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The morphine/heroin vaccine decreased the heroin-induced antinociceptive and reinforcing effects in three inbred strains mouse
•M6-TT vaccine decrease the heroin-induced analgesia in three inbred mouse strain.•M6-TT vaccine decrease heroin-locomotor sensitization in three inbred mouse strain.•M6-TT vaccine decrease heroin-induced place-preference in three inbred mouse strain. Clinical trials have indicated that a vaccine mu...
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Published in: | International immunopharmacology 2021-09, Vol.98, p.107887-107887, Article 107887 |
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creator | Barbosa-Méndez, Susana Matus-Ortega, Maura Hernández-Miramontes, Ricardo Salazar-Juárez, Alberto |
description | •M6-TT vaccine decrease the heroin-induced analgesia in three inbred mouse strain.•M6-TT vaccine decrease heroin-locomotor sensitization in three inbred mouse strain.•M6-TT vaccine decrease heroin-induced place-preference in three inbred mouse strain.
Clinical trials have indicated that a vaccine must be immunogenic in genetically diverse human populations and that immunogenicity and protective efficacy in animal models are two key indices required for the approval of a new vaccine. Additionally, the immune response (immunogenicity) and immunoprotection are dependent on the mouse strain. Therefore, the objective of the present study was to determine the immune response (immunogenicity) and the protective efficacy (behavioral response) in three inbred mouse strains immunized with the M6TT vaccine.
Female BALB/c, C57Bl/6, and DBA/2 inbred mice were immunized with the M6-TT vaccine. A solid-phase antibody-capture ELISA was used to monitor antibody titer responses after each booster dose in vaccinated animals. The study used tail-flick testing to evaluate the antinociceptive effects induced by heroin. Additionally, heroin-induced locomotor activity and place preference were evaluated.
The M6-TT vaccine was able to generate a specific antibody titer in the three inbred mouse strains evaluated. The antibodies reduced the antinociceptive effect of different doses of heroin. In addition, they decreased the heroin-induced locomotor activity and place preference.
These findings suggest that the M6-TT vaccine generates a powerful immunogenic response capable of reducing the antinociceptive and reinforcing effects of heroin in different inbred mouse strains, which supports its possible future use in clinical trials in genetically diverse human populations. |
doi_str_mv | 10.1016/j.intimp.2021.107887 |
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Clinical trials have indicated that a vaccine must be immunogenic in genetically diverse human populations and that immunogenicity and protective efficacy in animal models are two key indices required for the approval of a new vaccine. Additionally, the immune response (immunogenicity) and immunoprotection are dependent on the mouse strain. Therefore, the objective of the present study was to determine the immune response (immunogenicity) and the protective efficacy (behavioral response) in three inbred mouse strains immunized with the M6TT vaccine.
Female BALB/c, C57Bl/6, and DBA/2 inbred mice were immunized with the M6-TT vaccine. A solid-phase antibody-capture ELISA was used to monitor antibody titer responses after each booster dose in vaccinated animals. The study used tail-flick testing to evaluate the antinociceptive effects induced by heroin. Additionally, heroin-induced locomotor activity and place preference were evaluated.
The M6-TT vaccine was able to generate a specific antibody titer in the three inbred mouse strains evaluated. The antibodies reduced the antinociceptive effect of different doses of heroin. In addition, they decreased the heroin-induced locomotor activity and place preference.
These findings suggest that the M6-TT vaccine generates a powerful immunogenic response capable of reducing the antinociceptive and reinforcing effects of heroin in different inbred mouse strains, which supports its possible future use in clinical trials in genetically diverse human populations.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2021.107887</identifier><identifier>PMID: 34186279</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Active vaccination ; Analgesics, Opioid ; Animal models ; Animals ; Antibodies ; Clinical trials ; Disease Models, Animal ; Enzyme-linked immunosorbent assay ; Female ; Heroin ; Heroin - adverse effects ; Heroin - immunology ; Human populations ; Humans ; Immune response ; Immune system ; Immunization ; Immunogenicity ; Immunogenicity, Vaccine ; Inbreeding ; Locomotor activity ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Inbred DBA ; Morphine ; Morphine - adverse effects ; Morphine - immunology ; M−TT vaccine ; Nociception ; Nociception, inbred mouse strain ; Opioid-Related Disorders - immunology ; Opioid-Related Disorders - therapy ; Pain perception ; Place preference ; Population genetics ; Populations ; Reinforcement, Psychology ; Solid phases ; Vaccines ; Vaccines - administration & dosage ; Vaccines - immunology</subject><ispartof>International immunopharmacology, 2021-09, Vol.98, p.107887-107887, Article 107887</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Sep 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-e463c7fd6d52c749b34096879829942e5d1f6826e22d1d8e0ed72c2ecf8a99b73</citedby><cites>FETCH-LOGICAL-c390t-e463c7fd6d52c749b34096879829942e5d1f6826e22d1d8e0ed72c2ecf8a99b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34186279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbosa-Méndez, Susana</creatorcontrib><creatorcontrib>Matus-Ortega, Maura</creatorcontrib><creatorcontrib>Hernández-Miramontes, Ricardo</creatorcontrib><creatorcontrib>Salazar-Juárez, Alberto</creatorcontrib><title>The morphine/heroin vaccine decreased the heroin-induced antinociceptive and reinforcing effects in three inbred strains mouse</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>•M6-TT vaccine decrease the heroin-induced analgesia in three inbred mouse strain.•M6-TT vaccine decrease heroin-locomotor sensitization in three inbred mouse strain.•M6-TT vaccine decrease heroin-induced place-preference in three inbred mouse strain.
Clinical trials have indicated that a vaccine must be immunogenic in genetically diverse human populations and that immunogenicity and protective efficacy in animal models are two key indices required for the approval of a new vaccine. Additionally, the immune response (immunogenicity) and immunoprotection are dependent on the mouse strain. Therefore, the objective of the present study was to determine the immune response (immunogenicity) and the protective efficacy (behavioral response) in three inbred mouse strains immunized with the M6TT vaccine.
Female BALB/c, C57Bl/6, and DBA/2 inbred mice were immunized with the M6-TT vaccine. A solid-phase antibody-capture ELISA was used to monitor antibody titer responses after each booster dose in vaccinated animals. The study used tail-flick testing to evaluate the antinociceptive effects induced by heroin. Additionally, heroin-induced locomotor activity and place preference were evaluated.
The M6-TT vaccine was able to generate a specific antibody titer in the three inbred mouse strains evaluated. The antibodies reduced the antinociceptive effect of different doses of heroin. In addition, they decreased the heroin-induced locomotor activity and place preference.
These findings suggest that the M6-TT vaccine generates a powerful immunogenic response capable of reducing the antinociceptive and reinforcing effects of heroin in different inbred mouse strains, which supports its possible future use in clinical trials in genetically diverse human populations.</description><subject>Active vaccination</subject><subject>Analgesics, Opioid</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Clinical trials</subject><subject>Disease Models, Animal</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Female</subject><subject>Heroin</subject><subject>Heroin - adverse effects</subject><subject>Heroin - immunology</subject><subject>Human populations</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Immunogenicity, Vaccine</subject><subject>Inbreeding</subject><subject>Locomotor activity</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred DBA</subject><subject>Morphine</subject><subject>Morphine - adverse effects</subject><subject>Morphine - immunology</subject><subject>M−TT vaccine</subject><subject>Nociception</subject><subject>Nociception, inbred mouse strain</subject><subject>Opioid-Related Disorders - immunology</subject><subject>Opioid-Related Disorders - therapy</subject><subject>Pain perception</subject><subject>Place preference</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Reinforcement, Psychology</subject><subject>Solid phases</subject><subject>Vaccines</subject><subject>Vaccines - administration & dosage</subject><subject>Vaccines - immunology</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU1P5DAMhiMEAhb4BytUicteOiRpmo8LEhrtlzQSFzhHbeLuZDRNS9KOtBd-O0ZlOXDYU2zneW3LLyFfGV0xyuTtbhXiFPpxxSlnWFJaqyNyzrTSJVO0Psa4lqqslTRn5EvOO0qxLtgpOasE05Irc05eHrdQ9EMatyHC7RbSEGJxaJzDtPDgEjQZfDEhtXyWIfrZYanB6XFwwcE4hQNg7osEIXZDQvGfAroO3JQL7DdtEwAGbUJdnlITYsahc4ZLctI1-wxX7-8Fefrx_XH9q9w8_Py9vt-UrjJ0KkHIyqnOS19zp4RpK0GN1MpobozgUHvWSc0lcO6Z10DBK-44uE43xrSquiDflr5jGp5nyJPtQ3aw3zcRcA_LayGNpoZqRG8-obthThG3Q0oJTblgNVJioVwack7Q2TGFvkl_LaP2zR-7s4s_9s0fu_iDsuv35nPbg_8Q_TMEgbsFALzGIUCy2QWIePCQ8JzWD-H_E14B2oSkzQ</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Barbosa-Méndez, Susana</creator><creator>Matus-Ortega, Maura</creator><creator>Hernández-Miramontes, Ricardo</creator><creator>Salazar-Juárez, Alberto</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202109</creationdate><title>The morphine/heroin vaccine decreased the heroin-induced antinociceptive and reinforcing effects in three inbred strains mouse</title><author>Barbosa-Méndez, Susana ; Matus-Ortega, Maura ; Hernández-Miramontes, Ricardo ; Salazar-Juárez, Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-e463c7fd6d52c749b34096879829942e5d1f6826e22d1d8e0ed72c2ecf8a99b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Active vaccination</topic><topic>Analgesics, Opioid</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Clinical trials</topic><topic>Disease Models, Animal</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Female</topic><topic>Heroin</topic><topic>Heroin - adverse effects</topic><topic>Heroin - immunology</topic><topic>Human populations</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunization</topic><topic>Immunogenicity</topic><topic>Immunogenicity, Vaccine</topic><topic>Inbreeding</topic><topic>Locomotor activity</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred DBA</topic><topic>Morphine</topic><topic>Morphine - adverse effects</topic><topic>Morphine - immunology</topic><topic>M−TT vaccine</topic><topic>Nociception</topic><topic>Nociception, inbred mouse strain</topic><topic>Opioid-Related Disorders - immunology</topic><topic>Opioid-Related Disorders - therapy</topic><topic>Pain perception</topic><topic>Place preference</topic><topic>Population genetics</topic><topic>Populations</topic><topic>Reinforcement, Psychology</topic><topic>Solid phases</topic><topic>Vaccines</topic><topic>Vaccines - administration & dosage</topic><topic>Vaccines - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbosa-Méndez, Susana</creatorcontrib><creatorcontrib>Matus-Ortega, Maura</creatorcontrib><creatorcontrib>Hernández-Miramontes, Ricardo</creatorcontrib><creatorcontrib>Salazar-Juárez, Alberto</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology 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>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbosa-Méndez, Susana</au><au>Matus-Ortega, Maura</au><au>Hernández-Miramontes, Ricardo</au><au>Salazar-Juárez, Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The morphine/heroin vaccine decreased the heroin-induced antinociceptive and reinforcing effects in three inbred strains mouse</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2021-09</date><risdate>2021</risdate><volume>98</volume><spage>107887</spage><epage>107887</epage><pages>107887-107887</pages><artnum>107887</artnum><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>•M6-TT vaccine decrease the heroin-induced analgesia in three inbred mouse strain.•M6-TT vaccine decrease heroin-locomotor sensitization in three inbred mouse strain.•M6-TT vaccine decrease heroin-induced place-preference in three inbred mouse strain.
Clinical trials have indicated that a vaccine must be immunogenic in genetically diverse human populations and that immunogenicity and protective efficacy in animal models are two key indices required for the approval of a new vaccine. Additionally, the immune response (immunogenicity) and immunoprotection are dependent on the mouse strain. Therefore, the objective of the present study was to determine the immune response (immunogenicity) and the protective efficacy (behavioral response) in three inbred mouse strains immunized with the M6TT vaccine.
Female BALB/c, C57Bl/6, and DBA/2 inbred mice were immunized with the M6-TT vaccine. A solid-phase antibody-capture ELISA was used to monitor antibody titer responses after each booster dose in vaccinated animals. The study used tail-flick testing to evaluate the antinociceptive effects induced by heroin. Additionally, heroin-induced locomotor activity and place preference were evaluated.
The M6-TT vaccine was able to generate a specific antibody titer in the three inbred mouse strains evaluated. The antibodies reduced the antinociceptive effect of different doses of heroin. In addition, they decreased the heroin-induced locomotor activity and place preference.
These findings suggest that the M6-TT vaccine generates a powerful immunogenic response capable of reducing the antinociceptive and reinforcing effects of heroin in different inbred mouse strains, which supports its possible future use in clinical trials in genetically diverse human populations.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34186279</pmid><doi>10.1016/j.intimp.2021.107887</doi><tpages>1</tpages></addata></record> |
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subjects | Active vaccination Analgesics, Opioid Animal models Animals Antibodies Clinical trials Disease Models, Animal Enzyme-linked immunosorbent assay Female Heroin Heroin - adverse effects Heroin - immunology Human populations Humans Immune response Immune system Immunization Immunogenicity Immunogenicity, Vaccine Inbreeding Locomotor activity Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA Morphine Morphine - adverse effects Morphine - immunology M−TT vaccine Nociception Nociception, inbred mouse strain Opioid-Related Disorders - immunology Opioid-Related Disorders - therapy Pain perception Place preference Population genetics Populations Reinforcement, Psychology Solid phases Vaccines Vaccines - administration & dosage Vaccines - immunology |
title | The morphine/heroin vaccine decreased the heroin-induced antinociceptive and reinforcing effects in three inbred strains mouse |
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