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Customized T-cell treatment is generally safe for people living with HIV, and outcomes are comparable to those of HIV-negative people.
The woman’s leukemia is in remission and she remains free of detectable HIV more than a year after stopping antiretroviral treatment.
The drug, which blocks entry of HBV into liver cells, also prevents HDV replication.
Researchers hope to combine gene editing with a less toxic stem cell transplant. Findings may apply to cancer and other illnesses.
Cancer and HIV are invaders that the immune system fails to detect, and the similarities don’t end there.
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