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1.
PLoS One ; 19(6): e0305279, 2024.
Article in English | MEDLINE | ID: mdl-38861585

ABSTRACT

OBJECTIVES: Chlamydia trachomatis (chlamydia) is one of the most reported bacterial sexually transmitted infections (STI) worldwide. Chlamydia can cause long term complications such as pelvic inflammatory disease (PID), ectopic pregnancy (EP) and tubal factor infertility (TFI). Changing testing strategies, for example reduced asymptomatic testing, influence chlamydia surveillance, highlighting the need for exploring alternative ways of monitoring chlamydia. We investigated the possibility of introducing routine surveillance of chlamydia related long term complications. METHODS: A qualitative study including 15 in-depth interviews with a purposive sample of gynaecologists, general practitioners (GP), sexual health and emergency doctors was conducted in the Netherlands in 2021-2022. A semi-structured interview guide focused on experiences with diagnosis and registration of PID, EP and TFI and how a change in asymptomatic chlamydia testing strategy might influence this. Interviews were transcribed and analysed using a thematic approach. RESULTS: Analysis showed that gynaecologists most frequently reported diagnosing PID, EP and TFI. Other professions rarely diagnose these complications, with emergency doctors only diagnosing EP. Most respondents reported unique registration codes for PID and EP, but the coding for TFI is more ambiguous. They reflected that diagnosis and registration of PID, EP and TFI are handled differently within their professions. Most respondents acknowledged registration in diagnostic codes as a useful surveillance tool. They expressed concerns in representativeness (e.g. differences in interpretation of diagnosis criteria) and data quality for surveillance. CONCLUSIONS: Patient files of gynaecologists are likely to be most complete for monitoring trends of diagnosed chlamydia related long term complications in the Netherlands. However, when establishing a chlamydia complication surveillance system, professionals should be engaged in further standardizing diagnosis and registration practices. This will improve the quality and interpretability of complication surveillance and facilitate comparison between countries.


Subject(s)
Chlamydia Infections , Chlamydia trachomatis , Pelvic Inflammatory Disease , Humans , Netherlands/epidemiology , Female , Chlamydia Infections/diagnosis , Chlamydia Infections/epidemiology , Chlamydia Infections/microbiology , Pelvic Inflammatory Disease/microbiology , Pelvic Inflammatory Disease/epidemiology , Pelvic Inflammatory Disease/diagnosis , Chlamydia trachomatis/isolation & purification , Male , Qualitative Research , Pregnancy , Pregnancy, Ectopic/diagnosis , Pregnancy, Ectopic/epidemiology , Pregnancy, Ectopic/microbiology , Adult , Middle Aged
2.
Immun Inflamm Dis ; 12(6): e1300, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38896093

ABSTRACT

OBJECTIVE: The sequelae of pelvic inflammatory disease (SPID) are major causes of secondary infertility. Modified Hongteng Baijiang decoction (MHTBD) has produced positive results in the treatment of patients with chronic pelvic inflammatory disease; however, its role in SPID remains elusive. Therefore, this study clarified the role of MHTBD in SPID pathogenesis. METHODS: The main components in MHTBD were analyzed by using liquid chromatography‒mass spectrometry (LC/MS). An SPID rat model was established, and the rats were treated with different doses of MHTBD (0.504 g of raw drug/kg, 1.008 g of raw drug/kg, and 2.016 g of raw drug/kg). Endometrial pinopodes were observed via scanning electron microscopy, endometrial thickness and inflammatory cell infiltration were assessed via HE staining, and the expression of estrogen receptor (ER), progesterone receptor (PR), integrin ß3 (ITGB3), and CD31 in the endometrium was detected by using immunohistochemistry. Western blot analysis was used to detect the protein expression of LIF, JAK2, p-JAK2, STAT3, and p-STAT3 in the endometrium. Moreover, the changes in the gut microbiota were analyzed via 16S rRNA sequencing. RESULTS: MHTBD improved endometrial receptivity, attenuated endometrial pathologic damage, reduced inflammatory cell infiltration, decreased ER and PR expression in the endometrium, and promoted the expression of LIF, p-JAK2, and p-STAT3 in the endometrium (p < .05) in SPID rats. Additionally, MHTBD treatment affected the composition of the gut microbiota in SPID rats. Furthermore, MHTBD attenuated endometrial receptivity and pathological damage in SPID rats by promoting the LIF/JAK2/STAT3 pathway. CONCLUSION: MHTBD attenuates SPID in rats by promoting the LIF/JAK2/STAT3 pathway and improving the composition of the gut microbiota. MHTBD may be a valuable drug for SPID therapy.


Subject(s)
Drugs, Chinese Herbal , Gastrointestinal Microbiome , Janus Kinase 2 , Pelvic Inflammatory Disease , STAT3 Transcription Factor , Signal Transduction , Animals , Female , Rats , Disease Models, Animal , Drugs, Chinese Herbal/pharmacology , Drugs, Chinese Herbal/therapeutic use , Endometrium/pathology , Endometrium/metabolism , Endometrium/drug effects , Endometrium/microbiology , Gastrointestinal Microbiome/drug effects , Janus Kinase 2/metabolism , Pelvic Inflammatory Disease/drug therapy , Pelvic Inflammatory Disease/microbiology , Rats, Sprague-Dawley , Signal Transduction/drug effects , STAT3 Transcription Factor/metabolism , Male
3.
Nat Commun ; 15(1): 3756, 2024 May 04.
Article in English | MEDLINE | ID: mdl-38704381

ABSTRACT

The human pathogen Neisseria gonorrhoeae ascends into the upper female reproductive tract to cause damaging inflammation within the Fallopian tubes and pelvic inflammatory disease (PID), increasing the risk of infertility and ectopic pregnancy. The loss of ciliated cells from the epithelium is thought to be both a consequence of inflammation and a cause of adverse sequelae. However, the links between infection, inflammation, and ciliated cell extrusion remain unresolved. With the use of ex vivo cultures of human Fallopian tube paired with RNA sequencing we defined the tissue response to gonococcal challenge, identifying cytokine, chemokine, cell adhesion, and apoptosis related transcripts not previously recognized as potentiators of gonococcal PID. Unexpectedly, IL-17C was one of the most highly induced genes. Yet, this cytokine has no previous association with gonococcal infection nor pelvic inflammatory disease and thus it was selected for further characterization. We show that human Fallopian tubes express the IL-17C receptor on the epithelial surface and that treatment with purified IL-17C induces pro-inflammatory cytokine secretion in addition to sloughing of the epithelium and generalized tissue damage. These results demonstrate a previously unrecognized but critical role of IL-17C in the damaging inflammation induced by gonococci in a human explant model of PID.


Subject(s)
Fallopian Tubes , Gonorrhea , Inflammation , Interleukin-17 , Neisseria gonorrhoeae , Adult , Female , Humans , Cytokines/metabolism , Epithelium/pathology , Epithelium/microbiology , Fallopian Tubes/microbiology , Fallopian Tubes/pathology , Fallopian Tubes/immunology , Gonorrhea/immunology , Gonorrhea/microbiology , Gonorrhea/pathology , Inflammation/pathology , Inflammation/microbiology , Interleukin-17/metabolism , Neisseria gonorrhoeae/immunology , Neisseria gonorrhoeae/pathogenicity , Pelvic Inflammatory Disease/microbiology , Pelvic Inflammatory Disease/pathology , Pelvic Inflammatory Disease/immunology , Receptors, Interleukin-17/metabolism , Receptors, Interleukin-17/genetics
4.
Am J Reprod Immunol ; 90(2): e13754, 2023 08.
Article in English | MEDLINE | ID: mdl-37491918

ABSTRACT

PROBLEM: Interferon-epsilon (IFNε) is the only type I IFN constitutively expressed in the female reproductive tract and fluctuates across the menstrual cycle in humans. Mouse models show that IFNε protects against Chlamydia trachomatis, Herpes Simplex Virus, HIV, and Zika in mice, but human studies are limited. Bacterial sexually transmitted infections (STI) can ascend to the upper genital tract and cause pelvic inflammatory disease (PID) and subsequent infertility. However, the host immunological mechanisms that play a role in the ascension and infection of the endometrium in individuals with clinically suspected PID are not elucidated. METHOD OF STUDY: This pilot investigation determined if IFNε gene variants are associated with bacterial vaginosis (BV) and endometrial infection with C. trachomatis, Neisseria gonorrhoeae, and Mycoplasma genitalium using biospecimens from 154 self-report Black individuals who participated in the PID Evaluation and Clinical Health (PEACH) study. RESULTS: The T allele for rs2039381 was associated with endometrial STI infection (OR 2.7, 95% CI: 1.0-7.1) and the C allele for rs1125488 was inversely associated with BV (OR: .2, 95% CI: .05-.8). CONCLUSIONS: Few studies have examined IFNε gene variants, our study raises the possibility that IFNε gene variants may be a potential host contributor to STI pathogenesis.


Subject(s)
Chlamydia Infections , Mycoplasma Infections , Pelvic Inflammatory Disease , Sexually Transmitted Diseases , Vaginosis, Bacterial , Zika Virus Infection , Zika Virus , Female , Humans , Animals , Mice , Mycoplasma Infections/microbiology , Sexually Transmitted Diseases/genetics , Pelvic Inflammatory Disease/microbiology , Vaginosis, Bacterial/microbiology , Chlamydia trachomatis , Endometrium , Interferons/genetics
5.
Adv Emerg Nurs J ; 45(3): 222-229, 2023.
Article in English | MEDLINE | ID: mdl-37501275

ABSTRACT

Mycoplasma genitalium (MG) is a bacterium that can be spread through sexual contact with another person who is infected. If misdiagnosed and left untreated, this newer, emerging sexually transmitted infection (STI) can cause complications such as urethritis and pelvic inflammatory disease (PID) in both men and women. In males, MG can be asymptomatic and undetectable. In females, MG may present with nonspecific symptoms, such as dysuria, vaginal discharge, and/or pelvic pain. In addition to chlamydia and gonorrhea, MG may result in PID. Due to the complications of MG, health care providers in the emergency department setting need to consider this as a differential diagnosis when performing STI and vaginitis screenings on sexually active patients who may present with urinary or vaginal complaints. As patients with pelvic pain are frequently seen in the emergency department, providers need to be aware of the role that MG may play in STIs and the subsequent sequelae if not treated properly.


Subject(s)
Mycoplasma Infections , Mycoplasma genitalium , Pelvic Inflammatory Disease , Sexually Transmitted Diseases , Male , Humans , Female , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/complications , Pelvic Inflammatory Disease/microbiology , Chlamydia trachomatis , Mycoplasma Infections/complications , Mycoplasma Infections/diagnosis , Mycoplasma Infections/microbiology , Sexually Transmitted Diseases/complications , Sexually Transmitted Diseases/diagnosis , Sexually Transmitted Diseases/microbiology , Pelvic Pain
6.
Infect Dis Clin North Am ; 37(2): 267-288, 2023 06.
Article in English | MEDLINE | ID: mdl-37005162

ABSTRACT

Chlamydia trachomatis infection ("chlamydia") is the most commonly diagnosed bacterial sexually transmitted infection globally, occurring in the genitals (urethra or vagina/cervix), rectum, or pharynx. If left untreated in women, genital chlamydia can ascend into the upper genital tract causing pelvic inflammatory disease, increasing their risk for ectopic pregnancy, infertility, and chronic pelvic pain. In men, chlamydia can cause epididymitis and proctitis. However, chlamydia is asymptomatic in over 80% of cases. This article provides an update on the epidemiology, natural history, and clinical manifestations of chlamydia in adults and discusses the current approaches to its management and control policy.


Subject(s)
Chlamydia Infections , Pelvic Inflammatory Disease , Male , Pregnancy , Adult , Humans , Female , Chlamydia trachomatis , Chlamydia Infections/diagnosis , Chlamydia Infections/drug therapy , Chlamydia Infections/epidemiology , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/epidemiology , Pelvic Inflammatory Disease/microbiology , Age Factors
7.
Rev. chil. infectol ; 39(5): 654-655, oct. 2022.
Article in Spanish | LILACS | ID: biblio-1431698

ABSTRACT

Neisseria gonorrhoeae se considera uno de los agentes causales más importantes de la enfermedad pélvica inflamatoria (EPI) produciendo síntomas leves e inespecíficos, lo cual la convierte en un desafío diagnóstico. Se presenta un caso de una pelviperitonitis gonocócica aguda con dolor difuso, distensión abdominal, fiebre. El único hallazgo destacable fue un líquido peritoneal y endocervical purulento con reactantes de fase aguda elevados. El cultivo del líquido endocervical y peritoneal fue positivo para N. gonorrhoeae. En mujeres sexualmente activas y con sospecha de EPI es importante descartar enfermedades de transmisión sexual.


Neisseria gonorrhoeae is considered one of the most important causal agents of pelvic inflammatory disease, producing mild and nonspecific symptoms, which makes it a diagnostic challenge. A case of acute gonococcal pelviperitonitis with abdominal distension, fever and diffuse pain is presented. The only noteworthy finding was purulent peritoneal and endocervical fluid with elevated acute-phase reactants. Endocervical and peritoneal fluid culture showed infection with N. gonorrhoeae. Therefore, in sexually active women with suspected PID, it is important to rule out sexually transmitted diseases.


Subject(s)
Humans , Female , Young Adult , Gonorrhea/microbiology , Pelvic Inflammatory Disease/microbiology , Neisseria gonorrhoeae/isolation & purification , Gonorrhea/diagnosis , Gonorrhea/drug therapy , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/drug therapy , Anti-Bacterial Agents/therapeutic use
8.
Obstet Gynecol Clin North Am ; 49(3): 551-579, 2022 Sep.
Article in English | MEDLINE | ID: mdl-36122985

ABSTRACT

Pelvic inflammatory disease (PID) is an ascending polymicrobial infection of the upper female genital tract. The presentation of PID varies from asymptomatic cases to severe sepsis. The diagnosis of PID is often one of exclusion. Primary treatment for PID includes broad-spectrum antibiotics with coverage against gonorrhea, chlamydia, and common anaerobic and aerobic bacteria. If not clinically improved by antibiotics, percutaneous drain placement can promote efficient source control, as is often the case with large tubo-ovarian abscesses. Ultimately, even with treatment, PID can result in long-term morbidity, including chronic pelvic pain, infertility, and ectopic pregnancy.


Subject(s)
Pelvic Inflammatory Disease , Pregnancy, Ectopic , Anti-Bacterial Agents/therapeutic use , Disease Progression , Female , Humans , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/microbiology , Pelvic Inflammatory Disease/therapy , Pregnancy , Pregnancy, Ectopic/diagnosis , Pregnancy, Ectopic/therapy
9.
Sex Transm Infect ; 98(2): 115-120, 2022 03.
Article in English | MEDLINE | ID: mdl-33782146

ABSTRACT

BACKGROUND: Risk of pelvic inflammatory disease associated with Chlamydia trachomatis and Mycoplasma genitalium is increased after termination of pregnancy (TOP) and may be increased after insertion of intrauterine devices (IUDs). Screening prior to these procedures is recommended only for C. trachomatis. We examined C. trachomatis and M. genitalium prevalence and associated factors among women presenting to a pregnancy termination and contraception service over 10 years. METHODS: Retrospective analysis of clinical data collected from 17 573 women aged 15-45 years in 2009-2019 and for 266 M. genitalium positive women tested for macrolide resistance-associated mutations in 2016-2019. RESULTS: C. trachomatis and M. genitalium prevalence was 3.7% and 3.4%, respectively. In multivariable analyses, shared risk factors were younger age (p<0.001, for both C. trachomatis and M. genitalium), socioeconomic disadvantage (p=0.045 and p=0.008, respectively) and coinfection (p<0.001, for both sexually transmitted infections), with 10.1% of C. trachomatis positive women also positive for M. genitalium. Additional risk factors were earlier year of visit (p=0.001) for C. trachomatis and for M. genitalium residing outside a major city (p=0.013). The proportion of M. genitalium infections tested between 2016 and 2019 with macrolide resistance-associated mutations was 32.7%. CONCLUSIONS: Given the high level of antimicrobial resistance and the prevalence of coinfection, testing C. trachomatis positive women for M. genitalium could be considered in this setting to prevent further spread of resistant infections. Further research is required into the causal link between M. genitalium and pelvic inflammatory disease in women undergoing TOP and IUD insertion.


Subject(s)
Abortion, Induced/statistics & numerical data , Ambulatory Care Facilities/statistics & numerical data , Chlamydia Infections/epidemiology , Contraception/statistics & numerical data , Mycoplasma Infections/epidemiology , Adolescent , Adult , Chlamydia trachomatis/genetics , Chlamydia trachomatis/isolation & purification , Coinfection/epidemiology , Coinfection/microbiology , Drug Resistance, Bacterial/genetics , Female , Humans , Middle Aged , Mycoplasma genitalium/genetics , Mycoplasma genitalium/isolation & purification , Pelvic Inflammatory Disease/etiology , Pelvic Inflammatory Disease/microbiology , Pelvic Inflammatory Disease/prevention & control , Pregnancy , Prevalence , Retrospective Studies , Young Adult
10.
Dis Mon ; 68(3): 101287, 2022 Mar.
Article in English | MEDLINE | ID: mdl-34521505

ABSTRACT

Pelvic inflammatory disease (PID) is an infection of the female upper genital tract that is typically polymicrobial with classic core involvement of Neisseria gonorrhoeae and/or Chlamydia trachomatis, though other endogenous flora from the vagino-cervical areas can be involved as well. It is often a sexually transmitted disease but other etiologic routes are also noted. A variety of risk factors have been identified including adolescence, young adulthood, adolescent cervical ectropion, multiple sexual partners, immature immune system, history of previous PID, risky contraceptive practices and others. An early diagnosis and prompt treatment are necessary to reduce risks of PID complications such as chronic pelvic pain, ectopic pregnancy and infertility. Current management principles of PID are also reviewed. It is important for clinicians to screen sexually active females for common sexually transmitted infections such as Chlamydia trachomatis and provide safer sex education to their adolescent and young adult patients. Clinicians should provide comprehensive management to persons with PID and utilize established guidelines such as those from the US Centers for Disease Control and Prevention (CDC).


Subject(s)
Anti-Bacterial Agents/therapeutic use , Bacterial Infections/drug therapy , Bacterial Infections/microbiology , Bacterial Infections/physiopathology , Pelvic Inflammatory Disease/drug therapy , Pelvic Inflammatory Disease/microbiology , Pelvic Inflammatory Disease/physiopathology , Adolescent , Adult , Bacterial Infections/epidemiology , Female , Humans , Pelvic Inflammatory Disease/epidemiology , Pregnancy , Risk Factors , Young Adult
12.
PLoS One ; 16(9): e0257627, 2021.
Article in English | MEDLINE | ID: mdl-34543349

ABSTRACT

OBJECTIVES: Most research into the management of pelvic inflammatory disease (PID) is in younger women and focuses on sexually transmitted pathogens such as N. gonorrhoeae or C. trachomatis. Non-sexually transmitted bacterial pathogens and PID in older women are rarely examined. The objective of this study is to explore cervical culture pathogens in women of different age groups in a medical center in eastern Taiwan. METHODS: We enrolled patients whose medical records were diagnosed with PID (ICD-9-CM 614.0 [N70.01-03], 614.1[N70.11-13], 614.9 [N73.5, N73.9]) at our hospital from October 2014 to March 2020. Patients were divided into three groups according to age: the age <25 years, age 25-44 years, and the ≥ 45 years group. Chi-square test, ANOVA and logistic regression were used for statistical analysis. In subgroup analysis, endocervical pathogens were further stratified into vaginal, respiratory, enteric, skin, oral, and other. RESULTS: A total of 96 patients were included in the study. There were 31 patients in the age ≥ 45 years group, 52 patients in the age 25-44 years group, and 13 patients in the age <25 years group. Vagina and enteric pathogens were the most common pathogens among all groups. The isolated respiratory and other pathogens were more in the age ≥ 45 years group than in the other two groups. Prevotella bivia was more common in the age <25 years and 25-44 years groups. CONCLUSIONS: This may be due to different pathogeneses of PID in the age ≥ 45 years patients. Our study can be used as a reference for antibiotic choice of non-sexually transmitted PID and to prevent long-term sequelae of PID.


Subject(s)
Pelvic Inflammatory Disease/microbiology , Prevotella/isolation & purification , Adult , Cross-Sectional Studies , Female , Humans , Logistic Models , Lung/microbiology , Middle Aged , Pelvic Inflammatory Disease/diagnosis , Retrospective Studies , Skin/microbiology , Taiwan , Vagina/microbiology , Vagina/pathology , Young Adult
13.
Pol J Microbiol ; 70(3): 345-357, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34584529

ABSTRACT

Human vaginal microorganisms play an important role in maintaining good health throughout the human life cycle. An imbalance in the vaginal microbiota is associated with an increased risk of pelvic inflammatory disease (PID). This study aimed to characterize and compare vaginal microbial profiles of premenopausal Korean women with and without PID. 74 Korean premenopausal female vaginal samples were obtained; 33 were from healthy women (a control group) and 41 from PID patients. Vaginal fluid samples were collected from the vaginal wall and posterior cervix and then analyzed by 16S ribosomal ribonucleic acid (rRNA) gene-based amplicon sequencing. Results showed a significant difference between the vaginal microbial communities of the two groups (Jensen-Shannon, p = 0.014; Bray-Curtis, p = 0.009; Generalized UniFrac, p = 0.007; UniFrac, p = 0.008). Lactobacillus accounted for the highest percentage (61.0%) of the control group but was significantly decreased (34.9%) in PID patients; this was the most significant difference among all bacterial communities (p = 0.028, LDA effect size = 5.129). In addition, in the PID patient group, species diversity significantly increased (Simpson, p = 0.07) as the proportion of various pathogens increased evenly, resulting in a polymicrobial infection. Similarly, lactate, which constituted the highest percentage of the organic acids in the control group, was significantly decreased in the PID patient group (p = 0.04). The present study's findings will help understand PID from the microbiome perspective and are expected to contribute to the development of more efficient PID diagnosis and treatment modalities.


Subject(s)
Bacterial Physiological Phenomena , Biodiversity , Microbiota/physiology , Pelvic Inflammatory Disease/microbiology , Vagina/microbiology , Adult , Bacteria/genetics , Female , Humans , RNA, Ribosomal, 16S , Republic of Korea
14.
J Infect Dis ; 224(12 Suppl 2): S23-S28, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396398

ABSTRACT

Pelvic inflammatory disease (PID) is a syndrome that causes substantial morbidity, including chronic pelvic pain, to women globally. While limited data are available from low- and middle-income countries, national databases from the United States and Europe suggest that PID incidence may be decreasing but the rate of decrease may differ by the etiologic cause. Recent studies of women with PID have reported that fewer than half of women receiving a diagnosis of PID have gonococcal or chlamydial infection, while Mycoplasma genitalium, respiratory pathogens, and the constellation of bacteria associated with bacterial vaginosis may account for a substantial fraction of PID cases. The clinical diagnosis of PID is nonspecific, creating an urgent need to develop noninvasive tests to diagnose PID. Advances in serologic testing for Chlamydia trachomatis and Neisseria gonorrhoeae could advance epidemiologic studies, while the development of vaccines against these sexually transmitted pathogens could affect incident PID and associated morbidity.


Subject(s)
Pelvic Inflammatory Disease , Chlamydia Infections/complications , Chlamydia Infections/diagnosis , Chlamydia Infections/epidemiology , Chlamydia Infections/microbiology , Chlamydia trachomatis/isolation & purification , Female , Gonorrhea/diagnosis , Gonorrhea/epidemiology , Humans , Incidence , Neisseria gonorrhoeae , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/epidemiology , Pelvic Inflammatory Disease/etiology , Pelvic Inflammatory Disease/microbiology , United States/epidemiology
15.
J Infect Dis ; 224(12 Suppl 2): S96-S102, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396399

ABSTRACT

Pelvic inflammatory disease and infertility frequently develop after female genital tract infection with Neisseria gonorrhoeae, but determining their etiology from among various possibilities presents difficulties. Exploitation of serology to identify the causative agent is complicated by numerous factors, and no immunological test currently exists to determine unequivocally whether an individual currently is, or has been, infected with N. gonorrhoeae. The extensive antigenic variability of N. gonorrhoeae and its expression of antigens shared with other Neisseria species commonly carried in humans render problematic an assay that is specific for all gonococcal strains. However, novel conserved gonococcal antigens identified for potential vaccines may find additional application in diagnostic assays. N. gonorrhoeae also interferes with the adaptive immune response, and antibody responses to uncomplicated infection are usually weak. Elucidating the mechanisms whereby N. gonorrhoeae manipulates the human immune system may lead to improved understanding of the pathogenesis of pelvic inflammatory disease and infertility.


Subject(s)
Gonorrhea/diagnosis , Immunity , Infertility , Neisseria gonorrhoeae , Pelvic Inflammatory Disease/microbiology , Adaptive Immunity , Antigens , Cytokines , Female , Humans , Infertility/etiology , Infertility/immunology
16.
J Infect Dis ; 224(12 Suppl 2): S80-S85, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396401

ABSTRACT

Chlamydia trachomatis (CT) causes pelvic inflammatory disease, which may result in tubal factor infertility (TFI) in women. Serologic assays may be used to determine the proportion of women with and without TFI who have had previous CT infection and to generate estimates of infertility attributable to chlamydia. Unfortunately, most existing CT serologic assays are challenged by low sensitivity and, sometimes, specificity for prior CT infection; however, they are currently the only available tests available to detect prior CT infection. Modeling methods such as finite mixture modeling may be a useful adjunct to quantitative serologic data to obtain better estimates of CT-related infertility. In this article, we review CT serological assays, including the use of antigens preferentially expressed during upper genital tract infection, and suggest future research directions. These methodologic improvements, coupled with creation of new biomarkers for previous CT infection, should improve our understanding of chlamydia's contribution to female infertility.


Subject(s)
Antibodies, Bacterial/immunology , Chlamydia Infections/complications , Chlamydia trachomatis/immunology , Infertility, Female/etiology , Pelvic Inflammatory Disease/complications , Antibodies, Bacterial/blood , Biomarkers , Chlamydia trachomatis/isolation & purification , Female , Humans , Infertility, Female/blood , Infertility, Female/microbiology , Pelvic Inflammatory Disease/microbiology , Serology
17.
J Infect Dis ; 224(12 Suppl 2): S137-S144, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396403

ABSTRACT

BACKGROUND: Pelvic inflammatory disease (PID) leads to long-term reproductive consequences for cisgender women. Bacterial vaginosis (BV) and behavioral factors may play a role in PID pathogenesis. We assessed associations between BV, behavioral factors, and incident PID. METHODS: We analyzed participants (N = 2956) enrolled in the National Institutes of Health Longitudinal Study of Vaginal Flora, a cohort of nonpregnant cisgender women followed quarterly for 12 months. PID was defined by at least 1 of the following: cervical motion tenderness, uterine tenderness, or adnexal tenderness (160 cases). We tested associations between BV (measured using Nugent and Amsel criteria) and PID at the subsequent visit. Sociodemographic factors, sexual behaviors, and Chlamydia trachomatis (CT), untreated at baseline and concurrent with BV, were covariates in Cox proportional hazards models. Adjusting for the few Neisseria gonorrhoeae and Trichomonas vaginalis cases did not alter results. RESULTS: In multivariable modeling, Nugent-BV (adjusted hazard ratio [aHR], 1.53 [95% confidence interval {CI}, 1.05-2.21]), symptomatic Amsel-BV (aHR, 2.15 [95% CI, 1.23-3.75]), and vaginal douching (aHR, 1.47 [95% CI, 1.03-2.09]) were associated with incident PID. CONCLUSIONS: BV was associated with incident PID in a large prospective cohort, controlling for behavioral factors and sexually transmitted infections (STIs). Larger studies on how BV, STIs, behaviors, and host responses interactively affect PID risk are needed.


Subject(s)
Pelvic Inflammatory Disease/epidemiology , Sexual Behavior , Vagina/microbiology , Vaginosis, Bacterial/epidemiology , Adolescent , Adult , Alabama/epidemiology , Female , Humans , Longitudinal Studies , Pelvic Inflammatory Disease/microbiology , Prospective Studies , Sexual Partners , Sociodemographic Factors , Vaginosis, Bacterial/complications , Young Adult
18.
J Infect Dis ; 224(12 Suppl 2): S152-S160, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396408

ABSTRACT

Murine models of Neisseria gonorrhoeae lower reproductive tract infection are valuable systems for studying N. gonorrhoeae adaptation to the female host and immune responses to infection. These models have also accelerated preclinical testing of candidate therapeutic and prophylactic products against gonorrhea. However, because N. gonorrhoeae infection is restricted to the murine cervicovaginal region, there is a need for an in vivo system for translational work on N. gonorrhoeae pelvic inflammatory disease (PID). Here we discuss the need for well-characterized preclinical upper reproductive tract infection models for developing candidate products against N. gonorrhoeae PID, and report a refinement of the gonorrhea mouse model that supports sustained upper reproductive tract infection. To establish this new model for vaccine testing, we also tested the licensed meningococcal 4CMenB vaccine, which cross-protects against murine N. gonorrhoeae lower reproductive tract infection, for efficacy against N. gonorrhoeae in the endometrium and oviducts following transcervical or vaginal challenge.


Subject(s)
Anti-Infective Agents/administration & dosage , Gonorrhea/prevention & control , Pelvic Inflammatory Disease/prevention & control , Reproductive Tract Infections/microbiology , Animals , Disease Models, Animal , Female , Gonorrhea/drug therapy , Mice , Neisseria gonorrhoeae/immunology , Pelvic Inflammatory Disease/microbiology
19.
J Infect Dis ; 224(12 Suppl 2): S56-S63, 2021 08 16.
Article in English | MEDLINE | ID: mdl-34396410

ABSTRACT

While infection by Neisseria gonorrhoeae is often asymptomatic in women, undetected infections can ascend into the upper genital tract to elicit an inflammatory response that manifests as pelvic inflammatory disease, with the outcomes depending on the intensity and duration of inflammation and whether it is localized to the endometrial, fallopian tube, ovarian, and/or other tissues. This review examines the contribution of N. gonorrhoeae versus other potential causes of pelvic inflammatory disease by considering new insights gained through molecular, immunological, and microbiome-based analyses, and the current epidemiological burden of infection, with an aim to highlighting key areas for future study.


Subject(s)
Chlamydia Infections/epidemiology , Gonorrhea/epidemiology , Neisseria gonorrhoeae/isolation & purification , Pelvic Inflammatory Disease/epidemiology , Chlamydia Infections/complications , Endometritis/microbiology , Endometrium/microbiology , Endometrium/pathology , Fallopian Tubes/microbiology , Female , Gonorrhea/diagnosis , Humans , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/microbiology
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