Priming agents transiently reduce the clearance of cell-free DNA to improve liquid biopsies

Carmen Martin-Alonso(Harvard–MIT Division of Health Sciences and Technology), Shervin Tabrizi(Broad Institute), Kan Xiong(Broad Institute), Timothy Blewett(Broad Institute), Sainetra Sridhar(Broad Institute), Andjela Crnjac(Broad Institute), Sahil Patel(Broad Institute), Zhenyi An(Broad Institute), Ahmet Bekdemir(Massachusetts Institute of Technology), Douglas Shea(Broad Institute), Shih‐Ting Wang(Massachusetts Institute of Technology), Sergio A. Rodriguez‐Aponte(Massachusetts Institute of Technology), Christopher A. Naranjo(Massachusetts Institute of Technology), Justin Rhoades(Broad Institute), Jesse D. Kirkpatrick(Harvard–MIT Division of Health Sciences and Technology), Heather E. Fleming(Massachusetts Institute of Technology), Ava P. Amini(Microsoft (United States)), Todd R. Golub(Broad Institute), J. Christopher Love(Broad Institute), Sangeeta N. Bhatia(Broad Institute), Viktor A. Adalsteinsson(Broad Institute)
Science
January 18, 2024
Cited by 157Open Access
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Abstract

Liquid biopsies enable early detection and monitoring of diseases such as cancer, but their sensitivity remains limited by the scarcity of analytes such as cell-free DNA (cfDNA) in blood. Improvements to sensitivity have primarily relied on enhancing sequencing technology ex vivo. We sought to transiently augment the level of circulating tumor DNA (ctDNA) in a blood draw by attenuating its clearance in vivo. We report two intravenous priming agents given 1 to 2 hours before a blood draw to recover more ctDNA. Our priming agents consist of nanoparticles that act on the cells responsible for cfDNA clearance and DNA-binding antibodies that protect cfDNA. In tumor-bearing mice, they greatly increase the recovery of ctDNA and improve the sensitivity for detecting small tumors.


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