4 results on '"Haven, Kathryn"'
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2. Activated CD4+ T cells and CD14hiCD16+ monocytes correlate with antibody response following influenza virus infection in humans
- Author
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Wong, Sook-San, primary, Oshansky, Christine M., additional, Guo, Xi-Zhi J., additional, Ralston, Jacqui, additional, Wood, Timothy, additional, Reynolds, Gary E., additional, Seeds, Ruth, additional, Jelley, Lauren, additional, Waite, Ben, additional, Jeevan, Trushar, additional, Zanin, Mark, additional, Widdowson, Marc-Alain, additional, Huang, Q. Sue, additional, Thomas, Paul G., additional, Webby, Richard J., additional, Turner, Nikki, additional, Baker, Michael, additional, Grant, Cameron, additional, McArthur, Colin, additional, Roberts, Sally, additional, Trenholmes, Adrian, additional, Wong, Conroy, additional, Taylor, Susan, additional, Thompson, Mark, additional, Gross, Diane, additional, Duque, Jazmin, additional, Haven, Kathryn, additional, Aley, Debbie, additional, Muponisi, Pamela, additional, Chand, Bhamita, additional, Chen, Yan, additional, Plewes, Laurel, additional, Sawtell, Frann, additional, Lawrence, Shirley, additional, Cogcoy, Reniza, additional, Smith, Jo, additional, Gravidez, Franie, additional, Ma, Mandy, additional, Chamberlin, Shona, additional, Davey, Kirstin, additional, Knowles, Tania, additional, McLeish, Jo-Ann, additional, Todd, Angela, additional, Bocacao, Judy, additional, Gunn, Wendy, additional, Kawakami, Pamela, additional, Walker, Susan, additional, Madge, Robyn, additional, Moore, Nicole, additional, Rahnama, Fahimeh, additional, Qiao, Helen, additional, Tse, Fifi, additional, Zibaei, Mahtab, additional, Korrapadu, Tirzah, additional, Optland, Louise, additional, and Dela Cruz, Cecilia, additional
- Published
- 2021
- Full Text
- View/download PDF
3. A chest radiograph scoring system in patients with severe acute respiratory infection: a validation study.
- Author
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Taylor, Emma, Haven, Kathryn, Reed, Peter, Bissielo, Ange, Harvey, Dave, McArthur, Colin, Bringans, Cameron, Freundlich, Simone, Joan, R., Ingram, H., Perry, David, Wilson, Francessa, Milne, David, Modahl, Lucy, Sue Huang, Q., Gross, Diane, Widdowson, Marc-Alain, and Grant, Cameron C.
- Subjects
RADIOGRAPHY ,SARS treatment ,VALIDATION therapy ,ATELECTASIS ,HEART rate monitoring - Abstract
Background: The term severe acute respiratory infection (SARI) encompasses a heterogeneous group of respiratory illnesses. Grading the severity of SARI is currently reliant on indirect disease severity measures such as respiratory and heart rate, and the need for oxygen or intensive care. With the lungs being the primary organ system involved in SARI, chest radiographs (CXRs) are potentially useful for describing disease severity. Our objective was to develop and validate a SARI CXR severity scoring system. Methods: We completed validation within an active SARI surveillance project, with SARI defined using the World Health Organization case definition of an acute respiratory infection with a history of fever, or measured fever of ≥ 38 °C; and cough; and with onset within the last 10 days; and requiring hospital admission. We randomly selected 250 SARI cases. Admission CXR findings were categorized as: 1 = normal; 2 = patchy atelectasis and/or hyperinflation and/or bronchial wall thickening; 3 = focal consolidation; 4 = multifocal consolidation; and 5 = diffuse alveolar changes. Initially, four radiologists scored CXRs independently. Subsequently, a pediatrician, physician, two residents, two medical students, and a research nurse independently scored CXR reports. Inter-observer reliability was determined using a weighted Kappa (κ) for comparisons between radiologists; radiologists and clinicians; and clinicians. Agreement was defined as moderate (κ > 0.4-0.6), good (κ > 0.6-0.8) and very good (κ > 0.8-1.0). Results: Agreement between the two pediatric radiologists was very good (κ = 0.83, 95 % CI 0.65-1.00) and between the two adult radiologists was good (κ = 0.75, 95 % CI 0.57-0. 93). Agreement of the clinicians with the radiologists was moderate-to-good (pediatrician:κ = 0.65; pediatric resident:κ = 0.69; physician:κ = 0.68; resident:κ = 0.67; research nurse:κ = 0.49, medical students: κ = 0.53 and κ = 0.56). Agreement between clinicians was good-to-very good (pediatrician vs. physician:κ = 0.85; vs. pediatric resident:κ = 0.81; vs. medicine resident:κ = 0.76; vs. research nurse:κ = 0.75; vs. medical students:κ = 0.63 and 0.66). Following review of discrepant CXR report scores by clinician pairs, κ values for radiologist-clinician agreement ranged from 0.59 to 0.70 and for clinician-clinician agreement from 0.97 to 0.99. Conclusions: This five-point CXR scoring tool, suitable for use in poorly- and well-resourced settings and by clinicians of varying experience levels, reliably describes SARI severity. The resulting numerical data enables epidemiological comparisons of SARI severity between different countries and settings. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
4. Activated CD4+T cells and CD14hiCD16+monocytes correlate with antibody response following influenza virus infection in humans
- Author
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Wong, Sook-San, Oshansky, Christine M., Guo, Xi-Zhi J., Ralston, Jacqui, Wood, Timothy, Reynolds, Gary E., Seeds, Ruth, Jelley, Lauren, Waite, Ben, Jeevan, Trushar, Zanin, Mark, Widdowson, Marc-Alain, Huang, Q. Sue, Thomas, Paul G., Webby, Richard J., Turner, Nikki, Baker, Michael, Grant, Cameron, McArthur, Colin, Roberts, Sally, Trenholmes, Adrian, Wong, Conroy, Taylor, Susan, Thompson, Mark, Gross, Diane, Duque, Jazmin, Haven, Kathryn, Aley, Debbie, Muponisi, Pamela, Chand, Bhamita, Chen, Yan, Plewes, Laurel, Sawtell, Frann, Lawrence, Shirley, Cogcoy, Reniza, Smith, Jo, Gravidez, Franie, Ma, Mandy, Chamberlin, Shona, Davey, Kirstin, Knowles, Tania, McLeish, Jo-Ann, Todd, Angela, Bocacao, Judy, Gunn, Wendy, Kawakami, Pamela, Walker, Susan, Madge, Robyn, Moore, Nicole, Rahnama, Fahimeh, Qiao, Helen, Tse, Fifi, Zibaei, Mahtab, Korrapadu, Tirzah, Optland, Louise, and Dela Cruz, Cecilia
- Abstract
The failure to mount an antibody response following viral infection or seroconversion failure is a largely underappreciated and poorly understood phenomenon. Here, we identified immunologic markers associated with robust antibody responses after influenza virus infection in two independent human cohorts, SHIVERS and FLU09, based in Auckland, New Zealand and Memphis, Tennessee, USA, respectively. In the SHIVERS cohort, seroconversion significantly associates with (1) hospitalization, (2) greater numbers of proliferating, activated CD4+T cells, but not CD8+T cells, in the periphery during the acute phase of illness, and (3) fewer inflammatory monocytes (CD14hiCD16+) by convalescence. In the FLU09 cohort, fewer CD14hiCD16+monocytes during early illness in the nasal mucosa were also associated with the generation of influenza-specific mucosal immunoglobulin A (IgA) and IgG antibodies. Our study demonstrates that seroconversion failure after infection is a definable immunological phenomenon, associated with quantifiable cellular markers that can be used to improve diagnostics, vaccine efficacy, and epidemiologic efforts.
- Published
- 2021
- Full Text
- View/download PDF
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