIE in dogs.
Eleven dogs with CIE and 6 healthy beagle controls (CO).
Retrospective case-control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double-labeled immunofluorescence was used to investigate colocalization of Ki-67 and CD3 in epithelium and lamina propria (LP) of villi and crypts.
Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3-7) compared to CO (all 0; P < .001). The Ki-67/CD3 double-positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm
; IQR, 0-0.54) versus CO (0.08 cells/mm
; IQR, 0-0.26; P = .044). A significant correlation was found between CCECAI and the Ki-67/CD3 ratio in the LP of the crypt region (r = 0.670; P = .012) in dogs with CIE.
The Ki-67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki-67/CD3 could be a useful tool for detection of CIE. BackgroundT cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE.ObjectiveTo investigate Ki‐67 in relation to T cells as a marker for CIE in dogs.AnimalsEleven dogs with CIE and 6 healthy beagle controls (CO).MethodsRetrospective case‐control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double‐labeled immunofluorescence was used to investigate colocalization of Ki‐67 and CD3 in epithelium and lamina propria (LP) of villi and crypts.ResultsDogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3‐7) compared to CO (all 0; P < .001). The Ki‐67/CD3 double‐positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm2; IQR, 0‐0.54) versus CO (0.08 cells/mm2; IQR, 0‐0.26; P = .044). A significant correlation was found between CCECAI and the Ki‐67/CD3 ratio in the LP of the crypt region (r = 0.670; P = .012) in dogs with CIE.Conclusions and Clinical ImportanceThe Ki‐67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki‐67/CD3 could be a useful tool for detection of CIE. Abstract Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE. Objective To investigate Ki‐67 in relation to T cells as a marker for CIE in dogs. Animals Eleven dogs with CIE and 6 healthy beagle controls (CO). Methods Retrospective case‐control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double‐labeled immunofluorescence was used to investigate colocalization of Ki‐67 and CD3 in epithelium and lamina propria (LP) of villi and crypts. Results Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3‐7) compared to CO (all 0; P < .001). The Ki‐67/CD3 double‐positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm 2 ; IQR, 0‐0.54) versus CO (0.08 cells/mm 2 ; IQR, 0‐0.26; P = .044). A significant correlation was found between CCECAI and the Ki‐67/CD3 ratio in the LP of the crypt region ( r = 0.670; P = .012) in dogs with CIE. Conclusions and Clinical Importance The Ki‐67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki‐67/CD3 could be a useful tool for detection of CIE. Abstract Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE. Objective To investigate Ki‐67 in relation to T cells as a marker for CIE in dogs. Animals Eleven dogs with CIE and 6 healthy beagle controls (CO). Methods Retrospective case‐control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double‐labeled immunofluorescence was used to investigate colocalization of Ki‐67 and CD3 in epithelium and lamina propria (LP) of villi and crypts. Results Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3‐7) compared to CO (all 0; P < .001). The Ki‐67/CD3 double‐positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm2; IQR, 0‐0.54) versus CO (0.08 cells/mm2; IQR, 0‐0.26; P = .044). A significant correlation was found between CCECAI and the Ki‐67/CD3 ratio in the LP of the crypt region (r = 0.670; P = .012) in dogs with CIE. Conclusions and Clinical Importance The Ki‐67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki‐67/CD3 could be a useful tool for detection of CIE. Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki‐67 is an indicator for cell growth but there are only a few studies in dogs with CIE. Objective To investigate Ki‐67 in relation to T cells as a marker for CIE in dogs. Animals Eleven dogs with CIE and 6 healthy beagle controls (CO). Methods Retrospective case‐control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double‐labeled immunofluorescence was used to investigate colocalization of Ki‐67 and CD3 in epithelium and lamina propria (LP) of villi and crypts. Results Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3‐7) compared to CO (all 0; P < .001). The Ki‐67/CD3 double‐positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm2; IQR, 0‐0.54) versus CO (0.08 cells/mm2; IQR, 0‐0.26; P = .044). A significant correlation was found between CCECAI and the Ki‐67/CD3 ratio in the LP of the crypt region (r = 0.670; P = .012) in dogs with CIE. Conclusions and Clinical Importance The Ki‐67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki‐67/CD3 could be a useful tool for detection of CIE. |
Author | Tichy, Alexander Luckschander‐Zeller, Nicole Karlovits, Sonja Burgener, Iwan A. Walter, Ingrid Kummer, Stefan Allenspach, Karin Richter, Barbara Manz, Anita |
AuthorAffiliation | 2 Department of Veterinary Clinical Sciences, College of Veterinary Medicine Iowa State University Ames Iowa 4 Department of Biomedical Sciences University of Veterinary Medicine Vienna Austria 3 VetCore Facility for Research University of Veterinary Medicine Vienna Austria 1 Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine University of Veterinary Medicine Vienna Austria 5 Department for Pathobiology, Institute of Pathology University of Veterinary Medicine Vienna Austria |
AuthorAffiliation_xml | – name: 5 Department for Pathobiology, Institute of Pathology University of Veterinary Medicine Vienna Austria – name: 1 Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine University of Veterinary Medicine Vienna Austria – name: 2 Department of Veterinary Clinical Sciences, College of Veterinary Medicine Iowa State University Ames Iowa – name: 4 Department of Biomedical Sciences University of Veterinary Medicine Vienna Austria – name: 3 VetCore Facility for Research University of Veterinary Medicine Vienna Austria |
Author_xml | – sequence: 1 givenname: Sonja orcidid: 0000-0002-8420-2042 surname: Karlovits fullname: Karlovits, Sonja email: sonja.karlovits@chello.at organization: University of Veterinary Medicine – sequence: 2 givenname: Anita surname: Manz fullname: Manz, Anita organization: University of Veterinary Medicine – sequence: 3 givenname: Karin surname: Allenspach fullname: Allenspach, Karin organization: Iowa State University – sequence: 4 givenname: Ingrid surname: Walter fullname: Walter, Ingrid organization: University of Veterinary Medicine – sequence: 5 givenname: Stefan surname: Kummer fullname: Kummer, Stefan organization: University of Veterinary Medicine – sequence: 6 givenname: Alexander surname: Tichy fullname: Tichy, Alexander organization: University of Veterinary Medicine – sequence: 7 givenname: Barbara surname: Richter fullname: Richter, Barbara organization: University of Veterinary Medicine – sequence: 8 givenname: Iwan A. orcidid: 0000-0002-8516-0040 surname: Burgener fullname: Burgener, Iwan A. organization: University of Veterinary Medicine – sequence: 9 givenname: Nicole surname: Luckschander‐Zeller fullname: Luckschander‐Zeller, Nicole organization: University of Veterinary Medicine |
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CitedBy_id | crossref_primary_10_1016_j_vetimm_2024_110740 crossref_primary_10_1111_jvim_16436 crossref_primary_10_1093_ibd_izab064 crossref_primary_10_3390_ani12101263 |
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T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as... T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker... Abstract Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen... BackgroundT cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a... BACKGROUNDT cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a... Abstract Background T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen... |
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SubjectTerms | Animals Antibiotics Antigens Biopsy canine Case-Control Studies CD3 antigen CD3 Complex - blood Cell cycle Cytokines diagnostic marker Diarrhea Dog Diseases - blood Dogs Endoscopy Epithelium Feces Hypotheses Immunofluorescence Inflammation Inflammatory bowel disease Inflammatory Bowel Diseases - blood Inflammatory Bowel Diseases - diagnosis Inflammatory Bowel Diseases - veterinary Interactive learning intestinal inflammation Ki-67 Antigen - blood Lamina propria Lymphocytes Lymphocytes T Male Microscopy Mucosa Pathogenesis Proteins Retrospective Studies SMALL ANIMAL T cells Variables Veterinary medicine Vomiting |
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Title | Ki‐67/CD3 ratio in the diagnosis of chronic inflammatory enteropathy in dogs |
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