“…In particular, RBDs of TcdA and TcdB have been evaluated for their ability to induce protective immunity. 25,[32][33][34] Recent studies have indicated that the N-terminal GT domain of TcdB can serve as an excellent immunogen. 35,36 This notion was initially supported by our recent construction of a chimeric recombinant vaccine against TcdA and TcdB, i.e., cTxAB, in which the original RBD of a full-length TcdB was replaced with the corresponding portion of TcdA.…”