Submitted by Cássio da Cruz Nogueira (cassionogueirakk@gmail.com) on 2017-10-04T15:02:02Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_EstudoEpidemiologicoInfeccao.pdf: 1728040 bytes, checksum: 0fe6edf6cc8bc4638801d79c202c2fad (MD5) / Approved for entry into archive by Irvana Coutinho (irvana@ufpa.br) on 2017-10-05T14:50:27Z (GMT) No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_EstudoEpidemiologicoInfeccao.pdf: 1728040 bytes, checksum: 0fe6edf6cc8bc4638801d79c202c2fad (MD5) / Made available in DSpace on 2017-10-05T14:50:27Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_EstudoEpidemiologicoInfeccao.pdf: 1728040 bytes, checksum: 0fe6edf6cc8bc4638801d79c202c2fad (MD5) Previous issue date: 2016-04-27 / CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico / O câncer do colo uterino é um problema de saúde pública mundial. Apesar do fácil rastreamento e apresentar altas taxas de cura, quando detectado no início, ainda é responsável pelo óbito de aproximadamente 230 mil mulheres, sendo mais de 80% ocorridos nos países em desenvolvimento. Portanto, o objetivo desta pesquisa consistiu em realizar um estudo acerca da prevalência da infecção genital pelo Papilomavírus Humano (HPV) e os fatores de risco associados em mulheres residentes no município de Bragança, no Estado do Pará. Trata-se de um estudo clínico observacional transversal e analítico, realizado no Hospital Regional de Bragança Antônio Maria Zaccaria e nas unidades de saúde daquele município, por meio da coleta de dados através de um formulário clínico epidemiológico e colheita de amostras biológicas de células do colo uterino, para então detecção do HPV com a técnica de biologia molecular conhecida como “Nested-PCR. A prevalência do HPV foi de 37,5% nas mulheres no município de Bragança, tendo os seguintes subtipos identificados: 11, 16, 18, 31, 35, 52 e 58. Destes, os mais prevalentes foram o 16 e o 35, além de três casos de coinfecção de subtipos. Em relação aos fatores de risco, não houve nenhuma associação com a infecção pelo HPV, porém foi possível traçar um perfil das mulheres infectadas. Essas mulheres eram predominantemente casadas, com faixa etária entre 18 e 25 anos, possuíam alta escolaridade, não tabagistas, porém etilistas, apresentaram coitarca a partir dos 15 anos, mais de 5 parceiros sexuais ao longo da vida, um ou mais parceiros no último ano, sendo pelo menos um parceiro novo; não faziam uso regular de contraceptivos, tiveram até duas gestações, um parto, pelo menos um aborto e estavam realizando o primeiro exame de PCCU. Como conclusão, verificou-se uma alta prevalência do HPV nessas mulheres, e com este perfil em relação aos fatores de risco, pode-se elaborar ações em saúde voltada para a população de Bragança, visando minimizar a transmissão deste vírus e o desenvolvimento de câncer de colo uterino. / The cervical cancer is a problem of global public health. Despite the easy tracking and have high cure rates when detected early, it is still responsible for the death of approximately 230,000 women, of which 80% occurred in developing countries. Therefore, the objective of this research was to conduct a study of the prevalence of genital infection with human papillomavirus (HPV) and associated risk factors in women living in the city of Bragança, in the state of Pará. It was a cross-sectional observational clinical study and analytical, held in Bragança Regional Hospital Antonio Maria Zaccaria and in health units that municipality, through data collection was conducted with a clinical epidemiological form and collection of biological samples of cervical cells, and then the detection of HPV molecular biology technique known as "nested PCR (polymerase chain reaction). The prevalence of HPV was 37.5% in women from Bragança city, having identified subtypes: 11, 16, 18, 31, 35, 52 and 58, the most prevalent were 16 and 35 and three cases coinfection of subtypes. Infected women were predominantly married, were between 18 and 25, had high levels of education, non-smokers, but were alcoholic, had first sexual intercourse after 15 years, more than 5 partners in life, one or more sexual partners in the last year, and at least one new partner, did not make regular use of contraceptives, they had up to two pregnancies, childbirth, at least one abortion and were taking the first examination of PCCU. A high prevalence of HPV in these women was found but no risk factors was associated with statistically. However, one can trace a profile of the infected women to support health actions and minimize the transmission of this virus through educational activities, mainly focused on the proper use of condoms, in addition to increasing nastiness for cervical cancer in especially the awareness of the preventive test.

No description available.

Le virus du papillome humain (HPV) est l’infection sexuellement transmise la plus fréquente au monde. Plusieurs études ont établi son implication dans l’étiologie de pratiquement tous les cancers du col de l’utérus, une maladie qui constitue un problème de santé majeur dans les pays pauvres. Le HPV est également responsable de 90% des cancers de l’anus, 40-50% des cancers du pénis, de la vulve et du vagin, et 30% des cancers de la tête et du cou. L’objectif général de cette thèse est de combler les lacunes relatives aux connaissances sur la distribution génotypique du HPV dans les lésions néoplasiques cervicales utérines et de la tête et du cou, plus particulièrement en Afrique. Les objectifs spécifiques sont les suivants: 1) analyser la distribution génotypique du HPV dans les cancers du col de l’utérus et faire une analyse comparative de cette distribution dans cinq pays africains en fonction de la prévalence du VIH; 2) évaluer la présence du HPV dans les cancers de la tête et du cou au Sénégal; 3) faire une revue de la littérature et une méta-analyse sur la distribution du HPV dans les cancers de la tête et du cou dans toutes les régions du monde. Pour le premier et le second objectifs, qui découlent d’un large projet international coordonné par l’Institut Catalan d’Oncologie pour l’Organisation Mondiale de la Santé (OMS), une étude transversale multicentrique a été menée au Mali et au Sénégal pour collecter des blocs de paraffine de patientes diagnostiquées entre 2001 et 2010 du cancer invasif du col et des cancers de la tête et du cou. Pour le troisième objectif, une revue exhaustive de la littérature a permis d’identifier tous les articles qui ont été publiés sur les cancers de la tête et du cou dans tous les pays du monde et d’effectuer une méta-analyse sur la prévalence de l’ADN du HPV selon le site du cancer et la région géographique. Notre analyse montre que les principaux types de HPV ciblés dans les vaccins prophylactiques (HPV16/18) représentent la majorité des types de HPV détectés dans le cancer invasif du col de l’utérus en Afrique subsaharienne. Par contre, le HPV45 vient au second rang dans certains pays d’Afrique, dont le Mali et le Sénégal. Nos données suggèrent également que le VIH aurait un rôle dans la contribution relative du HPV18 et HPV45 dans le développement du cancer du col de l’utérus. Au Sénégal, notre étude montre que la prévalence du HPV dans les cancers de la tête et du cou est très faible et ne semble pas jouer un rôle important dans l’oncogenèse. Finalement, la méta-analyse a mesuré la prévalence des HPV dans les cancers de la cavité orale, de l’oropharynx, du larynx et de l’hypopharynx, et confirme l’importante contribution relative du HPV16 dans ces cancers. Globalement, cette thèse permet de mieux comprendre l’impact potentiel des vaccins prophylactiques sur l’incidence des cancers associés au HPV. / Human papillomavirus (HPV) infection is the most common sexually transmitted infection worldwide. Several studies have shown its involvement in the etiology of virtually all cancers of the cervix, which is a major health problem in poor countries. HPV is also responsible for 90% of anal cancers, 40-50% of penile, vulvar and vaginal cancers, and 30% of head and neck cancers. The overall objective of this thesis is to fill the gaps in knowledge on the genotype distribution of HPV in anogenital and head and neck neoplasia, especially in sub-Saharan Africa. The specific objectives are to: 1) analyze HPV genotype distribution in cervical cancer and compare this distribution in five African countries according to HIV prevalence; 2) evaluate the presence of HPV in cancers of the head and neck in Senegal; 3) review the literature on the distribution of HPV in cancers of the head and neck in all regions of the world and perform a meta-analysis. For the first and second objectives, which were derived from a larger international project coordinated by the Catalan Institute of Oncology for the World Health Organization (WHO), a cross-sectional multicentric study was conducted to collect paraffin-embedded blocks of invasive cervical cancer and head and neck cancer diagnosed between 2001 and 2010 in Mali and Senegal. For the third objective, a comprehensive search of the literature was conducted to identify all articles published to date on head and neck cancer. A meta-analysis was performed to estimate the prevalence of HPV DNA according to cancer site and geographical region. Our analysis shows that the main HPV types targeted in the prophylactic vaccines (HPV16/18) accounted for the majority of the HPV types found in invasive cervical cancer in sub-Saharan Africa. Our data also suggests that HIV may play a role in the contribution of HPV18 and HPV45 to the development of cervical cancer. However, HPV45 ranks second in many African countries, notably in Mali and Senegal. In Senegal, our study shows that HPV DNA prevalence in head and neck cancer is very low and is not importantly involved in the oncogenesis. Finally, the meta-analysis measured the prevalence of HPV in cancers of the oral cavity, oropharynx, larynx and hypopharynx, and confirmed the significant relative contribution of HPV16 in these cancers. Overall, this thesis contributes to a better understanding of the potential impact of HPV prophylactic vaccines on the incidence of HPV-associated cancers.

Chez les mammifères, les cellules apoptotiques peuvent être complètement dégradées par des cellules phagocytaires spécialisées ou servir de vecteur d'ADN Le transfert d'oncogènes via les cellules apoptotiques aboutit à la transformation des cellules receveuses uniquement si celles-ci sont déficientes en p53. Sachant que Fniicogène E6 des papillomavirus humains (HPV) à haut risque induit la dégradation de p53, il est concevable que son transfert par la cellule apoptotique soit à l'origine d'un mécanisme alternatif de carcinogenèse associée aux HPV. Afin de confirmer cette hypothèse, l'apoptose de cellules dérivées de cancer du col de l'utérus, abriiam ou non des séquences d'HPV, a été induite. En collaboration avec l'équipe de Patrick Sandoz du laboratoire d'optique de FEMTO-ST, nous avons adapté leur inicr;système référencé en position à l'observation automatisée de Finternalisation des cellules apoptotiques. Nous avons aussi déterminé que les cellules apoptotiques son! phagocytées par les fîbroblastes quel que soit leur statut virologique. Seules les cellules apoptotiques dérivées de cellules abritant de l'ADN d'HPV transforment les cellules receveuses. L'expression de l'ADN viral, dont E6, dans les fîbroblastes transformés ainsi que la perte d'expression des protéines p53 et p21 suggère que les oncogènes d'HPV pourraient être à l'origine de la transformation. Les résultats présentés dans ces travaux mettent en évidence un nouveau mécanisme de carcinogenèse associée aux HPV via la phagocytose des cellules apoptotiques, potentiellement impliqué dans la transformation de cellules primaires et la progression des tumeurs associées aux HPV. / Apoptotic cells in mammals may be completely degraded by specialized phagocytic cells or serve as a DNA vector. The oncogene transfer via apoptotic cells leads to the transformation of récipient cells but only when they are p53 deficient. As the E6 oncogene of high-risk human papillomavirus (HPV) leads to p53 dégradation, its transfer from apoptotic cells may be the cause of an alternative mechanism of HPV-associated carcinogenesis. To confirm this hypothesis, we induced apoptosis of cervical cancer cells that may harbor HPV sequences. In collaboration with Patrick Sandoz's team at the FEMTO-ST optical laboratory, we used their position-referenced microsystem for the automated observation of apoptotic cell internalization. We also found that apoptotic cells are phagocytized by fibroblasts regardless of their virological status. Only apoptotic cells from cells harboring HPV DNA transform recipient cells. Viral DNA expression, including E6, in transformed fibroblasts and the loss of p53 and p21 protein expression suggest that HPV oncogènes may cause transformation. These results highlight a new mechanism of HPV-associated carcinogenesis via apoptotic cell phagocytosis. This mechanism may be involved in thé transformation of primary cells and the progression of HPV-associated tumors.

L’infection génitale par le Virus du Papillome Humain (VPH) est l’infection transmissible sexuellement la plus fréquente. Sa prévalence la plus élevée est retrouvée chez les femmes en âge de procréer. Bien que la littérature expérimentale s’accorde sur la plausibilité biologique de l’effet du VPH sur les issues négatives de grossesse, les résultats des études observationnelles sont équivoques. Parmi ces issues négatives figure l’accouchement prématuré qui reste une cause majeure de mortalité périnatale et de morbidité à vie dans le monde. La présente thèse avait alors pour but de faire la lumière sur la qualité de la littérature actuelle sur les issues négatives de grossesse en lien avec le VPH en général et d’approfondir l’association entre le VPH et l’accouchement prématuré en particulier. À cette fin, trois objectifs de recherche étaient visés, à savoir: 1) évaluer systématiquement l’ampleur de l’association entre l’infection VPH et les issues négatives de grossesse dans la littérature et la qualité des évidences sur ces relations, 2) estimer l’association entre l’infection VPH pendant la grossesse et l’accouchement prématuré et 3) identifier les déterminants de la transmission du VPH dans le placenta chez les femmes infectées par le VPH au niveau vaginal. Trois analyses ont été menées pour répondre à chacun des objectifs. D’abord, nous avons effectué une revue systématique et des méta-analyses pour chacune des issues négatives de grossesse suivantes: avortement spontané, rupture prématurée et/ou préterme et des membranes, accouchement prématuré, faible poids de naissance, retard de croissance intra-utérine, troubles hypertensifs gestationnels et mortinaissance. Ensuite, en utilisant les données des femmes éligibles de la cohorte prospective HERITAGE (n=899), nous avons estimé l’association entre l’infection VPH (pendant la grossesse et dans le placenta) et l’accouchement prématuré. Dans un modèle de régression logistique, un ajustement pour la confusion a été assuré par pondération par l’inverse de probabilité de l’infection VPH au premier trimestre en fonction des caractéristiques maternelles. Enfin, l’analyse des déterminants du VPH dans le placenta a été réalisée sur l’échantillon de la cohorte de femmes positives au VPH au premier trimestre de grossesse (n=354) en utilisant un modèle d’équations d’estimation généralisée. La revue systématique et les méta-analyses ont montré que l’infection VPH est associée à plusieurs issues négatives de grossesse dont l’accouchement prématuré. Cependant, ces résultats doivent être interprétés avec prudence, compte tenu des limites dans certaines études en raison d’erreur de mesure de l’exposition au VPH, d’une détection du VPH en dehors de la période de grossesse, et d’un contrôle insuffisant pour la confusion. Les résultats de notre étude de cohorte prospective ont montré que la persistance des VPH16/18 pendant la grossesse et la présence du VPH dans le placenta sont associées à l’accouchement prématuré avec un odds ratio ajusté (aOR) de 3,72 (IC 95% 1,47-9,39) et 2,53 (IC 95% 1,06- 6,03) respectivement. Cet effet est indépendant des antécédents de traitement de dysplasies cervicales. Par ailleurs, la présence du VPH dans le placenta est associée à l’origine ethnique autre que blanc (aOR 1,78; IC 95% 1,08-2,96), aux anomalies cervicales (aOR 1,92; IC 95% 1,14-3,24), à l’infection génitale ou urinaire (aOR 2,32; IC 95% 1,15-4,68), à la coinfection VPH au 1er trimestre (aOR 2,56; IC 95% 1,72-3,83), à la persistance d’un VPH à haut risque autre que les génotypes 16/18 (2,31; IC 95% 1,20-4,45) et à la persistance des VPH-16/18 pendant la grossesse (aOR 4,55; IC 95% 2,40-8,66). Dans l’ensemble, les résultats de cette thèse apportent de nouvelles connaissances sur l’infection VPH vaginale pendant la grossesse et dans le placenta. L’association entre l’accouchement prématuré et la persistance du VPH-16/18 en cours de grossesse ou l’infection VPH dans le placenta indique qu’un certain nombre d’accouchements prématurés, jusque-là inexpliqués, pourraient être en lien avec le VPH. Cet effet direct de l’infection VPH sur l’accouchement prématuré vient s’ajouter à celui, déjà montré, du traitement cervical des lésions dysplasiques. Le VPH placentaire est associé aux marqueurs d’une réponse immunitaire inadéquate contre le VPH vaginal. Nos résultats plaident en faveur de la couverture vaccinale optimale contre le VPH dans le but d’alléger le fardeau des naissances prématurées. / Human Papillomavirus (HPV) genital infection is the most common sexually transmitted infection. Its highest prevalence is found in women of childbearing age. Although experimental studies agree on the biological plausibility of detrimental effect of HPV on pregnancy outcomes, observational studies yielded contradictory findings. Among these negative outcomes there is preterm delivery, which remains a major cause of perinatal mortality and lifelong morbidity worldwide. Therefore, this thesis aimed to shed light on the quality of the current literature on negative outcomes related to HPV in general and specifically to further investigate the association between HPV and preterm birth. We targeted three research objectives: 1) systematic assessment of the association between HPV infection and negative pregnancy outcomes in the literature and the quality of the evidence on these relationships, 2) estimate the association between HPV infection during pregnancy and preterm delivery; and 3) to identify the determinants of HPV transmission in the placenta in women infected with in the first trimester. Three analyzes were carried out to meet each of the objectives. We performed a systematic review and meta-analyzes for each of the following negative pregnancy outcomes: spontaneous abortion, premature and / or preterm rupture and membranes, preterm birth, low birth weight, intra-uterine growth retardation, pregnancy induced hypertensive disorders and stillbirth. Using data from eligible women in the HERITAGE prospective cohort (n = 899), we assessed the association between HPV infection (during pregnancy and in the placenta) and preterm birth. In a logistic regression model, we adjusted for confounding by inverse propensity treatment weighting of HPV infection in the first trimester based on maternal characteristics. Finally, the analysis of the determinants of HPV in the placenta was performed on the sample of the cohort of HPV positive women in the first trimester of pregnancy (n = 354) using a generalized estimation equations model. The systematic review and meta-analyzes showed that HPV infection is associated with several negative pregnancy outcomes including preterm birth. However, these results should be interpreted with caution, given the limitations in some studies regarding misclassification of HPV exposure, inappropriate HPV time-point detection, and insufficient control for confusion. Our prospective cohort study showed that the persistence of HPV16/18 during pregnancy and the presence of any HPV in the placenta are associated with preterm birth with an adjusted odds ratio (aOR) of 3.72 (CI 95 % 1.47-9.39) and 2.53 (95% CI 1.06-6.03) respectively. These findings are independent of the history of cervical dysplasia treatment. In addition, the presence of any HPV in the placenta is associated with ethnic origin other than white (aOR 1.78; 95% CI 1.08-2.96), cervical abnormalities (aOR 1.92; 95% CI 1.14-3.24), genital or urinary infection (aOR 2.32; 95% CI 1.15-4.68), HPV coinfection in the 1st trimester (aOR 2.56; 95% CI 1.72-3.83), persistence of high-risk HPV other than genotypes 16/18 (2.31; 95% CI 1.20-4.45) and persistence of HPV-16/18 during pregnancy (aOR 4.55; 95% CI 2.40-8.66). Overall, our findings provide new evidence on vaginal HPV infection during pregnancy and in the placenta. The association between preterm birth and persistence of HPV-16/18 during pregnancy or any HPV infection in the placenta indicates that a number of unexplained preterm deliveries may be related to HPV. This direct effect of HPV infection on preterm birth is in addition to that already shown of cervical treatment of dysplastic lesions. Placental HPV is associated with markers of an inadequate immune response against vaginal HPV. Our results argue in favor of an increase in vaccine coverage against HPV in order to reduce the burden of preterm births.

MSc (Microbiology) / Department of Microbiology / Background: Prostate cancer (PCA) is a major health concern in males, particularly those above 40 years old. It is the most common form of cancer in males worldwide, including South Africa. In South Africa, the rate of histologically diagnosed prostate cancer is 40 per 100 000 in whites and 14 per 100 000 in blacks, and 1 in 8 men will develop PCA in their lifetime. Several reports have suggested the association of viruses in the pathogenesis of prostate cancer. Objectives: This study was aimed at identifying Hepatitis B virus (HBV), human papilloma virus (HPV) and human herpes virus type 8 (HHV-8), implicated in other forms of cancer, in a cohort of South African patients with either PCA or benign prostatic hyperplasia (BPH); and to seek possible associations thereof. Methods: The study group comprised 187 male patients recruited from Polokwane Hospital presenting with either PCA (staged by Gleason scores) or BPH. Enzyme-linked immunosorbent assay was used to detect antibodies to HHV-8 and HPV; and to detect hepatitis B surface antigen (HBsAg) in the plasma of the study subjects. Total DNA was extracted from plasma and targeted for the identification of HBV and HHV-8 DNA by nested PCR protocols. The HBV nested PCR protocol amplifies a 336bp fragment of the overlapping surface polymerase gene of HBV. The HHV-8 nested protocol amplifies a 233bp fragment of the ORF 26 gene of HHV-8. Amplified DNA products were purified, sequenced by the Sanger protocol and phylogenetically analysed for viral genotypes. The Chi-square test was used to infer statistically significant differences in the level of detection of viruses and the stage of prostate cancer development. Results: Of the 187 participants, a seroprevalence of 4.8% (9/187, HBsAg), 5.3% (10/187, HPV IgG antibody) and 27% (33/124, HHV-8 IgG antibody) were observed. HBsAg was detected more in individuals with BPH than those without and this was statistically significant at ( 2=6.0, p< 0.05). HHV-8 DNA was detected more in individuals in the 60-79 years age range and this was statistically significant at ( 2=61.1, p< 0.05). Occult HBV infection (that is the presence of HBV DNA in the absence of HBsAg) was detected in 23/178 (12.9%) of patients. Taking into account occult HBV infection, the overall prevalence of HBV was 17.7%. HBV genotype E was more prevalent (86.7%) followed by genotype A (13.3%). HHV-8 genotypes K and R were inferred. Apparently, this is the first report on the identification of HHV-8 genotypes K and R from South Africa. Conclusion: The current study has demonstrated for the first time, the presence of genotypes K and R of HHV-8 in South Africa. This study also suggests that there is a high level of occult genotype E HBV infection. Future studies will explore the virome in prostate cancer biopsies.

Contexte : La littérature suggère que le virus du papillome humain (VPH) puisse être transmis verticalement. Or, le mécanisme exact de transmission verticale demeure inconnu et les données ne permettent pas de savoir dans quelle mesure la transmission verticale est affectée par le mode d’accouchement. L’objectif de l’étude était de mesurer l’association entre le mode d’accouchement et la détection d’ADN du VPH chez les bébés. Méthode : Nous avons utilisé les données de 1052 femmes enceintes de la cohorte HERITAGE. Des échantillons vaginaux auto-collectés ont été obtenus chez les mères durant la grossesse, et des échantillons des muqueuses de la bouche, la gorge, les yeux et de la région anogénitale ont été collectés chez les bébés à la naissance et à 3 mois. Nous avons inclus les 282 femmes ayant eu un test VPH positif au premier et troisième trimestre de grossesse. Tous les échantillons ont été analysés pour la détection d’ADN du VPH par la méthode de réaction de polymérase en chaîne (PCR) avec le test Linear ArrayMC. Les informations sur l’accouchement ont été collectées dans les dossiers médicaux. L’association entre le mode d’accouchement et la transmission verticale du VPH a été mesurée par régressions logistiques. Résultats : La probabilité de transmission verticale du VPH a été de 8,9% (25/282), soit 3,7% (3/81) pour les césariennes et 10,9% (22/201) pour les accouchements vaginaux. Chez 21 des 25 enfants positifs au VPH (84%), il y avait au moins un génotype concordant avec leur mère, et tous sont nés par accouchement vaginal. Une augmentation significative du risque de transmission verticale du VPH a été observée pour l’accouchement vaginal, en comparaison avec la césarienne (OR ajusté: 3,63, intervalles de confiance à 95% (IC 95%): 1,03-12,82). Nous n’avons pas observé d’association significative entre la césarienne suivant la rupture des membranes et le risque de transmission, lorsque comparé avec la césarienne avec membranes intactes (OR ajusté : 1,31, IC 95% : 0,10-17,76). Il n’y a pas eu d’association entre la durée écoulée entre la rupture des membranes et la naissance (en heures continues) et le risque de transmission verticale (OR : 1,00, IC 95% : 0,97-1,02). Conclusion : L’accouchement par césarienne a été associé à un risque significativement plus faible de transmission du VPH chez les bébés. La transmission verticale du VPH surviendrait principalement lors du passage dans le canal vaginal car très peu d’enfants nés par césarienne ont été infectés au VPH. Puisque la rupture des membranes avant la césarienne et la durée entre la rupture des membranes et la naissance n’ont pas été associées à un risque de transmission du VPH plus élevé, nos résultats suggèrent que la transmission par infection ascendante après rupture des membranes est probablement rare. / Background: The literature suggests that human papillomavirus (HPV) can be transmitted vertically. However, the exact mechanism of vertical transmission remains unknown and the data do not allow us to know to what extent vertical transmission is affected by the mode of delivery. The aim of the study was to measure the association between mode of delivery and the detection of HPV DNA in infants. Method: We used data from 1052 pregnant women from the HERITAGE cohort. Self-collected vaginal samples were obtained from mothers during pregnancy, and specimens from the mucous membranes of the mouth, throat, eyes and anogenital region were collected from infants at birth and at 3 months. We included 282 women who had both positive HPV tests in the first and third trimester of pregnancy. All samples were analyzed for detection of HPV DNA by the polymerase chain reaction (PCR) method with the Linear ArrayTM assay. Information about the delivery was collected from medical records. The association between the mode of delivery and HPV detection in infants was measured using logistic regressions. Results: The probability of transmission of HPV was 8.9% (25/282); 3.7% (3/81) for caesarean sections and 10.9% (22/201) for vaginal deliveries. In 21 of 25 HPV positive infants (84%), there was at least one genotype concordant with their mother, and all were born vaginally. A significant increase in the risk of transmission of HPV was observed for vaginal delivery, compared to caesarean section (adjusted OR: 3.63, 95% confidence intervals (95% CI): 1.03-12.82). We found no significant increase in the risk of HPV transmission for caesarean section following rupture of membranes, compared to caesarean section with intact membranes (adjusted OR: 1.31, 95% CI: 0.10-17.76). There was no association between the time between rupture of membranes and birth (in continuous hours) and the risk of vertical transmission (OR: 1.00, 95% CI: 0.97-1.02). Conclusion: Caesarean delivery is associated with a significantly lower risk of HPV vertical transmission. Vertical transmission is thought to occur mainly during passage through the vaginal canal, because very few infants born by caesarean section have been infected with HPV. Since rupture of membranes before caesarean section and the time between ruptured membranes and birth have not been associated with a higher risk of HPV transmission, our results suggest that transmission by ascending infection after rupture of membranes is unlikely.

Indiana University-Purdue University Indianapolis (IUPUI) / Cervical cancer is caused by the persistent infection of human papilloma virus (HPV) in the cervix epithelium. Although effective preventative care is available, the widespread nature of infection and the variety of HPV strains unprotected by HPV vaccines necessitate a better understanding of the disease for development of new therapies. A major tumor suppressing mechanism is the inhibition of cell division by tissue structure; however, the underlining molecular circuitry for this regulation remains unclear. Recently, the Yap transcriptional co-activator has emerged as a key growth promoter that mediates contact growth arrest and limits organ size. Thus, we aimed to uncover upstream signals that connect tissue organization to Yap regulation in the inhibition of cervical cancer. Two events that disrupt tissue structure were examined including the loss of the tumor suppressor LKB1 and the expression of the viral oncogene HPV16-E6. We identified that Yap mediates cell growth regulation downstream of both LKB1 and E6. Restoration of LKB1 expression in HeLa cervical cancer cells, which lack this tumor suppressor, or shRNA knockdown of LKB1 in NTERT immortalized normal human dermal keratinocytes, demonstrated that LKB1 promotes Yap phosphorylation, nuclear exclusion, and proteasomal degradation. The ability of phosphorylation-defective Yap mutants to rescue LKB1 phenotypes, such as reduced cell proliferation and cell size, suggest that Yap inhibition contributes to LKB1 tumor suppressor function(s). Interestingly, LKB1’s suppression of Yap activity required neither the canonical Yap kinases, Lats1/2, nor metabolic downstream targets of LKB1, AMPK and mTORC1. Instead, the scaffolding protein NF2 was required for LKB1 to induce a specific actin cytoskeleton structure that associates with Yap suppression. Meanwhile, HPV16-E6 promoted Yap activation in all stages of keratinocyte differentiation. E6 activated the Rap1 small GTPase, which in turn promoted Yap activity. Since Rap1 does not mediate differentiation inhibition caused by E6, E6 may play a role in promoting cell growth through Rap1-Yap activation rather than preventing growth arrest through the disruption of differentiation. Altogether, the LKB1-NF2-Yap and E6-Rap1-Yap pathways represent two examples of a novel phenomenon, whereby the structure of a cell directly influences its gene expression and proliferation.

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This thesis focuses on gynecopathology. It consists of a collection of seven papers published in pathology journals with impact factor. Introduction section contains selection of examples showing scientific application of molecular genetic methods. Further on the aims of individual research projects are described. The first project comprises histomophologic study of skin endometriosis addressing "mullerian" differentiation. A case report of a rare tumor namely borderline papillary serous tumor of the fimbriated end of the fallopian tube follows with molecular genetic analysis of KRAS, BRAF and p53 gene mutation status. Prospective longitudinal study on high grade squamous dysplasia (HSIL) of the cervix in HPV vaccinated women, so called DAV (dysplasia after vaccination), aims to elucidate pathogenesis of this phenomenon. Two other studies focus on incidence of fumarate hydratase deficient leiomyomas of the uterus and hereditary leiomyomatosis and renal cell carcinoma syndrome (HLRCC). The aim of those studies is to improve our diagnostic capability and increase detection rate of the patients with HLRCC syndrome. Finally a new subtype of HSIL namely bizarre cell dysplasia is described in two separate studies. Conclusion remarks contemplate the role of molecular genetics in surgical pathology.