Cross Alan S, Opal Steven M, Palardy John E, Drabick Joseph J, Warren H Shaw, Huber Christian, Cook Pamela, Bhattacharjee Apurba K
Department of Medicine, Center for Vaccine Development, University of Maryland School of Medicine, 685 W. Baltimore Street, HSF 480, Baltimore, MD 21201, USA.
Vaccine. 2003 Nov 7;21(31):4576-87. doi: 10.1016/s0264-410x(03)00483-3.
We previously observed that a detoxified Escherichia coli O111, Rc chemotype J5 lipopolysaccharide (J5dLPS)/group B meningococcal outer membrane protein (OMP) vaccine protected animals from experimental lethal sepsis when immune antibodies were given passively as treatment at the onset of fever or when vaccine was given actively as prophylaxis. To test the safety and immunogenicity of this vaccine, we administered doses of 5, 10 and 25 microg (based on dLPS) of vaccine at days 0, 28 and 56 to 24 human subjects (8 per group). Temperatures of 100.3, 99.5 and 99.4 degrees F occurred in three subjects. At 24h, pain at the injection site was moderate in 38%, mild in 44% and not present in 18%, while at 48 h, it was 1, 25 and 73%, respectively. No alterations in baseline renal, hepatic or hematologic functions occurred. There were two to three times mean-fold increases in anti-J5dLPS IgG (range: 1.9-5.1) and IgM (range: 1.2-9.2) levels in subjects receiving the 10 and 25 microg doses. At 12-month follow-up, three of the original responders had continued elevation of antibody levels. A 25 microg booster dose of vaccine did not increase antibody levels among those responders and did not elicit antibodies among three subjects with no previous antibody response. The plasma from the six volunteers inhibited LPS-induced cytokine generation in human whole blood ex vivo. We conclude that this J5dLPS/OMP vaccine was safe and well-tolerated with transient, local pain at the injection site. Vaccine formulations with different adjuvants are currently under investigation.
我们之前观察到,一种解毒的大肠杆菌O111、Rc化学型J5脂多糖(J5dLPS)/B群脑膜炎球菌外膜蛋白(OMP)疫苗,在发热开始时被动给予免疫抗体作为治疗,或主动给予疫苗作为预防时,可保护动物免受实验性致死性败血症。为了测试该疫苗的安全性和免疫原性,我们在第0、28和56天给24名人类受试者(每组8人)分别接种了5、10和25微克(基于dLPS)剂量的疫苗。三名受试者体温分别达到了100.3、99.5和99.4华氏度。在24小时时,注射部位疼痛程度为中度的受试者占38%,轻度的占44%,无疼痛的占18%;而在48小时时,相应比例分别为1%、25%和73%。基线时的肾脏、肝脏或血液学功能未发生改变。接受10微克和25微克剂量的受试者中,抗J5dLPS IgG(范围:1.9 - 5.1)和IgM(范围:1.2 - 9.2)水平平均升高了两到三倍。在12个月的随访中,最初有反应的受试者中有三人抗体水平持续升高。对这三名有反应的受试者给予25微克的疫苗加强剂量,并未提高抗体水平,且在三名之前无抗体反应的受试者中也未引发抗体。六名志愿者的血浆在体外可抑制人全血中LPS诱导的细胞因子生成。我们得出结论,这种J5dLPS/OMP疫苗是安全的,耐受性良好,注射部位有短暂的局部疼痛。目前正在研究不同佐剂的疫苗配方。