Abstract:
:Ebola virus (EBOV) gained public notoriety in the last decade largely as a consequence of the highly publicized isolation of a new EBOV species in a suburb of Washington, DC, in 1989, together with the dramatic clinical presentation of EBOV infection and high case-fatality rate in Africa (near 90% in some outbreaks), and the unusual and striking morphology of the virus. Furthermore, there are no vaccines or effective therapies currently available. Progress in understanding the origins of the pathophysiological changes that make EBOV infections of humans so devastating has been slow, primarily because these viruses require special containment for safe research. However, an increasing understanding of the mechanisms of EBOV pathogenesis, facilitated by the development of new tools to elucidate critical regulatory elements in the viral life cycle, is providing new targets that can be exploited for therapeutic interventions. Notably, identifying factors triggering the haemorrhagic complications that characterise EBOV infections led to the development of a strategy to modulate coagulopathy; this therapeutic modality successfully mitigated the effects of EBOV haemorrhagic fever in nonhuman primates. This review summarises our current understanding of EBOV pathogenesis and discusses various approaches to therapeutic intervention based on our current understanding of how EBOV produces a lethal infection.
journal_name
Expert Rev Mol Medjournal_title
Expert reviews in molecular medicineauthors
Geisbert TW,Hensley LEdoi
10.1017/S1462399404008300keywords:
subject
Has Abstractpub_date
2004-09-21 00:00:00pages
1-24issue
20issn
1462-3994pii
S1462399404008300journal_volume
6pub_type
杂志文章,评审abstract::Familial Alzheimer's disease (FAD) accounts for 5-10% of deaths from Alzheimer's disease (AD), and approximately 50% of these cases have been definitely linked to missense mutations in three genes, encoding the amyloid precursor protein (APP), presenilin 1 (PS1) and presenilin 2 (PS2). Of these, the vast majority of F...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399402005008
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abstract::Multiple sclerosis (MS) is an autoimmune disease with an important genetic component. The strongest genetic association is with the major histocompatibility complex (MHC) region. Several MHC alleles predispose to the disease, the most prominent of which are certain alleles in the HLA-DR2 haplotype. Functional and stru...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399405008914
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abstract::Humans and other vertebrates exhibit left-right (LR) asymmetric arrangement of the internal organs, and failure to establish normal LR asymmetry leads to internal laterality disorders, including situs inversus and heterotaxy. Situs inversus is complete mirror-imaged arrangement of the internal organs along LR axis, wh...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2014.22
更新日期:2015-01-27 00:00:00
abstract::Engineered tissue derived from ocular surface stem cells (SCs) are a cutting edge biotechnology for repair and restoration of severely damaged eyes as a result of ocular surface dysfunction because of SC failure. Ex-vivo SC expansion techniques have advanced significantly since the first patients were treated in the l...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2013.5
更新日期:2013-06-25 00:00:00
abstract::Since the discovery of noncoding small RNAs such as microRNAs (miRNAs), and their roles as potential tumour suppressors or oncogenes, post-transcriptional and translational control of gene expression have become increasingly important in cancer research. Given that over a third of coding genes, as estimated by computa...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399410001663
更新日期:2010-10-14 00:00:00
abstract::The mammalian target of rapamycin mTOR is a central element in an evolutionary conserved signalling pathway that regulates cell growth, survival and proliferation, orchestrating signals originating from growth factors, nutrients or particular stress stimuli. Two important modulators of mTOR activity are the AKT and ER...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399408000586
更新日期:2008-02-04 00:00:00
abstract::Muscle fibres are very specialised cells with a complex structure that requires a high level of organisation of the constituent proteins. For muscle contraction to function properly, there is a need for not only sarcomeres, the contractile structures of the muscle fibre, but also costameres. These are supramolecular s...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2015.9
更新日期:2015-06-19 00:00:00
abstract::Angptl2 is a multifaceted protein, displaying both physiological and pathological functions, in which scientific and clinical interest is growing exponentially within the past few years. Its physiological functions are not well understood, but angptl2 was first acknowledged for its pro-angiogenic and antiapoptotic cap...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2014.19
更新日期:2014-11-24 00:00:00
abstract::Atherosclerosis is a pathological process that takes place in the major arteries and is the underlying cause of heart attacks, stroke and peripheral artery disease. The earliest detectable lesions, called fatty streaks, contain macrophage foam cells that are derived from recruited monocytes. More-advanced atherosclero...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章
doi:10.1017/S1462399401003696
更新日期:2001-11-05 00:00:00
abstract::Polydactyly is one of the most common inherited limb abnormalities, characterised by supernumerary fingers or toes. It results from disturbances in the normal programme of the anterior-posterior axis of the developing limb, with diverse aetiology and variable inter- and intra-familial clinical features. Polydactyly ca...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2015.18
更新日期:2015-10-30 00:00:00
abstract::Carcinoma of the stomach is one of the most prevalent cancer types in the world today. Only a limited number of biomarkers are available for detection and prognostic evaluation of gastric cancer. New advances in identifying molecular biomarkers are essential. Two major forms of gastric cancer are distinguished accordi...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399402004337
更新日期:2002-03-21 00:00:00
abstract::Advances in molecular biology and immunology have renewed interest in the development of vaccines for the treatment or prevention of cancer. Research over the past 10 years has focused on the identification of suitable tumour antigens to use as targets for a variety of vaccine strategies. Carcinoembryonic antigen (CEA...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章
doi:10.1017/S146239940000168X
更新日期:2000-04-19 00:00:00
abstract::Appropriately functioning adipose tissue is essential for human health, a fact most clearly illustrated by individuals with lipodystrophy, who have impaired adipose development and often suffer severe metabolic disease as a result. Humans with obesity display a similar array of metabolic problems. This reflects failur...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399410001547
更新日期:2010-08-02 00:00:00
abstract::Epithelial ovarian cancer comprises several subtypes of tumours that exhibit diverse histopathological features. The intriguing assumption by many epithelial ovarian cancers of specialised features of nonovarian tissue lineages has promoted considerable debate as to whether these tumours arise from the deceptively sim...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399407000324
更新日期:2007-05-04 00:00:00
abstract::Infants born with severe combined immune deficiencies are prone to life-threatening infections and, without treatment, do not survive beyond the first year of life. Haematopoietic stem cell transplantation from a fully matched donor offers the possibility of cure. In the absence of a suitable matched donor, haploident...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399404007884
更新日期:2004-07-02 00:00:00
abstract::Acute kidney injury (AKI) is a serious clinical condition with no effective treatment. Tubular cells are key targets in AKI. Tubular cells and, specifically, proximal tubular cells are extremely rich in mitochondria and mitochondrial changes had long been known to be a feature of AKI. However, only recent advances in ...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2014.14
更新日期:2014-08-08 00:00:00
abstract::Invariant natural killer T (iNKT) cells are innate lymphocytes whose functions are regulated by self and foreign glycolipid antigens presented by the antigen-presenting molecule CD1d. Activation of iNKT cells in vivo results in rapid release of copious amounts of effector cytokines and chemokines with which they regul...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399408000732
更新日期:2008-07-07 00:00:00
abstract::Experimental and human studies have shown that proteinuria contributes to the progression of renal disease. Overexposure to filtered proteins promotes the expression and release of chemokines by tubular epithelial cells, thus leading to inflammatory cell recruitment and renal impairment. This review focuses on recent ...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2014.3
更新日期:2014-02-17 00:00:00
abstract::The human brain is a highly complex organ with remarkable energy demands. Although it represents only 2% of the total body weight, it accounts for 20% of all oxygen consumption, reflecting its high rate of metabolic activity. Mitochondria have a crucial role in the supply of energy to the brain. Consequently, their de...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399410001456
更新日期:2010-04-19 00:00:00
abstract::The HEDGEHOG-GLI (HH-GLI) signalling is a key pathway critical in embryonic development, stem cell biology and tissue homeostasis. In recent years, aberrant activation of HH-GLI signalling has been linked to several types of cancer, including those of the skin, brain, lungs, prostate, gastrointestinal tract and blood....
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2015.3
更新日期:2015-02-09 00:00:00
abstract::Ectopic pregnancy is defined as a pregnancy implanted outside the uterus, and >98% implant in the Fallopian tube. It has a major clinical and socioeconomic impact worldwide. The diagnosis of ectopic pregnancy is often difficult and resource intensive owing to a lack of accurate biomarkers, and there is a need for impr...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/erm.2011.2
更新日期:2012-03-02 00:00:00
abstract::Human tumours emerge as the result of multiple genetic and epigenetic aberrations that allow the proto-cancer cell to escape normal social control. Many signal transduction pathways become constitutively active during this process, and one whose importance is increasingly being appreciated involves phosphoinositide 3-...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399405009361
更新日期:2005-06-06 00:00:00
abstract::Antiphospholipid (aPL) antibodies (Abs) are associated with thrombosis and pregnancy loss in antiphospholipid syndrome (APS), a disorder initially characterised in patients with systemic lupus erythematosus (SLE) but now known to occur in the absence of other autoimmune disease. There is strong evidence that aPL Abs a...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399407000506
更新日期:2007-11-13 00:00:00
abstract::Genomic imprinting is an epigenetic marking of genes in the parental germline that ensures the stable transmission of monoallelic gene expression patterns in a parent-of-origin-specific manner. Epigenetic marking systems are thus able to regulate gene activity independently of the underlying DNA sequence. Several impr...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399410001717
更新日期:2011-01-25 00:00:00
abstract::Autoimmune diseases of the central nervous system (CNS) involve the migration of abnormal numbers of self-directed leukocytes across the blood-brain barrier that normally separates the CNS from the immune system. The cardinal lesion associated with neuroinflammatory diseases is the perivascular infiltrate, which compr...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399407000397
更新日期:2007-07-19 00:00:00
abstract::The major histocompatibility complex (MHC) harbours genes whose primary function in regulating immune responsiveness to infection is to present foreign antigens to cytotoxic T lymphocytes (CTLs) and T helper cells. In the case of infection by human immunodeficiency virus (HIV), defining the optimal HIV epitopes that a...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399403005957
更新日期:2003-02-24 00:00:00
abstract::Infantile haemangioma is the most common tumour of infancy, yet the origin of these lesions remains controversial and the predictable life cycle is poorly understood. Much new information on infantile haemangiomas has emerged over the past decade, but experts continue to debate fundamental features, including cell of ...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S146239940700052X
更新日期:2007-11-29 00:00:00
abstract::Several genetic loci appear to be involved in susceptibility to autoimmune disease. Some loci are disease specific, whereas others appear to exert a general effect on the autoimmune disease process. Despite a large number of studies of many different diseases, consistent associations with multiple autoimmune disorders...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399405009981
更新日期:2005-10-17 00:00:00
abstract::Many viruses, with distinct replication strategies, activate DNA-damage response pathways, including the lentivirus human immunodeficiency virus (HIV) and the DNA viruses Epstein-Barr virus (EBV), herpes simplex virus 1, adenovirus and SV40. DNA-damage response pathways involving DNA-dependent protein kinase, ataxia-t...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399406010544
更新日期:2006-03-03 00:00:00
abstract::Transthyretin (TTR) is a transport protein for thyroid hormones and vitamin A and might have an important role in the nervous system. However, TTR can undergo a conformational change and form amyloid fibrils, in both acquired and hereditary forms of systemic amyloidosis. More than 80 TTR mutations have been associated...
journal_title:Expert reviews in molecular medicine
pub_type: 杂志文章,评审
doi:10.1017/S1462399402004647
更新日期:2002-05-14 00:00:00