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dc.contributor.author
Saavedra-Avila, Noemi A.
dc.contributor.author
Pigni, Natalia Belen

dc.contributor.author
Caldwell, Donald R.
dc.contributor.author
Chena Becerra, Florencia
dc.contributor.author
Intano, Jose
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Ng, Tony W.
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Chennamadhavuni, Divya
dc.contributor.author
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
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Bioquímica y Biología Molecular

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Ciencias Biológicas

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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
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