Ho P S, Kwang J, Lee Y K
Department of Microbiology, National University of Singapore, 5 Science Drive 2, Singapore 117597, Singapore.
Vaccine. 2005 Feb 3;23(11):1335-42. doi: 10.1016/j.vaccine.2004.09.015.
Lactobacillus casei strain Shirota was selected as a bacterial carrier for the development of live mucosal vaccines against coronavirus. A 75 kDa fragment of transmissible gastroenteritis coronavirus (TGEV) spike glycoprotein S was used as the model coronavirus antigen. The S glycoprotein was cloned into a Lactobacillus/E. coli shuttle vector (pLP500) where expression and secretion of the glycoprotein S from the recombinant lactobacilli was detected via immunoblotting. Oral immunization of BALB/c mice with recombinant LcS that constitutively expresses the 75 kDa fragment of the glycoprotein S, induced both local mucosal and systemic immune responses against TGEV. Maximum titers of IgG (8.38+/-0.19 ng/ml of serum) and IgA (64.82+/-2.9 ng/ml of intestinal water) were attained 32 days post oral inturbation. The induced antibodies demonstrated neutralizing effects on TGEV infection.
干酪乳杆菌代田株被选作开发抗冠状病毒活黏膜疫苗的细菌载体。将传染性胃肠炎冠状病毒(TGEV)刺突糖蛋白S的一个75 kDa片段用作模型冠状病毒抗原。将糖蛋白S克隆到乳酸杆菌/大肠杆菌穿梭载体(pLP500)中,通过免疫印迹检测重组乳酸杆菌中糖蛋白S的表达和分泌。用组成性表达糖蛋白S的75 kDa片段的重组LcS对BALB/c小鼠进行口服免疫,诱导了针对TGEV的局部黏膜和全身免疫反应。口服灌胃后32天达到IgG(血清8.38±0.19 ng/ml)和IgA(肠液64.82±2.9 ng/ml)的最高滴度。诱导产生的抗体对TGEV感染具有中和作用。