Millett B, Sullivan A M, Morimoto M, Parsons G
T Cell Diagnostics, Inc., Woburn, MA.
Biotechniques. 1994 Dec;17(6):1166-71.
Tumor necrosis factor alpha (TNF alpha) is a polypeptide cytokine produced primarily by monocytes and macrophages. It is involved in a wide variety of immune reactions. Measurement of TNF alpha originally depended upon bioassays that are of varying reliability and reproducibility. Early immunoassays for TNF alpha required handling of radioisotopes and costly disposal of radioactive waste. Subsequent use of enzymes as reporter molecules in enzyme immunoassay (EIA) has eliminated the burden of radioisotope handling and its associated costs. However, EIA has presented new challenges. Use of thimerosal as a preservative in EIAs may require high disposal costs due to its mercury content. In addition, many EIAs lack the sensitivity achievable in radioimmunoassay (RIA). We have developed a simple microplate enzyme-linked immunosorbent assay (ELISA) for the detection of TNF alpha in serum, plasma and culture supernatants. Our high affinity capture antibody has enabled us to achieve a sensitivity of 1.5 pg/mL. The assay is calibrated to the World Health Organization (W.H.O.) first international standard for TNF alpha (87/650) and exhibits excellent precision and reproducibility. Tetramethylbenzidine is used to generate the colored end product of the reaction, and thimerosal has been removed from all components.
肿瘤坏死因子α(TNFα)是一种主要由单核细胞和巨噬细胞产生的多肽细胞因子。它参与多种免疫反应。TNFα的测量最初依赖于可靠性和可重复性各不相同的生物测定法。早期针对TNFα的免疫测定需要处理放射性同位素以及对放射性废物进行昂贵的处置。随后在酶免疫测定(EIA)中使用酶作为报告分子消除了处理放射性同位素的负担及其相关成本。然而,EIA带来了新的挑战。在EIA中使用硫柳汞作为防腐剂可能因其汞含量而需要高昂的处置成本。此外,许多EIA缺乏放射免疫测定(RIA)所能达到的灵敏度。我们开发了一种简单的微孔板酶联免疫吸附测定(ELISA)法,用于检测血清、血浆和培养上清液中的TNFα。我们的高亲和力捕获抗体使我们能够达到1.5 pg/mL的灵敏度。该测定法已按照世界卫生组织(W.H.O.)TNFα的首个国际标准(87/650)进行校准,具有出色的精密度和可重复性。使用四甲基联苯胺生成反应的有色终产物,并且所有组分中均已去除硫柳汞。