Iophysical studies and may become an important tool for identification of hAQP1 modulators.AcknowledgmentsThe authors thank David S ensen for excellent technical assistance, Dr. David Drew for generous gift of the GFP expression plasmid, pET20bGFP-8His and Dr. Jakob Winther for the anti-GFP ntibody.Author ContributionsConceived and designed the experiments: JB PSP PAP. Performed the experiments: JB PSP PAP. Analyzed the data: JB CHN PSP PAP. Contributed reagents/materials/analysis tools: JB PSP CHN PAP. Wrote the paper: JB CHN PAP.
The human immunodeficiency virus (HIV) is a sexuallytransmitted infection (STD) having a great impact around the world due to the large amount of people living with such infection (34.2 million) and the frequent appearance of new cases (2.5 million in 2011) [1]. It is characterized by affecting immune system CD4+ cells, thereby leading to a reduction in the body’s efficiency regarding the presentation of a response against other pathogens, making an individual more vulnerable to other types of infection [2]. Some studies have suggested that women living with HIV/ AIDS have Epigenetic Reader Domain increased frequency and incidence of single and multiple infections caused by human papillomavirus (HPV) [3]; the natural history of infection becomes altered, thereby leading to an increased risk of developing cervical 
cancer (CC) and contributing towards this type of cancer being the most frequently diagnosed in HIV-positive women [4]. This relationship may be due to: higher HPV exposure in HIV-infected women, increased frequency of main risk factors involved in CC development or therole of HIV-related immunosuppression in favoring carcinogenesis [5]. The immunosuppression can be attenuated through using antiretroviral therapy which favors balanced counts of 18055761 CD4 lymphocytes, however, this therapy has not been consistently implicated in the reduction of HPV-related diseases [6]. The CC incidence in the Colombian 15755315 general population is 36.4 cases/year/100,000 women [7]; the disease onset occurs approximately between 7 and 12 years after initial HPV infection [8]. These clinical features are altered in women infected simultaneously with HPV and HIV where a short-term clinical outcome usually occurs, involving lesions developing more aggressively, slower HPV infection regression rates and poorer responses to treatment [9]; such factors mean that pre-cancerous lesions could reach 60 (evolving in less than 3 years) [10]. Cervical Epigenetics cytology is the most widely used strategy for reducing the cervical cancer burden around the world [11]. However, this screening test has reduced impact in HIV-infected women, as this group has a greater probability of becoming infected with HPV and developing cervical lesions [12], which has led to cytologicalHPV in HIV-Infected Women Paired Samplesscreening guidelines being rewritten, now including a test every six months during the first year followed by a yearly check-up scheme if no lesions are observed [13]. Nevertheless, cytology coverage in this group of women is poor and insufficient [10], therefore, monitoring programs that allow the constant screening in extended time periods is thus suggested, considering the high risk associated with this group of women. In view of the above, the use of complementary techniques to the Papanicolau test could represent a useful tool in detecting women at risk. Some of these methods are non-invasive, such as self-sampling, 
as when they are used in screening programs they could.Iophysical studies and may become an important tool for identification of hAQP1 modulators.AcknowledgmentsThe authors thank David S ensen for excellent technical assistance, Dr. David Drew for generous gift of the GFP expression plasmid, pET20bGFP-8His and Dr. Jakob Winther for the anti-GFP ntibody.Author ContributionsConceived and designed the experiments: JB PSP PAP. Performed the experiments: JB PSP PAP. Analyzed the data: JB CHN PSP PAP. Contributed reagents/materials/analysis tools: JB PSP CHN PAP. Wrote the paper: JB CHN PAP.
The human immunodeficiency virus (HIV) is a sexuallytransmitted infection (STD) having a great impact around the world due to the large amount of people living with such infection (34.2 million) and the frequent appearance of new cases (2.5 million in 2011) [1]. It is characterized by affecting immune system CD4+ cells, thereby leading to a reduction in the body’s efficiency regarding the presentation of a response against other pathogens, making an individual more vulnerable to other types of infection [2]. Some studies have suggested that women living with HIV/ AIDS have increased frequency and incidence of single and multiple infections caused by human papillomavirus (HPV) [3]; the natural history of infection becomes altered, thereby leading to an increased risk of developing cervical cancer (CC) and contributing towards this type of cancer being the most frequently diagnosed in HIV-positive women [4]. This relationship may be due to: higher HPV exposure in HIV-infected women, increased frequency of main risk factors involved in CC development or therole of HIV-related immunosuppression in favoring carcinogenesis [5]. The immunosuppression can be attenuated through using antiretroviral therapy which favors balanced counts of 18055761 CD4 lymphocytes, however, this therapy has not been consistently implicated in the reduction of HPV-related diseases [6]. The CC incidence in the Colombian 15755315 general population is 36.4 cases/year/100,000 women [7]; the disease onset occurs approximately between 7 and 12 years after initial HPV infection [8]. These clinical features are altered in women infected simultaneously with HPV and HIV where a short-term clinical outcome usually occurs, involving lesions developing more aggressively, slower HPV infection regression rates and poorer responses to treatment [9]; such factors mean that pre-cancerous lesions could reach 60 (evolving in less than 3 years) [10]. Cervical cytology is the most widely used strategy for reducing the cervical cancer burden around the world [11]. However, this screening test has reduced impact in HIV-infected women, as this group has a greater probability of becoming infected with HPV and developing cervical lesions [12], which has led to cytologicalHPV in HIV-Infected Women Paired Samplesscreening guidelines being rewritten, now including a test every six months during the first year followed by a yearly check-up scheme if no lesions are observed [13]. Nevertheless, cytology coverage in this group of women is poor and insufficient [10], therefore, monitoring programs that allow the constant screening in extended time periods is thus suggested, considering the high risk associated with this group of women. In view of the above, the use of complementary techniques to the Papanicolau test could represent a useful tool in detecting women at risk. Some of these methods are non-invasive, such as self-sampling, as when they are used in screening programs they could.
