|  | 
  
    
    
      | 
          LT(R192G)         |  
      | Vaxjo ID | 379 |  
      | Vaccine Adjuvant Name | LT(R192G) |  
      | Adjuvant VO ID | VO_0005528 |  
      | Description | microorganism derived adjuvant that induces mixed Th1/Th2 response |  
      | Stage of Development | Clinical Trial |  
      | Host Species for Testing | Human |  
      | Second Host Species for Testing | Mouse |  
      | Components | heat-labile toxin derived from a clone of E. coil JM 83 |  
      | Structure | mutation of wild type LT of arginine 192 to glycine |  
      | Preparation | final product was lyophilized in vials containing 1,000 µg of protein per vial |  
      | Dosage | 2 µg |  
      | Function | enhances DC activation, cytokine secretion |  
	  | References | Lu et al., 2002: Lu X, Clements JD, Katz JM. Mutant Escherichia coli heat-labile enterotoxin [LT(R192G)] enhances protective humoral and cellular immune responses to orally administered inactivated influenza vaccine. Vaccine. 2002; 20(7-8); 1019-1029. [PubMed: 11803061]. NCT00090688: Clinicaltrials.gov [https://www.clinicaltrials.gov/study/NCT00090688] Riddle et al., 2020: Riddle MS, Maciel M Jr, Porter CK, Poole ST, Gutierrez RL, Gormley R, Laird RM, Sebeny PJ, Dori KE, Greenleaf ME, Hoq F, Turiansky GW, Jarell A, Hawk D, Tribble D, Savarino SJ. A first in human clinical trial assessing the safety and immunogenicity of transcutaneously delivered enterotoxigenic Escherichia coli fimbrial tip adhesin with heat-labile enterotoxin with mutation R192G. Vaccine. 2020; 38(45); 7040-7048. [PubMed: 32978003]. |  |