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Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells
Antibody-mediated targeting of antigen to specific antigen presenting cells (APC) receptors is an attractive strategy to enhance T cell immune responses to weak immunogenic antigens. Here, we describe the characterization of two monoclonal antibodies (mAb) against different epitopes of porcine sialo...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
EDP Sciences
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695033/ https://www.ncbi.nlm.nih.gov/pubmed/19081005 http://dx.doi.org/10.1051/vetres:2008052 |
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author | Revilla, Concepción Poderoso, Teresa Martínez, Paloma Álvarez, Belén López-Fuertes, Laura Alonso, Fernando Ezquerra, Angel Domínguez, Javier |
author_facet | Revilla, Concepción Poderoso, Teresa Martínez, Paloma Álvarez, Belén López-Fuertes, Laura Alonso, Fernando Ezquerra, Angel Domínguez, Javier |
author_sort | Revilla, Concepción |
collection | PubMed |
description | Antibody-mediated targeting of antigen to specific antigen presenting cells (APC) receptors is an attractive strategy to enhance T cell immune responses to weak immunogenic antigens. Here, we describe the characterization of two monoclonal antibodies (mAb) against different epitopes of porcine sialoadhesin (Sn) and evaluate in vitro the potential of targeting this receptor for delivery of antigens to APC for T cell stimulation. The specificity of these mAb was determined by amino acid sequence analysis of peptides derived from the affinity purified antigen. Porcine Sn is expressed by macrophages present in the border between white and red pulp of the spleen and in the subcapsular sinus of lymph nodes, an appropriate location for trapping blood and lymph-borne antigens. It is also expressed by alveolar macrophages and monocyte-derived dendritic cells (MoDC). Blood monocytes are negative for this molecule, but its expression can be induced by treatment with IFN-a. MAb bound to Sn is rapidly endocytosed. MAb to sialoadhesin induced in vitro T cell proliferation at concentrations 100-fold lower than the non-targeting control mAb when using T lymphocytes from pigs immunized with mouse immunoglobulins as responder cells and IFN-a treated monocytes or MoDC as APC, suggesting a role of sialoadhesin in antigen uptake and/or delivery into the presentation pathway in APC. |
format | Text |
id | pubmed-2695033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | EDP Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-26950332009-06-29 Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells Revilla, Concepción Poderoso, Teresa Martínez, Paloma Álvarez, Belén López-Fuertes, Laura Alonso, Fernando Ezquerra, Angel Domínguez, Javier Vet Res Original Article Antibody-mediated targeting of antigen to specific antigen presenting cells (APC) receptors is an attractive strategy to enhance T cell immune responses to weak immunogenic antigens. Here, we describe the characterization of two monoclonal antibodies (mAb) against different epitopes of porcine sialoadhesin (Sn) and evaluate in vitro the potential of targeting this receptor for delivery of antigens to APC for T cell stimulation. The specificity of these mAb was determined by amino acid sequence analysis of peptides derived from the affinity purified antigen. Porcine Sn is expressed by macrophages present in the border between white and red pulp of the spleen and in the subcapsular sinus of lymph nodes, an appropriate location for trapping blood and lymph-borne antigens. It is also expressed by alveolar macrophages and monocyte-derived dendritic cells (MoDC). Blood monocytes are negative for this molecule, but its expression can be induced by treatment with IFN-a. MAb bound to Sn is rapidly endocytosed. MAb to sialoadhesin induced in vitro T cell proliferation at concentrations 100-fold lower than the non-targeting control mAb when using T lymphocytes from pigs immunized with mouse immunoglobulins as responder cells and IFN-a treated monocytes or MoDC as APC, suggesting a role of sialoadhesin in antigen uptake and/or delivery into the presentation pathway in APC. EDP Sciences 2009 2008-12-12 /pmc/articles/PMC2695033/ /pubmed/19081005 http://dx.doi.org/10.1051/vetres:2008052 Text en © INRA, EDP Sciences, 2009 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted use, distribution, and reproduction in any noncommercial medium, provided the original work is properly cited. |
spellingShingle | Original Article Revilla, Concepción Poderoso, Teresa Martínez, Paloma Álvarez, Belén López-Fuertes, Laura Alonso, Fernando Ezquerra, Angel Domínguez, Javier Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title | Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title_full | Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title_fullStr | Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title_full_unstemmed | Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title_short | Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells |
title_sort | targeting to porcine sialoadhesin receptor improves antigen presentation to t cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695033/ https://www.ncbi.nlm.nih.gov/pubmed/19081005 http://dx.doi.org/10.1051/vetres:2008052 |
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