Clinical Study | Open Access
Chlamydia trachomatis and Mycoplasma genitalium Plasma Antibodies in Relation to Epithelial Ovarian Tumors
Objective. To assess associations of Chlamydia trachomatis and Mycoplasma genitalium antibodies with epithelial ovarian tumors. Methods. Plasma samples from 291 women, undergoing surgery due to suspected ovarian pathology, were analyzed with respect to C. trachomatis IgG and IgA, chlamydial Heat Shock Protein 60-1 (cHSP60-1) IgG and M. genitalium IgG antibodies. Women with borderline tumors (), ovarian carcinoma (), or other pelvic malignancies () were matched to four healthy controls each. Results. Overall, there were no associations of antibodies with EOC. However, chlamydial HSP60-1 IgG antibodies were associated with type II ovarian cancer () in women with plasma samples obtained >1 year prior to diagnosis (). M. genitalium IgG antibodies were associated with borderline ovarian tumors (). Conclusion. Chlamydial HSP60-1 IgG and M. genitalium IgG antibodies are in this study associated with epithelial ovarian tumors in some subsets, which support the hypothesis linking upper-genital tract infections and ovarian tumor development.
Ovarian cancer is the sixth most common cancer among females and the most lethal gynaecologic malignancy with a 16–51% five-year survival rate globally . No firm conclusions are established on the etiology of ovarian cancer, while 5–10% are attributable to genetic predisposition [2, 3]. Microorganisms causing chronic inflammatory disease have become increasingly investigated in the last decade as possible cancer initiators/promoters. Helicobacter pylori has been linked to gastric cancer, human papillomavirus to cervical cancer, and Hepatitis B and C virus to liver cancer . Chlamydia trachomatis (C. trachomatis) is considered a cofactor in cervical cancer and is primarily associated with squamos cell carcinoma of the cervix [5–7]. The role of persistent infection, leading to chronic inflammation, in the pathogenesis of ovarian cancer has received very little consideration, although a history of pelvic inflammatory disease (PID) is in a case-control study correlated to higher risk for ovarian cancer . C. trachomatis, the most common cause of PID in the developed world [9–11], is the genital infectious agent that has most often been addressed as a possible tumor initiator/promoter of the ovaries [12–15].
Primary infection with C. trachomatis, the most prevalent sexually transmitted bacterium worldwide with an estimated 90 million new cases occurring each year , is often asymptomatic and may persist for several months or years . There is evidence that chlamydial bacteria express high levels of chlamydial heat shock protein 60 (cHSP60), suggested to be antiapoptotic, during persistent infections [18, 19], and serum cHSP60 IgG antibodies are in several studies associated with tubal factor infertility (TFI) [20–24]. Mycoplasma genitalium (M. genitalium) is another sexually transmitted microorganism that has been associated with PID and TFI [25, 26]. Similar to C. trachomatis infections, disease caused by M. genitalium is often asymptomatic and it often remains undetected .
It has been proposed that ovarian tumors can be classified into two groups, type I and type II, based on clinical behavior, pathology, molecular genetic differences, and different precursors [28, 29]. Type II tumors constitute most ovarian carcinomas and are rapidly growing, highly aggressive neoplasms that lack well-defined precursor lesions. Many of the type II tumors, are suggested to originate in the tubal fimbria or peritoneum , are associated with tubal intraepithelial carcinoma (TIC) and “p53 signatures” and originate in the secretory cells . Both C. trachomatis and M. genitalium are especially adept at maintaining long-term relationships with their hosts, modulating and evading the immune system, and are shown to cause infections and inflammation of the fallopian tubes [32–34]. Hence, there is a possibility that these infections might play a role in carcinogenesis of the ovary, particularly the type II carcinomas .
Given the incomplete biological explanations for the etiology of ovarian cancer and the hypothesis of chronic infection and inflammation as part of ovarian tumor pathogenesis we estimated the associations of plasma C. trachomatis IgG, IgA, and cHSP60 IgG and plasma M. genitalium IgG antibodies with ovarian tumors.
2. Materials and Methods
This study is in part a cohort study to compare the prevalence of antibodies in women with different diagnoses going through surgery due to suspected ovarian pathology, and in part a case-control study to compare the antibody prevalence in women with ovarian tumors with matched controls. The study is approved by the Human Ethics Committee of the Medical Faculty, Umeå University, Sweden.
2.1. Study Population
From 1993 through 2001, 430 women who underwent surgery at the Department of Obstetrics and Gynecology, University Hospital of Umeå, Sweden, due to suspected ovarian pathology were included in the study after oral and written informed consent. The women were mainly from Västerbotten County in northern Sweden. In 238 cases, plasma samples drawn in connection with surgery were available. For another 53 cases, prospective plasma samples (maximum 5.1 years prior to diagnosis) from the Northern Sweden Health and Disease Study (NSHDS) were available and included in the analyses. In total, plasma samples were available for 291 women (Figure 1). In cases of borderline ovarian tumors (BOT), epithelial ovarian cancer (EOC), and other malignancies, control plasma samples from the Medical Biobank of Northern Sweden were matched with respect to age (±1 year) and date of plasma-sampling (±3 months). Age criteria had to be relaxed to ±2 years in 49 out of 271 controls (18%), date of plasma-sampling to ±6 months in 4 controls (1%) and both age and date of plasma-sampling in 4 controls (1%). The control plasma samples were collected as part of the NSHDS, which is a population-based, prospective health survey cohort in Västerbotten County, which has been previously reported in detail . The NSHDS serves the same population as the University Hospital of Umeå regarding ovarian tumor surgery. Control subjects were alive and without a cancer diagnosis (except basalioma) at the time of the diagnosis of the index case. Four matched controls per case were analyzed.
2.2. C. trachomatis Antibody Analyses
C. trachomatis-specific IgG and IgA antibodies, as well as Chlamydia pneumoniae (C. pneumoniae) IgG antibodies, were determined by the microimmunofluorescence (MIF) test (MRL Diagnostics/Focus, Cypress, CA, USA) specific for serovar D-K, according to the instructions of the manufacturer. Briefly, plasma dilutions at 1/40 (IgG) and 1/16 (IgA) were used. A weak specific immunofluorescence signal in the 1/40 (IgG) and 1/16 (IgA) dilution was reported as positive in 1/20 and 1/8, respectively. Detection of cHSP60 type I (cHSP60-1) IgG antibodies was performed using the commercial cHSP60-1 IgG ELISA technique (Medac, Germany). Protocol and validation criteria of the assay were followed according to the manufacturer’s instructions. Briefly, patient plasmas were diluted 1/50 and tested in duplicate. Cut off was defined as the mean optical density (OD) value of the negative control plus 0.350 and results are presented as plus (+) or minus (−). Plasma presenting OD values ±10% of the cut off value were interpreted as indeterminant and were excluded from analysis.
2.3. M. genitalium Antibody Analysis
M. genitalium IgG antibodies were detected using a M. genitalium Lipid associated membrane protein-enzyme immuno assay (LAMP-EIA) as previously described . Briefly, 100 μL of plasma samples diluted 1/50 in blocking solution was used. Serum from a patient with a M. genitalium—PCR positive result in the urogenital tract specimen was used as a positive control, and pooled sera from blood donors were used as a negative control in each run. The cut off level was set to 0.3 OD and was determined as 3-standard deviations above the negative-control mean.
2.4. Clinical Characteristics and Histopathologic Diagnosis
Information on histopathologic diagnosis, according to the World Health Organization classification , as well as data on clinical characteristics, was extracted from the medical records. Histopathologic diagnoses were reviewed by a specialist in gynecologic pathology (EL) at the Department of Laboratory Medicine, Clinical Pathology, University Hospital of Umeå. A reclassification according to the proposed hypothesis of a type I and a type II ovarian pathogenetic pathway  was done. The type I tumor group consisted of low-grade serous carcinomas and mucinous, endometrioid and clear cell carcinomas. The type II tumor group consisted of ovarian moderate and high-grade serous carcinomas, malignant mixed mesodermal tumors and undifferentiated carcinomas, as well as serous high-grade or undifferentiated peritoneal and fallopian tube cancers.
2.5. Statistical Analysis
Statistical analyses were performed using the SPSS software (version 17.0). The pearson Chi-square, and when the expected frequency was <5, Fisher’s exact test was used to analyze differences between groups with dichotomous data. Fisher’s exact confidence intervals were calculated for the prevalence estimates. Mann-Whitney U test was applied to analyze continuous data not normally distributed. A 2-sided P value of less than .05 was considered significant. Odd ratios (OR) and 95% confidence intervals (CI) were calculated using binary logistic regression analysis.
Clinical characteristics of the women going through ovarian surgery are described in Table 1. Demographic data are not complete, as indicated in the table, particularly among women with benign conditions, but the antibody prevalence was similar in women with or without demographic data. However, women with data on hormone replacement therapy (HRT) use presented C. trachomatis IgG () and cHSP60-1 IgG () more often than women lacking these data. Women with HRT data were younger (). Women with PID data more often presented C. trachomatis IgG () and cHSP60-1 IgG () antibodies. C. trachomatis IgG antibodies were associated with ever smoking () and HRT use (), while cHSP60-1 IgG antibodies were associated with ever smoking () and older age at menarche (). No other associations of antibodies with demographic data were found.
| Values are presented as medians and range (minimum and maximum values of age, menarche, menopause, parity, and BMI); or number and percentage of patients in each group (0 children, ≥3 children, oral contraceptive pill use ≥1 year, past or current HRT use, past or current smoking, history of PID: prospective plasma samples>1 year prior to diagnosis, type I pathogenetic pathway, and type II pathogenetic pathway). |
BOT: borderline ovarian tumor; EOC: epithelial ovarian cancer; HRT: hormone replacement therapy; PID: pelvic inflammatory disease; BMI: body mass index; SSPC: Serous Surface Papillary Carcinoma.
aVariable with partial missing data.
bMann-Whitney U test.
cFisher’s exact test.
Cases where no plasma samples or controls were available (Figure 1) had the same distribution of diagnoses as cases with matched controls. Reasons for lacking a plasma sample were mostly due to human error when including women about to have surgery. Difficulties in finding controls depend either on high age (>72 years) of the case () and/or a plasma sample from the first years of the study (1993–1995) (). No differences were found in the prevalence of antibodies between cases with or without matched controls.
The prevalence of C. pneumoniae IgG antibodies was 79.8% (95% CI: 76.2%–82.4%) and no covariations of C. trachomatis IgG, IgA, or cHSP60-1 IgG antibodies with C. pneumoniae IgG antibodies were found. C. trachomatis IgG and cHSP60-1 IgG antibodies were associated with a 74% concordance rate.
The prevalence of C. trachomatis IgG, cHSP60-1 IgG, and M. genitalium IgG antibodies among all women tested, including matched controls, are given in Table 2.
| BOT: borderline ovarian tumors; EOC: epithelial ovarian cancer.|
aCases with matched controls available.
bFour controls per case from the NSHDS (Northern Sweden Health and Disease Study) were matched with respect to age and date of plasma-sampling.
cA few subjects had cHSP60 IgG antibody results that were indeterminant and therefore excluded from the statistical analyses. Assigning them extreme values (all positive or negative) did not change the main outcomes.
dEpithelial ovarian cancer with plasma samples drawn 1.3 to 5.1 years prior to diagnosis.
Pearson Chi-square, and when the expected frequency was <5, Fisher’s exact test was used.
Notably, there is a significantly higher prevalence of M. genitalium IgG antibodies among women with borderline tumors compared with matched controls and women with benign conditions. Three of the four cases positive in M. genitalium IgG were also positive in cHSP60-1 IgG. In the subgroup of ovarian cancer cases that had prospective plasma samples collected more than one year prior to diagnosis , cHSP60-1 IgG antibodies were more prevalent among cases compared with women with benign conditions. The prevalence of plasma C. trachomatis IgA antibodies among all cases was 9.6% (95% CI: 6.5%–13.6%) with no association with ovarian tumors.
The antibody prevalences among women with type I tumors, or any of the histological subgroups of EOC, were not raised compared with neither matched controls nor women with benign conditions when plasma samples drawn in connection with diagnosis was analyzed (data not shown). The results of the antibody analyses for the type II ovarian tumors are described in Table 3. In plasma samples drawn in connection with diagnosis in type II tumors, there was no evidently higher prevalence of cHSP60-1 IgG antibodies compared with matched controls or women with benign conditions. However, when prospective plasma samples of the type II tumor group () were analyzed, the prevalence of cHSP60-1 IgG antibodies was significantly higher than in controls. Six out of seven cases were cHSP60-1 IgG antibody-positive. The clinical characteristics of this subgroup are presented in Table 4. The one woman that was cHSP60-1 IgG antibody-negative had an undifferentiated ovarian cancer. Assigning indeterminant cHSP60-1 IgG antibody results either positive or negative values did not change the main outcomes.
aCases with matched controls available.|
bFour controls per case from the NSHDS (Northern Sweden Health and Disease Study) were matched with respect to age and date of plasma-sampling.
cA few subjects had cHSP60 IgG antibody results that were indeterminant and therefore excluded from the statistical analyses. Assigning them extreme values (all positive or all negative) did not change the main outcomes.
dA subgroup of type II malignancies where plasma samples were drawn 1.3 to 5.1 years prior to diagnosis.
The Pearson chi-square was used first,and when the expected frequency was <5, Fisher’s exact test was used.
|Values are presented as medians and range (minimum and maximum values of age, menarche, menopause, parity, and BMI); or number and percentage of patients in each group (0 children, ≥3 children, oral contraceptive pill use ≥1 year, past or current HRT use, past or current smoking, history of PID). |
HRT: hormone replacement therapy; PID: pelvic inflammatory disease; BMI: body mass index; SSPC: Serous Surface Papillary Carcinoma.
aMissing data in one case.
In this analysis of a cohort of women going through surgery due to suspected ovarian pathology, we found an association of plasma cHSP60-1 IgG antibodies with type II ovarian tumors when prospective plasma samples were analyzed. Additionally, an association of plasma M. genitalium IgG antibodies with borderline ovarian tumors was detected. Neither C. trachomatis IgG nor IgA was significantly associated with any type of tumors in this cohort.
Strengths of this study are the population-based selection of case and control subjects with controls matched with respect to age and time of plasma-sampling. Moreover, the cohort was relatively homogeneous, the collection and storage of blood samples was standardized, the measurement of antibodies was performed in a research laboratory with laboratory personnel unaware of case-control status, the C. trachomatis IgG and IgA antibody test method is serovariant D-K specific, a standardized cHSP60-1 IgG test method was used, and the M. genitalium IgG method has no cross-reactivity to M. pneumoniae. Limitations of the study include the small number of subjects with eligible plasma samples and matched controls, making subgroup analysis and analysis of combinations of antibodies difficult. Incomplete data on clinical characteristics reduces the possibility to correct for potential confounders. However, the subgroup of women with type II carcinoma and prospectively drawn plasma samples did not seem to stand out concerning their clinical characteristics. The plasma samples in cases were mostly drawn within a few days prior to surgery. Analyzing plasma samples drawn more than one year prior to diagnosis might have been a more plausible approach considering the result of the subgroup analysis of cases with prospectively drawn plasma samples and previous studies regarding C. trachomatis and cervical cancer [39–41].
The association of cHSP60-1 IgG antibodies with ovarian cancer, and the slightly higher prevalence of C. trachomatis IgG antibodies, is consistent with the findings of an association of high levels of serum C. trachomatis IgG and cHSP60-1 IgG antibodies with ovarian cancer in a population-based case-control study . Wong et al., however, did not find an association of Chlamydia serum IgG, IgA, or IgM antibodies with epithelial ovarian cancer , maybe because the test method applied was not C. trachomatis specific and detected antibodies to all chlamydial species including C. pneumoniae. Serum C. trachomatis IgG antibodies were not associated with ovarian cancer in the recent study by Ness et al. , rather, a protective effect in younger-age groups was found. In that study, serum samples obtained after cancer treatment were analyzed possibly masking an association. Chlamydial HSP60-1 IgG antibodies were the antibodies most clearly associated with ovarian type II tumors in this study. Chlamydial HSP60 expression is found to be increased in prolonged infections with C. trachomatis and is suggested to have an antiapoptotic effect. This effect facilitates the survival of the bacteria within the host [18, 19], but at the same time it facilitates the survival of DNA-damaged cells leading to increased risk for cancer initiation .
The subgroup of women with prospectively drawn plasma samples displayed larger differences in antibody prevalence between cases and controls than women with plasma samples drawn at the time of diagnosis. Similar to this, concerning cervical cancer, Naucler et al. observed a positive correlation between C. trachomatis IgG antibodies and cases observed during followup, but not with cases identified at baseline ; cHSP60-1 IgG antibodies have been associated with cervical cancer in cases with long lag time ; and C. trachomatis DNA in Pap smears taken many years before diagnosis have been associated with cervical cancer . A conceivable explanation for this might be that C. trachomatis exerts its effect many years, or decades, before the cancer is overt and that antibodies might decline over time [43–46].
Type II tumors are suggested to originate in the secretory cells of the tubal fimbria in a significant percentage of tumors [30, 31, 47, 48]. The secretory cells are the cell type where chlamydial inclusions have been detected in experimental models [49, 50] and the bacteria are known to cause damage to the tubal fimbria. Therefore, it seems plausible that this subgroup was the one associated with cHSP60-1 IgG antibodies. However, the subgroup of women with prospective plasma samples was small, which will raise concern that this result is due to chance.
Plasma C. trachomatis IgA antibodies displayed varying and low prevalence in all groups and were not associated with the finding of ovarian tumors. IgA antibodies, in contrast to IgG and cHSP60-1 IgG, are more likely to reflect an active on-going phase of the infection which might be passed several years before the tumor is overt.
The association between M. genitalium IgG antibodies and borderline ovarian tumors might represent a typeIerror since a Bonferroni correction eliminates the significance of the results. M. genitalium is not previously studied in relation to ovarian cancer even though Mycoplasma DNA (PCR targeting 15 different species) was found in 59% of ovarian cancer tissues . On the other hand, in a study by Quirk et al., Mycoplasma ribosomal DNA (11 different Mycoplasma species but not M. genitalium) was found not associated with ovarian tumors . In vitro, M. genitalium can cause inflammatory changes of the epithelium to the human Fallopian tubes .
The prevalence of cHSP60-1 IgG antibodies was in this study relatively high compared with the prevalence of C. trachomatis IgG antibodies, particularly in the subgroup of women with type II carcinoma. This is different from the findings in most other studies and might reflect differences in laboratory methods. Another explanation is that the C. trachomatis, infections that will eventually lead to carcinomatous changes, produce higher amounts of cHSP60 or produces cHSP60 for a more protracted period of time inducing the production of cHSP60-1 IgG antibodies. Alternatively, there is a difference in the host immune system that leads both to the continuous production of cHSP60-1 IgG antibodies and renders the host more susceptible to carcinomatous changes. This might be the case, if for example, an autoimmune cross-reaction to the human HSP60  has a pathological role to play.
In conclusion, we have identified an association of plasma cHSP60-1 IgG antibodies with type II ovarian tumors in the subgroup of women with plasma samples drawn more than one year prior to surgery. This novel finding points toward another possible explanation of the etiology of ovarian neoplasia. M. genitalium was weakly associated with borderline ovarian tumors. Defining C. trachomatis and M. genitalium as disease precursors would have great impact on the importance of preventing, diagnosing, and treating C. trachomatis and M. genitalium infections to reduce not only fertility related morbidity and chronic pelvic pain, but also ovarian tumor development. However, the results have to be confirmed in larger studies and in studies with prospective plasma samples, and the mechanisms by which the bacteria might initiate or promote tumor development have to be clarified. Nevertheless, this study provides support to the intriguing hypothesis of a link between upper-genital tract infectious agents such as C. trachomatis, possibly M. genitalium, and ovarian tumor development.
This study was supported by grants from Lion’s Cancer Research Foundation at Umeå University, Sweden; Kempe Foundation, Umeå, Sweden; Organon Research Foundation, Sweden; Anna Cederbergh Foundation for Medical Research, Sweden. The authors would like to thank Peter Lindgren for enrolling the patients and collecting plasma samples, Lennart Nyström for help and support with statistical considerations, and Nitesh Mistry, Elisabeth Dahlberg, Birgitta Ekblom, Pernilla Andersson, and Lena Jansson for their skilful technical assistance. The study was conducted at the Department of Clinical Science/Obstetsrics & Gynecology, Department of Medical Biosciences/Pathology, Department of Clinical Microbiology/Virology and Public Health and Clinical Medicine, Nutritional research Umeå and Clinical Research Centre, Örebro University Hospital Örebro, Sweden.
- R. Sankaranarayanan and J. Ferlay, “Worldwide burden of gynaecological cancer: the size of the problem,” Best Practice and Research: Clinical Obstetrics and Gynaecology, vol. 20, no. 2, pp. 207–225, 2006.
- A. Berchuck, J. M. Schildkraut, J. R. Marks, and P. A. Futreal, “Managing hereditary ovarian cancer risk,” Cancer, vol. 86, no. 11, pp. 2517–2524, 1999.
- C. La Vecchia, “Epidemiology of ovarian cancer: a summary review,” The European Journal of Cancer Prevention, vol. 10, no. 2, pp. 125–129, 2001.
- S. F. Moss and M. J. Blaser, “Mechanisms of disease: inflammation and the origins of cancer,” Nature Clinical Practice Oncology, vol. 2, no. 2, pp. 90–97, 2005.
- M. M. Madeleine, T. Anttila, S. M. Schwartz et al., “Risk of cervical cancer associated with Chlamydia trachomatis antibodies by histology, HPV type and HPV cofactors,” International Journal of Cancer, vol. 120, no. 3, pp. 650–655, 2007.
- P. Koskela, T. Anttila, T. Bjørge et al., “Chlamydia trachomatis infection as a risk factor for invasive cervical cancer,” International Journal of Cancer, vol. 85, no. 1, pp. 35–39, 2000.
- T. Anttila, P. Saikku, P. Koskela et al., “Serotypes of Chlamydia trachomatis and risk for development of cervical squamous cell carcinoma,” Journal of the American Medical Association, vol. 285, no. 1, pp. 47–51, 2001.
- H. A. Risch and G. R. Howe, “Pelvic inflammatory disease and the risk of epithelial ovarian cancer,” Cancer Epidemiology Biomarkers and Prevention, vol. 4, no. 5, pp. 447–451, 1995.
- L. Westrom and P. Wolner-Hanssen, “Pathogenesis of pelvic inflammatory disease,” Genitourinary Medicine, vol. 69, no. 1, pp. 9–17, 1993.
- “Tubal infertility: serologic relationship to past chlamydial and gonococcal infection. World Health Organization Task Force on the Prevention and Management of Infertility,” Sexually Transmitted Diseases, vol. 22, no. 2, pp. 71–77, 1995.
- S. Barrett and C. Taylor, “A review on pelvic inflammatory disease,” International Journal of STD and AIDS, vol. 16, no. 11, pp. 715–721, 2005.
- J. Paavonen, “Chlamydia trachomatis and cancer,” Sexually Transmitted Infections, vol. 77, no. 3, pp. 154–156, 2001.
- R. B. Ness, M. T. Goodman, C. Shen, and R. C. Brunham, “Serologic evidence of past infection with Chlamydia trachomatis, in relation to ovarian cancer,” Journal of Infectious Diseases, vol. 187, no. 7, pp. 1147–1152, 2003.
- R. B. Ness, C. Shen, D. Bass et al., “Chlamydia trachomatis serology in women with and without ovarian cancer,” Infectious Diseases in Obstetrics and Gynecology, vol. 2008, Article ID 219672, 5 pages, 2008.
- A. Wong, A. B. Maclean, S. J. Furrows, G. L. Ridgway, P. J. Hardiman, and C. W. Perrett, “Could epithelial ovarian cancer be associated with chlamydial infection?” The European Journal of Gynaecological Oncology, vol. 28, no. 2, pp. 117–120, 2007.
- WHO, Global Prevalence and Incidence of Selected Curable Sexually Transmitted Infections. Overview and Estimates, World Health Organization, Geneva, Switzerland, 2001.
- P. Mpiga and M. Ravaoarinoro, “Chlamydia trachomatis persistence: an update,” Microbiological Research, vol. 161, no. 1, pp. 9–19, 2006.
- W. L. Beatty, G. I. Byrne, and R. P. Morrison, “Morphologic and antigenic characterization of interferon gamma-mediated persistent Chlamydia trachomatis infection in vitro,” Proceedings of the National Academy of Sciences of the United States of America, vol. 90, no. 9, pp. 3998–4002, 1993.
- D. Dean and V. C. Powers, “Persistent Chlamydia trachomatis infections resist apoptotic stimuli,” Infection and Immunity, vol. 69, no. 4, pp. 2442–2447, 2001.
- P. Claman, L. Honey, R. W. Peeling, P. Jessamine, and B. Toye, “The presence of serum antibody to the chlamydial heat shock protein (CHSP60) as a diagnostic test for tubal factor infertility,” Fertility and Sterility, vol. 67, no. 3, pp. 501–504, 1997.
- J. E. den Hartog, J. A. Land, F. R. Stassen, A. G. Kessels, and C. A. Bruggeman, “Serological markers of persistent C. trachomatis infections in women with tubal factor subfertility,” Human Reproduction, vol. 20, no. 4, pp. 986–990, 2005.
- S. Dieterle and J. Wollenhaupt, “Humoral immune response to the chlamydial heat shock proteins hsp60 and hsp70 in Chlamydia-associated chronic salpingitis with tubal occlusion,” Human Reproduction, vol. 11, no. 6, pp. 1352–1356, 1996.
- A. Idahl, L. Abramsson, U. Kumlin, J. A. Liljeqvist, and J. I. Olofsson, “Male serum Chlamydia trachomatis IgA and IgG, but not heat shock protein 60 IgG, correlates with negatively affected semen characteristics and lower pregnancy rates in the infertile couple,” International Journal of Andrology, vol. 30, no. 2, pp. 99–107, 2007.
- A. Tiitinen, H. M. Surcel, M. Halttunen et al., “Chlamydia trachomatis and chlamydial heat shock protein 60-specific antibody and cell-mediated responses predict tubal factor infertility,” Human Reproduction, vol. 21, no. 6, pp. 1533–1538, 2006.
- H. F. Clausen, J. Fedder, M. Drasbek et al., “Serological investigation of Mycoplasma genitalium in infertile women,” Human Reproduction, vol. 16, no. 9, pp. 1866–1874, 2001.
- H. F. Svenstrup, J. Fedder, S. E. Kristoffersen, B. Trolle, S. Birkelund, and G. Christiansen, “Mycoplasma genitalium, Chlamydia trachomatis and tubal factor infertility—a prospective study,” Fertility and Sterility, vol. 90, no. 3, pp. 513–520, 2008.
- L. Falk, H. Fredlund, and J. S. Jensen, “Signs and symptoms of urethritis and cervicitis among women with or without Mycoplasma genitalium or Chlamydia trachomatis infection,” Sexually Transmitted Infections, vol. 81, no. 1, pp. 73–78, 2005.
- I. M. Shih and R. J. Kurman, “Ovarian tumorigenesis: a proposed model based on morphological and molecular genetic analysis,” The American Journal of Pathology, vol. 164, no. 5, pp. 1511–1518, 2004.
- R. J. Kurman, K. Visvanathan, R. Roden, T. C. Wu, and I. M. Shih, “Early detection and treatment of ovarian cancer: shifting from early stage to minimal volume of disease based on a new model of carcinogenesis,” The American Journal of Obstetrics and Gynecology, vol. 198, no. 4, pp. 351–356, 2008.
- C. P. Crum, R. Drapkin, A. Miron et al., “The distal fallopian tube: a new model for pelvic serous carcinogenesis,” Current Opinion in Obstetrics and Gynecology, vol. 19, no. 1, pp. 3–9, 2007.
- Y. Lee, A. Miron, R. Drapkin et al., “A candidate precursor to serous carcinoma that originates in the distal fallopian tube,” Journal of Pathology, vol. 211, no. 1, pp. 26–35, 2007.
- S. F. Dallo and J. B. Baseman, “Intracellular DNA replication and long-term survival of pathogenic mycoplasmas,” Microbial Pathogenesis, vol. 29, no. 5, pp. 301–309, 2000.
- R. J. Hogan, S. A. Mathews, S. Mukhopadhyay, J. T. Summersgill, and P. Timms, “Chlamydial persistence: beyond the biphasic paradigm,” Infection and Immunity, vol. 72, no. 4, pp. 1843–1855, 2004.
- G. I. Byrne and D. M. Ojcius, “Chlamydia and apoptosis: life and death decisions of an intracellular pathogen,” Nature Reviews Microbiology, vol. 2, no. 10, pp. 802–808, 2004.
- J. T. Quirk and J. M. Kupinski, “Chronic infection, inflammation and epithelial ovarian cancer,” Medical Hypotheses, vol. 57, no. 4, pp. 426–428, 2001.
- R. Palmqvist, G. Hallmans, S. Rinaldi et al., “Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden,” Gut, vol. 50, no. 5, pp. 642–646, 2002.
- M. Jurstrand, J. S. Jensen, A. Magnuson, F. Kamwendo, and H. Fredlund, “A serological study of the role of Mycoplasma genitalium in pelvic inflammatory disease and ectopic pregnancy,” Sexually Transmitted Infections, vol. 83, no. 4, pp. 319–323, 2007.
- F. A. Tavassoli and P. Devilee, World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of the Breast and Female Genital Organs, IARC Press, Lyon, France, 2003.
- P. Naucler, H. C. Chen, K. Persson et al., “Seroprevalence of human papillomaviruses and Chlamydia trachomatis and cervical cancer risk: nested case-control study,” Journal of General Virology, vol. 88, part 3, pp. 814–822, 2007.
- J. Paavonen, K. P. Karunakaran, Y. Noguchi et al., “Serum antibody response to the heat shock protein 60 of Chlamydia trachomatis in women with developing cervical cancer,” The American Journal of Obstetrics and Gynecology, vol. 189, no. 5, pp. 1287–1292, 2003.
- K. L. Wallin, F. Wiklund, T. Luostarinen et al., “A population-based prospective study of Chlamydia trachomatis infection and cervical carcinoma,” International Journal of Cancer, vol. 101, no. 4, pp. 371–374, 2002.
- V. Di Felice, S. David, F. Cappello, F. Farina, and G. Zummo, “Is chlamydial heat shock protein 60 a risk factor for oncogenesis?” Cellular and Molecular Life Sciences, vol. 62, no. 1, pp. 4–9, 2005.
- M. Puolakkainen, E. Vesterinen, E. Purola, P. Saikku, and J. Paavonen, “Persistence of chlamydial antibodies after pelvic inflammatory disease,” Journal of Clinical Microbiology, vol. 23, no. 5, pp. 924–928, 1986.
- A. Clad, H. M. Freidank, M. Kunze et al., “Detection of seroconversion and persistence of Chlamydia trachomatis antibodies in five different serological tests,” The European Journal of Clinical Microbiology and Infectious Diseases, vol. 19, no. 12, pp. 932–937, 2000.
- B. Piura, B. Sarov, and I. Sarov, “Persistence of antichlamydial antibodies after treatment of acute salpingitis with doxycycline,” The European Journal of Obstetrics Gynecology and Reproductive Biology, vol. 48, no. 2, pp. 117–121, 1993.
- W. Chaim, Z. Edelstein, B. Sarov, and I. Sarov, “The long term follow-up of asymptomatic women with Chlamydia trachomatis,” Archives of Gynecology and Obstetrics, vol. 251, no. 4, pp. 159–164, 1992.
- R. J. Kurman and I. M. Shih, “Pathogenesis of ovarian cancer: lessons from morphology and molecular biology and their clinical implications,” International Journal of Gynecological Pathology, vol. 27, no. 2, pp. 151–160, 2008.
- D. W. Kindelberger, Y. Lee, A. Miron et al., “Intraepithelial carcinoma of the fimbria and pelvic serous carcinoma: evidence for a causal relationship,” The American Journal of Surgical Pathology, vol. 31, no. 2, pp. 161–169, 2007.
- D. L. Patton, S. A. Halbert, C. C. Kuo, S. P. Wang, and K. K. Holmes, “Host response to primary Chlamydia trachomatis infection of the fallopian tube in pig-tailed monkeys,” Fertility and Sterility, vol. 40, no. 6, pp. 829–840, 1983.
- D. L. Patton, D. V. Landers, and J. Schachter, “Experimental Chlamydia trachomatis salpingitis in mice: initial studies on the characterization of the leukocyte response to chlamydial infections,” Journal of Infectious Diseases, vol. 159, no. 6, pp. 1105–1110, 1989.
- P. J. Chan, I. M. Seraj, T. H. Kalugdan, and A. King, “Prevalence of mycoplasma conserved DNA in malignant ovarian cancer detected using sensitive PCR-ELISA,” Gynecologic Oncology, vol. 63, no. 2, pp. 258–260, 1996.
- J. T. Quirk, J. M. Kupinski, and R. A. DiCioccio, “Detection of Mycoplasma ribosomal DNA sequences in ovarian tumors by nested PCR,” Gynecologic Oncology, vol. 83, no. 3, pp. 560–562, 2001.
- A. Baczynska, P. Funch, J. Fedder, H. J. Knudsen, S. Birkelund, and G. Christiansen, “Morphology of human Fallopian tubes after infection with Mycoplasma genitalium and Mycoplasma hominis—in vitro organ culture study,” Human Reproduction, vol. 22, no. 4, pp. 968–979, 2007.
- A. Neuer, S. D. Spandorfer, P. Giraldo, S. Dieterle, Z. Rosenwaks, and S. S. Witkin, “The role of heat shock proteins in reproduction,” Human Reproduction Update, vol. 6, no. 2, pp. 149–159, 2000.
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