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Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype

Aluminum hydroxide (alum) is the most widely used adjuvant in human vaccines. Nevertheless, it is virtually unknown whether alum acts on B cells. In the present study, we explored the direct effect of alum on Ig expression by murine B cells in vitro. LPS-activated mouse spleen B cells were cultured...

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Autores principales: Jin, Bo-Ra, Kim, Sun-Jin, Lee, Jeong-Min, Kang, Seong-Ho, Han, Hye-Ju, Jang, Young-Saeng, Seo, Goo-young, Kim, Pyeung-Hyeun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607705/
https://www.ncbi.nlm.nih.gov/pubmed/23559895
http://dx.doi.org/10.4110/in.2013.13.1.10
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author Jin, Bo-Ra
Kim, Sun-Jin
Lee, Jeong-Min
Kang, Seong-Ho
Han, Hye-Ju
Jang, Young-Saeng
Seo, Goo-young
Kim, Pyeung-Hyeun
author_facet Jin, Bo-Ra
Kim, Sun-Jin
Lee, Jeong-Min
Kang, Seong-Ho
Han, Hye-Ju
Jang, Young-Saeng
Seo, Goo-young
Kim, Pyeung-Hyeun
author_sort Jin, Bo-Ra
collection PubMed
description Aluminum hydroxide (alum) is the most widely used adjuvant in human vaccines. Nevertheless, it is virtually unknown whether alum acts on B cells. In the present study, we explored the direct effect of alum on Ig expression by murine B cells in vitro. LPS-activated mouse spleen B cells were cultured with alum, and the level of isotype-specific Ig secretion, IgG1 secreting cell numbers, and Ig germ-line transcripts (GLT) were measured using ELISA, ELISPOT, and RT-PCR, respectively. Alum consistently enhanced total IgG1 production, numbers of IgG1 secreting cells, and GLTγ1 expression. These results demonstrate that alum can directly cause IgG1 isotype switching leading to IgG1 production.
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spelling pubmed-36077052013-04-04 Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype Jin, Bo-Ra Kim, Sun-Jin Lee, Jeong-Min Kang, Seong-Ho Han, Hye-Ju Jang, Young-Saeng Seo, Goo-young Kim, Pyeung-Hyeun Immune Netw Original Article Aluminum hydroxide (alum) is the most widely used adjuvant in human vaccines. Nevertheless, it is virtually unknown whether alum acts on B cells. In the present study, we explored the direct effect of alum on Ig expression by murine B cells in vitro. LPS-activated mouse spleen B cells were cultured with alum, and the level of isotype-specific Ig secretion, IgG1 secreting cell numbers, and Ig germ-line transcripts (GLT) were measured using ELISA, ELISPOT, and RT-PCR, respectively. Alum consistently enhanced total IgG1 production, numbers of IgG1 secreting cells, and GLTγ1 expression. These results demonstrate that alum can directly cause IgG1 isotype switching leading to IgG1 production. The Korean Association of Immunologists 2013-02 2013-02-28 /pmc/articles/PMC3607705/ /pubmed/23559895 http://dx.doi.org/10.4110/in.2013.13.1.10 Text en Copyright © 2013 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jin, Bo-Ra
Kim, Sun-Jin
Lee, Jeong-Min
Kang, Seong-Ho
Han, Hye-Ju
Jang, Young-Saeng
Seo, Goo-young
Kim, Pyeung-Hyeun
Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title_full Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title_fullStr Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title_full_unstemmed Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title_short Alum Directly Modulates Murine B Lymphocytes to Produce IgG1 Isotype
title_sort alum directly modulates murine b lymphocytes to produce igg1 isotype
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607705/
https://www.ncbi.nlm.nih.gov/pubmed/23559895
http://dx.doi.org/10.4110/in.2013.13.1.10
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