A preliminary study on the application of PspA as a carrier for group A meningococcal polysaccharide

This study aimed to explore the feasibility of pneumococcal surface protein A (PspA) as a carrier protein. Three recombinant pneumococcal surface proteins from three different clades were expressed by the prokaryotic expression system and conjugated to group A meningococcal polysaccharide (GAMP) to...

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Veröffentlicht in:PloS one 2019-07, Vol.14 (7), p.e0218427-e0218427
Hauptverfasser: Wang, Lichan, Tan, Yajun, Wei, Chen, Zhang, Huajie, Luo, Peng, Zhang, Shumin, Ma, Xiao
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Tan, Yajun
Wei, Chen
Zhang, Huajie
Luo, Peng
Zhang, Shumin
Ma, Xiao
description This study aimed to explore the feasibility of pneumococcal surface protein A (PspA) as a carrier protein. Three recombinant pneumococcal surface proteins from three different clades were expressed by the prokaryotic expression system and conjugated to group A meningococcal polysaccharide (GAMP) to generate three polysaccharide-protein conjugates. The conjugates, unconjugated proteins, GAMP, and GAMP-TT vaccine bulk (used as positive control) were immunized into mice, and their immune effects were assessed by the methods of enzyme-linked immunosorbent assay (ELISA), flow cytometry (FCM), and serum bactericidal assay (SBA). The results showed that the polysaccharide-protein conjugates could produce higher levels of anti-GAMP IgG titers (P < 0.05), higher ratios of Th1/Th2 (P < 0.05), and higher levels of serum bactericidal activity (P < 0.05), compared with the unconjugated GAMP. The conjugation of PspAs to GAMP also enhanced the anti-PspA responses compared with unconjugated PspAs except for PspA3. In conclusion, the results indicated that the three PspAs were appropriate carrier proteins, as demonstrated by the characteristics of T-cell dependent responses to the GAMP, and might protect against group A of epidemic cerebrospinal meningitis.
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Three recombinant pneumococcal surface proteins from three different clades were expressed by the prokaryotic expression system and conjugated to group A meningococcal polysaccharide (GAMP) to generate three polysaccharide-protein conjugates. The conjugates, unconjugated proteins, GAMP, and GAMP-TT vaccine bulk (used as positive control) were immunized into mice, and their immune effects were assessed by the methods of enzyme-linked immunosorbent assay (ELISA), flow cytometry (FCM), and serum bactericidal assay (SBA). The results showed that the polysaccharide-protein conjugates could produce higher levels of anti-GAMP IgG titers (P &lt; 0.05), higher ratios of Th1/Th2 (P &lt; 0.05), and higher levels of serum bactericidal activity (P &lt; 0.05), compared with the unconjugated GAMP. The conjugation of PspAs to GAMP also enhanced the anti-PspA responses compared with unconjugated PspAs except for PspA3. 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Three recombinant pneumococcal surface proteins from three different clades were expressed by the prokaryotic expression system and conjugated to group A meningococcal polysaccharide (GAMP) to generate three polysaccharide-protein conjugates. The conjugates, unconjugated proteins, GAMP, and GAMP-TT vaccine bulk (used as positive control) were immunized into mice, and their immune effects were assessed by the methods of enzyme-linked immunosorbent assay (ELISA), flow cytometry (FCM), and serum bactericidal assay (SBA). The results showed that the polysaccharide-protein conjugates could produce higher levels of anti-GAMP IgG titers (P &lt; 0.05), higher ratios of Th1/Th2 (P &lt; 0.05), and higher levels of serum bactericidal activity (P &lt; 0.05), compared with the unconjugated GAMP. The conjugation of PspAs to GAMP also enhanced the anti-PspA responses compared with unconjugated PspAs except for PspA3. 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Tan, Yajun ; Wei, Chen ; Zhang, Huajie ; Luo, Peng ; Zhang, Shumin ; Ma, Xiao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c641t-ffdf1a9807d50f1e04260ab499fa0e5a0c29c67337de06bbc33f77939505f5813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antigens</topic><topic>Bacterial proteins</topic><topic>Bacterial Proteins - immunology</topic><topic>Bacterial Proteins - pharmacology</topic><topic>Bactericidal activity</topic><topic>Biology and Life Sciences</topic><topic>Conjugates</topic><topic>Conjugation</topic><topic>Diphtheria</topic><topic>Diphtheria toxoid</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Enzymes</topic><topic>Epidemics</topic><topic>Feasibility studies</topic><topic>Female</topic><topic>Flow cytometry</topic><topic>Food</topic><topic>Genetic aspects</topic><topic>Immunity (Disease)</topic><topic>Immunization</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin G - immunology</topic><topic>Immunoglobulins</topic><topic>Laboratories</topic><topic>Lymphocytes T</topic><topic>Medical immunity</topic><topic>Medicine and Health Sciences</topic><topic>Meningitis</topic><topic>Meningococcal Infections - immunology</topic><topic>Meningococcal Infections - prevention &amp; 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Three recombinant pneumococcal surface proteins from three different clades were expressed by the prokaryotic expression system and conjugated to group A meningococcal polysaccharide (GAMP) to generate three polysaccharide-protein conjugates. The conjugates, unconjugated proteins, GAMP, and GAMP-TT vaccine bulk (used as positive control) were immunized into mice, and their immune effects were assessed by the methods of enzyme-linked immunosorbent assay (ELISA), flow cytometry (FCM), and serum bactericidal assay (SBA). The results showed that the polysaccharide-protein conjugates could produce higher levels of anti-GAMP IgG titers (P &lt; 0.05), higher ratios of Th1/Th2 (P &lt; 0.05), and higher levels of serum bactericidal activity (P &lt; 0.05), compared with the unconjugated GAMP. The conjugation of PspAs to GAMP also enhanced the anti-PspA responses compared with unconjugated PspAs except for PspA3. In conclusion, the results indicated that the three PspAs were appropriate carrier proteins, as demonstrated by the characteristics of T-cell dependent responses to the GAMP, and might protect against group A of epidemic cerebrospinal meningitis.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31291272</pmid><doi>10.1371/journal.pone.0218427</doi><tpages>e0218427</tpages><orcidid>https://orcid.org/0000-0002-5078-6393</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Antibodies, Bacterial - immunology
Antigens
Bacterial proteins
Bacterial Proteins - immunology
Bacterial Proteins - pharmacology
Bactericidal activity
Biology and Life Sciences
Conjugates
Conjugation
Diphtheria
Diphtheria toxoid
Enzyme-linked immunosorbent assay
Enzymes
Epidemics
Feasibility studies
Female
Flow cytometry
Food
Genetic aspects
Immunity (Disease)
Immunization
Immunoglobulin G
Immunoglobulin G - immunology
Immunoglobulins
Laboratories
Lymphocytes T
Medical immunity
Medicine and Health Sciences
Meningitis
Meningococcal Infections - immunology
Meningococcal Infections - prevention & control
Meningococcal Vaccines - immunology
Meningococcal Vaccines - pharmacology
Mice
Mice, Inbred BALB C
Neisseria meningitidis - immunology
Physiological aspects
Polysaccharides
Polysaccharides, Bacterial - immunology
Polysaccharides, Bacterial - pharmacology
Preliminary Data
Prevention
Properties
Protein A
Proteins
PspA protein
Quality
Research and Analysis Methods
Salmonella
Serum bactericidal activity
Streptococcus infections
Surface protein A
T cells
Tetanus
Tetanus toxoid
Toxins
Transport proteins
Typhoid
Vaccines
Vaccines, Conjugate - immunology
Vaccines, Conjugate - pharmacology
title A preliminary study on the application of PspA as a carrier for group A meningococcal polysaccharide
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T13%3A39%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20preliminary%20study%20on%20the%20application%20of%20PspA%20as%20a%20carrier%20for%20group%20A%20meningococcal%20polysaccharide&rft.jtitle=PloS%20one&rft.au=Wang,%20Lichan&rft.date=2019-07-10&rft.volume=14&rft.issue=7&rft.spage=e0218427&rft.epage=e0218427&rft.pages=e0218427-e0218427&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0218427&rft_dat=%3Cgale_plos_%3EA592865312%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2256214705&rft_id=info:pmid/31291272&rft_galeid=A592865312&rft_doaj_id=oai_doaj_org_article_782b734ab6664ced903f7e191301b9c6&rfr_iscdi=true