CAR Macrophages for SARS-CoV-2 Immunotherapy.

ABSTRACT: Targeted therapeutics for the treatment of coronavirus disease 2019 (COVID-19), especially severe cases, are currently lacking. As macrophages have unique effector functions as a first-line defense against invading pathogens, we genetically armed human macrophages with chimeric antigen receptors (CARs) to reprogram their phagocytic activity against SARS-CoV-2. After investigation of CAR constructs with different intracellular receptor domains, we found that although cytosolic domains from MERTK (CAR_MERTK) did not trigger antigen-specific cellular phagocytosis or killing effects, unlike those from MEGF10, FcRγ and CD3ζ did, these CARs all mediated similar SARS-CoV-2 clearance in vitro. Notably, we showed that CAR_MERTK macrophages reduced the virion load without upregulation of proinflammatory cytokine expression. These results suggest that CAR_MERTK drives an 'immunologically silent' scavenger effect in macrophages and pave the way for further investigation of CARs for the treatment of individuals with COVID-19, particularly those with severe cases at a high risk of hyperinflammation.

SUBMITTER: Fu W 

PROVIDER: S-EPMC8343226 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature