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MICA-specific nanobodies for diagnosis and immunotherapy of MICA+ tumors.
Verhaar, Elisha R; Knoflook, Anouk; Pishesha, Novalia; Liu, Xin; van Keizerswaard, Willemijn J C; Wucherpfennig, Kai W; Ploegh, Hidde L.
Afiliação
  • Verhaar ER; Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Knoflook A; Department of Cell and Chemical Biology, Leiden University Medical Centre, Leiden, Netherlands.
  • Pishesha N; Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Liu X; Division of Immunology, Boston Children's Hospital, Boston, MA, United States.
  • van Keizerswaard WJC; Department of Pediatrics, Harvard Medical School, Boston, MA, United States.
  • Wucherpfennig KW; Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Ploegh HL; Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Front Immunol ; 15: 1368586, 2024.
Article em En | MEDLINE | ID: mdl-38550583
ABSTRACT
MICA and MICB are Class I MHC-related glycoproteins that are upregulated on the surface of cells in response to stress, for instance due to infection or malignant transformation. MICA/B are ligands for NKG2D, an activating receptor on NK cells, CD8+ T cells, and γδ T cells. Upon engagement of MICA/B with NKG2D, these cytotoxic cells eradicate MICA/B-positive targets. MICA is frequently overexpressed on the surface of cancer cells of epithelial and hematopoietic origin. Here, we created nanobodies that recognize MICA. Nanobodies, or VHHs, are the recombinantly expressed variable regions of camelid heavy chain-only immunoglobulins. They retain the capacity of antigen recognition but are characterized by their stability and ease of production. The nanobodies described here detect surface-disposed MICA on cancer cells in vitro by flow cytometry and can be used therapeutically as nanobody-drug conjugates when fused to the Maytansine derivative DM1. The nanobody-DM1 conjugate selectively kills MICA positive tumor cells in vitro.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Anticorpos de Domínio Único / Neoplasias Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Anticorpos de Domínio Único / Neoplasias Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos