Immunoprotectivity of an antigenic construct derived from Omp۳۴ against A. baumanniiin murine pneumonia model

Acinetobacter baumannii which causes various hospital infections, has become a major problem fortreatment due to its antibiotic resistance even to colistin, and has led researchers to design polyvalent vaccinesusing different antigens with natural adjuvants such as chitosan, which increase the efficiency andimmunogenicity.

کلیدواژه ها:

Acinetobacter baumannii ، Omp۳۴ ، L۳X۵ ، Chitosan ، Vaccine ، Pneumonia