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dc.contributor.author
Saavedra-Avila, Noemi A.  
dc.contributor.author
Pigni, Natalia Belen  
dc.contributor.author
Caldwell, Donald R.  
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Chena Becerra, Florencia  
dc.contributor.author
Intano, Jose  
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Ng, Tony W.  
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Chennamadhavuni, Divya  
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Porcelli, Steven A.  
dc.contributor.author
Gascón, José A.  
dc.contributor.author
Howell, Amy R.  
dc.date.available
2025-05-12T10:13:49Z  
dc.date.issued
2024-03  
dc.identifier.citation
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  
dc.identifier.issn
1554-8929  
dc.identifier.uri
http://hdl.handle.net/11336/260992  
dc.description.abstract
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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
INKT  
dc.subject
GLYCOLIPID  
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KRN7000  
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MODEL  
dc.subject.classification
Bioquímica y Biología Molecular  
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Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
A Humanized Mouse Model Coupled with Computational Analysis Identifies Potent Glycolipid Agonist of Invariant NKT Cells  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2025-05-09T16:21:26Z  
dc.identifier.eissn
1554-8937  
dc.journal.volume
19  
dc.journal.number
4  
dc.journal.pagination
926-937  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Maryland  
dc.description.fil
Fil: Saavedra-Avila, Noemi A.. Albert Einstein College of Medicine; Estados Unidos  
dc.description.fil
Fil: Pigni, Natalia Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Ciencia y Tecnología de Alimentos Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Ciencia y Tecnología de Alimentos Córdoba; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Caldwell, Donald R.. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Chena Becerra, Florencia. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Intano, Jose. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Ng, Tony W.. Albert Einstein College of Medicine; Estados Unidos  
dc.description.fil
Fil: Chennamadhavuni, Divya. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Porcelli, Steven A.. Albert Einstein College of Medicine; Estados Unidos  
dc.description.fil
Fil: Gascón, José A.. University of Connecticut; Estados Unidos  
dc.description.fil
Fil: Howell, Amy R.. University of Connecticut; Estados Unidos  
dc.journal.title
ACS Chemical Biology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acschembio.3c00736  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acschembio.3c00736