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1.
J Am Soc Cytopathol ; 11(1): 21-30, 2022.
Article de Anglais | MEDLINE | ID: mdl-34625384

RÉSUMÉ

INTRODUCTION: Although anal cancer is more common in women, most of the studies on the role of high-risk human papillomavirus (hrHPV) infection in anal squamous lesions have focused on high-risk male patients. Therefore, we compared the genotype profile and clinicopathologic correlation of hrHPV infection in human immunodeficiency virus-positive (HIV+) men and women. MATERIALS AND METHODS: We retrospectively analyzed 2254 HIV+ patients (1931 men and 323 women) who had undergone anal Papanicolaou tests at our institution; 1189 of them also had follow-up biopsy data available. HPV genotyping was performed using the Roche Cobas system and correlated with the cytologic and histologic diagnosis. RESULTS: Compared with the HIV+ men, the HIV+ women had a significantly lower rate of hrHPV infection (67.5% versus 78.5%; P < 0.0001) but a significantly higher rate of high-grade squamous intraepithelial lesions (HSILs) on anal Papanicolaou tests (4.6% versus 2.5%; P < 0.05). Other high-risk HPV (ohrHPV), as a group, is much more common than HPV16 or HPV18 in both genders. HIV+ women had significantly lower HPV16 and ohrHPV infection rates than did HIV+ men. However, the HPV18 infection rates were similar between HIV+ women and HIV+ men. For both genders, the rates of HSILs or high-grade anal intraepithelial neoplasia (AIN2-3) were significantly increased when coinfection of ohrHPV with either HPV16 or HPV18 was present. CONCLUSIONS: Although both HIV+ men and HIV+ women have an increased risk of hrHPV infection, HIV+ women have different hrHPV genotype profiles and higher rates of high-grade lesions. Coinfection with different genotypes of hrHPV can significantly increase the risk of HSILs or AIN2-3 in both genders and could requires vigilant clinical and laboratory follow-up.


Sujet(s)
Alphapapillomavirus/génétique , Canal anal/virologie , Co-infection/virologie , Infections à VIH/complications , Infections à papillomavirus/complications , Adulte , Canal anal/cytologie , Canal anal/anatomopathologie , Biopsie , Co-infection/diagnostic , Co-infection/anatomopathologie , Études transversales , Femelle , Techniques de génotypage , Infections à VIH/virologie , Humains , Mâle , Adulte d'âge moyen , Infections à papillomavirus/virologie , Études rétrospectives , Facteurs de risque , Facteurs sexuels
2.
J. coloproctol. (Rio J., Impr.) ; 41(3): 222-227, July-Sept. 2021. tab
Article de Anglais | LILACS | ID: biblio-1346422

RÉSUMÉ

Introduction: Anal intraepithelial neoplasia (AIN) is a premalignant lesion of the anal canal associated with HPV, with a higher prevalence in immunosuppressed individuals. Patients with inflammatory bowel disease (IBD) are at potential risk for their development, due to the use of immunosuppressants and certain characteristics of the disease. Method: This is a prospective, cross-sectional, and interventional study that included 53 patients with IBD treated at a tertiary outpatient clinic, who underwent anal smear for cytology in order to assess the prevalence of AIN and associated risk factors. Results: Forty-eight samples were negative for dysplasia and 2 were positive (4%). Both positive samples occurred in women, with Crohn's disease (CD), who were immunosuppressed and had a history of receptive anal intercourse. Discussion: The prevalence of anal dysplasia in IBD patients in this study is similar to that described in low-risk populations. Literature data are scarce and conflicting and there is no evidence to recommend screening with routine anal cytology in patients with IBD. Female gender, history of receptive anal intercourse, immunosuppression and CD seem to be risk factors. (AU)


Sujet(s)
Humains , Mâle , Femelle , Adolescent , Adulte , Adulte d'âge moyen , Sujet âgé , Canal anal/traumatismes , Tumeurs de l'anus/épidémiologie , Maladies inflammatoires intestinales , Canal anal/cytologie , Maladie de Crohn
3.
Nat Commun ; 12(1): 2761, 2021 05 12.
Article de Anglais | MEDLINE | ID: mdl-33980830

RÉSUMÉ

At numerous locations of the body, transition zones are localized at the crossroad between two types of epithelium and are frequently associated with neoplasia involving both type of tissues. These transition zones contain cells expressing markers of adult stem cells that can be the target of early transformation. The mere fact that transition zone cells can merge different architecture with separate functions implies for a unique plasticity that these cells must display in steady state. However, their roles during tissue regeneration in normal and injured state remain unknown. Here, by using in vivo lineage tracing, single-cell transcriptomics, computational modeling and a three-dimensional organoid culture system of transition zone cells, we identify a population of Krt17+ basal cells with multipotent properties at the squamo-columnar anorectal junction that maintain a squamous epithelium during normal homeostasis and can participate in the repair of a glandular epithelium following tissue injury.


Sujet(s)
Canal anal/cytologie , Homéostasie , Rectum/cytologie , Régénération , Cellules souches/physiologie , Animaux , Différenciation cellulaire , Lignage cellulaire , Plasticité cellulaire , Humains , Muqueuse intestinale/cytologie , Kératine-17/génétique , Kératine-17/métabolisme , Souris , Organoïdes/cytologie , Cellules souches/cytologie , Cellules souches/métabolisme , Facteurs de transcription/génétique , Facteurs de transcription/métabolisme , Cicatrisation de plaie
4.
Nat Commun ; 12(1): 2147, 2021 04 12.
Article de Anglais | MEDLINE | ID: mdl-33846309

RÉSUMÉ

Tissue mononuclear phagocytes (MNP) are specialised in pathogen detection and antigen presentation. As such they deliver HIV to its primary target cells; CD4 T cells. Most MNP HIV transmission studies have focused on epithelial MNPs. However, as mucosal trauma and inflammation are now known to be strongly associated with HIV transmission, here we examine the role of sub-epithelial MNPs which are present in a diverse array of subsets. We show that HIV can penetrate the epithelial surface to interact with sub-epithelial resident MNPs in anogenital explants and define the full array of subsets that are present in the human anogenital and colorectal tissues that HIV may encounter during sexual transmission. In doing so we identify two subsets that preferentially take up HIV, become infected and transmit the virus to CD4 T cells; CD14+CD1c+ monocyte-derived dendritic cells and langerin-expressing conventional dendritic cells 2 (cDC2).


Sujet(s)
Canal anal/cytologie , Antigènes CD/métabolisme , Cellules dendritiques/métabolisme , Système génital/cytologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/physiologie , Lectines de type C/métabolisme , Lectines liant le mannose/métabolisme , Monocytes/métabolisme , Lymphocytes T CD4+/immunologie , Forme de la cellule , Collagenases/métabolisme , Derme/métabolisme , Infections à VIH/immunologie , Infections à VIH/virologie , Humains , Antigènes CD14/métabolisme , Muqueuse/métabolisme , Phagocytes/métabolisme , Phénotype , Récepteurs CCR5/métabolisme , Lectine-1 de type Ig liant l'acide sialique/métabolisme , Transcription génétique
5.
Ann Diagn Pathol ; 50: 151670, 2021 Feb.
Article de Anglais | MEDLINE | ID: mdl-33310590

RÉSUMÉ

BACKGROUND: Anal cytology (AC) is accepted as a practical screening modality for anal cancer. However, studies suggest that AC and anal biopsy dysplasia correlation is less robust than in cervicovaginal specimens. The current study goals were to look at our institutional experience in a subset of ACs and correlate with surgical pathology (SP), as well as evaluate their Human Papillomavirus (HPV) status. METHODS: 377 ACs from 169 patients (151 males and 18 females) from 2008 to 2017 were included. HPV genotyping (n = 47) and SP within one year of AC (n = 58) were reviewed. RESULTS: AC/SP was discrepant in 22 cases (37.9%), with a tendency towards AC underestimating the degree of dysplasia. Specifically, any abnormality on AC was 93.8% sensitive for detecting high-grade dysplasia (HGD). However, when requiring a high-grade AC diagnosis, the sensitivity decreases to 12.5%. "Other high-risk HPV" was the most common genotype (57.4%). When considered with all AC with a high-grade diagnosis, co-testing with HPV improved the sensitivity for HGD to 56.3%. Sensitivity improved further to 87.5% when only considering cases with both AC and HPV testing, and were high-risk HPV positive. Furthermore, following review and consensus diagnosis, 8 cases changed from "Discrepant" to "Agreed", reducing the discrepancy rate to 24.1%. Remaining discrepancies were explained by sampling error. CONCLUSION: Given the enhanced sensitivity of AC and HPV testing together, and sampling error seen with AC leading to underestimating dysplasia, we recommend AC and HPV co-testing, as well as describing confounding factors in AC reports and obtaining consensus opinion in equivocal cases.


Sujet(s)
Canal anal/cytologie , Canal anal/anatomopathologie , Tumeurs de l'anus/diagnostic , Cytodiagnostic/méthodes , Papillomaviridae/génétique , Anatomopathologie chirurgicale/méthodes , Centres hospitaliers universitaires , Adulte , Canal anal/virologie , Tumeurs de l'anus/anatomopathologie , Tumeurs de l'anus/virologie , Biopsie/méthodes , Cytodiagnostic/statistiques et données numériques , Femelle , Génotype , Humains , Mâle , Infections à papillomavirus/complications , Infections à papillomavirus/diagnostic , Anatomopathologie chirurgicale/statistiques et données numériques , Études rétrospectives , Sensibilité et spécificité
6.
ACS Sens ; 5(4): 1132-1139, 2020 04 24.
Article de Anglais | MEDLINE | ID: mdl-32133842

RÉSUMÉ

The group B Streptococcus (GBS) is a type of pathogen that seriously threatens the health of mothers and infants. Prompt and timely diagnosis is crucial for good patient outcomes. However, the traditional bacterial culture and polymerase chain reaction methods are limited by their speed and involve complex operating procedures. Herein, we successfully established an integrated microfluidic sample-to-answer system for nucleic acid-based detection of GBS directly in vaginal/anal swab samples. Meanwhile, we demonstrated a dynamical reaction mechanism of Bst/FEN1-based nucleic acid amplification, which differs from traditional Bst-based isothermal amplification strategies. The system integrates cell lysis and nucleic acid purification, separation, amplification, and detection, enabling rapid (about 45 min to the entire analysis) and highly accurate (98% accuracy) analysis in a clinical setting. Experimental results show that the system offers a good detection limit (500 CFU/mL), perfect specificity (no cross-reactivity with 25 other common pathogens), excellent stability (coefficient of variation less than 3%), and good anti-interference performance. This novel system holds great potential as a nucleic acid-based diagnostic tool in clinical applications for detecting not only GBS but also other types of pathogens.


Sujet(s)
Canal anal/composition chimique , Microfluidique/méthodes , Techniques d'amplification d'acides nucléiques/méthodes , Infections à streptocoques/diagnostic , Vagin/composition chimique , Canal anal/cytologie , Femelle , Humains , Limite de détection , Mâle , Vagin/cytologie
7.
Cancer Cytopathol ; 127(6): 407-413, 2019 06.
Article de Anglais | MEDLINE | ID: mdl-31145557

RÉSUMÉ

BACKGROUND: The incidence of squamous cell carcinoma of the anal canal has been increasing in high-risk populations. To the authors' knowledge, there is no international consensus regarding screening for squamous cell carcinoma of the anal canal, but screening is commonly comprised of a Papanicolaou (Pap) test in combination with digital anorectal examination followed by high-resolution anoscopy if necessary. The current study focused on individuals living with HIV and particularly on women living with HIV. METHODS: In this 5-year retrospective study, the authors identified 5982 Pap tests, 1848 of which had follow-up biopsy within 6 months. The rate of atypical squamous cells of undetermined significance was 42%, and approximately 38.1% of cases with this interpretation were diagnosed as high-grade squamous intraepithelial lesions on follow-up biopsy. In addition, 82 women with anal cytology had long-term follow-up (>10 years) available. RESULTS: The authors investigated a relationship between cervicovaginal human papillomavirus (HPV) results, cervical pathology, CD4 T-cell count, and CD4/8 ratio with the anal cytology interpretation. A statistical correlation was noted between the CD4 count and the CD4/8 ratio and the presence of anal dysplasia. Nearly one-half of the women without cervicovaginal HPV positivity presented with anal dysplasia. CONCLUSIONS: The results of the current study demonstrated that, among women living with HIV, screening for anal dysplasia should not be eschewed, regardless of lower genital tract pathology and/or HPV status. To the authors' knowledge, the current study is the largest reported retrospective anal cytology cohort in individuals living with HIV.


Sujet(s)
Canal anal/anatomopathologie , Tumeurs de l'anus/diagnostic , Infections à VIH/complications , Infections à papillomavirus/diagnostic , États précancéreux/diagnostic , Canal anal/cytologie , Canal anal/imagerie diagnostique , Tumeurs de l'anus/immunologie , Tumeurs de l'anus/anatomopathologie , Tumeurs de l'anus/virologie , Cellules malpighiennes atypiques du col utérin/anatomopathologie , Consensus , Toucher rectal , Femelle , Études de suivi , Infections à VIH/immunologie , Humains , Mâle , Dépistage de masse/normes , Adulte d'âge moyen , Test de Papanicolaou/normes , Papillomaviridae/immunologie , Papillomaviridae/isolement et purification , Infections à papillomavirus/immunologie , Infections à papillomavirus/anatomopathologie , Infections à papillomavirus/virologie , Guides de bonnes pratiques cliniques comme sujet , États précancéreux/immunologie , États précancéreux/anatomopathologie , États précancéreux/virologie , Proctoscopie/normes , Études rétrospectives , Facteurs sexuels
8.
Colorectal Dis ; 21(1): 38-47, 2019 01.
Article de Anglais | MEDLINE | ID: mdl-30047583

RÉSUMÉ

AIM: We aimed to isolate and propagate internal and external anal sphincter progenitor cells from the human anal sphincter, with or without radiotherapy, for tailored cell therapy of faecal incontinence. METHODS: Sphincter progenitor cells were isolated from normal internal and external anal sphincters collected from 10 patients with rectal cancer who had undergone abdominoperineal resection with (n = 6) or without (n = 4) preoperative chemoradiotherapy. The isolated cells and differentiated muscle fibres were identified using immunofluorescence assay, western blotting and reverse transcription polymerase chain reaction (RT-PCR). The proliferation of progenitor cells with and without radiotherapy was compared by quantitative 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. RESULTS: The immunofluorescence assay before differentiation confirmed that the internal anal sphincter progenitor cells expressed CD34 and neural-glial antigen 2 (NG2), whereas the external anal sphincter progenitor cells expressed CD34 and PAX7. After differentiation, the internal anal sphincter progenitor cells expressed desmin, calponin and α-smooth muscle actin, whereas the external anal sphincter progenitor cells expressed desmin, myogenic factor 4 and myosin heavy chain. The differential expression profiles of both cell types were confirmed by western blotting and RT-PCR. MTT assays showed that the viability of internal and external anal sphincter progenitor cells was significantly lower in the radiotherapy group than that in the nonradiotherapy group. CONCLUSIONS: This study describes the differential harvest internal and external sphincter muscle progenitor cells from human anal sphincters. We confirm that radiotherapy decreases the viability of internal and external anal sphincter progenitor cells.


Sujet(s)
Canal anal/cytologie , Prolifération cellulaire , Survie cellulaire , Chimioradiothérapie , Fibres musculaires squelettiques/cytologie , Myocytes du muscle lisse/cytologie , Tumeurs du rectum/thérapie , Cellules souches/cytologie , Actines/métabolisme , Sujet âgé , Sujet âgé de 80 ans ou plus , Canal anal/métabolisme , Antigènes/métabolisme , Antigènes CD34/métabolisme , Protéines de liaison au calcium/métabolisme , Études cas-témoins , Thérapie cellulaire et tissulaire , Desmine/métabolisme , Incontinence anale/thérapie , Femelle , Humains , Mâle , Protéines des microfilaments/métabolisme , Adulte d'âge moyen , Fibres musculaires squelettiques/métabolisme , Myocytes du muscle lisse/métabolisme , Myogénine/métabolisme , Chaînes lourdes de myosine/métabolisme , Traitement néoadjuvant , Facteur de transcription PAX7/métabolisme , Proctectomie , Protéoglycanes/métabolisme , RT-PCR , Cellules souches/métabolisme ,
9.
Rev. chil. cir ; 70(6): 523-528, dic. 2018. tab, graf
Article de Espagnol | LILACS | ID: biblio-978025

RÉSUMÉ

Introducción: El cáncer anal ha experimentado un aumento de incidencia en los últimos años. Está mediado por el VPH y precedido de cambios precancerosos planteando la posibilidad de dirigir los esfuerzos preventivos hacia los grupos de alto riesgo. Sigue siendo controvertida la indicación de cribado y los métodos de detección ideales. Objetivo: Validar las pruebas de cribado implementadas en la actualidad comparadas con la biopsia como "gold standard". Material y Métodos: Estudio transversal con recogida de datos prospectiva, en una cohorte de hombres VIH+ que tienen sexo con hombres, pertenecientes al Hospital Gregorio Marañón e Infanta Leonor en un periodo de 2 años. Resultados: Se seleccionaron 179 pacientes con 286 visitas a la consulta de screening en las que se llevaron a cabo 3 pruebas de cribado en paralelo (citología anal, genotipado del VPH y anoscopia de alta resolución (AAR) con toma de biopsia dirigida sobre zona sospechosa o aleatoria). La sensibilidad y especificidad para la detección de displasia de alto grado y cáncer y su grado de concordancia con la biopsia fue la siguiente: citología 3,23%/94,43% (k: 0,03), genotipado de VPH de alto riesgo 90,32%/27,45% (k: 0,05), AAR 32,26%/87,45 (k: 0, 17) siendo el rendimiento diagnóstico de las tres pruebas muy bajo. Conclusión: La citología presenta un rendimiento diagnóstico muy bajo comparado con el genotipado que representa el mayor. A la luz de nuestros resultados, los protocolos clínicos tal y como vienen desarrollándose en la actualidad deberían de ser abandonados.


Introduction: The incidence of anal cancer has increased in recent years. It is mediated by HPV and preceded by precancerous changes, raising the possibility of directing preventive efforts towards high-risk groups. The indication of screening remains controversial and which methods would be the ideal ones. Objective: To validate the screening tests established actually, comparing it with the biopsy considered as the "gold standard". Materials and Methods: A cross-sectional study was performed, with prospective data collection in a cohort of VIH+ patients, who have male homosexual anal relations, belonging to Gregorio Marañón and Infanta Leonor Hospitals in a period of 2 years. Results: A total of 179 patients were selected with 286 visits to the screening Outpatient Clinic in which 3 parallel screening tests were performed (anal cytology, HPV genotyping and high resolution anoscopy (AAR) with a biopsy directed on a suspicious or random area). The sensitivity and specificity for the detection of high-grade dysplasia and cancer and their degree of agreement with the biopsy was as follows: cytology 3.23%/94.43% (k: 0.03), high HPV genotyping. risk 90.32%/27.45% (k: 0.05), AAR 32.26%/87.45 (k: 0, 17), the diagnostic accuracy of the three tests being very low. Conclusion: Cytology shows a very low diagnostic accuracy compared to the genotype that represents the highest one. In light of our results, clinical protocols as they are currently being developed should be abandoned.


Sujet(s)
Humains , Mâle , Adulte , Tumeurs de l'anus/anatomopathologie , Carcinome épidermoïde/anatomopathologie , Dépistage de masse/méthodes , Homosexualité masculine , Canal anal/cytologie , Canal anal/anatomopathologie , Canal anal/virologie , Canal anal/imagerie diagnostique , Tumeurs de l'anus/virologie , Papillomaviridae/génétique , États précancéreux , Biopsie , Carcinome épidermoïde/virologie , Carcinome épidermoïde/imagerie diagnostique , Études transversales , Valeur prédictive des tests , Courbe ROC , Techniques cytologiques , Sensibilité et spécificité , Séropositivité VIH , Proctoscopie/méthodes , Infections à papillomavirus/anatomopathologie , Dépistage précoce du cancer/méthodes , Techniques de génotypage
10.
Papillomavirus Res ; 5: 180-191, 2018 06.
Article de Anglais | MEDLINE | ID: mdl-29723682

RÉSUMÉ

Human papillomaviruses (HPVs) co-evolve slowly with the human host and each HPV genotype displays epithelial tropisms. We assessed the evolution of intra HPV genotype variants within samples, and their association to anogenital site, cervical cytology and HIV status. Variability in the L1 gene of 35 HPV genotypes was characterized phylogenetically using maximum likelihood, and portrayed by phenotype. Up to a thousand unique variants were identified within individual samples. In-depth analyses of the most prevalent genotypes, HPV16, HPV18 and HPV52, revealed that the high diversity was dominated by a few abundant variants. This suggests high intra-host mutation rates. Clades of HPV16, HPV18 and HPV52 were associated to anatomical site and HIV co-infection. Particularly, we observed that one HPV16 clade was specific to vaginal cells and one HPV52 clade was specific to anal cells. One major HPV52 clade, present in several samples, was strongly associated with cervical neoplasia. Overall, our data suggest that tissue tropism and HIV immunosuppression are strong shapers of HPV evolution.


Sujet(s)
Alphapapillomavirus/génétique , Variation génétique , Tropisme viral/génétique , Adulte , Alphapapillomavirus/classification , Canal anal/cytologie , Canal anal/virologie , Protéines de capside/génétique , Col de l'utérus/cytologie , Col de l'utérus/virologie , Co-infection/virologie , Évolution moléculaire , Femelle , Génotype , Infections à VIH/complications , Humains , Mutation , Protéines des oncogènes viraux/génétique , Infections à papillomavirus/virologie , Phylogenèse , Vagin/cytologie , Vagin/virologie , Jeune adulte
11.
Clin Infect Dis ; 67(8): 1262-1268, 2018 09 28.
Article de Anglais | MEDLINE | ID: mdl-29659752

RÉSUMÉ

Background: Information on the performance of anal cytology in women who are high risk for human papillomavirus-related lesions and the factors that might influence cytology are largely lacking. Methods: Retrospective study including all new referrals of women with a previous history of anogenital neoplasia from January 2012 to July 2017, with concomitant anal cytology and high-resolution anoscopy with or without biopsies. Results: Six hundred and thirty six anal cytology samples and 323 biopsies obtained from 278 women were included. Overall sensitivity and specificity of "any abnormality" on anal cytology to predict any abnormality in histology was 47% (95% confidence interval [CI], 41%-54%) and 84% (95% CI, 73%-91%), respectively. For detecting high-grade squamous intraepithelial lesions (HSIL)/cancer, sensitivity was 71% (95% CI, 61%-79%) and specificity was 73% (95% CI, 66%-79%). There was a poor concordance between cytological and histological grades (κ = 0.147). Cytology had a higher sensitivity to predict HSIL/cancer in immunosuppressed vs nonimmunosuppressed patients (92% vs 60%, P = .002). The sensitivity for HSIL detection was higher when 2 or more quadrants were affected compared with 1 (86% vs 57%, P = .006). A previous history of vulvar HSIL/cancer (odds ratio [OR], 1.71, 1.08-2.73; P = .023), immunosuppression (OR, 1.88, 1.17-3.03; P = .009), and concomitant genital HSIL/cancer (OR, 2.51, 1.47-4.29; P = .001) were risk factors for abnormal cytology. Conclusions: Women characteristics can influence the performance of anal cytology. The sensitivity for detecting anal HSIL/cancer was higher in those immunosuppressed and with more extensive disease.


Sujet(s)
Canal anal/cytologie , Canal anal/anatomopathologie , Tumeurs de l'anus/diagnostic , Techniques cytologiques/normes , Proctoscopie/normes , Adulte , Biopsie , Femelle , Infections à VIH/complications , Techniques histologiques/normes , Humains , Adulte d'âge moyen , Odds ratio , Infections à papillomavirus , Études prospectives , Études rétrospectives , Facteurs de risque , Sensibilité et spécificité
12.
Papillomavirus Res ; 5: 143-149, 2018 06.
Article de Anglais | MEDLINE | ID: mdl-29626643

RÉSUMÉ

BACKGROUND: Men who have sex with men (MSM) are at increased risk for anal cancer. In cervical cancer screening, patterns of repeated cytology results are used to identify low- and high-risk women, but little is known about these patterns for anal cytology among MSM. METHODS: We analyzed Multicenter AIDS Cohort Study (MACS) data for MSM who were offered anal cytology testing annually (HIV-positive) or every 2 years (HIV-negative) for 4 years. RESULTS: Following an initial negative (normal) cytology, the frequency of a second negative cytology was lower among HIV-positive MSM with CD4 ≥ 500 (74%) or CD4 < 500 (68%) than HIV-negative MSM (83%) (p < 0.001). After an initial abnormal cytology, the frequency of a second abnormal cytology was highest among HIV-positive MSM with CD4 < 500 (70%) compared to CD4 ≥ 500 (53%) or HIV-negative MSM (46%) (p = 0.003). Among HIV-positive MSM with at least three results, 37% had 3 consecutive negative results; 3 consecutive abnormal results were more frequent among CD4 < 500 (22%) than CD4 ≥ 500 (10%) (p = 0.008). CONCLUSIONS: More than one-third of HIV-positive MSM have consistently negative anal cytology over three years. Following abnormal anal cytology, a repeated cytology is commonly negative in HIV-negative or immunocompetent HIV-positive men, while persistent cytological abnormality is more likely among HIV-positive men with CD4 < 500.


Sujet(s)
Canal anal/cytologie , Tumeurs de l'anus/diagnostic , Dépistage précoce du cancer/méthodes , Infections à VIH/complications , Homosexualité masculine , Canal anal/anatomopathologie , Tumeurs de l'anus/virologie , Épithélioma in situ/diagnostic , Épithélioma in situ/virologie , Études de cohortes , Cytodiagnostic/méthodes , Infections à VIH/anatomopathologie , Séropositivité VIH/sang , Humains , Mâle , Adulte d'âge moyen
13.
Sex Transm Dis ; 45(4): 266-271, 2018 04.
Article de Anglais | MEDLINE | ID: mdl-29528986

RÉSUMÉ

BACKGROUND: The quadrivalent human papillomavirus (HPV) vaccine (qHPV; types 6, 11, 16, 18) is indicated for men and women aged 9 to 26 years to prevent HPV associated anogenital high-grade squamous intraepithelial lesions (HSIL) and cancer. ACTG 5298 was a randomized placebo controlled Phase 3 study in human immunodeficiency virus (HIV)-infected men who have sex with men, and women of qHPV to prevent persistent anal HPV infection. Baseline data are presented here. METHODS: Human immunodeficiency virus-infected men who have sex with men, and women 27 years or older without previous anogenital or oral cancer were enrolled. Baseline anal cytology, high-resolution anoscopy and collection of anal, oral, and vaginal specimens for HPV genotyping were performed and acceptability assessed. RESULTS: Five hundred seventy-five (575) participants were enrolled (82% men and 18% women). Median age was 47 years. Race/ethnicity was 46% white, 31% black, and 20% Hispanic. Plasma HIV-1 RNA was less than 50 copies/mL in 83% and median CD4 T count was 602 cells/µL. Abnormal anal cytology was detected in 62%, with corresponding HSIL on biopsy (bHSIL) in 33%. Anal HPV 6, 11, 16, and 18 were detected in 25%, 13%, 32%, and 18% of the participants, respectively. Prevalence of 0, 1, 2, 3, and 4 qHPV types was 40%, 38%, 17%, 4%, and 1%, respectively. Oral infection with 1 or more qHPV type was detected in 10% of the participants. Study procedures were generally acceptable. CONCLUSIONS: At study baseline, there was a high prevalence of abnormal anal cytology, bHSIL, and HPV infection. Sixty percent of the participants had anal infection with preventable qHPV types.


Sujet(s)
Canal anal/anatomopathologie , Canal anal/virologie , Infections à VIH/virologie , Vaccin recombinant quadrivalent contre les papillomavirus humains de type 6, 11, 16 et 18/administration et posologie , Canal anal/cytologie , Tumeurs de l'anus/épidémiologie , Tumeurs de l'anus/virologie , Numération des lymphocytes CD4 , Méthode en double aveugle , Femelle , Infections à VIH/complications , Infections à VIH/épidémiologie , Homosexualité masculine , Humains , Mâle , Adulte d'âge moyen , Papillomaviridae/génétique , Papillomaviridae/isolement et purification , Infections à papillomavirus/épidémiologie , Lésions malpighiennes intra-épithéliales du col utérin/épidémiologie , Lésions malpighiennes intra-épithéliales du col utérin/anatomopathologie , Lésions malpighiennes intra-épithéliales du col utérin/virologie
14.
Cancer Cytopathol ; 126(2): 136-144, 2018 02.
Article de Anglais | MEDLINE | ID: mdl-29053225

RÉSUMÉ

BACKGROUND: Longitudinal studies of histological outcomes after anal cytological screening in men who have sex with men (MSM) are rare. This study measured the positive predictive values (PPVs) of each level of baseline cytological abnormality in MSM in Sydney, Australia, over a 12-month period. METHODS: The Study of the Prevention of Anal Cancer is a 3-year prospective study of the natural history of anal human papillomavirus infection in MSM at least 35 years old. For each participant with a baseline cytological abnormality, the worst histology was recorded at the baseline high-resolution anoscopy and at 6 and 12 months. PPVs for a histological high-grade squamous intraepithelial lesion (HSIL) diagnosis were calculated for each level of baseline cytological abnormality at each time point. RESULTS: Among 424 men who completed 3 visits, the PPV of a cytological HSIL increased from 71.6% at the baseline to 86.4% at 6 months and to 92.6% at 12 months (P < .001). For cytological atypical squamous cells, cannot rule out high-grade squamous intraepithelial lesion (ASC-H), the PPV increased from 51.5% at the baseline to 69.7% at 6 months and to 75.8% at 12 months (P = .004). At each time point, the PPV of a cytological HSIL was significantly higher than the PPV of ASC-H. The PPV of low-grade cytology reports was significantly lower than the PPV of ASC-H at each time point. CONCLUSIONS: In a cohort of MSM, a baseline histological HSIL diagnosis after an HSIL cytoprediction is high, and it increases with further examinations over the course of 12 months. Lower levels of cytological abnormalities have significantly lower PPVs. These data can inform patient management and the quality assessment of each aspect of the screening pathway. Cancer Cytopathol 2018;126:136-44. © 2017 American Cancer Society.


Sujet(s)
Tumeurs de l'anus/anatomopathologie , Carcinome épidermoïde/anatomopathologie , Infections à papillomavirus/anatomopathologie , Minorités sexuelles/statistiques et données numériques , Adulte , Sujet âgé , Canal anal/cytologie , Canal anal/anatomopathologie , Canal anal/virologie , Tumeurs de l'anus/diagnostic , Tumeurs de l'anus/épidémiologie , Tumeurs de l'anus/virologie , Australie/épidémiologie , Carcinome épidermoïde/diagnostic , Carcinome épidermoïde/épidémiologie , Carcinome épidermoïde/virologie , Humains , Incidence , Études longitudinales , Mâle , Adulte d'âge moyen , Grading des tumeurs , Papillomaviridae/isolement et purification , Infections à papillomavirus/diagnostic , Infections à papillomavirus/virologie , Valeur prédictive des tests , Études prospectives
15.
Sci Rep ; 7(1): 1477, 2017 05 03.
Article de Anglais | MEDLINE | ID: mdl-28469189

RÉSUMÉ

The present study focused on the role of microRNA-139-5p (miRNA-139-5p) in the regulation of basal tone in internal anal sphincter (IAS). Applying genome-wide miRNA microarrays on the phenotypically distinct smooth muscle cells (SMCs) within the rat anorectrum, we identified miRNA-139-5p as differentially expressed RNA repressor with highest expression in the purely phasic smooth muscle of anococcygeus (ASM) vs. the truly tonic smooth muscle of IAS. This pattern of miRNA-139-5p expression, previously shown to target ROCK2, was validated by target prediction using ingenuity pathway (IPA) and by qPCR analyses. Immunoblotting, immunocytochemistry (ICC), and functional assays using IAS tissues and cells subjected to overexpression/knockdown of miRNA-139-5p confirmed the inverse relationship between miRNA-139-5p and ROCK2 expressions/IAS tone. Overexpression of miRNA-139-5p caused a decrease, while knockdown by anti-miRNA-139-5p caused an increase in the IAS tone; these tissue contractile responses were confirmed by single-cell contraction using magnetic twisting cytometry (MTC). These findings suggest miRNA-139-5p is capable of significantly influencing the phenotypic tonicity in smooth muscle via ROCK2: a lack of tone in ASM may be associated with the suppression of ROCK2 by high expression of miRNA-139-5p, whereas basal IAS tone may be associated with the persistence of ROCK2 due to low expression of miRNA-139-5p.


Sujet(s)
Canal anal/métabolisme , microARN/génétique , Hypotonie musculaire/génétique , Myocytes du muscle lisse/métabolisme , rho-Associated Kinases/génétique , Canal anal/cytologie , Animaux , Antagomirs/génétique , Antagomirs/métabolisme , Cytophotométrie , Régulation de l'expression des gènes , microARN/agonistes , microARN/antagonistes et inhibiteurs , microARN/métabolisme , Contraction musculaire/physiologie , Hypotonie musculaire/métabolisme , Hypotonie musculaire/physiopathologie , Muscles lisses/cytologie , Muscles lisses/métabolisme , Myocytes du muscle lisse/cytologie , Oligoribonucléotides/génétique , Oligoribonucléotides/métabolisme , Phénotype , Rats , Rat Sprague-Dawley , Transduction du signal , Analyse sur cellule unique , rho-Associated Kinases/métabolisme
16.
Rev. cuba. cir ; 56(1): 27-36, ene.-mar. 2017. tab
Article de Espagnol | CUMED | ID: cum-72115

RÉSUMÉ

Introducción: la infección anal por el virus del papiloma humano, se ha convertido en una entidad muy frecuente y se ha demostrado su relación con el cáncer anal. Objetivo: estimar la prevalencia del virus del papiloma humano en pacientes atendidos en el servicio de coloproctología del Hospital Comandante Manuel Fajardo. Métodos: se realizó estudio observacional descriptivo y transversal en 102 pacientes sin patologías agudas anorrectales que dieron su consentimiento. El estudio se realizó desde enero de 2010 hasta diciembre 2013. Se aplicó entrevista a los pacientes, recogida de datos de historia clínica, examen físico anogenital y examen citológico anal. Las variables de estudio fueron: edad, color de la piel, estado civil, nivel escolar y factores de riesgo. Resultados: de 102 citologías realizadas, 29, (25,66 por ciento) fueron positivas a la infección anal por el virus del papiloma humano. La prevalencia de citologías positivas a la infección anal por el virus del papiloma humano según variables fue: sexo femenino: 57 (55,80 por ciento); edades entre 18 y 40 años; mestizos (35 por ciento); divorciados (55,55 por ciento); pacientes con nivel primario; portadores al VIH (73,07 por ciento). Conclusiones: la citología anal constituyó un procedimiento factible para la detección de la incidencia por la infección anal por el virus del papiloma humano y los factores de riesgo son similares a los encontrados en otras regiones y publicaciones(AU)


Introduction: Human papillomavirus anal infection has become a very common entity and been proved its relationship with anal cancer. Objective: To estimate the prevalence of HPV in patients treated by the coloproctology service at Manuel Fajardo Hospital. Methods: A observational, descriptive and cross-sectional study with 102 patients without any acute anorectal pathologies, and who gave their informed consent. The studied was conducted from January 2010 to December 2013. The patients were interviewed, clinical record data were gathered, anal-genital physical examination and anal-cytological examination were performed. The study variables were age, skin color, marital status, educational level and risk factors. Results: Out of 102 smear tests performed, 29 (25.66 por ciento) were Human papillomavirus anal infection-positive. The prevalence of Human papillomavirus anal infection-positive smears according to variables were: female sex (57, 55.80 por ciento), aged 18-40; mestizos (35 por ciento); divorced (55.55 por ciento); primary education patients; HIV-carriers (73.07 por ciento). Conclusions: Anal cytology was an effective procedure for detecting the incidence of HPVAI, and the risk factors are similar to those found in other regions and publications(AU)


Sujet(s)
Humains , Femelle , Jeune adulte , Adulte , Canal anal/cytologie , Infections à papillomavirus/épidémiologie , Études transversales , Collecte de données/méthodes , Épidémiologie Descriptive , Étude d'observation , Facteurs de risque
17.
Rev. cuba. cir ; 56(1): 27-36, ene.-mar. 2017. tab
Article de Espagnol | LILACS | ID: biblio-900962

RÉSUMÉ

Introducción: la infección anal por el virus del papiloma humano, se ha convertido en una entidad muy frecuente y se ha demostrado su relación con el cáncer anal. Objetivo: estimar la prevalencia del virus del papiloma humano en pacientes atendidos en el servicio de coloproctología del Hospital Comandante Manuel Fajardo. Métodos: se realizó estudio observacional descriptivo y transversal en 102 pacientes sin patologías agudas anorrectales que dieron su consentimiento. El estudio se realizó desde enero de 2010 hasta diciembre 2013. Se aplicó entrevista a los pacientes, recogida de datos de historia clínica, examen físico anogenital y examen citológico anal. Las variables de estudio fueron: edad, color de la piel, estado civil, nivel escolar y factores de riesgo. Resultados: de 102 citologías realizadas, 29, (25,66 por ciento) fueron positivas a la infección anal por el virus del papiloma humano. La prevalencia de citologías positivas a la infección anal por el virus del papiloma humano según variables fue: sexo femenino: 57 (55,80 por ciento); edades entre 18 y 40 años; mestizos (35 por ciento); divorciados (55,55 por ciento); pacientes con nivel primario; portadores al VIH (73,07 por ciento). Conclusiones: la citología anal constituyó un procedimiento factible para la detección de la incidencia por la infección anal por el virus del papiloma humano y los factores de riesgo son similares a los encontrados en otras regiones y publicaciones(AU)


Introduction: Human papillomavirus anal infection has become a very common entity and been proved its relationship with anal cancer. Objective: To estimate the prevalence of HPV in patients treated by the coloproctology service at Manuel Fajardo Hospital. Methods: A observational, descriptive and cross-sectional study with 102 patients without any acute anorectal pathologies, and who gave their informed consent. The studied was conducted from January 2010 to December 2013. The patients were interviewed, clinical record data were gathered, anal-genital physical examination and anal-cytological examination were performed. The study variables were age, skin color, marital status, educational level and risk factors. Results: Out of 102 smear tests performed, 29 (25.66 por ciento) were Human papillomavirus anal infection-positive. The prevalence of Human papillomavirus anal infection-positive smears according to variables were: female sex (57, 55.80 por ciento), aged 18-40; mestizos (35 por ciento); divorced (55.55 por ciento); primary education patients; HIV-carriers (73.07 por ciento). Conclusions: Anal cytology was an effective procedure for detecting the incidence of HPVAI, and the risk factors are similar to those found in other regions and publications(AU)


Sujet(s)
Humains , Canal anal/cytologie , Infections à papillomavirus/épidémiologie , Études transversales , Collecte de données/méthodes , Épidémiologie Descriptive , Étude d'observation , Facteurs de risque
18.
Appl Environ Microbiol ; 83(1)2017 01 01.
Article de Anglais | MEDLINE | ID: mdl-27742683

RÉSUMÉ

Our recent studies have shown that intimin and the locus of enterocyte effacement-encoded proteins do not play a role in Escherichia coli O157:H7 (O157) adherence to the bovine recto-anal junction squamous epithelial (RSE) cells. To define factors that play a contributory role, we investigated the role of curli, fimbrial adhesins commonly implicated in adherence to various fomites and plant and human epithelial cells, in O157 adherence to RSE cells. Specifically, we examined (i) wild-type strains of O157; (ii) curli variants of O157 strains; (iii) isogenic curli deletion mutants of O157; and (iv) adherence inhibition of O157 using anti-curlin sera. Results of these experiments conducted under stringent conditions suggest that curli do not solely contribute to O157 adherence to RSE cells and in fact demonstrate a modulating effect on O157 adherence to RSE cells in contrast to HEp-2 cells (human epidermoid carcinoma of the larynx cells with HeLa contamination). The absence of curli and presence of blocking anti-curli antibodies enhanced O157-RSE cell interactions among some strains, thus alluding to a spatial, tempering effect of curli on O157 adherence to RSE cells when present. At the same time, the presence or absence of curli did not alter RSE cell adherence patterns of another O157 strain. These observations are at variance with the reported role of curli in O157 adherence to human cell lines such as HEp-2 and need to be factored in when developing anti-adherence modalities for preharvest control of O157 in cattle. IMPORTANCE: This study demonstrated that O157 strains interact with epithelial cells in a host-specific manner. The fimbriae/adhesins that are significant for adherence to human cell lines may not have a role or may have a modulating role in O157 adherence to bovine cells. Targeting such adhesins may not prevent O157 attachment to bovine cells but instead may result in improved adherence. Hence, conducting host-specific evaluations is critical when selecting targets for O157 control strategies.


Sujet(s)
Adhésines bactériennes/métabolisme , Canal anal/microbiologie , Adhérence bactérienne , Protéines bactériennes/métabolisme , Cellules épithéliales/microbiologie , Escherichia coli O157/physiologie , Rectum/microbiologie , Adhésines bactériennes/génétique , Canal anal/cytologie , Animaux , Protéines bactériennes/génétique , Bovins , Lignée cellulaire tumorale , Cellules HeLa , Spécificité d'hôte , Humains , Rectum/cytologie
19.
J Forensic Sci ; 62(3): 585-592, 2017 May.
Article de Anglais | MEDLINE | ID: mdl-28008604

RÉSUMÉ

The persistence of sperm using confirmatory microscopic analysis, the persistence of sperm with tails, time since intercourse (TSI) analysis, and results from the acid phosphatase (AP) reaction from approximately 5581 swabs taken from circa 1450 sexual assault cases are presented. The observed proportions of sperm in the vagina and anus declines significantly after 48 h TSI, and sperm on oral swabs were observed up to 15 h TSI. The AP reaction as a predictor of sperm on intimate swabs is questioned. All AP reaction times gave a low true positive rate; 23% of sperm-positive swabs gave a negative AP reaction time. We show the AP reaction is an unsafe and an unreliable predictor of sperm on intimate swabs. We propose that TSI not AP informs precase assessment and the evaluative approach for sexual assault cases. To help inform an evaluative approach, TSI guidelines are presented.


Sujet(s)
Médecine légale/normes , Infractions sexuelles , Spermatozoïdes/cytologie , Acid phosphatase/analyse , Canal anal/cytologie , Femelle , Recommandations comme sujet , Humains , Irlande , Mâle , Microscopie , Bouche/cytologie , Manipulation d'échantillons , Spermatozoïdes/composition chimique , Facteurs temps , Vagin/cytologie
20.
J Infect Dis ; 213(3): 351-60, 2016 Feb 01.
Article de Anglais | MEDLINE | ID: mdl-26268855

RÉSUMÉ

BACKGROUND: Anal cancer rates are higher for human immunodeficiency virus (HIV)-infected adults than for uninfected adults. Limited published data exist characterizing the incidence of precursor lesions detected by anal cytology. METHODS: The Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy was a prospective cohort of 700 HIV-infected participants in 4 US cities. At baseline and annually thereafter, each participant completed a behavioral questionnaire, and healthcare professionals collected anorectal swabs for cytologic examination and human papillomavirus (HPV) detection and genotyping. RESULTS: Among 243 participants with negative baseline results of anal cytology, 37% developed abnormal cytology findings (incidence rate, 13.9 cases/100 person-years of follow-up; 95% confidence interval [CI], 11.3-16.9) over a median follow-up duration of 2.1 years. Rates among men having sex with men, among women, and among men having sex with women were 17.9 cases/person-years of follow-up (95% CI, 13.9-22.7), 9.4 cases/person-years of follow-up (95% CI, 5.6-14.9), and 8.9 cases/person-years of follow-up (95% CI, 4.8-15.6), respectively. In multivariable analysis, the number of persistent high-risk HPV types (adjusted hazard ratio [aHR], 1.17; 95% CI, 1.01-1.36), persistent high-risk HPV types except 16 or 18 (aHR, 2.46; 95% CI, 1.31-4.60), and persistent types 16 or 18 (aHR, 3.90; 95% CI, 1.78-8.54) remained associated with incident abnormalities. CONCLUSIONS: The incidence of abnormal anal cytology findings was high and more likely to develop among persons with persistent high-risk HPV.


Sujet(s)
Canal anal/cytologie , Agents antiVIH/usage thérapeutique , Infections à VIH/traitement médicamenteux , Adulte , Femelle , Infections à VIH/complications , Homosexualité masculine , Humains , Incidence , Mâle , Adulte d'âge moyen , Facteurs de risque
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