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- Publisher Website: 10.1093/infdis/jix290
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- PMID: 28633319
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Article: Immunotherapy Targeting Adenosine Synthase A Decreases Severity of Staphylococcus aureus Infection in Mouse Model
Title | Immunotherapy Targeting Adenosine Synthase A Decreases Severity of Staphylococcus aureus Infection in Mouse Model |
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Authors | |
Keywords | AdsA S. aureus Adenosine synthase A Immunotherapy |
Issue Date | 2017 |
Publisher | Oxford University Press. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/jid/ |
Citation | Journal of Infectious Diseases, 2017, v. 216, p. 245-253 How to Cite? |
Abstract | Staphylococcusaureus is a severe pathogen found in the community and in hospitals. Most notably, methicillin-resistant S. aureus (MRSA) is resistant to almost all antibiotics, which is a growing public health concern. The emergence of drug-resistant strains has prompted the search for alternative treatments such as immunotherapeutic approaches. Previous research showed that S. aureus exploit the immunomodulatory attributes of adenosine to escape host immunity. In this study, we investigated adenosine synthase A (AdsA), an S. aureus cell wall-anchored enzyme as possible targets for immunotherapy. Mice vaccinated with aluminum hydroxide-formulated recombinant AdsA (rAdsA) induced high-titer anti-AdsA antibodies, thereby providing consistent protection in 3 mouse infection models when challenged with 2 S. aureus strains. The importance of anti-AdsA antibody in protection was demonstrated by passive transfer experiments. Moreover, AdsA-specific antisera promote killing S. aureus by immune cells. Altogether, our data demonstrate that the AdsA is a promising target for vaccines and therapeutics development to alleviate severe S. aureus diseases. |
Persistent Identifier | http://hdl.handle.net/10722/246929 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 2.387 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhang, B | - |
dc.contributor.author | Cai, J | - |
dc.contributor.author | Yu, B | - |
dc.contributor.author | Xiong, L | - |
dc.contributor.author | Lin, Q | - |
dc.contributor.author | Yang, X | - |
dc.contributor.author | Xu, C | - |
dc.contributor.author | Zheng, S | - |
dc.contributor.author | Kao, RYT | - |
dc.contributor.author | Sze, KH | - |
dc.contributor.author | Yuen, KY | - |
dc.contributor.author | Huang, J | - |
dc.date.accessioned | 2017-10-18T08:19:32Z | - |
dc.date.available | 2017-10-18T08:19:32Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Journal of Infectious Diseases, 2017, v. 216, p. 245-253 | - |
dc.identifier.issn | 0022-1899 | - |
dc.identifier.uri | http://hdl.handle.net/10722/246929 | - |
dc.description.abstract | Staphylococcusaureus is a severe pathogen found in the community and in hospitals. Most notably, methicillin-resistant S. aureus (MRSA) is resistant to almost all antibiotics, which is a growing public health concern. The emergence of drug-resistant strains has prompted the search for alternative treatments such as immunotherapeutic approaches. Previous research showed that S. aureus exploit the immunomodulatory attributes of adenosine to escape host immunity. In this study, we investigated adenosine synthase A (AdsA), an S. aureus cell wall-anchored enzyme as possible targets for immunotherapy. Mice vaccinated with aluminum hydroxide-formulated recombinant AdsA (rAdsA) induced high-titer anti-AdsA antibodies, thereby providing consistent protection in 3 mouse infection models when challenged with 2 S. aureus strains. The importance of anti-AdsA antibody in protection was demonstrated by passive transfer experiments. Moreover, AdsA-specific antisera promote killing S. aureus by immune cells. Altogether, our data demonstrate that the AdsA is a promising target for vaccines and therapeutics development to alleviate severe S. aureus diseases. | - |
dc.language | eng | - |
dc.publisher | Oxford University Press. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/jid/ | - |
dc.relation.ispartof | Journal of Infectious Diseases | - |
dc.rights | Pre-print: Journal Title] ©: [year] [owner as specified on the article] Published by Oxford University Press [on behalf of xxxxxx]. All rights reserved. Pre-print (Once an article is published, preprint notice should be amended to): This is an electronic version of an article published in [include the complete citation information for the final version of the Article as published in the print edition of the Journal.] Post-print: This is a pre-copy-editing, author-produced PDF of an article accepted for publication in [insert journal title] following peer review. The definitive publisher-authenticated version [insert complete citation information here] is available online at: xxxxxxx [insert URL that the author will receive upon publication here]. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | AdsA | - |
dc.subject | S. aureus | - |
dc.subject | Adenosine synthase A | - |
dc.subject | Immunotherapy | - |
dc.title | Immunotherapy Targeting Adenosine Synthase A Decreases Severity of Staphylococcus aureus Infection in Mouse Model | - |
dc.type | Article | - |
dc.identifier.email | Cai, J: caijuice@hku.hk | - |
dc.identifier.email | Yu, B: ppayubin@hku.hk | - |
dc.identifier.email | Xiong, L: lfxiong@hku.hk | - |
dc.identifier.email | Lin, Q: qiubin@hku.hk | - |
dc.identifier.email | Kao, RYT: rytkao@hkucc.hku.hk | - |
dc.identifier.email | Sze, KH: khsze@hku.hk | - |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | - |
dc.identifier.email | Huang, J: jdhuang@hku.hk | - |
dc.identifier.authority | Kao, RYT=rp00481 | - |
dc.identifier.authority | Sze, KH=rp00785 | - |
dc.identifier.authority | Yuen, KY=rp00366 | - |
dc.identifier.authority | Huang, J=rp00451 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1093/infdis/jix290 | - |
dc.identifier.pmid | 28633319 | - |
dc.identifier.pmcid | PMC5853884 | - |
dc.identifier.scopus | eid_2-s2.0-85028373339 | - |
dc.identifier.hkuros | 280028 | - |
dc.identifier.hkuros | 293486 | - |
dc.identifier.volume | 216 | - |
dc.identifier.spage | 245 | - |
dc.identifier.epage | 253 | - |
dc.identifier.isi | WOS:000406832000014 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0022-1899 | - |