Saponin adjuvant enhancement of antigen-specific immune responses to an experimental HIV-1 vaccine

The adjuvant activity of a single highly purified saponin from the soap bark tree Quillaja saponaria was evaluated by using it as a component in an experimental vaccine containing rHIV-1 envelope protein (HIV-1 160D) adsorbed to alum. BALB/c mice immunized with experimental vaccine formulations cont...

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Veröffentlicht in:The Journal of immunology (1950) 1992-03, Vol.148 (5), p.1519-1525
Hauptverfasser: Wu, JY, Gardner, BH, Murphy, CI, Seals, JR, Kensil, CR, Recchia, J, Beltz, GA, Newman, GW, Newman, MJ
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container_end_page 1525
container_issue 5
container_start_page 1519
container_title The Journal of immunology (1950)
container_volume 148
creator Wu, JY
Gardner, BH
Murphy, CI
Seals, JR
Kensil, CR
Recchia, J
Beltz, GA
Newman, GW
Newman, MJ
description The adjuvant activity of a single highly purified saponin from the soap bark tree Quillaja saponaria was evaluated by using it as a component in an experimental vaccine containing rHIV-1 envelope protein (HIV-1 160D) adsorbed to alum. BALB/c mice immunized with experimental vaccine formulations containing the saponin adjuvant QS-21 produced significantly higher titers of antibodies than mice vaccinated with only the alum-adsorbed HIV-1 160D. Potent amnestic antibody responses to HIV-1 viral proteins were also induced. Ag-specific proliferative responses to recombinant proteins and to three variants of HIV-1 were significantly increased using QS-21 as an adjuvant. Alum-adsorbed HIV-1 160D failed to induce measurable proliferative responses to inactivated HIV-1 viruses, but group-specific proliferative responses were raised when the QS-21 adjuvant was used in the vaccine formulation. MHC class I restricted CTL specific for the immunodominant V-3 loop were induced but only when the QS-21 adjuvant was included in the vaccine formulation. The production of serine esterase by Ag-activated splenic mononuclear cells, indicating the maturation of precursor CTL, was used as a secondary measure of CTL activity, and this response was also increased. The specificity of antibody responses was not significantly broadened using QS-21; the adjuvant increased the immune recognition of epitopes throughout the HIV-1 glycoprotein 160. However, the specificity of the proliferation and serine esterase responses was broadened, suggesting that the QS-21 augmented cell-mediated immune responses specific for epitopes outside of the V-3 loop. Additionally, the QS-21 adjuvant appeared to induce recognition of weakly immunogenic epitopes that were not recognized using only alum-adsorbed HIV-1 160D. The ability of QS-21 to augment both antibody and cell-mediated immune responses suggests that this adjuvant could be a valuable component in subunit vaccines.
doi_str_mv 10.4049/jimmunol.148.5.1519
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BALB/c mice immunized with experimental vaccine formulations containing the saponin adjuvant QS-21 produced significantly higher titers of antibodies than mice vaccinated with only the alum-adsorbed HIV-1 160D. Potent amnestic antibody responses to HIV-1 viral proteins were also induced. Ag-specific proliferative responses to recombinant proteins and to three variants of HIV-1 were significantly increased using QS-21 as an adjuvant. Alum-adsorbed HIV-1 160D failed to induce measurable proliferative responses to inactivated HIV-1 viruses, but group-specific proliferative responses were raised when the QS-21 adjuvant was used in the vaccine formulation. MHC class I restricted CTL specific for the immunodominant V-3 loop were induced but only when the QS-21 adjuvant was included in the vaccine formulation. The production of serine esterase by Ag-activated splenic mononuclear cells, indicating the maturation of precursor CTL, was used as a secondary measure of CTL activity, and this response was also increased. The specificity of antibody responses was not significantly broadened using QS-21; the adjuvant increased the immune recognition of epitopes throughout the HIV-1 glycoprotein 160. However, the specificity of the proliferation and serine esterase responses was broadened, suggesting that the QS-21 augmented cell-mediated immune responses specific for epitopes outside of the V-3 loop. Additionally, the QS-21 adjuvant appeared to induce recognition of weakly immunogenic epitopes that were not recognized using only alum-adsorbed HIV-1 160D. 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The production of serine esterase by Ag-activated splenic mononuclear cells, indicating the maturation of precursor CTL, was used as a secondary measure of CTL activity, and this response was also increased. The specificity of antibody responses was not significantly broadened using QS-21; the adjuvant increased the immune recognition of epitopes throughout the HIV-1 glycoprotein 160. However, the specificity of the proliferation and serine esterase responses was broadened, suggesting that the QS-21 augmented cell-mediated immune responses specific for epitopes outside of the V-3 loop. Additionally, the QS-21 adjuvant appeared to induce recognition of weakly immunogenic epitopes that were not recognized using only alum-adsorbed HIV-1 160D. 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Psychology</subject><subject>Gene Products, env - immunology</subject><subject>HIV Antibodies - analysis</subject><subject>HIV Envelope Protein gp160</subject><subject>HIV-1 - immunology</subject><subject>human immunodeficiency virus 1</subject><subject>Lymphocyte Activation</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Protein Precursors - immunology</subject><subject>Saponins - pharmacology</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</subject><subject>Vaccines, Synthetic - immunology</subject><subject>Virology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctO3DAUhq0KBAPtE1RIXqCyytSOL3GWFSoXCYkFtFvL4xwzHiVOGk-Y8vY90xladqx85PP95_YT8pmzuWSy_rqKXTelvp1zaeZqzhWvP5AZV4oVWjN9QGaMlWXBK10dk5OcV4wxzUp5RI64EoYLOSOLBzf0KSbqmtX07NKaQlq65KEDjPtA8Ss-QSryAD6G6OnfpkBHyCjMkOm6R4jC7wHGuFW5lt7c_iw4fXbexwQfyWFwbYZP-_eU_Lj6_nh5U9zdX99efrsrvGJiXWgedO2cLIPwoVkoaHBaJbSCSuE6BkcWxviyNswwr2pfNc432qvgVSWdEKfky67uMPa_Jshr28XsoW1dgn7KtioNN1xW74Jcl1ziAREUO9CPfc4jBDvgim58sZzZrQX21QKLFlhltxag6mxfflp00PzX7G6O-fN93mXv2jDiuWP-hyk0sFYlYhc7bBmflps4gs2da1ssyu1ms3nT8A-98Z7q</recordid><startdate>19920301</startdate><enddate>19920301</enddate><creator>Wu, JY</creator><creator>Gardner, BH</creator><creator>Murphy, CI</creator><creator>Seals, JR</creator><creator>Kensil, CR</creator><creator>Recchia, J</creator><creator>Beltz, GA</creator><creator>Newman, GW</creator><creator>Newman, MJ</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19920301</creationdate><title>Saponin adjuvant enhancement of antigen-specific immune responses to an experimental HIV-1 vaccine</title><author>Wu, JY ; Gardner, BH ; Murphy, CI ; Seals, JR ; Kensil, CR ; Recchia, J ; Beltz, GA ; Newman, GW ; Newman, MJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-61f69aa42f3cfdb5ed0065365e756608153388c298080c59c7dacd6c5fc574a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adjuvants, Immunologic - pharmacology</topic><topic>AIDS Vaccines - immunology</topic><topic>AIDS/HIV</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Esterases - biosynthesis</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Products, env - immunology</topic><topic>HIV Antibodies - analysis</topic><topic>HIV Envelope Protein gp160</topic><topic>HIV-1 - immunology</topic><topic>human immunodeficiency virus 1</topic><topic>Lymphocyte Activation</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Protein Precursors - immunology</topic><topic>Saponins - pharmacology</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</topic><topic>Vaccines, Synthetic - immunology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, JY</creatorcontrib><creatorcontrib>Gardner, BH</creatorcontrib><creatorcontrib>Murphy, CI</creatorcontrib><creatorcontrib>Seals, JR</creatorcontrib><creatorcontrib>Kensil, CR</creatorcontrib><creatorcontrib>Recchia, J</creatorcontrib><creatorcontrib>Beltz, GA</creatorcontrib><creatorcontrib>Newman, GW</creatorcontrib><creatorcontrib>Newman, MJ</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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, JY</au><au>Gardner, BH</au><au>Murphy, CI</au><au>Seals, JR</au><au>Kensil, CR</au><au>Recchia, J</au><au>Beltz, GA</au><au>Newman, GW</au><au>Newman, MJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Saponin adjuvant enhancement of antigen-specific immune responses to an experimental HIV-1 vaccine</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1992-03-01</date><risdate>1992</risdate><volume>148</volume><issue>5</issue><spage>1519</spage><epage>1525</epage><pages>1519-1525</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>The adjuvant activity of a single highly purified saponin from the soap bark tree Quillaja saponaria was evaluated by using it as a component in an experimental vaccine containing rHIV-1 envelope protein (HIV-1 160D) adsorbed to alum. 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The production of serine esterase by Ag-activated splenic mononuclear cells, indicating the maturation of precursor CTL, was used as a secondary measure of CTL activity, and this response was also increased. The specificity of antibody responses was not significantly broadened using QS-21; the adjuvant increased the immune recognition of epitopes throughout the HIV-1 glycoprotein 160. However, the specificity of the proliferation and serine esterase responses was broadened, suggesting that the QS-21 augmented cell-mediated immune responses specific for epitopes outside of the V-3 loop. Additionally, the QS-21 adjuvant appeared to induce recognition of weakly immunogenic epitopes that were not recognized using only alum-adsorbed HIV-1 160D. The ability of QS-21 to augment both antibody and cell-mediated immune responses suggests that this adjuvant could be a valuable component in subunit vaccines.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>1538134</pmid><doi>10.4049/jimmunol.148.5.1519</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adjuvants, Immunologic - pharmacology
AIDS Vaccines - immunology
AIDS/HIV
Animals
Biological and medical sciences
Esterases - biosynthesis
Female
Fundamental and applied biological sciences. Psychology
Gene Products, env - immunology
HIV Antibodies - analysis
HIV Envelope Protein gp160
HIV-1 - immunology
human immunodeficiency virus 1
Lymphocyte Activation
Mice
Mice, Inbred BALB C
Microbiology
Protein Precursors - immunology
Saponins - pharmacology
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Vaccines, Synthetic - immunology
Virology
title Saponin adjuvant enhancement of antigen-specific immune responses to an experimental HIV-1 vaccine
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