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    <identifier>10.57760/sciencedb.07297</identifier>
    <datestamp>2023-02-10T10:56:02Z</datestamp>
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  <dc:date>2023-02-10</dc:date>
  <dc:title>Magnetic-acoustic sequentially actuated CAR T cell microrobots for precision navigation and in-situ antitumour immunoactivation</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.07297</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Despite its clinical success,&amp;nbsp;chimeric antigen receptor T (CAR T) cell immunotherapy remains limited in solid tumours, owing to harsh physical barriers and immunosuppressive microenvironments. Here we describe a CAR T cell-based live microrobot (M-CAR T) created by decorating CAR T with immunomagnetic beads using click conjugation. M-CAR Ts are capable of magnetic-acoustic actuation for precision tumour targeting and in-situ activation of antitumour immune responses. Sequential actuation endows M-CAR Ts with magnetically actuated anti-flow and obstacle avoidance capabilities as well as tumour tissue penetration driven by acoustic propulsion, enabling efficient migration and accumulation in artificial tumour models. In animal models, sequentially actuated M-CAR Ts achieved long-distance targeting and accumulated at the peritumoural area under programmable magnetic guidance, and subsequently acoustic tweezers actuated M-CAR Ts to migrate into deep tumour tissues, resulting in a 6.6-fold increase in accumulated exogenous CD8+ CAR T cells compared with that with no actuation. Anti-CD3/CD28 immunomagnetic beads in-situ stimulate infiltrated CAR T proliferation and activation in situ, significantly enhancing their antitumour efficacy. Thus, our sequential actuation-guided cell microrobot combines the merits of autonomous targeting and penetration of intelligent robots with in-situ immunoactivation of T cells, and holds considerable promise for precision navigation of cancer immunotherapies.</dc:description>
  <dc:subject>CAR T cell microrobots; magnetic-acoustic sequential actuation; active targeting; in-situ immunoactivation; tumour immunotherapy</dc:subject>
  <dc:creator>Hong Pan</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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