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1.
Artículo en Inglés | MEDLINE | ID: mdl-35469553

RESUMEN

Abstract: An outbreak of leptospirosis occurred in the Top End of the Northern Territory, Australia, during the wet season in early 2021. There were 14 outbreak cases; most were male (12/14; 86%) and non-Indigenous (13/14; 93%) with a median age of 22 years (range 19-52 years). We conducted a descriptive case series to investigate the outbreak. We determined that the outbreak was most likely due to higher than usual rainfall in a workplace with exposure to cattle, heightened by wearing clothing and footwear which offered little protection, with limited use of personal protective equipment (PPE). Increased and ongoing education for cattle industry workers, and promotion of the use of appropriate clothing and PPE, may minimise the risk of future outbreaks. Australia's national surveillance case definition for leptospirosis should be reviewed to incorporate the use of nucleic acid testing in the detection of leptospirosis.


Asunto(s)
Leptospira , Leptospirosis , Animales , Bovinos , Brotes de Enfermedades , Femenino , Humanos , Leptospirosis/diagnóstico , Leptospirosis/epidemiología , Leptospirosis/veterinaria , Masculino , Northern Territory/epidemiología , Estaciones del Año
2.
BMC Infect Dis ; 21(1): 929, 2021 Sep 08.
Artículo en Inglés | MEDLINE | ID: mdl-34496760

RESUMEN

BACKGROUND: Remote Australian Aboriginal and Torres Strait Islander communities have potential to be severely impacted by COVID-19, with multiple factors predisposing to increased transmission and disease severity. Our modelling aims to inform optimal public health responses. METHODS: An individual-based simulation model represented SARS-CoV2 transmission in communities ranging from 100 to 3500 people, comprised of large, interconnected households. A range of strategies for case finding, quarantining of contacts, testing, and lockdown were examined, following the silent introduction of a case. RESULTS: Multiple secondary infections are likely present by the time the first case is identified. Quarantine of close contacts, defined by extended household membership, can reduce peak infection prevalence from 60 to 70% to around 10%, but subsequent waves may occur when community mixing resumes. Exit testing significantly reduces ongoing transmission. Concurrent lockdown of non-quarantined households for 14 days is highly effective for epidemic control and reduces overall testing requirements; peak prevalence of the initial outbreak can be constrained to less than 5%, and the final community attack rate to less than 10% in modelled scenarios. Lockdown also mitigates the effect of a delay in the initial response. Compliance with lockdown must be at least 80-90%, however, or epidemic control will be lost. CONCLUSIONS: A SARS-CoV-2 outbreak will spread rapidly in remote communities. Prompt case detection with quarantining of extended-household contacts and a 14 day lockdown for all other residents, combined with exit testing for all, is the most effective strategy for rapid containment. Compliance is crucial, underscoring the need for community supported, culturally sensitive responses.


Asunto(s)
COVID-19 , Australia/epidemiología , Control de Enfermedades Transmisibles , Brotes de Enfermedades , Humanos , ARN Viral , SARS-CoV-2
4.
Emerg Infect Dis ; 26(12): 2844-2853, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-32985971

RESUMEN

The ability of health systems to cope with coronavirus disease (COVID-19) cases is of major concern. In preparation, we used clinical pathway models to estimate healthcare requirements for COVID-19 patients in the context of broader public health measures in Australia. An age- and risk-stratified transmission model of COVID-19 demonstrated that an unmitigated epidemic would dramatically exceed the capacity of the health system of Australia over a prolonged period. Case isolation and contact quarantine alone are insufficient to constrain healthcare needs within feasible levels of expansion of health sector capacity. Overlaid social restrictions must be applied over the course of the epidemic to ensure systems do not become overwhelmed and essential health sector functions, including care of COVID-19 patients, can be maintained. Attention to the full pathway of clinical care is needed, along with ongoing strengthening of capacity.


Asunto(s)
COVID-19/transmisión , Capacidad de Camas en Hospitales/estadística & datos numéricos , Pandemias/prevención & control , Capacidad de Reacción/organización & administración , Australia/epidemiología , COVID-19/epidemiología , Trazado de Contacto , Vías Clínicas/normas , Humanos , Unidades de Cuidados Intensivos/estadística & datos numéricos , Distanciamiento Físico , Salud Pública , Cuarentena/métodos
5.
BJPsych Bull ; 40(2): 97-102, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27087996

RESUMEN

Aims and method We used an online questionnaire to investigate medical students' perceptions of the apparent hierarchy between specialties, whether they have witnessed disparaging comments ('badmouthing' or 'bashing') against other specialists and whether this has had an effect on their career choice. Results In total, 960 students from 13 medical schools completed the questionnaire; they ranked medical specialties according to the level of badmouthing and answered questions on their experience of specialty bashing. Psychiatry and general practice attracted the greatest number of negative comments, which were made by academic staff, doctors and students. Twenty-seven per cent of students had changed their career choice as a direct result of bashing and a further 25.5% stated they were more likely to change their specialty choice. Although 80.5% of students condemned badmouthing as unprofessional, 71.5% believed that it is a routine part of practising medicine. Clinical implications Bashing of psychiatry represents another form of stigmatisation that needs to be challenged in medical schools. It not only has an impact on recruitment into the specialty, but also has the wider effect of stigmatising people with mental health disorders.

7.
J Tissue Eng Regen Med ; 10(8): 656-68, 2016 08.
Artículo en Inglés | MEDLINE | ID: mdl-23950083

RESUMEN

Spinal cord injury results in tissue necrosis in and around the lesion site, commonly leading to the formation of a fluid-filled cyst. This pathological end point represents a physical gap that impedes axonal regeneration. To overcome the obstacle of the cavity, we have explored the extent to which axonal substrates can be bioengineered through electrospinning, a process that uses an electrical field to produce fine fibres of synthetic or biological molecules. Recently, we demonstrated the potential of electrospinning to generate an aligned matrix that can influence the directionality and growth of axons. Here, we show that this matrix can be supplemented with nerve growth factor and chondroitinase ABC to provide trophic support and neutralize glial-derived inhibitory proteins. Moreover, we show how air-gap electrospinning can be used to generate a cylindrical matrix that matches the shape of the cord. Upon implantation in a completely transected rat spinal cord, matrices supplemented with NGF and chondroitinase ABC promote significant functional recovery. An examination of these matrices post-implantation shows that electrospun aligned monofilaments induce a more robust cellular infiltration than unaligned monofilaments. Further, a vascular network is generated in these matrices, with some endothelial cells using the electrospun fibres as a growth substrate. The presence of axons within these implanted matrices demonstrates that they facilitate axon regeneration following spinal cord injury. Collectively, these results demonstrate the potential of electrospinning to generate an aligned substrate that can provide trophic support, directional guidance cues and regeneration-inhibitory neutralizing compounds to regenerating axons following spinal cord injury. Copyright © 2016 John Wiley & Sons, Ltd.


Asunto(s)
Axones/metabolismo , Condroitina ABC Liasa , Factor de Crecimiento Nervioso , Traumatismos de la Médula Espinal/terapia , Regeneración de la Medula Espinal/efectos de los fármacos , Andamios del Tejido/química , Animales , Axones/patología , Condroitina ABC Liasa/química , Condroitina ABC Liasa/farmacología , Factor de Crecimiento Nervioso/química , Factor de Crecimiento Nervioso/farmacología , Ratas , Ratas Sprague-Dawley , Traumatismos de la Médula Espinal/metabolismo , Traumatismos de la Médula Espinal/patología
8.
BMC Immunol ; 10: 56, 2009 Oct 27.
Artículo en Inglés | MEDLINE | ID: mdl-19860908

RESUMEN

BACKGROUND: Leukocyte Ig-like receptors (LILR) are a family of innate immune receptors with immunomodulatory functions. High-level expression of the receptors LILRB2 (ILT4) and LILRB4 (ILT3) is a feature of tolerogenic antigen presenting cells and has been observed in cancer and transplant situations. There are relatively few studies regarding these receptors in the context of infection and it is not yet clear how LILRB4 exerts its inhibitory effects. RESULTS: We studied the effects of LILRB4 ligation on antigen presenting cell phenotype, and the expression of LILRB2 and LILRB4 on Salmonella-infected antigen presenting cells. Ligation of LILRB4 throughout in vitro culture of dendritic cells led to an upregulation of the co-stimulatory protein CD86. Alterations in the production of IL-8 and IL-10 by LILRB4-ligated macrophages were also observed. Infection with Salmonella typhimurium or TLR stimulation with Salmonella components led to an upregulation of LILRB2 and LILRB4. CONCLUSION: Our results indicate that the inhibitory effects of LILRB4 do not result from a failure to upregulate co-stimulatory proteins. In addition to the high level expression that can render antigen presenting cells tolerogenic, there may be a role for lower level expression and activity of LILRB2 and LILRB4 in response to TLR signalling during an immune response to bacterial infection.


Asunto(s)
Glicoproteínas de Membrana/biosíntesis , Receptores de Superficie Celular/metabolismo , Receptores Inmunológicos/biosíntesis , Infecciones por Salmonella/inmunología , Salmonella typhimurium/inmunología , Células Presentadoras de Antígenos/inmunología , Células Presentadoras de Antígenos/metabolismo , Células Presentadoras de Antígenos/patología , Antígeno B7-2/biosíntesis , Antígeno B7-2/genética , Antígeno B7-2/inmunología , Células Cultivadas , Células Dendríticas/inmunología , Células Dendríticas/metabolismo , Células Dendríticas/microbiología , Células Dendríticas/patología , Regulación hacia Abajo , Humanos , Inmunofenotipificación , Interleucina-10/metabolismo , Interleucina-8/metabolismo , Macrófagos/inmunología , Macrófagos/metabolismo , Macrófagos/patología , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/inmunología , Receptores de Superficie Celular/genética , Receptores de Superficie Celular/inmunología , Receptores Inmunológicos/genética , Receptores Inmunológicos/inmunología , Infecciones por Salmonella/genética , Infecciones por Salmonella/metabolismo , Infecciones por Salmonella/patología , Salmonella typhimurium/patogenicidad , Regulación hacia Arriba
9.
Eur J Immunol ; 39(11): 3195-206, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19658091

RESUMEN

Leucocyte Ig-like receptors (LILR) are a family of innate immune receptors expressed on myeloid and lymphoid cells that influence adaptive immune responses. We identified a common mechanism of alternative mRNA splicing, which generates transcripts that encode soluble protein isoforms of the majority of human LILR. These alternative splice variants lack transmembrane and cytoplasmic encoding regions, due to the transcription of a cryptic stop codon present in an intron 5' of the transmembrane encoding exon. The alternative LILR transcripts were detected in cell types that express their membrane-associated isoforms. Expression of the alternative LILRB1 transcript in transfected cells resulted in the release of a soluble approximately 65 Kd LILRB1 protein into culture supernatants. Soluble LILRB1 protein was also detected in the culture supernatants of monocyte-derived DC. In vitro assays suggested that soluble LILRB1 could block the interaction between membrane-associated LILRB1 and HLA-class I. Soluble LILRB1 may act as a dominant negative regulator of HLA-class I-mediated LILRB1 inhibition. Soluble isoforms of the other LILR may function in a comparable way.


Asunto(s)
Empalme Alternativo/genética , Empalme Alternativo/inmunología , Receptores Inmunológicos/genética , Receptores Inmunológicos/inmunología , Antígenos CD/genética , Western Blotting , Diferenciación Celular/genética , Diferenciación Celular/inmunología , Separación Celular , Codón , Células Dendríticas/citología , Células Dendríticas/inmunología , Citometría de Flujo , Expresión Génica , Humanos , Focalización Isoeléctrica , Receptor Leucocitario Tipo Inmunoglobulina B1 , Macrófagos/inmunología , Glicoproteínas de Membrana/genética , Monocitos/inmunología , Isoformas de Proteínas/genética , Isoformas de Proteínas/inmunología , ARN Mensajero/análisis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transcripción Genética
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