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Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii
BACKGROUND: Pneumocystis pneumonia (PcP), which is caused by Pneumocystis carinii, is a life-threatening infection that affects immunocompromised individuals. Unfortunately, chemoprophylaxis and dapsone are only effective for half of the patients with PcP, indicating that additional preventive metho...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236001/ https://www.ncbi.nlm.nih.gov/pubmed/34174820 http://dx.doi.org/10.1186/s12865-021-00436-6 |
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author | Tong, Tong Wang, Zhongxin Xu, Yuanhong Shen, Jilu |
author_facet | Tong, Tong Wang, Zhongxin Xu, Yuanhong Shen, Jilu |
author_sort | Tong, Tong |
collection | PubMed |
description | BACKGROUND: Pneumocystis pneumonia (PcP), which is caused by Pneumocystis carinii, is a life-threatening infection that affects immunocompromised individuals. Unfortunately, chemoprophylaxis and dapsone are only effective for half of the patients with PcP, indicating that additional preventive methods are needed. We predicated the pneumocystis surface protein A12 sequence 1–85 by DNAStar software and BepiPred, and identified it as a potential vaccine candidate by bioresearch. METHODS: We used recombinant A12(1–85) as antigen to immunized mice and detected serum titer of IgG, expression of inflammatory factors by EILSA, qRT-PCR and flow cytometry. RESULTS: Our results showed that immunization with recombinant A12(1–85) increased the serum titer of IgG, promoted the secretion of T lymphocytes, increased the expression of inflammatory factors, and elevated lung inflammatory injury in mice. CONCLUSIONS: Our findings suggest that A12(1–85) is a potential vaccine target for preventing Pneumocystis carinii. The evaluation of A12(1–85)-elicited antibodies in the prevention of PcP in humans deserves further investigation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12865-021-00436-6. |
format | Online Article Text |
id | pubmed-8236001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82360012021-06-28 Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii Tong, Tong Wang, Zhongxin Xu, Yuanhong Shen, Jilu BMC Immunol Research BACKGROUND: Pneumocystis pneumonia (PcP), which is caused by Pneumocystis carinii, is a life-threatening infection that affects immunocompromised individuals. Unfortunately, chemoprophylaxis and dapsone are only effective for half of the patients with PcP, indicating that additional preventive methods are needed. We predicated the pneumocystis surface protein A12 sequence 1–85 by DNAStar software and BepiPred, and identified it as a potential vaccine candidate by bioresearch. METHODS: We used recombinant A12(1–85) as antigen to immunized mice and detected serum titer of IgG, expression of inflammatory factors by EILSA, qRT-PCR and flow cytometry. RESULTS: Our results showed that immunization with recombinant A12(1–85) increased the serum titer of IgG, promoted the secretion of T lymphocytes, increased the expression of inflammatory factors, and elevated lung inflammatory injury in mice. CONCLUSIONS: Our findings suggest that A12(1–85) is a potential vaccine target for preventing Pneumocystis carinii. The evaluation of A12(1–85)-elicited antibodies in the prevention of PcP in humans deserves further investigation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12865-021-00436-6. BioMed Central 2021-06-27 /pmc/articles/PMC8236001/ /pubmed/34174820 http://dx.doi.org/10.1186/s12865-021-00436-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Tong, Tong Wang, Zhongxin Xu, Yuanhong Shen, Jilu Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title | Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title_full | Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title_fullStr | Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title_full_unstemmed | Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title_short | Immunization with Pneumocystis carinii A12(1–85) antigen activates immune function against P. carinii |
title_sort | immunization with pneumocystis carinii a12(1–85) antigen activates immune function against p. carinii |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236001/ https://www.ncbi.nlm.nih.gov/pubmed/34174820 http://dx.doi.org/10.1186/s12865-021-00436-6 |
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