Vaccination strategies against intracellular microbes

Leishmaniasis, malaria, tuberculosis, leprosy, typhoid and listeriosis are infections diseases which, together, cause enormous public health problems throughout the world. The etiologic agents of these diseases, Leishmania ssp., Plasmodium ssp., Mycobacterium tuberculosis, Mycobacterium leprae, Salm...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:FEMS immunology and medical microbiology 1993-08, Vol.7 (2), p.95-103
Hauptverfasser: Hess, Jürgen, Kaufmann, Stefan H.E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 103
container_issue 2
container_start_page 95
container_title FEMS immunology and medical microbiology
container_volume 7
creator Hess, Jürgen
Kaufmann, Stefan H.E.
description Leishmaniasis, malaria, tuberculosis, leprosy, typhoid and listeriosis are infections diseases which, together, cause enormous public health problems throughout the world. The etiologic agents of these diseases, Leishmania ssp., Plasmodium ssp., Mycobacterium tuberculosis, Mycobacterium leprae, Salmonella typhi/S. paratyphi or Listeria monocytogenes, respectively, are endowed with the capacity to utilize the intracellular habitat of various host cells, including macrophages, erythrocytes and liver cells. This intracellular habitat effectively protects them from antibody-mediated defence mechanisms, so that T lymphocytes are required for acquisition of antimicrobial protection. Protective immunity is best induced by viable vaccines, whereas soluble proteins are generally insufficient. In this review we will focus on immunity to tuberculosis and on the use of viable recombinant vaccines as multivalent carrier systems for the vaccination against various intracellular microbial infections. We will discuss new strategies to improve N, bovis BC and S. typhimurium aroA super(-) by genetic engineering, in order to evoke optimum protection.
doi_str_mv 10.1111/j.1574-695X.1993.tb00387.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75944128</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16948846</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3955-19f6ad20a0ab0219cd1a33e3704fe6920a44cfd4801f1dd2e20aa93816fbffa3</originalsourceid><addsrcrecordid>eNqVkFFLwzAQx4Moc04_gjBEfGu9NGmbCD7IcDqY-DLEt3BNk5HRddp0uH17U1b2KuYlcP_f5S4_Qm4oxDSc-1VM05xHmUw_Yyoli9sCgIk83p2Q4TE6JUOQiYhEwvk5ufB-BQBcAgzIQHCgnCVDkn6g1q7G1m3qsW8bbM3SGT_GJbrat2NXh5o2VbWtsBmvnW42hfGX5Mxi5c1Vf4_IYvq8mLxG8_eX2eRpHmkm0zSi0mZYJoCABSRU6pIiY4blwK3JZAg417bkAqilZZmYUEHJBM1sYS2yEbk7PPvVbL63xrdq7Xy3DNZms_UqTyXnNBF_gjSTXAieBfDhAIZ_eN8Yq74at8Zmryiozq1aqU6g6gSqzq3q3apdaL7up2yLtSmPrb3MkN_2OXqNlW2w1s4fMS4ZT3MI2OMB-3GV2f9jATWdvcmU_QLF8Zai</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16948846</pqid></control><display><type>article</type><title>Vaccination strategies against intracellular microbes</title><source>Oxford Journals Open Access Collection</source><source>MEDLINE</source><source>Wiley Online Library All Journals</source><source>Oxford University Press Journals Digital Archive Legacy</source><creator>Hess, Jürgen ; Kaufmann, Stefan H.E.</creator><creatorcontrib>Hess, Jürgen ; Kaufmann, Stefan H.E.</creatorcontrib><description>Leishmaniasis, malaria, tuberculosis, leprosy, typhoid and listeriosis are infections diseases which, together, cause enormous public health problems throughout the world. The etiologic agents of these diseases, Leishmania ssp., Plasmodium ssp., Mycobacterium tuberculosis, Mycobacterium leprae, Salmonella typhi/S. paratyphi or Listeria monocytogenes, respectively, are endowed with the capacity to utilize the intracellular habitat of various host cells, including macrophages, erythrocytes and liver cells. This intracellular habitat effectively protects them from antibody-mediated defence mechanisms, so that T lymphocytes are required for acquisition of antimicrobial protection. Protective immunity is best induced by viable vaccines, whereas soluble proteins are generally insufficient. In this review we will focus on immunity to tuberculosis and on the use of viable recombinant vaccines as multivalent carrier systems for the vaccination against various intracellular microbial infections. We will discuss new strategies to improve N, bovis BC and S. typhimurium aroA super(-) by genetic engineering, in order to evoke optimum protection.</description><identifier>ISSN: 0928-8244</identifier><identifier>EISSN: 1574-695X</identifier><identifier>DOI: 10.1111/j.1574-695X.1993.tb00387.x</identifier><identifier>PMID: 8401432</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Applied microbiology ; BCG Vaccine - immunology ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Humans ; Microbiology ; Mycobacterium bovis ; Salmonella typhimurium ; T lymphocyte ; T-Lymphocytes - immunology ; Tuberculosis ; Tuberculosis - prevention &amp; control ; Typhoid ; Typhoid Fever - prevention &amp; control ; Typhoid-Paratyphoid Vaccines - immunology ; Vaccination ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Vaccines, Synthetic - immunology</subject><ispartof>FEMS immunology and medical microbiology, 1993-08, Vol.7 (2), p.95-103</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3955-19f6ad20a0ab0219cd1a33e3704fe6920a44cfd4801f1dd2e20aa93816fbffa3</citedby><cites>FETCH-LOGICAL-c3955-19f6ad20a0ab0219cd1a33e3704fe6920a44cfd4801f1dd2e20aa93816fbffa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1574-695X.1993.tb00387.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1574-695X.1993.tb00387.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4934570$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8401432$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hess, Jürgen</creatorcontrib><creatorcontrib>Kaufmann, Stefan H.E.</creatorcontrib><title>Vaccination strategies against intracellular microbes</title><title>FEMS immunology and medical microbiology</title><addtitle>FEMS Immunol Med Microbiol</addtitle><description>Leishmaniasis, malaria, tuberculosis, leprosy, typhoid and listeriosis are infections diseases which, together, cause enormous public health problems throughout the world. The etiologic agents of these diseases, Leishmania ssp., Plasmodium ssp., Mycobacterium tuberculosis, Mycobacterium leprae, Salmonella typhi/S. paratyphi or Listeria monocytogenes, respectively, are endowed with the capacity to utilize the intracellular habitat of various host cells, including macrophages, erythrocytes and liver cells. This intracellular habitat effectively protects them from antibody-mediated defence mechanisms, so that T lymphocytes are required for acquisition of antimicrobial protection. Protective immunity is best induced by viable vaccines, whereas soluble proteins are generally insufficient. In this review we will focus on immunity to tuberculosis and on the use of viable recombinant vaccines as multivalent carrier systems for the vaccination against various intracellular microbial infections. We will discuss new strategies to improve N, bovis BC and S. typhimurium aroA super(-) by genetic engineering, in order to evoke optimum protection.</description><subject>Animals</subject><subject>Applied microbiology</subject><subject>BCG Vaccine - immunology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Mycobacterium bovis</subject><subject>Salmonella typhimurium</subject><subject>T lymphocyte</subject><subject>T-Lymphocytes - immunology</subject><subject>Tuberculosis</subject><subject>Tuberculosis - prevention &amp; control</subject><subject>Typhoid</subject><subject>Typhoid Fever - prevention &amp; control</subject><subject>Typhoid-Paratyphoid Vaccines - immunology</subject><subject>Vaccination</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>Vaccines, Synthetic - immunology</subject><issn>0928-8244</issn><issn>1574-695X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkFFLwzAQx4Moc04_gjBEfGu9NGmbCD7IcDqY-DLEt3BNk5HRddp0uH17U1b2KuYlcP_f5S4_Qm4oxDSc-1VM05xHmUw_Yyoli9sCgIk83p2Q4TE6JUOQiYhEwvk5ufB-BQBcAgzIQHCgnCVDkn6g1q7G1m3qsW8bbM3SGT_GJbrat2NXh5o2VbWtsBmvnW42hfGX5Mxi5c1Vf4_IYvq8mLxG8_eX2eRpHmkm0zSi0mZYJoCABSRU6pIiY4blwK3JZAg417bkAqilZZmYUEHJBM1sYS2yEbk7PPvVbL63xrdq7Xy3DNZms_UqTyXnNBF_gjSTXAieBfDhAIZ_eN8Yq74at8Zmryiozq1aqU6g6gSqzq3q3apdaL7up2yLtSmPrb3MkN_2OXqNlW2w1s4fMS4ZT3MI2OMB-3GV2f9jATWdvcmU_QLF8Zai</recordid><startdate>199308</startdate><enddate>199308</enddate><creator>Hess, Jürgen</creator><creator>Kaufmann, Stefan H.E.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><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>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199308</creationdate><title>Vaccination strategies against intracellular microbes</title><author>Hess, Jürgen ; Kaufmann, Stefan H.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3955-19f6ad20a0ab0219cd1a33e3704fe6920a44cfd4801f1dd2e20aa93816fbffa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Applied microbiology</topic><topic>BCG Vaccine - immunology</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Microbiology</topic><topic>Mycobacterium bovis</topic><topic>Salmonella typhimurium</topic><topic>T lymphocyte</topic><topic>T-Lymphocytes - immunology</topic><topic>Tuberculosis</topic><topic>Tuberculosis - prevention &amp; control</topic><topic>Typhoid</topic><topic>Typhoid Fever - prevention &amp; control</topic><topic>Typhoid-Paratyphoid Vaccines - immunology</topic><topic>Vaccination</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><topic>Vaccines, Synthetic - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hess, Jürgen</creatorcontrib><creatorcontrib>Kaufmann, Stefan H.E.</creatorcontrib><collection>Pascal-Francis</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>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS immunology and medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hess, Jürgen</au><au>Kaufmann, Stefan H.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaccination strategies against intracellular microbes</atitle><jtitle>FEMS immunology and medical microbiology</jtitle><addtitle>FEMS Immunol Med Microbiol</addtitle><date>1993-08</date><risdate>1993</risdate><volume>7</volume><issue>2</issue><spage>95</spage><epage>103</epage><pages>95-103</pages><issn>0928-8244</issn><eissn>1574-695X</eissn><abstract>Leishmaniasis, malaria, tuberculosis, leprosy, typhoid and listeriosis are infections diseases which, together, cause enormous public health problems throughout the world. The etiologic agents of these diseases, Leishmania ssp., Plasmodium ssp., Mycobacterium tuberculosis, Mycobacterium leprae, Salmonella typhi/S. paratyphi or Listeria monocytogenes, respectively, are endowed with the capacity to utilize the intracellular habitat of various host cells, including macrophages, erythrocytes and liver cells. This intracellular habitat effectively protects them from antibody-mediated defence mechanisms, so that T lymphocytes are required for acquisition of antimicrobial protection. Protective immunity is best induced by viable vaccines, whereas soluble proteins are generally insufficient. In this review we will focus on immunity to tuberculosis and on the use of viable recombinant vaccines as multivalent carrier systems for the vaccination against various intracellular microbial infections. We will discuss new strategies to improve N, bovis BC and S. typhimurium aroA super(-) by genetic engineering, in order to evoke optimum protection.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8401432</pmid><doi>10.1111/j.1574-695X.1993.tb00387.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0928-8244
ispartof FEMS immunology and medical microbiology, 1993-08, Vol.7 (2), p.95-103
issn 0928-8244
1574-695X
language eng
recordid cdi_proquest_miscellaneous_75944128
source Oxford Journals Open Access Collection; MEDLINE; Wiley Online Library All Journals; Oxford University Press Journals Digital Archive Legacy
subjects Animals
Applied microbiology
BCG Vaccine - immunology
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Humans
Microbiology
Mycobacterium bovis
Salmonella typhimurium
T lymphocyte
T-Lymphocytes - immunology
Tuberculosis
Tuberculosis - prevention & control
Typhoid
Typhoid Fever - prevention & control
Typhoid-Paratyphoid Vaccines - immunology
Vaccination
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Vaccines, Synthetic - immunology
title Vaccination strategies against intracellular microbes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T07%3A48%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Vaccination%20strategies%20against%20intracellular%20microbes&rft.jtitle=FEMS%20immunology%20and%20medical%20microbiology&rft.au=Hess,%20J%C3%BCrgen&rft.date=1993-08&rft.volume=7&rft.issue=2&rft.spage=95&rft.epage=103&rft.pages=95-103&rft.issn=0928-8244&rft.eissn=1574-695X&rft_id=info:doi/10.1111/j.1574-695X.1993.tb00387.x&rft_dat=%3Cproquest_cross%3E16948846%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16948846&rft_id=info:pmid/8401432&rfr_iscdi=true