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Protective Immunity in Mice Immunized With P. vivax MSP1 19 -Based Formulations and Challenged With P. berghei Expressing Pv MSP1 19
The lack of continuous cultures has been an obstacle delaying pre-clinical testing of vaccine formulations based on known antigens. In this study, we generated a model to test available formulations based on the MSP1 antigen. The strains ANKA and NK65 were modified to express MSP1 instead of the end...
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Published in: | Frontiers in immunology 2020, Vol.11, p.28 |
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container_title | Frontiers in immunology |
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creator | Dobrescu, Irina de Camargo, Tarsila Mendes Gimenez, Alba Marina Murillo, Oscar Amorim, Kelly Nazaré da Silva Marinho, Claudio Romero Farias Soares, Irene Silva Boscardin, Silvia Beatriz Bargieri, Daniel Youssef |
description | The lack of continuous
cultures has been an obstacle delaying pre-clinical testing of
vaccine formulations based on known antigens. In this study, we generated a model to test available formulations based on the
MSP1
antigen. The
strains ANKA and NK65 were modified to express
MSP1
instead of the endogenous
MSP1
. The hybrid parasites were used to challenge C57BL/6 or BALB/c mice immunized with
MSP1
-based vaccine formulations. The
MSP1
was correctly expressed in the
hybrid mutant lines as confirmed by immunofluorescence using anti-
MSP1
monoclonal antibodies and by Western blot. Replacement of the
MSP1
by the
MSP1
had no impact on asexual growth
. High titers of specific antibodies to
MSP1
were not sufficient to control initial parasitemia in the immunized mice, but late parasitemia control and a balanced inflammatory process protected these mice from dying, suggesting that an established immune response to
MSP1
in this model can help immunity mounted later during infection. |
doi_str_mv | 10.3389/fimmu.2020.00028 |
format | article |
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cultures has been an obstacle delaying pre-clinical testing of
vaccine formulations based on known antigens. In this study, we generated a model to test available formulations based on the
MSP1
antigen. The
strains ANKA and NK65 were modified to express
MSP1
instead of the endogenous
MSP1
. The hybrid parasites were used to challenge C57BL/6 or BALB/c mice immunized with
MSP1
-based vaccine formulations. The
MSP1
was correctly expressed in the
hybrid mutant lines as confirmed by immunofluorescence using anti-
MSP1
monoclonal antibodies and by Western blot. Replacement of the
MSP1
by the
MSP1
had no impact on asexual growth
. High titers of specific antibodies to
MSP1
were not sufficient to control initial parasitemia in the immunized mice, but late parasitemia control and a balanced inflammatory process protected these mice from dying, suggesting that an established immune response to
MSP1
in this model can help immunity mounted later during infection.</description><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2020.00028</identifier><identifier>PMID: 32153555</identifier><language>eng</language><publisher>Switzerland</publisher><subject>Animals ; Antibodies, Protozoan - immunology ; Antigens, Protozoan - immunology ; Female ; Immunogenicity, Vaccine ; Malaria Vaccines - immunology ; Malaria, Vivax - immunology ; Malaria, Vivax - parasitology ; Merozoite Surface Protein 1 - immunology ; Merozoite Surface Protein 1 - metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Parasitemia - immunology ; Plasmids - genetics ; Plasmodium berghei - genetics ; Plasmodium berghei - metabolism ; Plasmodium vivax - immunology ; Protozoan Proteins - immunology ; Transfection ; Treatment Outcome ; Vaccination</subject><ispartof>Frontiers in immunology, 2020, Vol.11, p.28</ispartof><rights>Copyright © 2020 Dobrescu, de Camargo, Gimenez, Murillo, Amorim, Marinho, Soares, Boscardin and Bargieri.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32153555$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dobrescu, Irina</creatorcontrib><creatorcontrib>de Camargo, Tarsila Mendes</creatorcontrib><creatorcontrib>Gimenez, Alba Marina</creatorcontrib><creatorcontrib>Murillo, Oscar</creatorcontrib><creatorcontrib>Amorim, Kelly Nazaré da Silva</creatorcontrib><creatorcontrib>Marinho, Claudio Romero Farias</creatorcontrib><creatorcontrib>Soares, Irene Silva</creatorcontrib><creatorcontrib>Boscardin, Silvia Beatriz</creatorcontrib><creatorcontrib>Bargieri, Daniel Youssef</creatorcontrib><title>Protective Immunity in Mice Immunized With P. vivax MSP1 19 -Based Formulations and Challenged With P. berghei Expressing Pv MSP1 19</title><title>Frontiers in immunology</title><addtitle>Front Immunol</addtitle><description>The lack of continuous
cultures has been an obstacle delaying pre-clinical testing of
vaccine formulations based on known antigens. In this study, we generated a model to test available formulations based on the
MSP1
antigen. The
strains ANKA and NK65 were modified to express
MSP1
instead of the endogenous
MSP1
. The hybrid parasites were used to challenge C57BL/6 or BALB/c mice immunized with
MSP1
-based vaccine formulations. The
MSP1
was correctly expressed in the
hybrid mutant lines as confirmed by immunofluorescence using anti-
MSP1
monoclonal antibodies and by Western blot. Replacement of the
MSP1
by the
MSP1
had no impact on asexual growth
. High titers of specific antibodies to
MSP1
were not sufficient to control initial parasitemia in the immunized mice, but late parasitemia control and a balanced inflammatory process protected these mice from dying, suggesting that an established immune response to
MSP1
in this model can help immunity mounted later during infection.</description><subject>Animals</subject><subject>Antibodies, Protozoan - immunology</subject><subject>Antigens, Protozoan - immunology</subject><subject>Female</subject><subject>Immunogenicity, Vaccine</subject><subject>Malaria Vaccines - immunology</subject><subject>Malaria, Vivax - immunology</subject><subject>Malaria, Vivax - parasitology</subject><subject>Merozoite Surface Protein 1 - immunology</subject><subject>Merozoite Surface Protein 1 - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Parasitemia - immunology</subject><subject>Plasmids - genetics</subject><subject>Plasmodium berghei - genetics</subject><subject>Plasmodium berghei - metabolism</subject><subject>Plasmodium vivax - immunology</subject><subject>Protozoan Proteins - immunology</subject><subject>Transfection</subject><subject>Treatment Outcome</subject><subject>Vaccination</subject><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFjk9LwzAYxoMgbujunuT9Aq1J3masV8eGHgYFBY8jW7P2lSYtSVo2z35we7Cwm6cHfs8fHsYeBU8RV_nziaztU8klTznncnXD5mK5zBKUMpuxRQhfI-ZZjojqjs1QCoVKqTn7KXwbzTHSYOBt3HAUL0AOdnScwLcp4ZNiDUUKAw36DLv3QoDIIXnRYTS3rbd9oyO1LoB2Jaxr3TTGVVfFg_FVbQg2586bEMhVUAzT0AO7PekmmMWf3rOn7eZj_Zp0_cGact95stpf9tNt_DfwC2j6Upc</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Dobrescu, Irina</creator><creator>de Camargo, Tarsila Mendes</creator><creator>Gimenez, Alba Marina</creator><creator>Murillo, Oscar</creator><creator>Amorim, Kelly Nazaré da Silva</creator><creator>Marinho, Claudio Romero Farias</creator><creator>Soares, Irene Silva</creator><creator>Boscardin, Silvia Beatriz</creator><creator>Bargieri, Daniel Youssef</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>2020</creationdate><title>Protective Immunity in Mice Immunized With P. vivax MSP1 19 -Based Formulations and Challenged With P. berghei Expressing Pv MSP1 19</title><author>Dobrescu, Irina ; de Camargo, Tarsila Mendes ; Gimenez, Alba Marina ; Murillo, Oscar ; Amorim, Kelly Nazaré da Silva ; Marinho, Claudio Romero Farias ; Soares, Irene Silva ; Boscardin, Silvia Beatriz ; Bargieri, Daniel Youssef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_321535553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antibodies, Protozoan - immunology</topic><topic>Antigens, Protozoan - immunology</topic><topic>Female</topic><topic>Immunogenicity, Vaccine</topic><topic>Malaria Vaccines - immunology</topic><topic>Malaria, Vivax - immunology</topic><topic>Malaria, Vivax - parasitology</topic><topic>Merozoite Surface Protein 1 - immunology</topic><topic>Merozoite Surface Protein 1 - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Parasitemia - immunology</topic><topic>Plasmids - genetics</topic><topic>Plasmodium berghei - genetics</topic><topic>Plasmodium berghei - metabolism</topic><topic>Plasmodium vivax - immunology</topic><topic>Protozoan Proteins - immunology</topic><topic>Transfection</topic><topic>Treatment Outcome</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dobrescu, Irina</creatorcontrib><creatorcontrib>de Camargo, Tarsila Mendes</creatorcontrib><creatorcontrib>Gimenez, Alba Marina</creatorcontrib><creatorcontrib>Murillo, Oscar</creatorcontrib><creatorcontrib>Amorim, Kelly Nazaré da Silva</creatorcontrib><creatorcontrib>Marinho, Claudio Romero Farias</creatorcontrib><creatorcontrib>Soares, Irene Silva</creatorcontrib><creatorcontrib>Boscardin, Silvia Beatriz</creatorcontrib><creatorcontrib>Bargieri, Daniel Youssef</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dobrescu, Irina</au><au>de Camargo, Tarsila Mendes</au><au>Gimenez, Alba Marina</au><au>Murillo, Oscar</au><au>Amorim, Kelly Nazaré da Silva</au><au>Marinho, Claudio Romero Farias</au><au>Soares, Irene Silva</au><au>Boscardin, Silvia Beatriz</au><au>Bargieri, Daniel Youssef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective Immunity in Mice Immunized With P. vivax MSP1 19 -Based Formulations and Challenged With P. berghei Expressing Pv MSP1 19</atitle><jtitle>Frontiers in immunology</jtitle><addtitle>Front Immunol</addtitle><date>2020</date><risdate>2020</risdate><volume>11</volume><spage>28</spage><pages>28-</pages><eissn>1664-3224</eissn><abstract>The lack of continuous
cultures has been an obstacle delaying pre-clinical testing of
vaccine formulations based on known antigens. In this study, we generated a model to test available formulations based on the
MSP1
antigen. The
strains ANKA and NK65 were modified to express
MSP1
instead of the endogenous
MSP1
. The hybrid parasites were used to challenge C57BL/6 or BALB/c mice immunized with
MSP1
-based vaccine formulations. The
MSP1
was correctly expressed in the
hybrid mutant lines as confirmed by immunofluorescence using anti-
MSP1
monoclonal antibodies and by Western blot. Replacement of the
MSP1
by the
MSP1
had no impact on asexual growth
. High titers of specific antibodies to
MSP1
were not sufficient to control initial parasitemia in the immunized mice, but late parasitemia control and a balanced inflammatory process protected these mice from dying, suggesting that an established immune response to
MSP1
in this model can help immunity mounted later during infection.</abstract><cop>Switzerland</cop><pmid>32153555</pmid><doi>10.3389/fimmu.2020.00028</doi></addata></record> |
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source | PubMed Central |
subjects | Animals Antibodies, Protozoan - immunology Antigens, Protozoan - immunology Female Immunogenicity, Vaccine Malaria Vaccines - immunology Malaria, Vivax - immunology Malaria, Vivax - parasitology Merozoite Surface Protein 1 - immunology Merozoite Surface Protein 1 - metabolism Mice Mice, Inbred BALB C Mice, Inbred C57BL Parasitemia - immunology Plasmids - genetics Plasmodium berghei - genetics Plasmodium berghei - metabolism Plasmodium vivax - immunology Protozoan Proteins - immunology Transfection Treatment Outcome Vaccination |
title | Protective Immunity in Mice Immunized With P. vivax MSP1 19 -Based Formulations and Challenged With P. berghei Expressing Pv MSP1 19 |
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