Barrett T J, Snyder J D, Blake P A, Feeley J C
J Clin Microbiol. 1982 Feb;15(2):235-7. doi: 10.1128/jcm.15.2.235-237.1982.
Because typhoid fever continues to be a major cause of illness in many developing countries, there is a clear need for a sensitive and specific test that will permit rapid laboratory diagnosis of the disease. An enzyme-linked immunosorbent assay (ELISA) has recently been developed and tested, both in the laboratory and in a clinical situation, for its ability to detect Vi antigen in urine. The ELISA was capable of detecting as little as 1 ng of purified Vi antigen per ml in urine, compared with 100 ng/ml detectable by a previously tested coagglutination method. It could also detect antigen in urine diluted as much as 1:1,024 in normal urine. In tests of urine specimens from six stool culture-positive persons in a small typhoid outbreak in the United States, the ELISA detected antigen in specimens from four of the six patients. The ELISA also proved to be specific, giving no false-positive results for specimens from 50 persons who did not have typhoid fever. The apparent high sensitivity and specificity of this ELISA make it a promising test for rapid diagnosis of typhoid fever.
由于伤寒热仍是许多发展中国家主要的致病原因,因此显然需要一种灵敏且特异的检测方法,以便能在实验室中快速诊断该疾病。最近研发并在实验室及临床环境中对一种酶联免疫吸附测定法(ELISA)进行了测试,以检测其在尿液中检测Vi抗原的能力。ELISA能够检测出尿液中每毫升低至1纳克的纯化Vi抗原,相比之下,之前测试的协同凝集法可检测出的浓度为每毫升100纳克。它还能检测出在正常尿液中稀释至1:1024的尿液中的抗原。在美国一次小型伤寒热暴发中,对六名粪便培养呈阳性者的尿液样本进行检测时,ELISA在六名患者中的四名患者样本中检测到了抗原。ELISA也被证明具有特异性,对50名未患伤寒热者的样本未给出假阳性结果。这种ELISA明显的高灵敏度和特异性使其成为快速诊断伤寒热的一种有前景的检测方法。