Prophylactic fenbendazole therapy does not affect the incidence and onset of type 1 diabetes in non-obese diabetic mice
Fenbendazole (FBZ) is a common, highly efficacious broad-spectrum anthelmintic drug used to treat and limit rodent pinworm infections. However, the effect of its prophylactic use on the immune response of rodents is largely undefined. The non-obese diabetic (NOD) mouse is a model commonly used to st...
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Veröffentlicht in: | International immunology 2006-03, Vol.18 (3), p.453-458 |
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description | Fenbendazole (FBZ) is a common, highly efficacious broad-spectrum anthelmintic drug used to treat and limit rodent pinworm infections. However, the effect of its prophylactic use on the immune response of rodents is largely undefined. The non-obese diabetic (NOD) mouse is a model commonly used to study type 1 diabetes (T1D). Parasitic infections will inhibit diabetes development in NOD mice; thus, in the presence of contamination, prophylactic treatment with anthelmintics must be considered to maintain experimental research. Herein, we investigated the prophylactic use of FBZ in NOD mice to determine its effect on the incidence and onset of diabetes, lymphocyte sub-populations and T cell proliferative responses. NOD mice were separated into control and treatment groups. The treatment group received a diet containing FBZ. Animals were monitored for the incidence and onset of T1D. At matched time points, diabetic and non-diabetic mice were killed and splenic lymphocytes analyzed for various cell sub-populations and mitogen-induced proliferative responses using flow cytometry. Treated and control mice were monitored >23 weeks with no detectable effects on the incidence or onset of diabetes. Moreover, no significant differences were detected in lymphocyte sub-populations and mitogen-induced CD4+ and CD8+ proliferative responses between control and treatment groups. These results suggest that prophylactic FBZ treatment does not significantly alter the incidence or onset of diabetes in NOD mice. The prophylactic use of FBZ, therefore, presents a viable approach for the prevention of pinworm infection in precious experimental animals with substantial scientific and economic benefits. |
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H. ; Shirwan, Haval</creator><creatorcontrib>Franke, Deanna D. H. ; Shirwan, Haval</creatorcontrib><description>Fenbendazole (FBZ) is a common, highly efficacious broad-spectrum anthelmintic drug used to treat and limit rodent pinworm infections. However, the effect of its prophylactic use on the immune response of rodents is largely undefined. The non-obese diabetic (NOD) mouse is a model commonly used to study type 1 diabetes (T1D). Parasitic infections will inhibit diabetes development in NOD mice; thus, in the presence of contamination, prophylactic treatment with anthelmintics must be considered to maintain experimental research. Herein, we investigated the prophylactic use of FBZ in NOD mice to determine its effect on the incidence and onset of diabetes, lymphocyte sub-populations and T cell proliferative responses. NOD mice were separated into control and treatment groups. The treatment group received a diet containing FBZ. Animals were monitored for the incidence and onset of T1D. At matched time points, diabetic and non-diabetic mice were killed and splenic lymphocytes analyzed for various cell sub-populations and mitogen-induced proliferative responses using flow cytometry. Treated and control mice were monitored >23 weeks with no detectable effects on the incidence or onset of diabetes. Moreover, no significant differences were detected in lymphocyte sub-populations and mitogen-induced CD4+ and CD8+ proliferative responses between control and treatment groups. These results suggest that prophylactic FBZ treatment does not significantly alter the incidence or onset of diabetes in NOD mice. The prophylactic use of FBZ, therefore, presents a viable approach for the prevention of pinworm infection in precious experimental animals with substantial scientific and economic benefits.</description><identifier>ISSN: 0953-8178</identifier><identifier>EISSN: 1460-2377</identifier><identifier>DOI: 10.1093/intimm/dxh385</identifier><identifier>PMID: 16415097</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Antinematodal Agents - therapeutic use ; autoimmunity ; CD4-Positive T-Lymphocytes - cytology ; CD4-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - cytology ; CD8-Positive T-Lymphocytes - immunology ; Cell Proliferation - drug effects ; CFSE carboxy-fluorescein diacetate succinimidyl ester ; diabetes ; Diabetes Mellitus, Type 1 - immunology ; Diabetes Mellitus, Type 1 - prevention & control ; FBZ fenbendazole ; Female ; fenbendazole ; Fenbendazole - therapeutic use ; Hypoglycemic Agents - therapeutic use ; Incidence ; Mice ; Mice, Inbred NOD ; Mitogens - immunology ; NOD non-obese diabetic ; PI proliferation index ; prophylactic therapy ; Spleen - cytology ; Spleen - drug effects ; T1D type 1 diabetes</subject><ispartof>International immunology, 2006-03, Vol.18 (3), p.453-458</ispartof><rights>Copyright Oxford University Press(England) Mar 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-f51d2b81528d64b3eef66383cfa2881c65f404c46c2b316224eeb177942eb62a3</citedby><cites>FETCH-LOGICAL-c416t-f51d2b81528d64b3eef66383cfa2881c65f404c46c2b316224eeb177942eb62a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16415097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Franke, Deanna D. H.</creatorcontrib><creatorcontrib>Shirwan, Haval</creatorcontrib><title>Prophylactic fenbendazole therapy does not affect the incidence and onset of type 1 diabetes in non-obese diabetic mice</title><title>International immunology</title><addtitle>Int. Immunol</addtitle><description>Fenbendazole (FBZ) is a common, highly efficacious broad-spectrum anthelmintic drug used to treat and limit rodent pinworm infections. However, the effect of its prophylactic use on the immune response of rodents is largely undefined. The non-obese diabetic (NOD) mouse is a model commonly used to study type 1 diabetes (T1D). Parasitic infections will inhibit diabetes development in NOD mice; thus, in the presence of contamination, prophylactic treatment with anthelmintics must be considered to maintain experimental research. Herein, we investigated the prophylactic use of FBZ in NOD mice to determine its effect on the incidence and onset of diabetes, lymphocyte sub-populations and T cell proliferative responses. NOD mice were separated into control and treatment groups. The treatment group received a diet containing FBZ. Animals were monitored for the incidence and onset of T1D. At matched time points, diabetic and non-diabetic mice were killed and splenic lymphocytes analyzed for various cell sub-populations and mitogen-induced proliferative responses using flow cytometry. Treated and control mice were monitored >23 weeks with no detectable effects on the incidence or onset of diabetes. Moreover, no significant differences were detected in lymphocyte sub-populations and mitogen-induced CD4+ and CD8+ proliferative responses between control and treatment groups. These results suggest that prophylactic FBZ treatment does not significantly alter the incidence or onset of diabetes in NOD mice. The prophylactic use of FBZ, therefore, presents a viable approach for the prevention of pinworm infection in precious experimental animals with substantial scientific and economic benefits.</description><subject>Animals</subject><subject>Antinematodal Agents - therapeutic use</subject><subject>autoimmunity</subject><subject>CD4-Positive T-Lymphocytes - cytology</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - cytology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Cell Proliferation - drug effects</subject><subject>CFSE carboxy-fluorescein diacetate succinimidyl ester</subject><subject>diabetes</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Diabetes Mellitus, Type 1 - prevention & control</subject><subject>FBZ fenbendazole</subject><subject>Female</subject><subject>fenbendazole</subject><subject>Fenbendazole - therapeutic use</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Incidence</subject><subject>Mice</subject><subject>Mice, Inbred NOD</subject><subject>Mitogens - immunology</subject><subject>NOD non-obese diabetic</subject><subject>PI proliferation index</subject><subject>prophylactic therapy</subject><subject>Spleen - cytology</subject><subject>Spleen - drug effects</subject><subject>T1D type 1 diabetes</subject><issn>0953-8178</issn><issn>1460-2377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhyBVZHLiFemzHTo6o0C3SSvRQBOrFcpyx1iWxQ-wVXX49qXZFpV56Gmnmmzd68wh5C-wjsFachVjCOJ71d1vR1M_ICqRiFRdaPycr1taiakA3J-RVzreMMcFb8ZKcgJJQs1avyJ-rOU3b_WBdCY56jB3G3v5NA9KyxdlOe9onzDSmQq336Mp9n4boQo_RIbWxpylmLDR5WvYTUqB9sB2WZSvEZTFWqcOMx-5yZQwOX5MX3g4Z3xzrKfl-8eX6_LLafFt_Pf-0qZwEVSpfQ8-7Bmre9Ep2AtErJRrhvOVNA07VXjLppHK8E6A4l4gdaN1Kjp3iVpySDwfdaU6_d5iLGUN2OAw2Ytplo7RqddPCkyDo5V_A1QK-fwTept0cFxMG2poxroAtUHWA3JxyntGbaQ6jnfcGmLnPzRxyM4fcFv7dUXTXjdg_0MegHgRDLnj3f27nX4sFoWtz-fPGfN6wm_X6hzQX4h9CpqUc</recordid><startdate>200603</startdate><enddate>200603</enddate><creator>Franke, Deanna D. 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H. ; Shirwan, Haval</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-f51d2b81528d64b3eef66383cfa2881c65f404c46c2b316224eeb177942eb62a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Antinematodal Agents - therapeutic use</topic><topic>autoimmunity</topic><topic>CD4-Positive T-Lymphocytes - cytology</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - cytology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Cell Proliferation - drug effects</topic><topic>CFSE carboxy-fluorescein diacetate succinimidyl ester</topic><topic>diabetes</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes Mellitus, Type 1 - prevention & control</topic><topic>FBZ fenbendazole</topic><topic>Female</topic><topic>fenbendazole</topic><topic>Fenbendazole - therapeutic use</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Incidence</topic><topic>Mice</topic><topic>Mice, Inbred NOD</topic><topic>Mitogens - immunology</topic><topic>NOD non-obese diabetic</topic><topic>PI proliferation index</topic><topic>prophylactic therapy</topic><topic>Spleen - cytology</topic><topic>Spleen - drug effects</topic><topic>T1D type 1 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Franke, Deanna D. H.</creatorcontrib><creatorcontrib>Shirwan, Haval</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Franke, Deanna D. H.</au><au>Shirwan, Haval</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prophylactic fenbendazole therapy does not affect the incidence and onset of type 1 diabetes in non-obese diabetic mice</atitle><jtitle>International immunology</jtitle><addtitle>Int. Immunol</addtitle><date>2006-03</date><risdate>2006</risdate><volume>18</volume><issue>3</issue><spage>453</spage><epage>458</epage><pages>453-458</pages><issn>0953-8178</issn><eissn>1460-2377</eissn><abstract>Fenbendazole (FBZ) is a common, highly efficacious broad-spectrum anthelmintic drug used to treat and limit rodent pinworm infections. However, the effect of its prophylactic use on the immune response of rodents is largely undefined. The non-obese diabetic (NOD) mouse is a model commonly used to study type 1 diabetes (T1D). Parasitic infections will inhibit diabetes development in NOD mice; thus, in the presence of contamination, prophylactic treatment with anthelmintics must be considered to maintain experimental research. Herein, we investigated the prophylactic use of FBZ in NOD mice to determine its effect on the incidence and onset of diabetes, lymphocyte sub-populations and T cell proliferative responses. NOD mice were separated into control and treatment groups. The treatment group received a diet containing FBZ. Animals were monitored for the incidence and onset of T1D. At matched time points, diabetic and non-diabetic mice were killed and splenic lymphocytes analyzed for various cell sub-populations and mitogen-induced proliferative responses using flow cytometry. Treated and control mice were monitored >23 weeks with no detectable effects on the incidence or onset of diabetes. Moreover, no significant differences were detected in lymphocyte sub-populations and mitogen-induced CD4+ and CD8+ proliferative responses between control and treatment groups. These results suggest that prophylactic FBZ treatment does not significantly alter the incidence or onset of diabetes in NOD mice. The prophylactic use of FBZ, therefore, presents a viable approach for the prevention of pinworm infection in precious experimental animals with substantial scientific and economic benefits.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>16415097</pmid><doi>10.1093/intimm/dxh385</doi><tpages>6</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Antinematodal Agents - therapeutic use autoimmunity CD4-Positive T-Lymphocytes - cytology CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - cytology CD8-Positive T-Lymphocytes - immunology Cell Proliferation - drug effects CFSE carboxy-fluorescein diacetate succinimidyl ester diabetes Diabetes Mellitus, Type 1 - immunology Diabetes Mellitus, Type 1 - prevention & control FBZ fenbendazole Female fenbendazole Fenbendazole - therapeutic use Hypoglycemic Agents - therapeutic use Incidence Mice Mice, Inbred NOD Mitogens - immunology NOD non-obese diabetic PI proliferation index prophylactic therapy Spleen - cytology Spleen - drug effects T1D type 1 diabetes |
title | Prophylactic fenbendazole therapy does not affect the incidence and onset of type 1 diabetes in non-obese diabetic mice |
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