In viral infections, viral particles attach themselves to the host cell membrane for invasion, hijacking host cell machinery to replicate. [9,10] In order to counteract these threats, biological neutralization represents a general strategy that deploys therapeutic agents to bind with the harmful molecules or pathogens, block their bioactivity, and thus prevent them from causing the diseases. [11][12][13][14] Therapeutic platforms, such as antisera, monoclonal antibodies, and small-molecule inhibitors, have been widely used for neutralization. [15][16][17][18][19] Despite their pivotal roles in treating numerous diseases, these platforms sometimes show inadequate efficacy. The reason is attributable, in part, to their design of focusing on the causative molecules or pathogens, which leads to narrow-spectrum neutralization solutions. For example, some antidotes are highly effective in treating poisoning, but most deadly toxicants do not have specific pharmacological antidotes. [12] In inflammatory disorders, existing agents neutralizing one or a few cytokines are insufficient to halt or reverse disease progression due to the multiplicity of cytokine targets and signaling network redundancy. [20] In bacterial infections, bacterial toxins display enormous diversity of molecular structures and epitopic targets. [21,22] In contrast, current neutralizing agents target specific toxin structures and require customized design for different toxins, making their wide applications impractical. Similarly, viral neutralization focuses heavily on specific viral species and therefore cannot be deployed across different species or families of viruses or may be rendered ineffective as the virus accumulates mutations and escapes treatments. [23] Overall, these challenges underscore the need for innovative biological neutralization approaches.Recently, the emergency of cell-membrane-coated nanoparticles offers a unique solution to address the challenges facing current biological neutralization technologies. [24] These nanoparticles are made by first deriving natural cell membranes and then coating them onto synthetic cores. Cell-membranecoated nanoparticles were first developed by coating red blood cell (RBC) membranes onto polymeric cores. [25] The goal was to replicate the long-circulation feature of natural RBCs desirable for drug delivery. However, the success of these biomimetic nanoparticles soon sparked the idea of using them as decoys of susceptible RBCs for biological neutralization. [26] All pathological agents must interact with host cells for their bioactivity.Biological neutralization represents a general strategy that deploys therapeutic agents to bind with harmful molecules or infectious pathogens, block their bioactivity, and thus prevent them from causing the diseases. Here, a comprehensive review of using cell-membrane-coated nanoparticles, namely "cellular nanosponges," as host decoys for a wide range of biological neutralization applications is provided. Compared to traditional neutralization strategies, the cellu...