Kessler Matthew J, Berard John D, Rawlins Richard G, Bercovitch Fred B, Gerald Melissa S, Laudenslager Mark L, Gonzalez-Martinez Janis
Center for Comparative Medicine, University of Virginia Health System, Charlottesville, Virginia, USA.
Am J Primatol. 2006 Jul;68(7):725-31. doi: 10.1002/ajp.20262.
Prior to 1985 tetanus was a major cause of mortality in the free-ranging colony of rhesus monkeys on Cayo Santiago, accounting for almost a quarter of annual deaths. In 1985 and 1986 all animals (except infants) received primary and booster doses, respectively, of tetanus toxoid. In subsequent years primary immunizations were given to all yearlings, and boosters were administered to all 2-year-old animals during the annual capture of the colony. The main objectives of the tetanus immunization program were to reduce the pain and suffering caused by tetanus infections and to decrease mortality in the colony. Other objectives were to evaluate the efficacy of the two-dose tetanus toxoid immunization protocol and to determine whether additional boosters might be required to provide adequate long-term protection against tetanus infections. The immediate effect of the mass immunization program was the elimination of clinical tetanus infections in the population and a 42.2% reduction in the overall mortality rate. Since the immunization program began, no cases of tetanus have been observed in the colony, except in two unimmunized infants, and it has not been necessary to give tertiary injections of tetanus toxoid to maintain protection against infection. A sample collected in 2004 of the original cohort of monkeys immunized in 1985 and 1986 showed that 93.3% (14/15) had protective tetanus antibody titers (>0.01 IU/ml) at the ages of 20-23 years, which is close to the life expectancy of the Cayo Santiago rhesus macaques. Two intramuscular doses of tetanus toxoid provided long-term, if not lifelong, protection against tetanus for rhesus monkeys living in a tropical clime where tetanus is enzootic and the risk of infection is great.
1985年以前,破伤风是圣地亚哥岛恒河猴自由放养群体中主要的致死原因,几乎占年死亡数的四分之一。1985年和1986年,所有动物(婴儿除外)分别接种了破伤风类毒素的初次和加强剂量。在随后的几年里,所有一岁的猴子都接受了初次免疫,并且在每年对猴群进行捕捉时,对所有两岁的动物都进行了加强免疫。破伤风免疫计划的主要目标是减轻破伤风感染所带来的痛苦并降低猴群的死亡率。其他目标是评估两剂破伤风类毒素免疫方案的效果,并确定是否可能需要额外的加强免疫来提供足够的长期保护以预防破伤风感染。大规模免疫计划的直接效果是消除了人群中的临床破伤风感染,总体死亡率降低了42.2%。自免疫计划开始以来,除了两只未免疫的婴儿外,在猴群中未观察到破伤风病例,并且没有必要注射第三剂破伤风类毒素来维持对感染的保护。2004年采集的1985年和1986年最初接种疫苗的猴群样本显示,在20 - 23岁时,93.3%(14/15)的猴子具有保护性破伤风抗体滴度(>0.01 IU/ml),这接近圣地亚哥岛恒河猴的预期寿命。两剂肌肉注射的破伤风类毒素为生活在破伤风地方流行且感染风险很大的热带气候中的恒河猴提供了长期(即便不是终身)的破伤风保护。