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Article Dans Une Revue Veterinary Research Année : 2009

Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells

Concepción Revilla
  • Fonction : Auteur
Teresa Poderoso
  • Fonction : Auteur
Paloma Martínez
  • Fonction : Auteur
Belén Álvarez
  • Fonction : Auteur
Laura López-Fuertes
  • Fonction : Auteur
Fernando Alonso
  • Fonction : Auteur
Angel Ezquerra
  • Fonction : Auteur
Javier Domínguez
  • Fonction : Auteur

Résumé

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.
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hal-00903080 , version 1 (11-05-2020)

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Concepción Revilla, Teresa Poderoso, Paloma Martínez, Belén Álvarez, Laura López-Fuertes, et al.. Targeting to porcine sialoadhesin receptor improves antigen presentation to T cells. Veterinary Research, 2009, 40 (3), ⟨10.1051/vetres:2008052⟩. ⟨hal-00903080⟩
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