CLEC9A and infection: Accordingly, TNTDNGR‐1 also reduced virus load in the lungs, indicating that DNGR‐1‐targeting provides an effective control of the infection spread as conventional Fc‐containing nAbs.[50, 51, 52, 62] TNTDNGR‐1 induced an early and efficient S‐specific IgM and S‐, RBD‐, and N‐specific IgG antibody response, while TNT treatment did not increase endogenous antibody induction over non‐treated animal levels.