Terho P, Meurman O
J Med Microbiol. 1981 Feb;14(1):77-87. doi: 10.1099/00222615-14-1-77.
A solid-phase radioimmunoassay (RIA) for IgG and IgA class antibodies to Chlamydia trachomatis was developed with C. trachomatis serotype L2 as antigen. The assay was sensitive, reproducible and correlated well with an immunofluorescence test (r = 0.85). Serum IgG antibodies were detected in 79% of Chlamydia isolation-positive versus 43% of isolation-negative male patients with urethritis, and and serum IgA antibodies in 53% and 21%, respectively. Urethral IgA antibodies, measured from specimens taken for chlamydial isolation, could be detected in 94% and 38%, respectively. From 737 male urethral and 909 female cervical secretions screened for the presence of IgA antibodies, about half were isolation and IgA negative. Only 4% (6/151) of male and 5.4% (2/37) of female isolation-positive specimens were IgA negative. The determination of local IgA antibodies may be used as a screening test in chlamydial genital infections.
以沙眼衣原体血清型L2为抗原,开发了一种用于检测沙眼衣原体IgG和IgA类抗体的固相放射免疫测定法(RIA)。该测定法灵敏、可重复,与免疫荧光试验相关性良好(r = 0.85)。在沙眼衣原体分离阳性的男性尿道炎患者中,79%检测到血清IgG抗体,而分离阴性的患者中这一比例为43%;血清IgA抗体的检测率分别为53%和21%。从用于衣原体分离的标本中测得的尿道IgA抗体,检测率分别为94%和38%。在737份男性尿道分泌物和909份女性宫颈分泌物中筛查IgA抗体的存在情况,约一半标本衣原体分离和IgA检测均为阴性。男性分离阳性标本中只有4%(6/151)、女性分离阳性标本中只有5.4%(2/37)为IgA阴性。局部IgA抗体的检测可作为衣原体性生殖器感染的筛查试验。