Artículo
A Humanized Mouse Model Coupled with Computational Analysis Identifies Potent Glycolipid Agonist of Invariant NKT Cells
Saavedra-Avila, Noemi A.; Pigni, Natalia Belen
; Caldwell, Donald R.; Chena Becerra, Florencia; Intano, Jose; Ng, Tony W.; Chennamadhavuni, Divya; Porcelli, Steven A.; Gascón, José A.; Howell, Amy R.

Fecha de publicación:
03/2024
Editorial:
American Chemical Society
Revista:
ACS Chemical Biology
ISSN:
1554-8929
e-ISSN:
1554-8937
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
Invariant natural killer T (iNKT) cells play an important role in many innate and adaptive immune responses, with potential applications in cancer immunotherapy. The glycolipid KRN7000, an α-galactosylceramide, potently activates iNKT cells but has shown limited anticancer effects in human clinical trials conducted so far. In spite of almost three decades of structure−activity relationship studies, no alternative glycolipid has yet emerged as a superior clinical candidate. One reason for the slow progress in this area is that standard mouse models do not accurately reflect the specific ligand recognition by human iNKT cells and their requirements for activation. Here we evaluated a series of KRN7000 analogues using a recently developed humanized mouse model that expresses a human αTCR chain sequence and human CD1d. In this process, a more stimulatory, previously reported but largely overlooked glycolipid was identified, and its activity was probed and rationalized via molecular simulations.
Palabras clave:
INKT
,
GLYCOLIPID
,
KRN7000
,
MODEL
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Articulos(ICYTAC)
Articulos de INST. DE CIENCIA Y TECNOLOGIA DE ALIMENTOS CORDOBA
Articulos de INST. DE CIENCIA Y TECNOLOGIA DE ALIMENTOS CORDOBA
Citación
Saavedra-Avila, Noemi A.; Pigni, Natalia Belen; Caldwell, Donald R.; Chena Becerra, Florencia; Intano, Jose; et al.; A Humanized Mouse Model Coupled with Computational Analysis Identifies Potent Glycolipid Agonist of Invariant NKT Cells; American Chemical Society; ACS Chemical Biology; 19; 4; 3-2024; 926-937
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