Host receptor-targeted therapeutic approach to counter pathogenic New World mammarenavirus infections.

Publication Type:

Journal Article


Nat Commun, Volume 13, Issue 1, p.558 (2022)


A549 Cells, Animals, Antibodies, Monoclonal, Antigens, CD, Arenaviridae, Chlorocebus aethiops, Hemorrhagic Fever, American, Host-Pathogen Interactions, Humans, Junin virus, Mice, Inbred C57BL, Mice, Transgenic, Molecular Docking Simulation, Protein Binding, Receptors, Transferrin, Vero Cells, Viral Envelope Proteins


<p>Five New World mammarenaviruses (NWMs) cause life-threatening hemorrhagic fever (HF). Cellular entry by these viruses is mediated by human transferrin receptor 1 (hTfR1). Here, we demonstrate that an antibody (ch128.1/IgG1) which binds the apical domain of hTfR1, potently inhibits infection of attenuated and pathogenic NWMs in vitro. Computational docking of the antibody Fab crystal structure onto the known structure of hTfR1 shows an overlapping receptor-binding region shared by the Fab and the viral envelope glycoprotein GP1 subunit that binds hTfR1, and we demonstrate competitive inhibition of NWM GP1 binding by ch128.1/IgG1 as the principal mechanism of action. Importantly, ch128.1/IgG1 protects hTfR1-expressing transgenic mice against lethal NWM challenge. Additionally, the antibody is well-tolerated and only partially reduces ferritin uptake. Our findings provide the basis for the development of a novel, host receptor-targeted antibody therapeutic broadly applicable to the treatment of HF of NWM etiology.</p>