The perfect mix: recent progress in adjuvant research
Key Points New vaccines are often less immunogenic than previous vaccines, and adjuvants are therefore required to assist in the induction of potent and persistent immune responses, to reduce the amount of antigen and limit the number of injections. Some new vaccines also need adjuvants that are cap...
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description | Key Points
New vaccines are often less immunogenic than previous vaccines, and adjuvants are therefore required to assist in the induction of potent and persistent immune responses, to reduce the amount of antigen and limit the number of injections.
Some new vaccines also need adjuvants that are capable of inducing potent cell-mediated immunity in addition to an antibody response, such as T helper (T
H
) 1 responses and cytotoxic T lymphocyte (CTL) responses.
Recent advances in basic immunology have demonstrated the crucial role of some innate immune signals in modulating — both quantitatively and qualitatively — the subsequent adaptive response. Among these, some agonists of Toll-like receptors (TLRs) would in theory constitute promising adjuvants.
Vaccine research can take advantage of these discoveries to design and develop more focused and efficient adjuvants, such as new synthetic agonists of TLRs.
Moreover, new formulations can combine different immunostimulants, including TLR agonists and non-TLR 'classical' adjuvants. These compounds can act in synergy, and targeting them towards antigen-presenting cells could further increase and focus their action.
In parallel, new biochemical and immunological tools and assays have been developed to characterize and evaluate these new adjuvants, both
in vitro
and
in vivo
. The combination of information obtained in several assays, for example in animal models and human primary or transformed cells, can provide more accurate information on the potency and safety of these new adjuvants before use on humans.
Vaccine research scientists can now chose between a larger panel of compounds and technologies to design and develop the formulation that would drive the most efficient and safest response with respect to each considered pathogen, keeping in mind that each antigen–adjuvant couple is unique.
In addition to improving our understanding of target antigens for vaccines and their correlates of protection, recent advances in immunological research, particularly in our understanding of innate immunity, have also had a major impact on adjuvant research. Bruno Guy reviews the practical applications of our increased understanding of the immune system in the design and development of more specific and focused adjuvants.
Developing efficient and safe adjuvants for use in human vaccines remains both a challenge and a necessity. Past approaches have been largely empirical and generally used a single type of adjuvant, such as |
doi_str_mv | 10.1038/nrmicro1681 |
format | Article |
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New vaccines are often less immunogenic than previous vaccines, and adjuvants are therefore required to assist in the induction of potent and persistent immune responses, to reduce the amount of antigen and limit the number of injections.
Some new vaccines also need adjuvants that are capable of inducing potent cell-mediated immunity in addition to an antibody response, such as T helper (T
H
) 1 responses and cytotoxic T lymphocyte (CTL) responses.
Recent advances in basic immunology have demonstrated the crucial role of some innate immune signals in modulating — both quantitatively and qualitatively — the subsequent adaptive response. Among these, some agonists of Toll-like receptors (TLRs) would in theory constitute promising adjuvants.
Vaccine research can take advantage of these discoveries to design and develop more focused and efficient adjuvants, such as new synthetic agonists of TLRs.
Moreover, new formulations can combine different immunostimulants, including TLR agonists and non-TLR 'classical' adjuvants. These compounds can act in synergy, and targeting them towards antigen-presenting cells could further increase and focus their action.
In parallel, new biochemical and immunological tools and assays have been developed to characterize and evaluate these new adjuvants, both
in vitro
and
in vivo
. The combination of information obtained in several assays, for example in animal models and human primary or transformed cells, can provide more accurate information on the potency and safety of these new adjuvants before use on humans.
Vaccine research scientists can now chose between a larger panel of compounds and technologies to design and develop the formulation that would drive the most efficient and safest response with respect to each considered pathogen, keeping in mind that each antigen–adjuvant couple is unique.
In addition to improving our understanding of target antigens for vaccines and their correlates of protection, recent advances in immunological research, particularly in our understanding of innate immunity, have also had a major impact on adjuvant research. Bruno Guy reviews the practical applications of our increased understanding of the immune system in the design and development of more specific and focused adjuvants.
Developing efficient and safe adjuvants for use in human vaccines remains both a challenge and a necessity. Past approaches have been largely empirical and generally used a single type of adjuvant, such as aluminium salts or emulsions. However, new vaccine targets often require the induction of well-defined cell-mediated responses in addition to antibodies, and thus new immunostimulants are required. Recent advances in basic immunology have elucidated how early innate immune signals can shape subsequent adaptive responses and this, coupled with improvements in biochemical techniques, has led to the design and development of more specific and focused adjuvants. In this Review, I discuss the research that has made it possible for vaccinologists to now be able to choose between a large panel of adjuvants, which potentially can act synergistically, and combine them in formulations that are specifically adapted to each target and to the relevant correlate(s) of protection.</description><identifier>ISSN: 1740-1526</identifier><identifier>EISSN: 1740-1534</identifier><identifier>DOI: 10.1038/nrmicro1681</identifier><identifier>PMID: 17558426</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adaptive immunity ; Adjuvants, Immunologic - chemistry ; Adjuvants, Immunologic - pharmacology ; Adjuvants, Immunologic - therapeutic use ; Aluminum ; Animals ; Antibodies ; Antigens ; Biomedical and Life Sciences ; Cells ; Cytokines ; Cytotoxicity ; Drug Design ; Emulsions ; Humans ; Immunity, Cellular - drug effects ; Immunology ; Infectious Diseases ; Life Sciences ; Lymphocytes ; Medical Microbiology ; Medical research ; Mice ; Microbiology ; Parasitology ; Pathogens ; Receptors, Cell Surface - drug effects ; review-article ; Toll-Like Receptors - drug effects ; Vaccines ; Vaccines - immunology ; Virology</subject><ispartof>Nature reviews. Microbiology, 2007-07, Vol.5 (7), p.396-397</ispartof><rights>Springer Nature Limited 2007</rights><rights>Copyright Nature Publishing Group Jul 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-ec841ba577106e7800c252772cdbc2898bf2a40113a1d22722a876ec79a16cf13</citedby><cites>FETCH-LOGICAL-c351t-ec841ba577106e7800c252772cdbc2898bf2a40113a1d22722a876ec79a16cf13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrmicro1681$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrmicro1681$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17558426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guy, Bruno</creatorcontrib><title>The perfect mix: recent progress in adjuvant research</title><title>Nature reviews. Microbiology</title><addtitle>Nat Rev Microbiol</addtitle><addtitle>Nat Rev Microbiol</addtitle><description>Key Points
New vaccines are often less immunogenic than previous vaccines, and adjuvants are therefore required to assist in the induction of potent and persistent immune responses, to reduce the amount of antigen and limit the number of injections.
Some new vaccines also need adjuvants that are capable of inducing potent cell-mediated immunity in addition to an antibody response, such as T helper (T
H
) 1 responses and cytotoxic T lymphocyte (CTL) responses.
Recent advances in basic immunology have demonstrated the crucial role of some innate immune signals in modulating — both quantitatively and qualitatively — the subsequent adaptive response. Among these, some agonists of Toll-like receptors (TLRs) would in theory constitute promising adjuvants.
Vaccine research can take advantage of these discoveries to design and develop more focused and efficient adjuvants, such as new synthetic agonists of TLRs.
Moreover, new formulations can combine different immunostimulants, including TLR agonists and non-TLR 'classical' adjuvants. These compounds can act in synergy, and targeting them towards antigen-presenting cells could further increase and focus their action.
In parallel, new biochemical and immunological tools and assays have been developed to characterize and evaluate these new adjuvants, both
in vitro
and
in vivo
. The combination of information obtained in several assays, for example in animal models and human primary or transformed cells, can provide more accurate information on the potency and safety of these new adjuvants before use on humans.
Vaccine research scientists can now chose between a larger panel of compounds and technologies to design and develop the formulation that would drive the most efficient and safest response with respect to each considered pathogen, keeping in mind that each antigen–adjuvant couple is unique.
In addition to improving our understanding of target antigens for vaccines and their correlates of protection, recent advances in immunological research, particularly in our understanding of innate immunity, have also had a major impact on adjuvant research. Bruno Guy reviews the practical applications of our increased understanding of the immune system in the design and development of more specific and focused adjuvants.
Developing efficient and safe adjuvants for use in human vaccines remains both a challenge and a necessity. Past approaches have been largely empirical and generally used a single type of adjuvant, such as aluminium salts or emulsions. However, new vaccine targets often require the induction of well-defined cell-mediated responses in addition to antibodies, and thus new immunostimulants are required. Recent advances in basic immunology have elucidated how early innate immune signals can shape subsequent adaptive responses and this, coupled with improvements in biochemical techniques, has led to the design and development of more specific and focused adjuvants. In this Review, I discuss the research that has made it possible for vaccinologists to now be able to choose between a large panel of adjuvants, which potentially can act synergistically, and combine them in formulations that are specifically adapted to each target and to the relevant correlate(s) of protection.</description><subject>Adaptive immunity</subject><subject>Adjuvants, Immunologic - chemistry</subject><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Adjuvants, Immunologic - therapeutic use</subject><subject>Aluminum</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Biomedical and Life Sciences</subject><subject>Cells</subject><subject>Cytokines</subject><subject>Cytotoxicity</subject><subject>Drug Design</subject><subject>Emulsions</subject><subject>Humans</subject><subject>Immunity, Cellular - drug effects</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Life Sciences</subject><subject>Lymphocytes</subject><subject>Medical Microbiology</subject><subject>Medical research</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Parasitology</subject><subject>Pathogens</subject><subject>Receptors, Cell Surface - drug effects</subject><subject>review-article</subject><subject>Toll-Like Receptors - drug effects</subject><subject>Vaccines</subject><subject>Vaccines - immunology</subject><subject>Virology</subject><issn>1740-1526</issn><issn>1740-1534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkM1Lw0AQxRdRbK2evEvw4EWjO5PsR71J8QsKXuo5bDaTNqVJ6m4i-t-70mJFPM0w8-O9x2PsFPg18ETfNK6urGtBathjQ1Apj0Ek6f7PjnLAjrxfco5CKDxkA1BC6BTlkInZgqI1uZJsF9XVx23kyFLTRWvXzh15H1VNZIpl_27CMRzIOLs4ZgelWXk62c4Re324n02e4unL4_PkbhrbREAXk9Up5EYoBVyS0pxbFKgU2iK3qMc6L9GkHCAxUCAqRKOVJKvGBqQtIRmxi41uSPPWk--yuvKWVivTUNv7THEJcgw6gOd_wGXbuyZkyxBTKYIJD9DlBgptee-ozNauqo37zIBn31Vmv6oM9NlWss9rKnbstrsAXG0AH17NnNzO8z-9L31tfYA</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Guy, Bruno</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070701</creationdate><title>The perfect mix: recent progress in adjuvant research</title><author>Guy, Bruno</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-ec841ba577106e7800c252772cdbc2898bf2a40113a1d22722a876ec79a16cf13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adaptive immunity</topic><topic>Adjuvants, Immunologic - chemistry</topic><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Adjuvants, Immunologic - therapeutic use</topic><topic>Aluminum</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>Biomedical and Life Sciences</topic><topic>Cells</topic><topic>Cytokines</topic><topic>Cytotoxicity</topic><topic>Drug Design</topic><topic>Emulsions</topic><topic>Humans</topic><topic>Immunity, Cellular - drug effects</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Life Sciences</topic><topic>Lymphocytes</topic><topic>Medical Microbiology</topic><topic>Medical research</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Parasitology</topic><topic>Pathogens</topic><topic>Receptors, Cell Surface - drug effects</topic><topic>review-article</topic><topic>Toll-Like Receptors - drug effects</topic><topic>Vaccines</topic><topic>Vaccines - immunology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guy, Bruno</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guy, Bruno</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The perfect mix: recent progress in adjuvant research</atitle><jtitle>Nature reviews. Microbiology</jtitle><stitle>Nat Rev Microbiol</stitle><addtitle>Nat Rev Microbiol</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>5</volume><issue>7</issue><spage>396</spage><epage>397</epage><pages>396-397</pages><issn>1740-1526</issn><eissn>1740-1534</eissn><abstract>Key Points
New vaccines are often less immunogenic than previous vaccines, and adjuvants are therefore required to assist in the induction of potent and persistent immune responses, to reduce the amount of antigen and limit the number of injections.
Some new vaccines also need adjuvants that are capable of inducing potent cell-mediated immunity in addition to an antibody response, such as T helper (T
H
) 1 responses and cytotoxic T lymphocyte (CTL) responses.
Recent advances in basic immunology have demonstrated the crucial role of some innate immune signals in modulating — both quantitatively and qualitatively — the subsequent adaptive response. Among these, some agonists of Toll-like receptors (TLRs) would in theory constitute promising adjuvants.
Vaccine research can take advantage of these discoveries to design and develop more focused and efficient adjuvants, such as new synthetic agonists of TLRs.
Moreover, new formulations can combine different immunostimulants, including TLR agonists and non-TLR 'classical' adjuvants. These compounds can act in synergy, and targeting them towards antigen-presenting cells could further increase and focus their action.
In parallel, new biochemical and immunological tools and assays have been developed to characterize and evaluate these new adjuvants, both
in vitro
and
in vivo
. The combination of information obtained in several assays, for example in animal models and human primary or transformed cells, can provide more accurate information on the potency and safety of these new adjuvants before use on humans.
Vaccine research scientists can now chose between a larger panel of compounds and technologies to design and develop the formulation that would drive the most efficient and safest response with respect to each considered pathogen, keeping in mind that each antigen–adjuvant couple is unique.
In addition to improving our understanding of target antigens for vaccines and their correlates of protection, recent advances in immunological research, particularly in our understanding of innate immunity, have also had a major impact on adjuvant research. Bruno Guy reviews the practical applications of our increased understanding of the immune system in the design and development of more specific and focused adjuvants.
Developing efficient and safe adjuvants for use in human vaccines remains both a challenge and a necessity. Past approaches have been largely empirical and generally used a single type of adjuvant, such as aluminium salts or emulsions. However, new vaccine targets often require the induction of well-defined cell-mediated responses in addition to antibodies, and thus new immunostimulants are required. Recent advances in basic immunology have elucidated how early innate immune signals can shape subsequent adaptive responses and this, coupled with improvements in biochemical techniques, has led to the design and development of more specific and focused adjuvants. In this Review, I discuss the research that has made it possible for vaccinologists to now be able to choose between a large panel of adjuvants, which potentially can act synergistically, and combine them in formulations that are specifically adapted to each target and to the relevant correlate(s) of protection.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>17558426</pmid><doi>10.1038/nrmicro1681</doi><tpages>2</tpages></addata></record> |
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subjects | Adaptive immunity Adjuvants, Immunologic - chemistry Adjuvants, Immunologic - pharmacology Adjuvants, Immunologic - therapeutic use Aluminum Animals Antibodies Antigens Biomedical and Life Sciences Cells Cytokines Cytotoxicity Drug Design Emulsions Humans Immunity, Cellular - drug effects Immunology Infectious Diseases Life Sciences Lymphocytes Medical Microbiology Medical research Mice Microbiology Parasitology Pathogens Receptors, Cell Surface - drug effects review-article Toll-Like Receptors - drug effects Vaccines Vaccines - immunology Virology |
title | The perfect mix: recent progress in adjuvant research |
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