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Smart Immune Cells: Tumor Destruction Breakthrough

Smart Immune Cells: Tumor Destruction Breakthrough

June 27, 2025 Health

USC ⁢engineers ​have revolutionized cancer treatment wiht EchoBack⁣ CAR T-cells,⁢ a cutting-edge CAR T-cell ‍therapy designed ⁢to⁤ precisely⁢ target and ‍destroy solid tumors.Unlike conventional methods, these smart immune cells,⁢ activated by ultrasound, can attack tumors ‍for five days, offering enhanced efficacy and safety. This ⁣breakthrough in cancer immunotherapy, published in Cell, marks ⁢a meaningful step forward in treating previously resistant ‌cancers. Pioneering research, led by Peter Yingxiao Wang, utilizes ultrasound ⁣control, ​potentially‌ reducing treatment ​frequency. These innovative T-cells ⁤show great ⁢promise,particularly against prostate cancer. News Directory 3 is excited to cover this groundbreaking advancement in medical science. Could⁢ this lead the charge in personalized cancer treatment? Discover⁤ what’s next …

Key Points

  • USC engineers created ⁤EchoBack CAR T-cells for​ targeted cancer ‌treatment.
  • EchoBack cells attack tumors for five days, unlike standard CAR T-cells.
  • Ultrasound​ activates ⁣the cells, enhancing safety and effectiveness.
  • The new technology ​shows promise for treating solid tumors like prostate cancer.

USC Engineers⁣ develop EchoBack CAR T-Cell Therapy for Solid Tumors

⁢‍ Updated June 27,2025
⁣

Los Angeles-USC biomedical engineers have engineered a⁢ new type of ⁢immune cell,the “EchoBack CAR T-cell,” designed⁤ to target and destroy ‌solid ​tumors with unprecedented precision. This innovative cancer immunotherapy approach, detailed ⁣in the ⁤journal⁢ Cell, offers a potential breakthrough⁢ in treating cancers​ previously resistant to ⁣immunotherapy, while safeguarding healthy tissues.

CAR T-cell therapy, which has ‌shown success against blood cancers ‍like leukemia, involves extracting a patient’s T-cells, genetically modifying them ⁣to enhance thier cancer-fighting‌ abilities, and ​then ‍reintroducing them ⁣into the body.⁣ Peter Yingxiao Wang leads pioneering research ​in this area at USC’s alfred E. Mann Department of⁤ Biomedical Engineering.

The‍ Wang Lab’s latest innovation, the echoback⁤ CAR T-cell, can attack tumor‌ cells five times longer than ⁢conventional CAR T-cells.Focused ultrasound remotely‌ controls these cells, possibly increasing treatment safety and efficacy. This novel role⁤ for ultrasound in cancer ​therapy could revolutionize treatment protocols.

Longwei Liu, assistant ⁤professor at the USC Viterbi School ​of Engineering and lead ‌author, explained that first-generation ultrasound-controllable‌ CAR T-cells typically attacked cancer cells for only 24 hours. The EchoBack CAR T-cells,⁢ however, remain active for ⁣at least five days⁤ after ultrasound activation at the tumor site.

Liu noted the reduced treatment ⁤frequency as a major benefit. “With first-generation cells, patients⁣ might need daily hospital visits. The ⁢new generation could reduce visits to once every two‌ weeks, or even less.”

Wang hailed the development as ⁤a “breakthrough,” making ultrasound-controllable‍ CAR⁢ T-cells practical for real-world medical use.

The⁣ focused‌ ultrasound acts as⁣ an “on switch,” triggering ⁤the CAR T-cells to recognize and attack cancer cells after ‌a brief, 10-minute pulse.

Wang emphasized ⁣the long-lasting effect of the ultrasound stimulation, enabling the ⁢cells to effectively⁢ kill tumors locally. “It’s a milestone, migrating from ‍conceptual design to ‌a practical application system,” he said.

The cells are named ⁣’EchoBack-CAR’ due to​ their unique mechanism that echoes the ultrasound ⁢stimulation. This‍ feedback ⁤function ​allows them ‌to react to ⁤tumor⁤ cells, triggering ⁣activation and attack.

“When a tumor cell is nearby,‍ it signals our CAR ⁣T-cell, which then produces more ‍killing molecules,” liu explained.”This ‍also enhances safety, as the ‌CAR molecule degrades when the T-cells migrate out of ‌the tumor, preventing⁤ harm to⁤ normal tissue. We’ve engineered them‌ to be smart CAR T-cells.”

Lab experiments in mouse models tested the new CAR T-cells against prostate cancer and glioblastoma cells.

“The ultrasound controllable CAR, with ‍two rounds of stimulation, outperformed standard CAR⁢ T-cells,” Liu said. “When⁢ challenged repeatedly with tumor cells, standard CAR T-cells became weary, while our ultrasound⁤ controllable CAR maintained better function, less exhaustion, and enhanced ‌killing.”

USC Viterbi PhD students Peixiang He ⁤and Yuxuan Wang contributed considerably. The team collaborated with⁢ Yale University and the University of north Carolina at Chapel ‍Hill for single-cell sequencing. Qifa Zhou, a Zohrab A. Kaprielian Fellow ​in ⁤Engineering at USC, provided ultrasound technology expertise.

What’s​ next

The‌ team hopes to adapt this technology to treat other solid tumors, such as breast cancer and retinoblastoma, offering a modular tool for future immunotherapy applications. Liu envisions a future where “smart” CAR ⁣T-cells, responsive to ultrasound and tumor signals, provide meaningful benefits to‍ patients.

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Brain Tumor; Cancer; Prostate Cancer; Stem Cells; Lung Cancer; Lymphoma; Immune System; Skin Cancer

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