Abstract
Objectives:
to compare the percentage of collagen fibers in the autopsied women’s uterine body and cervix with and without the Acquired Immunodeficiency Syndrome (Aids).
Methods:
30 autopsied women’s medical files were selected from 1988 to 2013. 30 fragments of the uterine body and 30 cervix were collected and then divided into two groups, 15 with Aids and 15 without, The quantification of the collagen fibers of the uterine body and cervix was performed on slides stained with picrosirius, using the KS-300® system.
Results:
the percentage of collagen fibers was lower for cervix (U=336544; p=0.001) and higher for the uterine body (U=308726,5; p=0.004) in the retroviral group when compared to the group without the disease. The percentage was higher for cervix than the uterine body in the group with Aids (t=0,4793; p=0.0031). the same result was found in the group without Aids (t=2,397; p=0.0637).
Conclusions:
the increase in the percentage of collagen fibers in the uterine body of women with Aids’ indicates an immune response for viral infection and reveals a failure in keeping the infection restricted to the cervix. The interpretation of the histochemical and morphometric parameters can be useful in the diagnosis associated to HIV infection, contributing for clinical improvement and life expectancy.
Key words
Acquired immunodeficiency syndrome; Cervix; Collagen; Autopsy
Resumo
Objetivos:
comparar a porcentagem de fibras colágenas no corpo e colo uterino de mulheres autopsiadas com e sem a Síndrome da Imunodeficiência Adquirida (Aids).
Métodos:
foram selecionados 30 prontuários de mulheres autopsiadas no período de 1988 a 2013. Foram coletados 30 fragmentos do corpo uterino e 30 do colo uterino, dividido em dois grupos, 15 com Aids e 15 sem. A quantificação das fibras colágenas do corpo e colo uterino foi feita nas lâminas coradas por picrosirius, utilizando-se o sistema KS-300®.
Resultados:
a porcentagem de fibras colágenas foi menor no colo (U=336544; p=0,001) e maior no corpo uterino (U=308 726,5; p=0,004) no grupo com a retrovirose quando comparado ao grupo sem a doença. A porcentagem no grupo com Aids foi maior no colo uterino do que no corpo (t=0,4793; p=0,0031). Sendo o mesmo resultado encontrado para o grupo sem Aids (t=2.397; p=0,0637).
Conclusões:
um aumento da porcentagem de fibras colágenas no corpo uterino das mulheres com Aids indica uma resposta imune frente a infecção viral e revela uma falha em manter a infecção restrita ao colo. A interpretação dos parâmetros histoquímicos e morfométricos podem ser úteis no diagnóstico das condições associadas à infecção pelo HIV, contribuindo para a melhora clínica e expectativa de vida.
Palavras-chave
Síndrome da imunodeficiência adquirida; Colo do útero; Colágeno; Autópsia
Introduction
Sexually transmitted infections (STIs) continue to be a major public health problem in Brazil from 2007 to June 2016. 136,945 cases of human immunodeficiency virus (HIV) infection were reported in the Sistema de Notificagao de Lesoes (SINAN)11 Brasil. Ministério da Saúde. Departamento de DST, Aids e Hepatites Virais. Secretaria de Vigilância em Saúde. Boletim Epidemiológico: HIV e Aids. Brasília, DF; 2016. Ano V - n° 01-26. Available in file:///C:/Users/BIA/Downloads/boletim_2016_1_pdf_16375.pdf Accessed in 13-11-17. (Notification System on Lesions). And during this period, a total of 44,766 cases of only women, were reported by SINAN.11 Brasil. Ministério da Saúde. Departamento de DST, Aids e Hepatites Virais. Secretaria de Vigilância em Saúde. Boletim Epidemiológico: HIV e Aids. Brasília, DF; 2016. Ano V - n° 01-26. Available in file:///C:/Users/BIA/Downloads/boletim_2016_1_pdf_16375.pdf Accessed in 13-11-17.
Women with Acquired Immunodeficiency Syndrome (Aids) present a decrease on the cervical epithelium, esophageal and skin,22 Cavellani CL, Rocha LP, Silva RSC, Oliveira LF, Faria HA, Olegario JG, Correa RR, Teixeira VP. The influence of Aids on the morphometric and immune status of the uterine cervix of autopsied patients. Curr HIV Res. 2011; 9 (8): 606-12.
3 Rocha LP, Silva R, Olegario J, Correa R, Teixeira VPA, Cavellani CL. Esophageal epithelium of women with AIDS: Thickness and local immunity. Pathol Res Pract. 2010; 206 (4): 248-52.-44 Favarato GKNA, Silva ACS, Oliveira LFO, Ferraz, MLF, Teixeira VPA, Cavellani CL. Skin aging in patients with acquired immunodeficiency syndrome. Ann Diagn Pathol. 2016; 24 (10): 35-9. and the first line of defense against HIV acquisition in the female genital tract is the mucosal lining of the epithelial barrier.55 Wira CR, Rodriguez-Garcia M, Patel MV. The role of sex hormones in immune protection of the female reproductive tract. Nat Rev Immunol. 2015; 15: 217-30. Studies demonstrate that HIV can interact by means of gp120 with immune cells which activate local inflammatory responses and repairs.66 Dixon LJ, Barnes M, Tang H, Pritchard MT, Nagy LE. Kupffer cells in the liver. Compr Physiol. 2013; 3 (2): 785-97. However, sometimes this interaction may occur by producing inappropriate activations77 Del Cornò M, Cappon A, Donninelli G, Varano B, Marra F, Gessani S. HIV-1 gp120 signaling through TLR4 modulates innate immune activation in human macrophages and the biology of hepatic stellate cells. J Leukoc Biol. 2016; 100 (3): 599-606. and increase the production of collagen and monocyte chemoattractant protein (a macrophage chemoattractant).88 Tuyama AC, Hong F, Saiman Y, Wang C, Ozkok D, Mosoian A, Chen P, Chen BK, Klotman ME, Bansal MB. Human immunodeficiency virus (HIV)-1 infects human hepatic stellate cells and promotes collagen I and monocyte chemoattractant protein-1 expression: implications for the pathogenesis of HIV/hepatitis C virus-induced liver fibrosis. Hepatology. 2010; 52 (2): 612-22.
The cervix is a dense fibrous tissue that is located at the lowest part of the uterus.99 Bauer M, Mazza E, Nava A, Zeck W, Eder M, Bajka M, Cacho F, Lang U, Holzapfel GA. In Vivo Characterization of the Mechanics of Human Uterine Cervices. Ann N Y Acad Sci. 2007; 1101 (1): 186-202. The cervical mechanical activity has two functions: before childbirth, it should remain closed and resist to the mechanical load of the pregnancy and at the moment of childbirth it should be soft to be deformed and dilated allowing a passage for the fetus.1010 Myers KM, Feltovich H, Mazza E, Vink J, Bajka M, Wapner RJ, Hall TJ, House M. The mechanical role of the cervix in pregnancy. J Biomech. 2015; 48 (9): 1511-23. The organization of the collagen in the human cervical tissue plays an important role in the structural function of the tissue.1111 Yao W, Gan Y, Myers KM, Vink JY, Wapner RJ, Hendon CP. Collagen Fiber Orientation and Dispersion in the Upper Cervix of Non-Pregnant and Pregnant Women. PLoS ONE. 2016; 11 (11): e0166709.
The cervical collagen is like fibers in a hierarchical network embedded in a superficial viscous substance of glycosaminoglycans negatively charged and other proteins.1010 Myers KM, Feltovich H, Mazza E, Vink J, Bajka M, Wapner RJ, Hall TJ, House M. The mechanical role of the cervix in pregnancy. J Biomech. 2015; 48 (9): 1511-23. The collagen (types I and III) compose of 34 to 77% of dry weight,1212 Zork NM, Myers KM, Yoshida K, Cremers S, Jiang H, Ananth CV, Wapner RJ, Kitajewski J, Vink J. A systematic evaluation of collagen cross-links in the human cervix. Am J Obstet Gynecol. 2015; 212 (3): 321.e1-8.,1313 Feltovich H, Hall TJ. Quantitative imaging of the cervix: setting the bar. Ultrasound Obstet Gynecol. 2013; 41 (2): 121-8. with evidence in studies on human tissues that this dry weight content remains constantly during the gesta-tion.1414 Myers K, Socrate S, Tzeranis D, House M. Changes in the biochemical constituents and morphologic appearance of the human cervical stroma during pregnancy. Eur J Obstet Gynecol Reprod Biol. 2009; 144: S82-9. In general, the collagen fiber network is reported to be anisotropic with different orientations in distinct anatomical regions within the cervix.1515 Gan Y, Yao W, Myers KM, Vink JY, Wapner RJ, Hendon CP. Analyzing three-dimensional ultrastructure of human cervical tissue using optical coherence tomography. Biomed Opt Express. 2015; 6 (4): 1090-108.
Patients with Aids usually present an increased number of collagen fibers due to the deterioration of the natural immune mechanisms, the susceptibility to viral, fungal, bacterial, and parasitic agents as well as the occurrence of non-infectious inflammatory diseases.22 Cavellani CL, Rocha LP, Silva RSC, Oliveira LF, Faria HA, Olegario JG, Correa RR, Teixeira VP. The influence of Aids on the morphometric and immune status of the uterine cervix of autopsied patients. Curr HIV Res. 2011; 9 (8): 606-12.
The purpose of this study was to compare the percentage of collagen fibers in the uterine body and cervix of autopsied women with and without Aids. Thus, this study intends to contribute for a better understanding on the influence of Aids on uterine changes.
Method
This study was approved by the Research Ethics Committee at the Universidade Federal do Triangulo Mineiro (UFTM) under the protocol number 2689.
It is a quantitative, cross-sectional and descriptive study. We analyzed retrospectively a total of 482 autopsy protocols at the Hospital de Clinicas da Universidade Federal do Triangulo Mineiro (HC-UFTM), Uberaba City, Minas Gerais State in the period of 1988 to 2013. From these protocols, 15 autopsied women diagnosed with Aids were selected (Figure 1). The selection criteria were ages >18 years old and females. Women whose autopsy protocols were incomplete and did not have the uterus in good condition for analysis were excluded. In addition, for the selected group, the diagnosis for Aids was made by the evidence of at least one of the diseases defining the syndrome presented at the time of autopsy and the CD4+ T lymphocyte count below 200 cells/mm3.1616 Centers for Disease Control and Prevention. HIV/AIDS Surveillance Report. Atlanta, US. 2003; (Vol. 15): 40. Available in https://www.cdc.gov/hiv/pdf/library/reports/surveillance/cdc-hiv-surveillance-report-2003-vol-15.pdf.
https://www.cdc.gov/hiv/pdf/library/repo...
The anatomopathological diagnosis performed by the two medical pathologists also reported that the cause of death of all the selected women with Aids for the present study was infectious disease. For the comparison criteria, 15 autop-sied women without Aids were selected for a control group in the same period were paired for the study group according to the variables:, age, skin color (white or non-white) and the Body Mass Index (BMI).
In the cervix, a fragment of approximately 3 millimeters (mm) thick was removed by a mediated section. In the uterine body, a cut was made on the uterine wall where the epithelium was preserved and, a fragment of approximately 3 millimeters (mm) was removed. Thus, in both groups, 15 fragments of the uterine body and 15 fragments of the cervix constituted of 60 fragments altogether.
The fragments were fixed in 10% formaldehyde and dehydrated in increasing concentrations of alcohol (70 to 100%), diaphanized in xylol and included in paraffin. The slides were made in serial cut of 4μm thick. The fragments were put on the glass slides with poly-L-lysine® and processed for histochemistry.
To quantify the percentage of collagen fibers in the uterine body and cervix, the slides were stained with picrosirius and examined under 40x objective polarized light (1600x final increase), the digitalized image showed a constructed area of collagen, with an aspect of birefringence and a reddish coloration. The quantification was performed on the entire length of the slides using the KS-300® system, in which the observer marked the collagen fibers to obtain the percentage of these fibers by field area analyzed, and the number of fields varied from 18 to 42.
The statistical analysis used the SigmaStat® 2.03 software. The quantitative variables were tested for normality by Kolmogorov-Smirnov test. The parametric Student’s t-test was applied to compare the two groups with normal distribution and homogeneous variance variables. The non-parametric Mann-Whitney (U) test was used to compare the two groups with non-normal distribution and non-homogeneous variance variables. The differences were considered statistically significant with p<0.05.
Results
The groups were paired according to age (t=1.326; p<0.001), BMI (t=6.165; p<0.002) and skin color (white or non-white). Of the 30 women selected, the mean age was 37.40 ± 7.16 years old in the retroviral group and 38.20 ± 8.00 years old in the group without Aids and the age was between 25 and 49 years old in both groups. Among the women with Aids, 8 (53.3%) were classified as white, the same with the women without Aids. The BMI in the group with Aids was 22.20 ± 4.08 kg/m2 and in the group without Aids was 26.83 ± 4.86 kg/m2.
The percentage of collagen fibers in the cervix was significantly lower in the group with Aids (U=336544; p=0.001) (Table 1, Figure 2) when compared to the group without the disease.
Comparison of the percentage of collagen fibers of the cervix and the uterine body among a group of women with and without Aids.
Microscopic analysis of collagen fibers indicated by yellow arrows of the cervix through optic microscopy. (Picrosirius, 1600X).
(A) collagen fibers of a woman with Aids under common light; (B) collagen fibers of a woman with Aids under polarized light; (C) collagen fibers of a woman without Aids under common light; (D) collagen fibers of a woman without Aids under polarized light.
In the comparison of the percentage of collagen fibers in the uterine body, the group with Aids presented a significantly higher percentage than the group without Aids (U=308726; p=0.004) (Table 1, Figure 3).
Microscopic analysis of the collagen fibers indicated by yellow arrows of the uterine body by optic microscopy. (Picrosirius, 1600X).
(A) collagen fibers of a woman with Aids under common light; (B) collagen fibers of a woman with Aids under polarized light; (C) collagen fibers of a woman without Aids under common light; (D) collagen fibers of a woman without Aids under polarized light.
In the comparison of the percentage of collagen fibers in the cervix with the percentage of collagen fibers in the uterine body in the group of women with Aids, the percentage in the cervix was significantly higher (t=0.479; p=0.003) (Table 2). The same result was obtained in the group without Aids (t=2.397; p=0.064) (Table 2).
Comparison of the percentage of collagen fibers of the cervix and the percentage of collagen fibers of the uterine body in a group of women with and without Aids.
Table 3 shows the causes of death and possible infections present in both groups.
Description of the cause of death and other infections in a group of women with and without Aids.
Discussion
The women with Aids presented significantly a lower percentage of collagen fibers in the cervix when compared to the group without the syndrome. The comparison of the percentage of collagen fibers in the cervix with the percentage of collagen fibers in the uterine body in the group with Aids, the percentage in the uterine body was significantly higher. According to the medical literature, patients with Aids usually have an increase in the amount of collagen fibers. This increase is associated to the activation and inflammation of the immune system in a chronic form in these locations.22 Cavellani CL, Rocha LP, Silva RSC, Oliveira LF, Faria HA, Olegario JG, Correa RR, Teixeira VP. The influence of Aids on the morphometric and immune status of the uterine cervix of autopsied patients. Curr HIV Res. 2011; 9 (8): 606-12. The imbalance between CD4 and CD8 cells seen in HIV infection can lead to alterations in the cytokine profiles with the reduction in anti-fibrotic cytokines mediated by a decrease of the interferon (IFN)-gamma from Th1 cells and an increase in the profibrotic cytokines (IL-4, IL-5, IL-10 and IL-13) due to a relative increase in the TH2 signal.1717 Mastroianni CM, Lichtner M, Mascia C, Zuccalà P, Vullo V. Molecular mechanisms of liver fibrosis in HIV/HCV coinfection. Int J Mol Sci. 2014; 15 (6): 9184-208.,1818 Roszkiewicz J, Smolewska E. Kaleidoscope of autoimmune diseases in HIV infection. Rheumatol Int. 2016; 36: 1481-91.
In addition to the infectious process, other factors may also alter the levels of cytokines in the genital fluids, such as oral contraceptive use, pregnancy, age and the use of vaginal antiseptics.1919 Sturm-Ramirez K, Gaye-Diallo A, Eisen G, Mboup S, Kanki PJ. High levels of tumor necrosis factor-alpha and interleukin-1 beta in bacterial vaginosis may increase susceptibility to human immunodeficiency virus. J Infect Dis. 2000; 182 (2): 476-73. However, studies show that in chronic HIV infection, the epithelial cells, fibroblasts and the immune cells that reside in the female reproductive tract tissues contribute to the pool of cytokines, chemokines and growth factors present in the sexual hormones tissue environment, estradiol and proges-terone.2020 Wira CR, Rodriguez-Garcia M, Shen Z, Patel M, Fahey JV. The Role of Sex Hormones and the Tissue Environment in Immune Protection Against HIV in the Female Reproductive Tract. Am J Reprod Immunol. 2014; 72 (2): 171-81. Since fibroblasts respond to several immunological mediators, the immune alterations in patients with HIV could affect their functions, leading to modifications in the responses of producing and/or reducing collagen fibers.2121 Coimbra DD, Lustosa JC, Sarmento DF, Lima RB, Pessoa OMN. Colagenoma eruptivo em paciente HIV+. An Bras Dermatol. 2008; 83 (2): 141-5.
In this present study, a significantly higher percentage of collagen fibers was detected in the uterine body of patients with Aids when compared to the group without Aids. When the upper tract genital epithelial cells are exposed to HIV, the mucosal barrier is compromised and along with the pro-inflammatory cytokines secretion action by the epithelial cells.2222 Nazli A, Kafka JK, Ferreira VH, Anipindi V, Mueller K, Osborne BJ, Dizzell S, Chauvin S, Mian MF, Ouellet M, Tremblay MJ, Mossman KL, Ashkar AA, Kovacs C, Bowdish DM, Snider DP, Kaul R, Kaushic C. HIV-1 gp120 induces TLR2- and TLR4-mediated innate immune activa-tion in human female genital epithelium. J Immunol. 2013; 191 (8): 4246-58. The secretions by the epithelial cells from the female reproductive tract have significant effects in determining whether or not an HIV infection will occur. For example, many of these epithelial cell factors are chemokines/cytokines that attract/activate the immune cells at the location of the HIV infection.2323 Wira CR, Ghosh M, Smith JM, Shen L, Connor RI, Sundstrom P, Frechette GM, Hill ET, Fahey JV. Epithelial cell secretions from the human female reproductive tract inhibit sexually transmitted pathogens and Candida albi-cans but not Lactobacillus. Mucosal Immunol. 2011; 4 (3): 335-42. The number of activated HIV target cells (CD4+T cells, macrophages and dendritic cells) present at the point of the virus, may increase chances for the infection to occur. Alternatively, some of the same factors have anti-HIV activity and prevent the HIV infection to develop. This apparent paradox in relation to the HIV infection is dependent on many factors, including the quantity of the epithelial factors secretion is in the female reproductive tract, the presence of co-infecting pathogens, the presence of proteolytic enzymes, the sexual hormone balance, the activation of cells status, the interaction of other secreted factors by other cells as well as the epithelial cells and the present types of immune cells.2020 Wira CR, Rodriguez-Garcia M, Shen Z, Patel M, Fahey JV. The Role of Sex Hormones and the Tissue Environment in Immune Protection Against HIV in the Female Reproductive Tract. Am J Reprod Immunol. 2014; 72 (2): 171-81.
In the uterus during the proliferative phase, the aggregated lymphoid consist of cell groups CD4+ T or CD8+ discreet (300 cells). During the secreting phase,the aggregated lymphoid increased to 3,000-4,000 cells.2424 Wira CR, Fahey JV. A new strategy to understand how HIV infects women: identification of a window of vulnerability during the menstrual cycle. AIDS. 2008; 22 (15): 1909-17. These findings led us to propose a hypothesis of a “vulnerability window” (starting with ovulation and lasting between 7-10 days until the secreting phase of the cycle) what suggests that endocrine alterations modulate the immune protection in a way that increases the probability of the HIV infection and sexually transmitted infections (STI).2424 Wira CR, Fahey JV. A new strategy to understand how HIV infects women: identification of a window of vulnerability during the menstrual cycle. AIDS. 2008; 22 (15): 1909-17.,2020 Wira CR, Rodriguez-Garcia M, Shen Z, Patel M, Fahey JV. The Role of Sex Hormones and the Tissue Environment in Immune Protection Against HIV in the Female Reproductive Tract. Am J Reprod Immunol. 2014; 72 (2): 171-81.
Therefore, this percentage of increased collagen fibers in the uterine body in the group with Aids may be related to chronic HIV infection, since the induction of a cellular immune response characterized by the predominance of cytotoxic T lymphocytes, despite having a protective effect against HIV-1 genital infection,2525 Iqbal Sm, Ball TB, Kimani P, Thottingal P, Embree JE, Fowke KR, Plummer FA. Elevated T cell counts and RANTES expression in the genital mucosa of HIV-1-resis-tant Kenyan commercial sex workers. J Infect Dis. 2005; 192 (5): 728-38. are not sufficient to control viremia in patients with chronic infection.2626 Draenert R, Verril CL, Tang Y, Allen TM, Wurcel AG, Boczanowski M, Lechner A, Kim AY, Suscovich T, Brown NV, Addo MM, Walker BD. Persistent recognition of autol-ogous virus by high-avidity CD8 T cells in chronic, progressive human immunodeficiency virus type 1 infec-tion. J Virol. 2004; 78 (2): 630-41. Once deposited in the vagina, the sperm moves rapidly into the cervix, uterine body, Fallopian tubes and ovaries, potentially leading to an exposure over a large and phenotypically diverse mucosal surface.2727 Racicot K, Cardenas I, Wunsche V, Aldo P, Guller S, Means RE, Romero R, Mor G. Viral infection of the pregnant cervix predisposes to ascending bacterial infection. J Immunol. 2013; 191 (2): 934-41. These factors make women more vulnerable to sexually transmitted infections after sexual intercourse and may be responsible for the difficulty in establishing an efficient immunity against infections, since most sexually transmitted microorganisms are conveyed in large quantities of immunomodulatory seminal plasma.2828 Lima YAR, Alves MFC. O Sistema imune da mucosa do trato genital feminino e o impacto das doenças sexualmente transmissíveis. Rev Patol Trop. 2008; 37 (4): 295-309.
In the histochemical and morphometric analysis in this study on autopsied female patients with and without Aids, the percentage of collagen fibers in the uterine body was higher in women with Aids. This indicates that an immune response to viral infection induces a greater production of these fibers as a mechanism to repair the caused lesions. Moreover, it reveals a failure of the organism in the attempt to keep the infection restricted to the cervix.
The interpretation of the parameters evaluated in the uterine body and cervix can be very useful in the diagnosis in the conditions associated to HIV infection. This may contribute to the patient’s clinical conditions and life expectancy. In addition to favoring the development of therapeutic measurements that prevent the establishment of complications related to Aids.
Acknowledgments
This present study was supported by the Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) (National Council for Scientific and Technological Development), Coordenagao de Melhoramento de Pessoal de Ensino Superior (CAPES) (Coordination of Improving Personnel in Superior Education), Fundagao de Apoio a Pesquisa do Estado de Minas Gerais (FAPEMIG) (Research Support Foundation in Minas Gerais State) and Fundagao de Ensino e Pesquisa de Uberaba (FUNEPU).( Teaching and Research Foundation in Uberaba).
Referências
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1Brasil. Ministério da Saúde. Departamento de DST, Aids e Hepatites Virais. Secretaria de Vigilância em Saúde. Boletim Epidemiológico: HIV e Aids. Brasília, DF; 2016. Ano V - n° 01-26. Available in file:///C:/Users/BIA/Downloads/boletim_2016_1_pdf_16375.pdf Accessed in 13-11-17.
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2Cavellani CL, Rocha LP, Silva RSC, Oliveira LF, Faria HA, Olegario JG, Correa RR, Teixeira VP. The influence of Aids on the morphometric and immune status of the uterine cervix of autopsied patients. Curr HIV Res. 2011; 9 (8): 606-12.
-
3Rocha LP, Silva R, Olegario J, Correa R, Teixeira VPA, Cavellani CL. Esophageal epithelium of women with AIDS: Thickness and local immunity. Pathol Res Pract. 2010; 206 (4): 248-52.
-
4Favarato GKNA, Silva ACS, Oliveira LFO, Ferraz, MLF, Teixeira VPA, Cavellani CL. Skin aging in patients with acquired immunodeficiency syndrome. Ann Diagn Pathol. 2016; 24 (10): 35-9.
-
5Wira CR, Rodriguez-Garcia M, Patel MV. The role of sex hormones in immune protection of the female reproductive tract. Nat Rev Immunol. 2015; 15: 217-30.
-
6Dixon LJ, Barnes M, Tang H, Pritchard MT, Nagy LE. Kupffer cells in the liver. Compr Physiol. 2013; 3 (2): 785-97.
-
7Del Cornò M, Cappon A, Donninelli G, Varano B, Marra F, Gessani S. HIV-1 gp120 signaling through TLR4 modulates innate immune activation in human macrophages and the biology of hepatic stellate cells. J Leukoc Biol. 2016; 100 (3): 599-606.
-
8Tuyama AC, Hong F, Saiman Y, Wang C, Ozkok D, Mosoian A, Chen P, Chen BK, Klotman ME, Bansal MB. Human immunodeficiency virus (HIV)-1 infects human hepatic stellate cells and promotes collagen I and monocyte chemoattractant protein-1 expression: implications for the pathogenesis of HIV/hepatitis C virus-induced liver fibrosis. Hepatology. 2010; 52 (2): 612-22.
-
9Bauer M, Mazza E, Nava A, Zeck W, Eder M, Bajka M, Cacho F, Lang U, Holzapfel GA. In Vivo Characterization of the Mechanics of Human Uterine Cervices. Ann N Y Acad Sci. 2007; 1101 (1): 186-202.
-
10Myers KM, Feltovich H, Mazza E, Vink J, Bajka M, Wapner RJ, Hall TJ, House M. The mechanical role of the cervix in pregnancy. J Biomech. 2015; 48 (9): 1511-23.
-
11Yao W, Gan Y, Myers KM, Vink JY, Wapner RJ, Hendon CP. Collagen Fiber Orientation and Dispersion in the Upper Cervix of Non-Pregnant and Pregnant Women. PLoS ONE. 2016; 11 (11): e0166709.
-
12Zork NM, Myers KM, Yoshida K, Cremers S, Jiang H, Ananth CV, Wapner RJ, Kitajewski J, Vink J. A systematic evaluation of collagen cross-links in the human cervix. Am J Obstet Gynecol. 2015; 212 (3): 321.e1-8.
-
13Feltovich H, Hall TJ. Quantitative imaging of the cervix: setting the bar. Ultrasound Obstet Gynecol. 2013; 41 (2): 121-8.
-
14Myers K, Socrate S, Tzeranis D, House M. Changes in the biochemical constituents and morphologic appearance of the human cervical stroma during pregnancy. Eur J Obstet Gynecol Reprod Biol. 2009; 144: S82-9.
-
15Gan Y, Yao W, Myers KM, Vink JY, Wapner RJ, Hendon CP. Analyzing three-dimensional ultrastructure of human cervical tissue using optical coherence tomography. Biomed Opt Express. 2015; 6 (4): 1090-108.
-
16Centers for Disease Control and Prevention. HIV/AIDS Surveillance Report. Atlanta, US. 2003; (Vol. 15): 40. Available in https://www.cdc.gov/hiv/pdf/library/reports/surveillance/cdc-hiv-surveillance-report-2003-vol-15.pdf
» https://www.cdc.gov/hiv/pdf/library/reports/surveillance/cdc-hiv-surveillance-report-2003-vol-15.pdf -
17Mastroianni CM, Lichtner M, Mascia C, Zuccalà P, Vullo V. Molecular mechanisms of liver fibrosis in HIV/HCV coinfection. Int J Mol Sci. 2014; 15 (6): 9184-208.
-
18Roszkiewicz J, Smolewska E. Kaleidoscope of autoimmune diseases in HIV infection. Rheumatol Int. 2016; 36: 1481-91.
-
19Sturm-Ramirez K, Gaye-Diallo A, Eisen G, Mboup S, Kanki PJ. High levels of tumor necrosis factor-alpha and interleukin-1 beta in bacterial vaginosis may increase susceptibility to human immunodeficiency virus. J Infect Dis. 2000; 182 (2): 476-73.
-
20Wira CR, Rodriguez-Garcia M, Shen Z, Patel M, Fahey JV. The Role of Sex Hormones and the Tissue Environment in Immune Protection Against HIV in the Female Reproductive Tract. Am J Reprod Immunol. 2014; 72 (2): 171-81.
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21Coimbra DD, Lustosa JC, Sarmento DF, Lima RB, Pessoa OMN. Colagenoma eruptivo em paciente HIV+. An Bras Dermatol. 2008; 83 (2): 141-5.
-
22Nazli A, Kafka JK, Ferreira VH, Anipindi V, Mueller K, Osborne BJ, Dizzell S, Chauvin S, Mian MF, Ouellet M, Tremblay MJ, Mossman KL, Ashkar AA, Kovacs C, Bowdish DM, Snider DP, Kaul R, Kaushic C. HIV-1 gp120 induces TLR2- and TLR4-mediated innate immune activa-tion in human female genital epithelium. J Immunol. 2013; 191 (8): 4246-58.
-
23Wira CR, Ghosh M, Smith JM, Shen L, Connor RI, Sundstrom P, Frechette GM, Hill ET, Fahey JV. Epithelial cell secretions from the human female reproductive tract inhibit sexually transmitted pathogens and Candida albi-cans but not Lactobacillus. Mucosal Immunol. 2011; 4 (3): 335-42.
-
24Wira CR, Fahey JV. A new strategy to understand how HIV infects women: identification of a window of vulnerability during the menstrual cycle. AIDS. 2008; 22 (15): 1909-17.
-
25Iqbal Sm, Ball TB, Kimani P, Thottingal P, Embree JE, Fowke KR, Plummer FA. Elevated T cell counts and RANTES expression in the genital mucosa of HIV-1-resis-tant Kenyan commercial sex workers. J Infect Dis. 2005; 192 (5): 728-38.
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Publication Dates
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Publication in this collection
Jan-Mar 2018
History
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Received
17 July 2017 -
Accepted
02 Mar 2018