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The adjuvant effect of manganese on tuberculosis subunit vaccine Bfrb-GrpE
Protein subunit vaccines, lacking pathogen-associated molecular patterns that trigger immune responses, rely on adjuvants to induce robust immune responses against the target pathogen. Thus, selection of adjuvants plays a crucial role in the design of protein subunit vaccines. Recently, there has be...
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Published in: | npj vaccines 2024-12, Vol.9 (1), p.248 |
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creator | Zhou, Shuai Cao, Qianqian Zhang, Zunjing Du, Yunjie Hou, Yilin Zhang, Xiaojuan xie, Zhijun Zhou, Yuan Zhu, Bingdong Zhang, Ying Zhu, Aisong Niu, Hongxia |
description | Protein subunit vaccines, lacking pathogen-associated molecular patterns that trigger immune responses, rely on adjuvants to induce robust immune responses against the target pathogen. Thus, selection of adjuvants plays a crucial role in the design of protein subunit vaccines. Recently, there has been growing interest in utilizing cGAS-STING agonists as vaccine adjuvants. In this study, we investigated the adjuvant effect of manganese (Mn), a cGAS-STING agonist, on the tuberculosis subunit vaccine Bfrb-GrpE (BG) in a mouse model. Initially, mice were administered with BG-Mn(J), and its immunogenicity and protective efficacy were assessed six weeks after the final immunization. The results showed that Mn(J) enhanced both the cellular and humoral immune responses to the BG vaccine and conferred effective protection against
M. tuberculosis
H37Ra infection in mice, leading to a significant reduction of 2.0 ± 0.17 Log
10
CFU in spleens and 1.3 ± 0.17 Log
10
CFU in lungs compared to the PBS control group. Additionally, we assessed the BG-Mn(J) vaccine in a surrogate model of tuberculosis in rabbit skin model. The vaccination with BG-Mn(J) also provided effective protection in the rabbit model, as indicated by a decreased bacterial load at the infection site, minimal pathological damage, and accelerated healing. These findings suggest that Mn(J) holds promise as an adjuvant for tuberculosis vaccines, underscoring its potential to enhance vaccine efficacy and offer protection against tuberculosis infection. |
doi_str_mv | 10.1038/s41541-024-01049-x |
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M. tuberculosis
H37Ra infection in mice, leading to a significant reduction of 2.0 ± 0.17 Log
10
CFU in spleens and 1.3 ± 0.17 Log
10
CFU in lungs compared to the PBS control group. Additionally, we assessed the BG-Mn(J) vaccine in a surrogate model of tuberculosis in rabbit skin model. The vaccination with BG-Mn(J) also provided effective protection in the rabbit model, as indicated by a decreased bacterial load at the infection site, minimal pathological damage, and accelerated healing. These findings suggest that Mn(J) holds promise as an adjuvant for tuberculosis vaccines, underscoring its potential to enhance vaccine efficacy and offer protection against tuberculosis infection.</description><identifier>ISSN: 2059-0105</identifier><identifier>EISSN: 2059-0105</identifier><identifier>DOI: 10.1038/s41541-024-01049-x</identifier><identifier>PMID: 39702587</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/590 ; 631/326/590 ; Adjuvants ; Biomedical and Life Sciences ; Biomedicine ; Immunization ; Immunogenicity ; Infections ; Infectious Diseases ; Manganese ; Medical Microbiology ; Pathogens ; Public Health ; Tuberculosis ; Vaccine ; Vaccines ; Virology</subject><ispartof>npj vaccines, 2024-12, Vol.9 (1), p.248</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>Copyright Nature Publishing Group 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3147278994?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,38516,43895,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39702587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Shuai</creatorcontrib><creatorcontrib>Cao, Qianqian</creatorcontrib><creatorcontrib>Zhang, Zunjing</creatorcontrib><creatorcontrib>Du, Yunjie</creatorcontrib><creatorcontrib>Hou, Yilin</creatorcontrib><creatorcontrib>Zhang, Xiaojuan</creatorcontrib><creatorcontrib>xie, Zhijun</creatorcontrib><creatorcontrib>Zhou, Yuan</creatorcontrib><creatorcontrib>Zhu, Bingdong</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Zhu, Aisong</creatorcontrib><creatorcontrib>Niu, Hongxia</creatorcontrib><title>The adjuvant effect of manganese on tuberculosis subunit vaccine Bfrb-GrpE</title><title>npj vaccines</title><addtitle>npj Vaccines</addtitle><addtitle>NPJ Vaccines</addtitle><description>Protein subunit vaccines, lacking pathogen-associated molecular patterns that trigger immune responses, rely on adjuvants to induce robust immune responses against the target pathogen. Thus, selection of adjuvants plays a crucial role in the design of protein subunit vaccines. Recently, there has been growing interest in utilizing cGAS-STING agonists as vaccine adjuvants. In this study, we investigated the adjuvant effect of manganese (Mn), a cGAS-STING agonist, on the tuberculosis subunit vaccine Bfrb-GrpE (BG) in a mouse model. Initially, mice were administered with BG-Mn(J), and its immunogenicity and protective efficacy were assessed six weeks after the final immunization. The results showed that Mn(J) enhanced both the cellular and humoral immune responses to the BG vaccine and conferred effective protection against
M. tuberculosis
H37Ra infection in mice, leading to a significant reduction of 2.0 ± 0.17 Log
10
CFU in spleens and 1.3 ± 0.17 Log
10
CFU in lungs compared to the PBS control group. Additionally, we assessed the BG-Mn(J) vaccine in a surrogate model of tuberculosis in rabbit skin model. The vaccination with BG-Mn(J) also provided effective protection in the rabbit model, as indicated by a decreased bacterial load at the infection site, minimal pathological damage, and accelerated healing. These findings suggest that Mn(J) holds promise as an adjuvant for tuberculosis vaccines, underscoring its potential to enhance vaccine efficacy and offer protection against tuberculosis infection.</description><subject>631/250/590</subject><subject>631/326/590</subject><subject>Adjuvants</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Infections</subject><subject>Infectious Diseases</subject><subject>Manganese</subject><subject>Medical Microbiology</subject><subject>Pathogens</subject><subject>Public Health</subject><subject>Tuberculosis</subject><subject>Vaccine</subject><subject>Vaccines</subject><subject>Virology</subject><issn>2059-0105</issn><issn>2059-0105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><recordid>eNpdkUtLAzEUhYMottT-ARcScONmNK9JJkuVWpWCm7oOmUymTpmXyaTUf2_6EMXVvZf73cPhHgAuMbrFiGZ3nuGU4QQRliCMmEy2J2BMUCp3Y3r6px-BqfdrhBAWnKYCnYMRlQKRNBNj8Lr8sFAX67DR7QBtWVozwK6EjW5XurXewq6FQ8itM6HufOWhD3loqwFutDFVa-FD6fJk7vrZBTgrde3t9Fgn4P1ptnx8ThZv85fH-0XSY5JtkxTLnAtOuM0zrRHKJcYE4wIzyRjLhUGSSsaRMSUvqBBMMM55RoTUJrOM0wm4Oej2rvsM1g-qqbyxdR39dsEriuNJFrVYRK__oesuuDa621NEZFLuqKsjFfLGFqp3VaPdl_r5UgToAfBx1a6s-5XBSO3iUIc4VIxD7eNQW_oNmU14Bw</recordid><startdate>20241219</startdate><enddate>20241219</enddate><creator>Zhou, Shuai</creator><creator>Cao, Qianqian</creator><creator>Zhang, Zunjing</creator><creator>Du, Yunjie</creator><creator>Hou, Yilin</creator><creator>Zhang, Xiaojuan</creator><creator>xie, Zhijun</creator><creator>Zhou, Yuan</creator><creator>Zhu, Bingdong</creator><creator>Zhang, Ying</creator><creator>Zhu, Aisong</creator><creator>Niu, Hongxia</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20241219</creationdate><title>The adjuvant effect of manganese on tuberculosis subunit vaccine Bfrb-GrpE</title><author>Zhou, Shuai ; 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Thus, selection of adjuvants plays a crucial role in the design of protein subunit vaccines. Recently, there has been growing interest in utilizing cGAS-STING agonists as vaccine adjuvants. In this study, we investigated the adjuvant effect of manganese (Mn), a cGAS-STING agonist, on the tuberculosis subunit vaccine Bfrb-GrpE (BG) in a mouse model. Initially, mice were administered with BG-Mn(J), and its immunogenicity and protective efficacy were assessed six weeks after the final immunization. The results showed that Mn(J) enhanced both the cellular and humoral immune responses to the BG vaccine and conferred effective protection against
M. tuberculosis
H37Ra infection in mice, leading to a significant reduction of 2.0 ± 0.17 Log
10
CFU in spleens and 1.3 ± 0.17 Log
10
CFU in lungs compared to the PBS control group. Additionally, we assessed the BG-Mn(J) vaccine in a surrogate model of tuberculosis in rabbit skin model. The vaccination with BG-Mn(J) also provided effective protection in the rabbit model, as indicated by a decreased bacterial load at the infection site, minimal pathological damage, and accelerated healing. These findings suggest that Mn(J) holds promise as an adjuvant for tuberculosis vaccines, underscoring its potential to enhance vaccine efficacy and offer protection against tuberculosis infection.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>39702587</pmid><doi>10.1038/s41541-024-01049-x</doi><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/590 631/326/590 Adjuvants Biomedical and Life Sciences Biomedicine Immunization Immunogenicity Infections Infectious Diseases Manganese Medical Microbiology Pathogens Public Health Tuberculosis Vaccine Vaccines Virology |
title | The adjuvant effect of manganese on tuberculosis subunit vaccine Bfrb-GrpE |
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