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Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay

Understanding the mechanisms that maintain protective antibody levels after immunisation is important for vaccine design. In this study, we have determined the kinetics of plasma and memory B cells detectable in the blood of cattle immunised with model T-dependent or T-independent antigens. Immunisa...

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Autores principales: Grant, Clare FJ, Lefevre, Eric A, Carr, B Veronica, Prentice, Helen, Gubbins, Simon, Pollard, Andrew J, Charreyre, Catherine, Charleston, Bryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487944/
https://www.ncbi.nlm.nih.gov/pubmed/23050495
http://dx.doi.org/10.1186/1297-9716-43-68
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author Grant, Clare FJ
Lefevre, Eric A
Carr, B Veronica
Prentice, Helen
Gubbins, Simon
Pollard, Andrew J
Charreyre, Catherine
Charleston, Bryan
author_facet Grant, Clare FJ
Lefevre, Eric A
Carr, B Veronica
Prentice, Helen
Gubbins, Simon
Pollard, Andrew J
Charreyre, Catherine
Charleston, Bryan
author_sort Grant, Clare FJ
collection PubMed
description Understanding the mechanisms that maintain protective antibody levels after immunisation is important for vaccine design. In this study, we have determined the kinetics of plasma and memory B cells detectable in the blood of cattle immunised with model T-dependent or T-independent antigens. Immunisation with the T-D antigen resulted in an expansion of TNP-specific plasma cells post-TNP primary and booster immunisations, which was associated with increased titres of TNP-specific IgG antibodies. Although no TNP-specific memory B cells were detected in the T-D group following the primary immunisation, we detected an increase in the number of TNP-specific memory B cells post-TNP boost. In contrast, no TNP-specific plasma or memory B cells were detected after primary or secondary immunisation with the T-I antigen. We then investigated if immunisation with a third party antigen (tetanus toxin fragment C, TTC) would result in a bystander stimulation and increase the number of TNP-specific plasma and memory B cells in the T-D and/or T-I group. TTC immunisation in the T-D group resulted in a small increase in the number of TNP-specific plasma cells post-TTC primary immunisation and boost, and in an increase in the number of TNP-specific memory B cells post-TTC boost. This bystander effect was not observed in the animals previously immunised with the T-I antigen. In conclusion, the present study characterised for the first time the B cell response in cattle to immunisation with T-D and T-I antigens and showed that bystander stimulation of an established T-D B cell memory response may occur in cattle.
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spelling pubmed-34879442012-11-03 Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay Grant, Clare FJ Lefevre, Eric A Carr, B Veronica Prentice, Helen Gubbins, Simon Pollard, Andrew J Charreyre, Catherine Charleston, Bryan Vet Res Research Understanding the mechanisms that maintain protective antibody levels after immunisation is important for vaccine design. In this study, we have determined the kinetics of plasma and memory B cells detectable in the blood of cattle immunised with model T-dependent or T-independent antigens. Immunisation with the T-D antigen resulted in an expansion of TNP-specific plasma cells post-TNP primary and booster immunisations, which was associated with increased titres of TNP-specific IgG antibodies. Although no TNP-specific memory B cells were detected in the T-D group following the primary immunisation, we detected an increase in the number of TNP-specific memory B cells post-TNP boost. In contrast, no TNP-specific plasma or memory B cells were detected after primary or secondary immunisation with the T-I antigen. We then investigated if immunisation with a third party antigen (tetanus toxin fragment C, TTC) would result in a bystander stimulation and increase the number of TNP-specific plasma and memory B cells in the T-D and/or T-I group. TTC immunisation in the T-D group resulted in a small increase in the number of TNP-specific plasma cells post-TTC primary immunisation and boost, and in an increase in the number of TNP-specific memory B cells post-TTC boost. This bystander effect was not observed in the animals previously immunised with the T-I antigen. In conclusion, the present study characterised for the first time the B cell response in cattle to immunisation with T-D and T-I antigens and showed that bystander stimulation of an established T-D B cell memory response may occur in cattle. BioMed Central 2012 2012-10-10 /pmc/articles/PMC3487944/ /pubmed/23050495 http://dx.doi.org/10.1186/1297-9716-43-68 Text en Copyright ©2012 Grant et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Grant, Clare FJ
Lefevre, Eric A
Carr, B Veronica
Prentice, Helen
Gubbins, Simon
Pollard, Andrew J
Charreyre, Catherine
Charleston, Bryan
Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title_full Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title_fullStr Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title_full_unstemmed Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title_short Assessment of T-dependent and T-independent immune responses in cattle using a B cell ELISPOT assay
title_sort assessment of t-dependent and t-independent immune responses in cattle using a b cell elispot assay
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487944/
https://www.ncbi.nlm.nih.gov/pubmed/23050495
http://dx.doi.org/10.1186/1297-9716-43-68
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