Grasman Keith A
Methods Mol Biol. 2010;598:387-98. doi: 10.1007/978-1-60761-401-2_25.
Various methods have been adapted for assessing the effects of environmental contaminants on the structure and function of the immune system in wild and captive birds. This chapter describes two integrative functional assays that have been adapted to a variety of avian species and have proven to be sensitive biomarkers for immunotoxicological effects. The phytohemagglutinin (PHA) skin test measures T cell-mediated immunity. PHA is injected intra- or sub-dermally into the wing web of the elbow joint (or interdigitary skin or wattle). The PHA stimulates T lymphocytes to release cytokines that cause an inflammatory influx of leukocytes and fluid. The thickness of the wing web is measured before and 24 h after injection. A stimulation index, which reflects T cell function, is calculated as the increase in skin thickness caused by the PHA minus the increase caused by an injection of phosphate buffered saline (PBS) in the other wing web. In addition to its sensitivity to contaminants, ecological studies have shown that the PHA skin response is positively associated with rates of survival and colonization of new areas (i.e., ability to found new local populations) in wild birds.The sheep red blood cell (SRBC) hemagglutination assay measures the antibody response to immunization with SRBC antigens, integrating the functions of B lymphocytes, helper T lymphocytes, and macrophages. A SRBC suspension is injected i.v., and a blood sample is collected approximately 6 days later. Plasma (or serum) from the blood sample is serially diluted in a microtiter plate, and SRBCs are added. The magnitude of the antibody response is defined as the titer - the highest dilution of plasma in which the concentration of antibody is sufficient to agglutinate the SRBCs. Both IgM and IgG titers can be measured. This avian test is very similar in principle to the anti-SRBC ELISA and splenic plaque forming assays used for immunotoxicological testing in rodents. However, this avian hemagglutination assay does not require a species-specific secondary antibody (as does the ELISA), and this minimally invasive, nonlethal procedure is amenable to studies of protected species, as opposed to the splenic assay. The PHA and SRBC assays have been employed successfully in both the laboratory and field. In ecological studies birds must be recaptured 24 h or 6 days after the initial injections, limiting their use in some species. However, their sensitivity to a variety of contaminants and their ease of adaptability to a variety of species have made the PHA and SRBC tests some of the most commonly used assays for screening and monitoring immunotoxicity in birds.
人们采用了各种方法来评估环境污染物对野生和圈养鸟类免疫系统结构和功能的影响。本章介绍了两种综合功能检测方法,它们已适用于多种鸟类物种,并已被证明是免疫毒理学效应的敏感生物标志物。植物血凝素(PHA)皮肤试验可测量T细胞介导的免疫反应。将PHA皮内或皮下注射到肘关节的翼膜(或指间皮肤或肉垂)中。PHA刺激T淋巴细胞释放细胞因子,导致白细胞和液体的炎症性流入。在注射前和注射后24小时测量翼膜的厚度。计算反映T细胞功能的刺激指数,即PHA引起的皮肤厚度增加减去另一翼膜注射磷酸盐缓冲盐水(PBS)引起的增加。除了对污染物敏感外,生态学研究表明,PHA皮肤反应与野生鸟类的存活率和新区域的定殖率(即建立新的本地种群的能力)呈正相关。绵羊红细胞(SRBC)血凝试验测量对SRBC抗原免疫的抗体反应,整合了B淋巴细胞、辅助性T淋巴细胞和巨噬细胞的功能。静脉注射SRBC悬液,大约6天后采集血样。将血样中的血浆(或血清)在微量滴定板中进行系列稀释,然后加入SRBC。抗体反应的强度定义为效价——血浆的最高稀释度,其中抗体浓度足以凝集SRBC。IgM和IgG效价均可测量。这种鸟类检测方法在原理上与用于啮齿动物免疫毒理学检测的抗SRBC ELISA和脾斑形成试验非常相似。然而,这种鸟类血凝试验不需要物种特异性的二抗(如ELISA),而且这种微创、非致死性的程序适用于对受保护物种的研究,这与脾试验不同。PHA和SRBC检测已在实验室和野外成功应用。在生态学研究中,鸟类必须在初次注射后24小时或6天被重新捕获,这限制了它们在某些物种中的应用。然而,它们对多种污染物的敏感性以及对多种物种的易适应性,使得PHA和SRBC检测成为鸟类免疫毒性筛选和监测中最常用的检测方法之一。