LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 28

Search options

  1. Article: Determining

    Watson, Anna Louise / Woodford, John / Britton, Sumudu / Gupta, Rita / Whiley, David / McCarthy, Kate

    Diagnostics (Basel, Switzerland)

    2024  Volume 14, Issue 1

    Abstract: Background: Pneumocystis jirovecii: Methods: Retrospective audit of all positive : Results: Of the 82 positive qPCRs, 28 were categorised as high-probability PCP infection, 30 as uncertain PCP and 24 as colonisation. There was a significant ... ...

    Abstract Background: Pneumocystis jirovecii
    Methods: Retrospective audit of all positive
    Results: Of the 82 positive qPCRs, 28 were categorised as high-probability PCP infection, 30 as uncertain PCP and 24 as colonisation. There was a significant difference in qPCR values stratified by clinical category but not respiratory sample type. Current assay performance with a cutoff of 2.5 × 10
    Conclusions: A single qPCR cutoff cannot reliably determine
    Language English
    Publishing date 2024-01-04
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662336-5
    ISSN 2075-4418
    ISSN 2075-4418
    DOI 10.3390/diagnostics14010114
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Adapting malaria clinical trials infrastructure to implement COVID-19 epidemiology studies: Response to a public health emergency amid safe continuation of a research enterprise.

    Woodford, John / Sagara, Issaka / Dicko, Alassane / Duffy, Patrick E

    Frontiers in public health

    2022  Volume 10, Page(s) 959678

    MeSH term(s) COVID-19/epidemiology ; COVID-19/prevention & control ; Clinical Trials as Topic ; Humans ; Malaria/epidemiology ; Public Health
    Language English
    Publishing date 2022-07-26
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2711781-9
    ISSN 2296-2565 ; 2296-2565
    ISSN (online) 2296-2565
    ISSN 2296-2565
    DOI 10.3389/fpubh.2022.959678
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Posttreatment Transaminase Elevations in Controlled Human Malaria Infection and Naturally Acquired Malaria.

    Odedra, Anand / Woodford, John / Chalon, Stephan / Barber, Bridget E / McCarthy, James S

    The Journal of infectious diseases

    2021  Volume 225, Issue 5, Page(s) 926–927

    MeSH term(s) Humans ; Malaria/drug therapy ; Malaria, Falciparum/drug therapy ; Transaminases
    Chemical Substances Transaminases (EC 2.6.1.-)
    Language English
    Publishing date 2021-10-05
    Publishing country United States
    Document type Editorial ; Research Support, N.I.H., Intramural ; Comment
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiab502
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Haematological response in experimental human Plasmodium falciparum and Plasmodium vivax malaria.

    Woolley, Stephen D / Marquart, Louise / Woodford, John / Chalon, Stephan / Moehrle, Joerg J / McCarthy, James S / Barber, Bridget E

    Malaria journal

    2021  Volume 20, Issue 1, Page(s) 470

    Abstract: Background: Malaria-associated anaemia, arising from symptomatic, asymptomatic and submicroscopic infections, is a significant cause of morbidity worldwide. Induced blood stage malaria volunteer infection studies (IBSM-VIS) provide a unique opportunity ... ...

    Abstract Background: Malaria-associated anaemia, arising from symptomatic, asymptomatic and submicroscopic infections, is a significant cause of morbidity worldwide. Induced blood stage malaria volunteer infection studies (IBSM-VIS) provide a unique opportunity to evaluate the haematological response to early Plasmodium falciparum and Plasmodium vivax infection.
    Methods: This study was an analysis of the haemoglobin, red cell counts, and parasitaemia data from 315 participants enrolled in IBSM-VIS between 2012 and 2019, including 269 participants inoculated with the 3D7 strain of P. falciparum (Pf3D7), 15 with an artemisinin-resistant P. falciparum strain (PfK13) and 46 with P. vivax. Factors associated with the fractional fall in haemoglobin (Hb-FF) were evaluated, and the malaria-attributable erythrocyte loss after accounting for phlebotomy-related losses was estimated. The relative contribution of parasitized erythrocytes to the malaria-attributable erythrocyte loss was also estimated.
    Results: The median peak parasitaemia prior to treatment was 10,277 parasites/ml (IQR 3566-27,815), 71,427 parasites/ml [IQR 33,236-180,213], and 34,840 parasites/ml (IQR 13,302-77,064) in participants inoculated with Pf3D7, PfK13, and P. vivax, respectively. The median Hb-FF was 10.3% (IQR 7.8-13.3), 14.8% (IQR 11.8-15.9) and 11.7% (IQR 8.9-14.5) in those inoculated with Pf3D7, PfK13 and P. vivax, respectively, with the haemoglobin nadir occurring a median 12 (IQR 5-21), 15 (IQR 7-22), and 8 (IQR 7-15) days following inoculation. In participants inoculated with P. falciparum, recrudescence was associated with a greater Hb-FF, while in those with P. vivax, the Hb-FF was associated with a higher pre-treatment parasitaemia and later day of anti-malarial treatment. After accounting for phlebotomy-related blood losses, the estimated Hb-FF was 4.1% (IQR 3.1-5.3), 7.2% (IQR 5.8-7.8), and 4.9% (IQR 3.7-6.1) in participants inoculated with Pf3D7, PfK13, and P. vivax, respectively. Parasitized erythrocytes were estimated to account for 0.015% (IQR 0.006-0.06), 0.128% (IQR 0.068-0.616) and 0.022% (IQR 0.008-0.082) of the malaria-attributable erythrocyte loss in participants inoculated with Pf3D7, PfK13, and P. vivax, respectively.
    Conclusion: Early experimental P. falciparum and P. vivax infection resulted in a small but significant fall in haemoglobin despite parasitaemia only just at the level of microscopic detection. Loss of parasitized erythrocytes accounted for < 0.2% of the total malaria-attributable haemoglobin loss.
    MeSH term(s) Adult ; Anemia/drug therapy ; Anemia/parasitology ; Antimalarials/therapeutic use ; Erythrocytes/parasitology ; Female ; Humans ; Malaria, Falciparum/complications ; Malaria, Falciparum/drug therapy ; Malaria, Falciparum/parasitology ; Malaria, Vivax/complications ; Malaria, Vivax/drug therapy ; Malaria, Vivax/parasitology ; Male ; Middle Aged ; Parasitemia/drug therapy ; Parasitemia/parasitology ; Plasmodium falciparum/drug effects ; Plasmodium vivax/drug effects ; Young Adult
    Chemical Substances Antimalarials
    Language English
    Publishing date 2021-12-20
    Publishing country England
    Document type Journal Article
    ISSN 1475-2875
    ISSN (online) 1475-2875
    DOI 10.1186/s12936-021-04003-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Tracking SARS-CoV-2 seropositivity in rural communities using blood-fed mosquitoes: a proof-of-concept study.

    Krajacich, Benjamin J / Samaké, Djibril / Dao, Adama / Diallo, Moussa / Sanogo, Zana Lamissa / Yaro, Alpha Seydou / Zeguime, Amatigue / Poudiougo, Josué / Cissé, Kadiatou / Traoré, Mamadou / Dit Assitoun, Alassane / Faiman, Roy / Zaidi, Irfan / Woodford, John / Duffy, Patrick E / Lehmann, Tovi

    Frontiers in epidemiology

    2023  Volume 3, Page(s) 1243691

    Abstract: Background: The spread of SARS-CoV-2 cannot be well monitored and understood in areas without capacity for effective disease surveillance. Countries with a young population will have disproportionately large numbers of asymptomatic or pauci-symptomatic ... ...

    Abstract Background: The spread of SARS-CoV-2 cannot be well monitored and understood in areas without capacity for effective disease surveillance. Countries with a young population will have disproportionately large numbers of asymptomatic or pauci-symptomatic infections, further hindering detection of infection. Sero-surveillance on a country-wide scale by trained medical professionals may be limited in a resource-limited setting such as Mali. Novel ways of broadly sampling the human population in a non-invasive method would allow for large-scale surveillance at a reduced cost.
    Approach: Here we evaluate the collection of naturally blood-fed mosquitoes to test for human anti-SARS-CoV-2 antibodies in the laboratory and at five field locations in Mali.
    Results: Immunoglobulin-G antibodies to multiple SARS-CoV-2 antigens were readily detected in mosquito bloodmeals by bead-based immunoassay through at least 10 h after feeding [mean sensitivity of 0.92 (95% CI 0.78-1) and mean specificity of 0.98 (95% CI 0.88-1)], indicating that most blood-fed mosquitoes collected indoors during early morning hours (and likely to have fed the previous night) are viable samples for analysis. We found that reactivity to four SARS-CoV-2 antigens rose during the pandemic from pre-pandemic levels. The crude seropositivity of blood sampled via mosquitoes was 6.3% in October and November 2020 across all sites, and increased to 25.1% overall by February 2021, with the most urban site reaching 46.7%, consistent with independent venous blood-based sero-surveillance estimates.
    Conclusions: We have demonstrated that using mosquito bloodmeals, country-wide sero-surveillance of human diseases (both vector-borne and non-vector-borne) is possible in areas where human-biting mosquitoes are common, offering an informative, cost-effective, and non-invasive sampling option.
    Language English
    Publishing date 2023-12-13
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2674-1199
    ISSN (online) 2674-1199
    DOI 10.3389/fepid.2023.1243691
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Positron emission tomography and magnetic resonance imaging of the brain in experimental human malaria, a prospective cohort study.

    Woodford, John / Gillman, Ashley / Jenvey, Peter / Roberts, Jennie / Woolley, Stephen / Barber, Bridget E / Fernandez, Melissa / Rose, Stephen / Thomas, Paul / Anstey, Nicholas M / McCarthy, James S

    Scientific reports

    2022  Volume 12, Issue 1, Page(s) 5696

    Abstract: Cerebral malaria is the most serious manifestation of severe falciparum malaria. Sequestration of infected red blood cells and microvascular dysfunction are key contributing processes. Whether these processes occur in early stage disease prior to ... ...

    Abstract Cerebral malaria is the most serious manifestation of severe falciparum malaria. Sequestration of infected red blood cells and microvascular dysfunction are key contributing processes. Whether these processes occur in early stage disease prior to clinical manifestations is unknown. To help localize and understand these processes during the early stages of infection, we performed 18-F fluorodeoxyglucose positron emission tomography/magnetic resonance imaging in volunteers with Plasmodium falciparum induced blood stage malaria (IBSM) infection, and compared results to individuals with P. vivax infection, in whom coma is rare. Seven healthy, malaria-naïve participants underwent imaging at baseline, and at early symptom onset a median 9 days following inoculation (n = 4 P. falciparum, n = 3 P. vivax). Participants with P. falciparum infection demonstrated marked lability in radiotracer uptake across all regions of the brain, exceeding expected normal variation (within subject coefficient of variation (wCV): 14.4%) compared to the relatively stable uptake in participants with P. vivax infection (wCV: 3.5%). No consistent imaging changes suggestive of microvascular dysfunction were observed in either group. Neuroimaging in early IBSM studies is safe and technically feasible, with preliminary results suggesting that differences in brain tropism between P. falciparum and P. vivax may occur very early in infection.
    MeSH term(s) Brain/diagnostic imaging ; Brain/pathology ; Humans ; Magnetic Resonance Imaging ; Malaria, Cerebral/diagnostic imaging ; Malaria, Falciparum/diagnostic imaging ; Malaria, Falciparum/pathology ; Malaria, Vivax/pathology ; Plasmodium falciparum ; Plasmodium vivax ; Positron-Emission Tomography ; Prospective Studies
    Language English
    Publishing date 2022-04-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-022-09748-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Early Endothelial Activation Precedes Glycocalyx Degradation and Microvascular Dysfunction in Experimentally Induced Plasmodium falciparum and Plasmodium vivax Infection.

    Woodford, John / Yeo, Tsin W / Piera, Kim A / Butler, Kristy / Weinberg, J Brice / McCarthy, James S / Anstey, Nicholas M / Barber, Bridget E

    Infection and immunity

    2020  Volume 88, Issue 5

    Abstract: Endothelial activation and microvascular dysfunction are key pathogenic processes in severe malaria. We evaluated the early role of these processes in experimentally ... ...

    Abstract Endothelial activation and microvascular dysfunction are key pathogenic processes in severe malaria. We evaluated the early role of these processes in experimentally induced
    MeSH term(s) Adolescent ; Adult ; Angiopoietin-2/metabolism ; Biomarkers/metabolism ; Endothelial Cells/metabolism ; Female ; Glycocalyx/metabolism ; Humans ; Malaria, Falciparum/metabolism ; Malaria, Vivax/metabolism ; Male ; Microvessels/metabolism ; Middle Aged ; Plasmodium falciparum/pathogenicity ; Plasmodium vivax/pathogenicity ; Prospective Studies ; Young Adult
    Chemical Substances Angiopoietin-2 ; Biomarkers
    Language English
    Publishing date 2020-04-20
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/IAI.00895-19
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: The Dynamics of Liver Function Test Abnormalities after Malaria Infection: A Retrospective Observational Study.

    Woodford, John / Shanks, G Dennis / Griffin, Paul / Chalon, Stephan / McCarthy, James S

    The American journal of tropical medicine and hygiene

    2018  Volume 98, Issue 4, Page(s) 1113–1119

    Abstract: Liver dysfunction has long been recognized as a clinical feature of malaria. We have observed delayed elevation in the transaminase portion of liver function tests (LFTs) after treatment in some participants undergoing induced blood stage malaria ... ...

    Abstract Liver dysfunction has long been recognized as a clinical feature of malaria. We have observed delayed elevation in the transaminase portion of liver function tests (LFTs) after treatment in some participants undergoing induced blood stage malaria infection. We sought to determine whether similar LFT elevations occur after naturally acquired infection. We performed a retrospective audit of confirmed cases of
    MeSH term(s) Adult ; Alanine Transaminase/blood ; Aspartate Aminotransferases/blood ; Female ; Humans ; Liver/physiopathology ; Liver Function Tests ; Malaria/physiopathology ; Male ; Middle Aged ; Retrospective Studies
    Chemical Substances Aspartate Aminotransferases (EC 2.6.1.1) ; Alanine Transaminase (EC 2.6.1.2)
    Language English
    Publishing date 2018-02-08
    Publishing country United States
    Document type Journal Article ; Observational Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.17-0754
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Positron emission tomography and magnetic resonance imaging in experimental human malaria to identify organ-specific changes in morphology and glucose metabolism: A prospective cohort study.

    Woodford, John / Gillman, Ashley / Jenvey, Peter / Roberts, Jennie / Woolley, Stephen / Barber, Bridget E / Fernandez, Melissa / Rose, Stephen / Thomas, Paul / Anstey, Nicholas M / McCarthy, James S

    PLoS medicine

    2021  Volume 18, Issue 5, Page(s) e1003567

    Abstract: Background: Plasmodium vivax has been proposed to infect and replicate in the human spleen and bone marrow. Compared to Plasmodium falciparum, which is known to undergo microvascular tissue sequestration, little is known about the behavior of P. vivax ... ...

    Abstract Background: Plasmodium vivax has been proposed to infect and replicate in the human spleen and bone marrow. Compared to Plasmodium falciparum, which is known to undergo microvascular tissue sequestration, little is known about the behavior of P. vivax outside of the circulating compartment. This may be due in part to difficulties in studying parasite location and activity in life.
    Methods and findings: To identify organ-specific changes during the early stages of P. vivax infection, we performed 18-F fluorodeoxyglucose (FDG) positron emission tomography/magnetic resonance imaging (PET/MRI) at baseline and just prior to onset of clinical illness in P. vivax experimentally induced blood-stage malaria (IBSM) and compared findings to P. falciparum IBSM. Seven healthy, malaria-naive participants were enrolled from 3 IBSM trials: NCT02867059, ACTRN12616000174482, and ACTRN12619001085167. Imaging took place between 2016 and 2019 at the Herston Imaging Research Facility, Australia. Postinoculation imaging was performed after a median of 9 days in both species (n = 3 P. vivax; n = 4 P. falciparum). All participants were aged between 19 and 23 years, and 6/7 were male. Splenic volume (P. vivax: +28.8% [confidence interval (CI) +10.3% to +57.3%], P. falciparum: +22.9 [CI -15.3% to +61.1%]) and radiotracer uptake (P. vivax: +15.5% [CI -0.7% to +31.7%], P. falciparum: +5.5% [CI +1.4% to +9.6%]) increased following infection with each species, but more so in P. vivax infection (volume: p = 0.72, radiotracer uptake: p = 0.036). There was no change in FDG uptake in the bone marrow (P. vivax: +4.6% [CI -15.9% to +25.0%], P. falciparum: +3.2% [CI -3.2% to +9.6%]) or liver (P. vivax: +6.2% [CI -8.7% to +21.1%], P. falciparum: -1.4% [CI -4.6% to +1.8%]) following infection with either species. In participants with P. vivax, hemoglobin, hematocrit, and platelet count decreased from baseline at the time of postinoculation imaging. Decrements in hemoglobin and hematocrit were significantly greater in participants with P. vivax infection compared to P. falciparum. The main limitations of this study are the small sample size and the inability of this tracer to differentiate between host and parasite metabolic activity.
    Conclusions: PET/MRI indicated greater splenic tropism and metabolic activity in early P. vivax infection compared to P. falciparum, supporting the hypothesis of splenic accumulation of P. vivax very early in infection. The absence of uptake in the bone marrow and liver suggests that, at least in early infection, these tissues do not harbor a large parasite biomass or do not provoke a prominent metabolic response. PET/MRI is a safe and noninvasive method to evaluate infection-associated organ changes in morphology and glucose metabolism.
    MeSH term(s) Bone Marrow/metabolism ; Bone Marrow/parasitology ; Bone Marrow/pathology ; Female ; Glucose/metabolism ; Humans ; Liver/metabolism ; Liver/parasitology ; Liver/pathology ; Magnetic Resonance Imaging ; Malaria, Falciparum/parasitology ; Malaria, Falciparum/pathology ; Malaria, Falciparum/physiopathology ; Malaria, Vivax/parasitology ; Malaria, Vivax/pathology ; Malaria, Vivax/physiopathology ; Male ; Plasmodium falciparum ; Plasmodium vivax ; Positron-Emission Tomography ; Prospective Studies ; Queensland ; Spine/metabolism ; Spine/parasitology ; Spine/pathology ; Spleen/metabolism ; Spleen/parasitology ; Spleen/pathology ; Young Adult
    Chemical Substances Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2021-05-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2185925-5
    ISSN 1549-1676 ; 1549-1277
    ISSN (online) 1549-1676
    ISSN 1549-1277
    DOI 10.1371/journal.pmed.1003567
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Book: DISORDERS OF THE NERVOUS SYSTEM

    Reeves, Alexander G. / VALENSTEIN, EDWARD / Ochoa, José L. / WOODFORD, JOHN E.

    A PRIMER

    (INTERNAL MEDICINE SERIES)

    1981  

    Author's details ALEXANDER G. REEVES WITH CONTRIBUTIONS BY EDWARD VALENSTEIN, JOSE L. OCHOA, JOHN E. WOODFORD
    Series title INTERNAL MEDICINE SERIES
    Keywords NERVOUS SYSTEM DISEASES
    Size XI, 240 S. : ILL.
    Publisher YEAR BOOK MEDICAL
    Publishing place CHICAGO ; LONDON
    Document type Book
    Note INCLUDES BIBLIOGRAPHIES AND INDEX
    HBZ-ID HT002554228
    ISBN 0-8151-7136-6 ; 978-0-8151-7136-2
    Database Catalogue ZB MED Medicine, Health

    Kategorien

To top