Hechemy K E, Michaelson E E, Anacker R L, Zdeb M, Sasowski S J, Kleeman K T, Joseph J M, Patel J, Kudlac J, Elliott L B
J Clin Microbiol. 1983 Oct;18(4):938-46. doi: 10.1128/jcm.18.4.938-946.1983.
A latex-Rickettsia rickettsii test for detection of antibodies to Rocky Mountain spotted fever (RMSF) was evaluated during the 1980 RMSF season in 11 laboratories in nine states where the disease is endemic. In a double-blind study, all sera submitted to each laboratory for RMSF testing were also examined by the latex-R. rickettsii test. A portion of each specimen was then sent to the New York State laboratory for testing by latex-R. rickettsii and by the reference microimmunofluorescence test. Results were exchanged at the end of the examination period. At the usual ratio of reactive to nonreactive sera encountered in a diagnostic laboratory on a day-to-day basis, the efficiency of the latex-R. rickettsii test relative to microimmunofluorescence was 96.79% for New York and 93.30% for the collaborating laboratories. Both the latex and microimmunofluorescence tests detected antibodies to RMSF within 7 to 9 days of onset. With the latex-R. rickettsii test--but not necessarily with microimmunofluorescence--a high titer (greater than or equal to 128) on a single serum was diagnostic of active RMSF. Changes in serum titer for patients with multiple sera were similar for both tests. The test detects rickettsial antibodies in patients with active infection, but in most cases it does not detect antibody in patients with past infection. Test reactivity could not be uniquely linked to a particular immunoglobulin class.
1980年落基山斑疹热(RMSF)流行季节期间,在该病流行的九个州的11个实验室对一种用于检测落基山斑疹热抗体的乳胶 - 立氏立克次体试验进行了评估。在一项双盲研究中,提交给每个实验室进行RMSF检测的所有血清也通过乳胶 - 立氏立克次体试验进行检测。然后将每个标本的一部分送到纽约州实验室,用乳胶 - 立氏立克次体试验和参考微量免疫荧光试验进行检测。在检查期结束时交换结果。按照诊断实验室日常遇到的反应性血清与非反应性血清的通常比例,乳胶 - 立氏立克次体试验相对于微量免疫荧光试验的效率,纽约为96.79%,合作实验室为93.30%。乳胶试验和微量免疫荧光试验均在发病后7至9天内检测到RMSF抗体。对于乳胶 - 立氏立克次体试验(但不一定对于微量免疫荧光试验),单份血清中高滴度(大于或等于128)可诊断为活动性RMSF。两份或多份血清患者的血清滴度变化在两种试验中相似。该试验可检测活动性感染患者的立克次体抗体,但在大多数情况下不能检测既往感染患者的抗体。试验反应性不能唯一地与特定免疫球蛋白类别相关联。