Evaluation of multi-epitope recombinant protein as a candidate for a contraceptive vaccine
•The aim of this study was to evaluate a chimeric fusion protein containing IZUMO, SACA3 and PH-20 epitopes.•Lack of proper function of spermatogonia due to the presence of anti-sperm antibodies.•Infertility in male mice y producing anti-sperm antibodies. Contraceptive vaccine (CV) is a valuable, no...
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Veröffentlicht in: | Journal of reproductive immunology 2021-06, Vol.145, p.103325-103325, Article 103325 |
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creator | Mortazavi, Behnam Allahyari Fard, Najaf Karkhane, Ali Asghar Shokrpoor, Sara Heidari, Farid |
description | •The aim of this study was to evaluate a chimeric fusion protein containing IZUMO, SACA3 and PH-20 epitopes.•Lack of proper function of spermatogonia due to the presence of anti-sperm antibodies.•Infertility in male mice y producing anti-sperm antibodies.
Contraceptive vaccine (CV) is a valuable, non-invasive, and alternative method for purposeful contraception. Sperm antigens are useful targets for producing CVs due to their specialized expression in sperm. In this study, a recombinant protein containing three main sperm epitopes (IZUMO1, SACA3, and PH-20) was designed and evaluated as CV to control fertility in male mice. The chimeric recombinant protein was expressed and purified in E. coli. Male mice were immunized by 100 μg purified protein and sera were collected to assess IgG antibodies. Evaluating the reproductive performance, immunized male mice mated with normal-fertile female mice and mating rate and the number of newborns was studied. Immunized mice were sacrificed and necropsy and histopathology studies were conducted. The results revealed that the designed chimeric protein stimulated the immune system of the mice effectively. The level of IgG antibody was significantly higher in vaccinated mouse rather than control mouse. Eighty percent of the vaccinated mice became infertile and in the remaining ones, the number of children decreased to 4-6 offspring instead of 10–12 in normal mice. Histopathological studies showed that no organs including heart, brain, lung, liver, kidney and intestine were damaged. However, Normal spermatogenesis has been disrupted and necrotic spermatogonia cells were reported in Seminiferous tubules. We concluded that the designed chimeric protein containing IZUMO1, SACA3, and PH-20 epitopes can stimulate the immune system and cause male contraception without any side effects. |
doi_str_mv | 10.1016/j.jri.2021.103325 |
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Contraceptive vaccine (CV) is a valuable, non-invasive, and alternative method for purposeful contraception. Sperm antigens are useful targets for producing CVs due to their specialized expression in sperm. In this study, a recombinant protein containing three main sperm epitopes (IZUMO1, SACA3, and PH-20) was designed and evaluated as CV to control fertility in male mice. The chimeric recombinant protein was expressed and purified in E. coli. Male mice were immunized by 100 μg purified protein and sera were collected to assess IgG antibodies. Evaluating the reproductive performance, immunized male mice mated with normal-fertile female mice and mating rate and the number of newborns was studied. Immunized mice were sacrificed and necropsy and histopathology studies were conducted. The results revealed that the designed chimeric protein stimulated the immune system of the mice effectively. The level of IgG antibody was significantly higher in vaccinated mouse rather than control mouse. Eighty percent of the vaccinated mice became infertile and in the remaining ones, the number of children decreased to 4-6 offspring instead of 10–12 in normal mice. Histopathological studies showed that no organs including heart, brain, lung, liver, kidney and intestine were damaged. However, Normal spermatogenesis has been disrupted and necrotic spermatogonia cells were reported in Seminiferous tubules. We concluded that the designed chimeric protein containing IZUMO1, SACA3, and PH-20 epitopes can stimulate the immune system and cause male contraception without any side effects.</description><identifier>ISSN: 0165-0378</identifier><identifier>EISSN: 1872-7603</identifier><identifier>DOI: 10.1016/j.jri.2021.103325</identifier><identifier>PMID: 33930667</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Anti-sperm antibody ; Contraceptive vaccine ; Multi-epitope vaccine ; Sperm antigen</subject><ispartof>Journal of reproductive immunology, 2021-06, Vol.145, p.103325-103325, Article 103325</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-16e27f6438644b2d9338d04d2bb4d34cae0e5c1377f50b12344c6f09204353f23</citedby><cites>FETCH-LOGICAL-c353t-16e27f6438644b2d9338d04d2bb4d34cae0e5c1377f50b12344c6f09204353f23</cites><orcidid>0000-0001-7590-5179 ; 0000-0002-1862-2233</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jri.2021.103325$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33930667$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mortazavi, Behnam</creatorcontrib><creatorcontrib>Allahyari Fard, Najaf</creatorcontrib><creatorcontrib>Karkhane, Ali Asghar</creatorcontrib><creatorcontrib>Shokrpoor, Sara</creatorcontrib><creatorcontrib>Heidari, Farid</creatorcontrib><title>Evaluation of multi-epitope recombinant protein as a candidate for a contraceptive vaccine</title><title>Journal of reproductive immunology</title><addtitle>J Reprod Immunol</addtitle><description>•The aim of this study was to evaluate a chimeric fusion protein containing IZUMO, SACA3 and PH-20 epitopes.•Lack of proper function of spermatogonia due to the presence of anti-sperm antibodies.•Infertility in male mice y producing anti-sperm antibodies.
Contraceptive vaccine (CV) is a valuable, non-invasive, and alternative method for purposeful contraception. Sperm antigens are useful targets for producing CVs due to their specialized expression in sperm. In this study, a recombinant protein containing three main sperm epitopes (IZUMO1, SACA3, and PH-20) was designed and evaluated as CV to control fertility in male mice. The chimeric recombinant protein was expressed and purified in E. coli. Male mice were immunized by 100 μg purified protein and sera were collected to assess IgG antibodies. Evaluating the reproductive performance, immunized male mice mated with normal-fertile female mice and mating rate and the number of newborns was studied. Immunized mice were sacrificed and necropsy and histopathology studies were conducted. The results revealed that the designed chimeric protein stimulated the immune system of the mice effectively. The level of IgG antibody was significantly higher in vaccinated mouse rather than control mouse. Eighty percent of the vaccinated mice became infertile and in the remaining ones, the number of children decreased to 4-6 offspring instead of 10–12 in normal mice. Histopathological studies showed that no organs including heart, brain, lung, liver, kidney and intestine were damaged. However, Normal spermatogenesis has been disrupted and necrotic spermatogonia cells were reported in Seminiferous tubules. We concluded that the designed chimeric protein containing IZUMO1, SACA3, and PH-20 epitopes can stimulate the immune system and cause male contraception without any side effects.</description><subject>Anti-sperm antibody</subject><subject>Contraceptive vaccine</subject><subject>Multi-epitope vaccine</subject><subject>Sperm antigen</subject><issn>0165-0378</issn><issn>1872-7603</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kMFq3DAQhkVJaTbbPkAvQcdcvJU0suWlpxKSphDopb30ImRpDFpsyZHkhbx9tGySY0_DwPf_zHyEfOVsxxnvvh12h-R3ggledwDRfiAb3ivRqI7BBdlUpm0YqP6SXOV8YIwrtuefyCXAHljXqQ35d3c002qKj4HGkc7rVHyDiy9xQZrQxnnwwYRClxQL-kBNpoZaE5x3piAdYzrtMZRkLC7FH5EejbU-4GfycTRTxi-vc0v-3t_9uX1oHn___HX747Gx0EJpeIdCjZ2EvpNyEG4P0DsmnRgG6UBagwxby0GpsWUDFyCl7Ua2F0zW_ChgS27OvfXEpxVz0bPPFqfJBIxr1qIVrFccKr0l_IzaFHNOOOol-dmkZ82ZPinVB12V6pNSfVZaM9ev9eswo3tPvDmswPczgPXJo8eks_UYLDpfBRbtov9P_QtX64Yi</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Mortazavi, Behnam</creator><creator>Allahyari Fard, Najaf</creator><creator>Karkhane, Ali Asghar</creator><creator>Shokrpoor, Sara</creator><creator>Heidari, Farid</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7590-5179</orcidid><orcidid>https://orcid.org/0000-0002-1862-2233</orcidid></search><sort><creationdate>20210601</creationdate><title>Evaluation of multi-epitope recombinant protein as a candidate for a contraceptive vaccine</title><author>Mortazavi, Behnam ; Allahyari Fard, Najaf ; Karkhane, Ali Asghar ; Shokrpoor, Sara ; Heidari, Farid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-16e27f6438644b2d9338d04d2bb4d34cae0e5c1377f50b12344c6f09204353f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anti-sperm antibody</topic><topic>Contraceptive vaccine</topic><topic>Multi-epitope vaccine</topic><topic>Sperm antigen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mortazavi, Behnam</creatorcontrib><creatorcontrib>Allahyari Fard, Najaf</creatorcontrib><creatorcontrib>Karkhane, Ali Asghar</creatorcontrib><creatorcontrib>Shokrpoor, Sara</creatorcontrib><creatorcontrib>Heidari, Farid</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of reproductive immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mortazavi, Behnam</au><au>Allahyari Fard, Najaf</au><au>Karkhane, Ali Asghar</au><au>Shokrpoor, Sara</au><au>Heidari, Farid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of multi-epitope recombinant protein as a candidate for a contraceptive vaccine</atitle><jtitle>Journal of reproductive immunology</jtitle><addtitle>J Reprod Immunol</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>145</volume><spage>103325</spage><epage>103325</epage><pages>103325-103325</pages><artnum>103325</artnum><issn>0165-0378</issn><eissn>1872-7603</eissn><abstract>•The aim of this study was to evaluate a chimeric fusion protein containing IZUMO, SACA3 and PH-20 epitopes.•Lack of proper function of spermatogonia due to the presence of anti-sperm antibodies.•Infertility in male mice y producing anti-sperm antibodies.
Contraceptive vaccine (CV) is a valuable, non-invasive, and alternative method for purposeful contraception. Sperm antigens are useful targets for producing CVs due to their specialized expression in sperm. In this study, a recombinant protein containing three main sperm epitopes (IZUMO1, SACA3, and PH-20) was designed and evaluated as CV to control fertility in male mice. The chimeric recombinant protein was expressed and purified in E. coli. Male mice were immunized by 100 μg purified protein and sera were collected to assess IgG antibodies. Evaluating the reproductive performance, immunized male mice mated with normal-fertile female mice and mating rate and the number of newborns was studied. Immunized mice were sacrificed and necropsy and histopathology studies were conducted. The results revealed that the designed chimeric protein stimulated the immune system of the mice effectively. The level of IgG antibody was significantly higher in vaccinated mouse rather than control mouse. Eighty percent of the vaccinated mice became infertile and in the remaining ones, the number of children decreased to 4-6 offspring instead of 10–12 in normal mice. Histopathological studies showed that no organs including heart, brain, lung, liver, kidney and intestine were damaged. However, Normal spermatogenesis has been disrupted and necrotic spermatogonia cells were reported in Seminiferous tubules. We concluded that the designed chimeric protein containing IZUMO1, SACA3, and PH-20 epitopes can stimulate the immune system and cause male contraception without any side effects.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>33930667</pmid><doi>10.1016/j.jri.2021.103325</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7590-5179</orcidid><orcidid>https://orcid.org/0000-0002-1862-2233</orcidid></addata></record> |
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subjects | Anti-sperm antibody Contraceptive vaccine Multi-epitope vaccine Sperm antigen |
title | Evaluation of multi-epitope recombinant protein as a candidate for a contraceptive vaccine |
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