Solid-state batteries have fascinated the research community over the past decade, largely due to their improved safety properties and potential for high-energy density. Searching for fast ion conductors with sufficient electrochemical and chemical stabilities is at the heart of solid-state battery research and applications. Recently, significant progress has been made in solid-state electrolyte development. Sulfide-, oxide-, and halide-based electrolytes have been able to achieve high ionic conductivities of more than 10-3 S/cm at room temperature, which are comparable to liquid-based electrolytes. However, their stability toward Li metal anodes poses significant challenges for these electrolytes. The existence of non-Li cations that can be reduced by Li metal in these electrolytes hinders the application of Li anode and therefore poses an obstacle toward achieving high-energy density. The finding of antiperovskites as ionic conductors in recent years has demonstrated a new and exciting solution. These materials, mainly constructed from Li (or Na), O, and Cl (or Br), are lightweight and electrochemically stable toward metallic Li and possess promising ionic conductivity. Because of the structural flexibility and tunability, antiperovskite electrolytes are excellent candidates for solid-state battery applications, and researchers are still exploring the relationship between their structure and ion diffusion behavior. Herein, the recent progress of antiperovskites for solid-state batteries is reviewed, and the strategies to tune the ionic conductivity by structural manipulation are summarized. Major challenges and future directions are discussed to facilitate the development of antiperovskite-based solid-state batteries.