98%
921
2 minutes
20
HIV-exposed seronegative individuals (HESNs) are persons who remain seronegative despite repeated exposure to HIV, suggesting an in vivo resistance mechanism to HIV. Elucidation of endogenous factors responsible for this phenomenon may aid in the development of new classes of microbicides and therapeutics. We compared cervicovaginal protein abundance profiles between high-risk HESN and two control groups: low-risk HESN and HIV-positives. Four iTRAQ-based quantitative experiments were performed using samples classified based on presence/absence of particular gynaecological conditions. After statistical analysis, two proteins were shown to be differentially abundant between high-risk HESNs and control groups. Serpin A5, a serine proteinase inhibitor and Myeloblastin, a serine protease, were up- and downregulated, respectively. Commercially available ELISA assays were used to confirm differential Serpin A5 levels. These results suggest that HIV resistance in CVF of HESNs is the result of a delicate balance between two complementary mechanisms: downregulation of serine proteinases and upregulation of their inhibitors.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.virol.2014.04.015 | DOI Listing |
Am J Physiol Renal Physiol
September 2025
LVTS, INSERM U1148, Université Paris Cité and Université Sorbonne Paris Nord, F-75018 Paris.
Diabetic nephropathy (DN) is a multifactorial disease in which inflammation and angiogenesis play a crucial role. SerpinE2, or protease nexin-1 (PN-1), is a protease inhibitor of the serpin family, expressed by vascular and inflammatory cells. In this study, we addressed the role of SerpinE2 in DN, using the models of streptozotocin-induced type-1 and db/db type-2 diabetes.
View Article and Find Full Text PDFInnate Immun
September 2025
Departments of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
To determine whether (i) altered levels of acute-phase (APR)-, inflammation-, and extracellular matrix (ECM)-related in the amniotic fluid (AF) were associated with spontaneous preterm delivery (SPTD) in asymptomatic women with midtrimester short cervix (SCX) and (ii) if SPTD risk severity was related to the expression levels of inflammation-related proteins in the AF. This retrospective cohort study included 70 singleton pregnant women diagnosed with a SCX (<25 mm) at 17-25 weeks, who were subjected to amniocentesis to exclude intraamniotic inflammation (IAI; defined as AF interleukin [IL]-6 ≥ 2.6 ng/mL).
View Article and Find Full Text PDFCommun Biol
August 2025
Division of Histology and Neuroanatomy, Department of Anatomy and Physiology, Faculty of Medicine, Saga University, Saga, Japan.
The impact of allergic diseases on bone loss remains unclear because it is considered to result from the use of corticosteroids to ameliorate allergic inflammation. To explore the effects of allergic diseases on bone metabolism, we investigated long bones in ovalbumin (OVA)-induced asthmatic mice. Compared with that of vehicle-treated controls, the bone mass of OVA-induced asthmatic mice was lower.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
Center for Advanced Studies and Technologies (CAST), 'G d'Annunzio' University of Chieti-Pescara, Via 9, Luigi Polacchi 13, 66100 Chieti, Italy.
Early diagnosis of lung cancer, essential for reducing its high mortality rate, is currently challenging, partly due to the lack of specific biomarkers. Here, we attempted to develop a noninvasive and potentially sensitive screening method based on the proteomic analysis of unstimulated and stimulated saliva samples, collected by passive drooling and salivary swabs, respectively, from healthy heavy smokers enrolled in a nonprofit screening project. Protein content analyzed before and after sample cryopreservation for various periods and the associated two-dimensional electrophoresis revealed that protein extraction after short-term cryopreservation prevented the loss of detectable proteins.
View Article and Find Full Text PDFBiomolecules
August 2025
Division of Clinical Laboratory Science, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Alpha2-plasmin inhibitor (α2PI) has a heterogeneous structure due to proteolytic cleavages in the circulation. The C-terminally cleaved form loses the plasminogen binding site and is, therefore, a slow plasmin inhibitor (NPB-α2PI). As FXIII primarily crosslinks the plasminogen-binding intact form (PB-α2PI) to fibrin, the effect of NPB-α2PI on fibrinolysis has been less studied.
View Article and Find Full Text PDF