OBJECTIVE: To investigate the diagnosis of sexually transmitted infections (STIs) with human papillomavirus (HPV) infection and the presence of cytological changes in the cervix in a cohort of sexually active women in Greece. METHODS: Cervical cytology testing and the molecular typing of HPV and other STIs were performed for 345 sexually active women aged between 18 and 45 years (mean 33.2±7.2years) visiting a gynaecology clinic for routine cervical screening. The association of HPV and STI detection with cytological findings was investigated. RESULTS: HPV was detected in 61 women (17.7%) and STIs in 82 (23.8%). Ureaplasma spp was the most frequently detected pathogen, which was found in 63 (18.2%) women, followed by Mycoplasma spp (21 women, 25.6%) and Chlamydia trachomatis (five women, 6.1%). HPV positivity only (with no co-presence of STI) was associated with an abnormal cytology (odds ratio 6.9, p<0.001), while women who were negative for both HPV and STIs had a higher probability of a normal cytology (odds ratio 0.36, p<0.01). Sixteen out of the 63 (25.4%) women who tested positive for Ureaplasma spp, harboured a high-risk HPV type (odds ratio 2.3, p=0.02). CONCLUSIONS: In a population with a high prevalence of Ureaplasma spp, there was an association of this pathogen with high-risk HPV infection, a finding that needs further elucidation.
OBJECTIVE: To investigate the diagnosis of sexually transmitted infections (STIs) with human papillomavirus (HPV) infection and the presence of cytological changes in the cervix in a cohort of sexually active women in Greece. METHODS: Cervical cytology testing and the molecular typing of HPV and other STIs were performed for 345 sexually active women aged between 18 and 45 years (mean 33.2±7.2years) visiting a gynaecology clinic for routine cervical screening. The association of HPV and STI detection with cytological findings was investigated. RESULTS:HPV was detected in 61 women (17.7%) and STIs in 82 (23.8%). Ureaplasma spp was the most frequently detected pathogen, which was found in 63 (18.2%) women, followed by Mycoplasma spp (21 women, 25.6%) and Chlamydia trachomatis (five women, 6.1%). HPV positivity only (with no co-presence of STI) was associated with an abnormal cytology (odds ratio 6.9, p<0.001), while women who were negative for both HPV and STIs had a higher probability of a normal cytology (odds ratio 0.36, p<0.01). Sixteen out of the 63 (25.4%) women who tested positive for Ureaplasma spp, harboured a high-risk HPV type (odds ratio 2.3, p=0.02). CONCLUSIONS: In a population with a high prevalence of Ureaplasma spp, there was an association of this pathogen with high-risk HPV infection, a finding that needs further elucidation.
Community acquired respiratory viruses (CARV) are an important cause of morbidity and mortality among Hematopoietic Stem Cell Transplant recipients (HSCT). Reported incidence of CARV in HSCT varies from 4% on early days of antigen testing to ∼40% using PCR based detection. Most commonly detected viruses are Rhinovirus/enterovirus (22-34%), followed by Influenza, Respiratory Syncytial Virus (RSV) and Parainfluenza on similar range. Less frequently, with important morbidity associated are Coronavirus (3-11%), Adenovirus and Human metapneumovirus (HMPV).Influenza pneumonia have attributable mortality in HSCT ∼ 12%. Progression to lower respiratory tract infection (LRTI) can occur in one third of patients. However, perceived less aggressive viruses can progress to LRTI with equally precarious outcomes. For example, RSV have attributable mortality ∼ 15%, with some series describing mortality around 80% in untreated patients. Adenovirus disseminated infection has been reported around 50% in small series, with mortality ranging 23%. Associated risk factors for LRTI progression include age greater than 65, lymphopenia, neutropenia, unrelated donor and chronic graft versus host disease.Bacterial coinfection, bronchiolitis obliterans and decline in pulmonary function are complications frequently described after CARV infections. Allograft related shortcomings remained an important area of research.General preventive measures are recommended to reduce infection related complications. Great example is Influenza vaccination and antiviral prophylaxis in specific scenarios. Immunization for several other CARV remains in development and not commercially available. Impact of contact and respiratory precaution at level of health care has been documented in several studies and should be followed. Other interventions like palivizumab for RSV in adults still lacking enough data and difficult implementation due to cost.Therapeutic options are narrow given limited antiviral agents approved for the wide range of CARV. Influenza therapy is known to improve outcomes. Ribavirin (RBV) with or without IVIG has reported to beneficial for RSV, PIV and anecdotic reports for HMPV. RBV IV or inhaled (teratogenic and only FDA approved) administration poses a logistic challenge and associated to several side effects. Cidofovir for Adenovirus, ALN-RSV01 (RSV), DAS-181 (PIV), specific T-cell immunity therapies, among others, should accumulate more data to be suited for general use.
Authors: Marianna Martinelli; Rosario Musumeci; Illari Sechi; Giovanni Sotgiu; Andrea Piana; Federica Perdoni; Federica Sina; Robert Fruscio; Fabio Landoni; Clementina E Cocuzza Journal: Int J Environ Res Public Health Date: 2019-12-09 Impact factor: 3.390
Authors: Ongeziwe Taku; Adrian Brink; Tracy L Meiring; Keletso Phohlo; Charles B Businge; Zizipho Z A Mbulawa; Anna-Lise Williamson Journal: PeerJ Date: 2021-03-03 Impact factor: 2.984
Authors: H J Alotaibi; F N Almajhdi; A N Alsaleh; D A Obeid; H H Khayat; T A Al-Muammer; A M Tulbah; M B Alfageeh; M N Al-Ahdal; F S Alhamlan Journal: Saudi J Biol Sci Date: 2020-03-19 Impact factor: 4.219