Rapid Universal Detection of High‐Risk and Low‐Abundance Microbial Contaminations in CAR‐T Cell Therapy

Abstract Live microbial contamination poses high risks to cell and gene therapies, threatening manufacturing processes and patient safety. Rapid, sensitive detection of live microbes in complex environments, such as CAR‐T cell cultures, remains an urgent need. Here, an innovative sample‐to‐result workflow is introduced using digital loop‐mediated isothermal amplification (dLAMP), enhanced by Electrostatic Microfiltration (EM)‐based enrichment, for rapid sterility testing. By rationally designing primers targeting 16S and 18S rRNA, dLAMP assay enables both universal detection (covering >80% of known species) and strain‐specific identification of bacterial and fungal contaminants in CAR‐T cell spent medium and final products, directly from microorganism lysates. Enhanced by EM‐based enrichment of low‐abundance live microbes, the workflow achieves unparalleled sensitivity and speed, detecting contamination levels as low as 1 CFU/mL in complex CAR‐T cell cultures within 6 h. Compared to qPCR and 14‐day compendial methods, the approach demonstrates superior accuracy and significantly faster turnaround times. This workflow holds transformative potential for real‐time monitoring in cell therapy manufacturing and rapid safety assessments of CAR‐T cell products prior to patient infusion. Beyond cell therapy, the method is broadly applicable to infectious disease diagnostics, biomanufacturing monitoring, food safety, and environmental surveillance.