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Published on: August 11, 2012
Interpretation of Chlamydia trachomatis antibody response in chlamydial oculogenital infection
H C Patel1, B T Goh, N D Viswalingam
1Diagnostic Clinic, Moorfields Eye Hospital, London, UK.
Insights
The micro-immunofluorescence test detects chlamydial infections with high accuracy, but cross-reactivity between species is common. Serological diagnosis is useful, but results require careful interpretation due to potential cross-reactivity.
Area of Science:
- Ophthalmology
- Infectious Diseases
- Immunology
Background:
- Chlamydia trachomatis is a significant cause of ocular and genital infections.
- Accurate serological diagnosis is crucial for effective treatment and epidemiological studies.
- The micro-immunofluorescence (micro-IF) test is a key diagnostic tool for chlamydial infections.
Purpose of the Study:
- To evaluate the chlamydial antibody response using the micro-IF test in various infection groups.
- To assess antibody cross-reactivity between different Chlamydia species and serovars.
- To determine the diagnostic accuracy of the micro-IF test for chlamydial oculogenital infections.
Main Methods:
- Studied antibody responses in patients with genital, ocular, or combined oculogenital infections.
- Included control groups with adenovirus conjunctivitis and uninfected male partners.
- Analyzed antibody cross-reactivity against different Chlamydia species and serovars using the micro-IF test.
Main Results:
- High IgG antibody prevalence (94%) was observed in patients with chlamydial oculogenital infection.
- Significant cross-reactivity was noted between different Chlamydia species (71%) and C. trachomatis serovars (92%).
- The micro-IF test demonstrated high sensitivity and specificity for diagnosing chlamydial conjunctivitis and oculogenital infections.
Conclusions:
- The micro-IF test is a valuable adjunct for diagnosing chlamydial infections.
- Cross-reactivity necessitates caution when interpreting serological results, especially in epidemiological studies.
- Dual infections may elicit an anamnestic antibody response, influencing diagnostic interpretation.
Objective:
To study: (a) the chlamydial antibody response (to the D-K serovars) using the micro-immunofluorescence (micro-IF) test in the following groups: (I) chlamydial genital infection only, (II) chlamydial ocular infection only, (III) combined chlamydial ocular and genital infection (oculo-genital infection), (IV) chlamydial ocular infection with chlamydia-negative non-gonococcal urethritis, (V) adenovirus conjunctivitis (control group 1), (VI) male partners of group I-IV with no chlamydial oculogenital infection or non-gonococcal urethritis (control group 2) (b) the cross reactivity of antibodies in patients' sera between the three chlamydial species and within the serovars of C trachomatis in those with culture-positive chlamydial oculo-genital infection.
Setting:
oculogenital (diagnostic) clinic at Moorfields Eye Hospital, London, UK.
Subjects:
209 consecutive patients attending the clinic with Chlamydia trachomatis oculogenital infection and 86 patients with adenovirus conjunctivitis (control group 1) and 55 male partners with no evidence of chlamydial oculogenital infection or non-gonococcal urethritis (control group 2).
Results:
Of all the patients with proven chlamydial oculogenital infection, 10.5% (22/209) and 94% (197/209) had IgM and IgG antibodies respectively. The geometric mean IgG antibody titres (GMT) were 1:98, 1:123, 1:245 and 1:101 in groups I to IV respectively. The IgG GMT values seen in control groups 1 and 2 were 1:45 and 1:36 respectively. Only 2/86(2%) patients in group V (control group 1) had IgG chlamydial antibodies of 1:32 and 1:64, whilst only 1/55(1.8%) and 4/55(7.3%) of patients in group VI(control group 2) had chlamydial IgG antibody titres of > or = 1:256 and > or = 1:128 respectively. A four-fold rise or fall in IgG antibody titre occurred in 56%(107/192) of patient groups I-IV over 2-6 weeks. Low titre cross-reactive antibody responses against different chlamydial species and serovars were commonly seen; 71%(148/209) of all patients showed cross-reactivity with Chlamydia pneumoniae or psittaci species or both, whilst 92% (193/209) of patients showed some level of cross reactivity to other pooled serovars of C trachomatis (A-C and L 1-3).
Conclusions:
Serological diagnosis of chlamydial infection as evidenced by a positive IgM antibody response, high IgG titre (> or = 1:256) or > or = 4-fold rise or fall in IgG antibody titre was seen in 78%(163/209) of patients with culture-positive chlamydial oculogenital infection. Chlamydial IgG antibody titres of > or = 1:256 had a sensitivity of 42.6%, specificity of 98.2%, positive predictive value of 98.8% and a negative predictive value of 31% for chlamydial infection at any site, when considering groups I-IV and control group 2. In this study of 216 patients with conjunctivitis, a positive IgG antibody response (titre > or = 1:16) had a sensitivity of 98.5%, specificity of 97.7%, positive predictive value of 98.5% and a negative predictive value of 97.7%, for chlamydial conjunctivitis. Patients with dual chlamydial infection of conjunctiva and genital tract had a higher IgG GMT titre than those with ocular or genital infection alone: infection at a second site may produce an anamnestic response. Although the micro-IF test is a useful adjunct for the diagnosis of chlamydial infection, cross-reactivity between different chlamydial species and serovars is common. Chlamydial seroepidemiological studies should be interpreted with caution, as studies may attribute a serological response to a particular species or serovar in a setting where two or more are prevalent.
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