Fusco Luciano Sebastián, Rodríguez Juan Pablo, Teibler Pamela, Maruñak Silvana, Acosta Ofelia, Leiva Laura
Laboratorio de investigación en Proteínas (LabInPro), Facultad de Ciencias Exactas y Naturales y Agrimensura, Universidad Nacional del Nordeste (UNNE), Av. Libertad 5470, Corrientes 3400, Argentina; Facultad de Ciencias Veterinarias, Universidad Nacional del Nordeste (UNNE), Sargento Cabral 2139, Corrientes 3400, Argentina.
Laboratorio de investigación en Proteínas (LabInPro), Facultad de Ciencias Exactas y Naturales y Agrimensura, Universidad Nacional del Nordeste (UNNE), Av. Libertad 5470, Corrientes 3400, Argentina.
Biologicals. 2015 Jan;43(1):62-70. doi: 10.1016/j.biologicals.2014.09.001. Epub 2014 Nov 8.
Antivenoms are usually obtained by animal immunization with successive inoculations of increasing sublethal amounts of venom, which may impair the animal health. The high lethality of venom requires prolonged immunization plans with small amounts of venom. Thus, we propose an alternative plan that includes a pre-immunization of the animal with phospholipase A2, the main crotoxin component, which is responsible for the whole venom lethality. For comparison, three different immunization schemes were designed: high dose protocol (HDP; 0.5-27 mg of venom), low dose protocol (LDP; 0.1-7 mg of venom) and Mix protocol (MP; preimmunization 0.1-1.2 mg of crotalic PLA2, and then 4.5-8 mg of venom). Antibody titers were determined by ELISA, in blood plasma obtained from the marginal vein of the ear. The neutralizing ability of the different sera obtained by all protocols (HDS, LDS and MS) was tested against the most important pharmacological activities of whole venom: PLA2 activity, myotoxicity, thrombin like activity and lethality. MS showed the best neutralizing efficacy and at the same time, it was obtained by an immunization protocol that takes account of animal health care, since it requires low quantities of venoms in comparison to traditional protocols.
抗蛇毒血清通常是通过用逐渐增加的亚致死剂量的毒液连续接种来对动物进行免疫获得的,这可能会损害动物健康。毒液的高致死性需要采用使用少量毒液的长时间免疫计划。因此,我们提出了一种替代方案,包括先用磷脂酶A2(主要的响尾蛇毒素成分,它是整个毒液致死性的原因)对动物进行预免疫。为了进行比较,设计了三种不同的免疫方案:高剂量方案(HDP;0.5 - 27毫克毒液)、低剂量方案(LDP;0.1 - 7毫克毒液)和混合方案(MP;先用0.1 - 1.2毫克响尾蛇PLA2进行预免疫,然后用4.5 - 8毫克毒液)。通过ELISA在从耳缘静脉采集的血浆中测定抗体滴度。测试了所有方案(HDS、LDS和MS)获得的不同血清对整个毒液最重要的药理活性的中和能力:PLA2活性、肌毒性、凝血酶样活性和致死性。MS显示出最佳的中和效果,同时,它是通过一种考虑到动物健康护理的免疫方案获得的,因为与传统方案相比,它需要的毒液量较少。