Molecular dynamics at immune synapse lipid rafts influence the cytolytic behavior of CAR T cells

Chimeric antigen receptor T cells (CART) targeting CD19 through CD28.ζ signaling induce rapid lysis of leukemic blasts, contrasting with persistent tumor control exhibited by 4-1BB.ζ-CART. We reasoned that molecular dynamics at the CART immune synapse (CARIS) could explain differences in their tumor rejection kinetics. We observed that CD28.ζ-CART engaged in brief highly lethal CARIS and mastered serial killing, whereas 4-1BB.ζ-CART formed lengthy CARIS and relied on robust expansion and cooperative killing. We analyzed CARIS membrane lipid rafts (mLRs) and found that, upon tumor engagement, CD28.ζ-CAR molecules rapidly but transiently translocated into mLRs, mobilizing the microtubular organizing center and lytic granules to the CARIS. This enabled fast CART recovery and sensitivity to low target site density. In contrast, gradual accumulation of 4-1BB.ζ-CAR and LFA-1 molecules at mLRs built mechanically tonic CARIS mediating chronic Fas ligand-based killing. The differences in CD28.ζ- and 4-1BB.ζ-CARIS dynamics explain the distinct cytolytic behavior of CART and can guide engineering of more adaptive effective cellular products.

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Publication Details

Journal
Science Advances
Published
2025-01-10
DOI
https://doi.org/10.1126/sciadv.adq8114
Citations
13
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
13.59
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Molecular dynamics at immune synapse lipid rafts influence the cytolytic behavior of CAR T cells

Jessica C. H. Lee, Ilya Levental, Sujith K. Joseph, Ahmed Z. Gad et al.
13 citations
Science Advances
CAR-T cell therapy research
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article

Molecular dynamics at immune synapse lipid rafts influence the cytolytic behavior of CAR T cells

Jessica C. H. Lee, Ilya Levental, Sujith K. Joseph, Ahmed Z. Gad, Spyridoula Vasileiou, Ann M. Leen, Lea Godret-Miertschin, Melisa J. Montalvo, Nabil Ahmed, Meenakshi Hegde, Navin Varadarajan, Jessica S. Morris, Kandice R. Levental, Sybrina S. Kerr, Kristen Fousek, Alexandre F. Carisey, Rebecca M. Brock, Yongshuai Li, Mohammad H Abu-Arja, Maksim Mamonkin, Arash Saeedi, Madhuwanti Srinivasan, Shuo Xu, Harrison R. Berger, Malini Mukherjee, Mohamed F. Sheha, Amr M. Saadeldin
article en
13 citations

Abstract

Chimeric antigen receptor T cells (CART) targeting CD19 through CD28.ζ signaling induce rapid lysis of leukemic blasts, contrasting with persistent tumor control exhibited by 4-1BB.ζ-CART. We reasoned that molecular dynamics at the CART immune synapse (CARIS) could explain differences in their tumor rejection kinetics. We observed that CD28.ζ-CART engaged in brief highly lethal CARIS and mastered serial killing, whereas 4-1BB.ζ-CART formed lengthy CARIS and relied on robust expansion and cooperative killing. We analyzed CARIS membrane lipid rafts (mLRs) and found that, upon tumor engagement, CD28.ζ-CAR molecules rapidly but transiently translocated into mLRs, mobilizing the microtubular organizing center and lytic granules to the CARIS. This enabled fast CART recovery and sensitivity to low target site density. In contrast, gradual accumulation of 4-1BB.ζ-CAR and LFA-1 molecules at mLRs built mechanically tonic CARIS mediating chronic Fas ligand-based killing. The differences in CD28.ζ- and 4-1BB.ζ-CARIS dynamics explain the distinct cytolytic behavior of CART and can guide engineering of more adaptive effective cellular products.

Science AdvancesVol. 11(2)
Houston Methodist (US), Baylor College of Medicine (US), Methodist Hospital (US), Texas Children's Hospital (US), Children's Cancer Center (US), University of Houston (US), University of Virginia (US)
Good health and well-being
Openalex Percentile: Top 1%
CAR-T cell therapy research
13.59
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