Autor: |
Mamta K. Jain, Tauseef Rehman, P. Coburn, Alain G. DuChene, K. Quan, Paul F. Riska, Jennifer A. Whitaker, Adriana Sanchez, L. H. Makohon, Fred M. Gordin, Norman Markowitz, Julia A. Metcalf, Edward M. Gardner, C. Solorzano, John H. Beigel, Elizabeth Finley, A. Shoen, D. Bigley, J. Moghe, T. Petersen, Marie L. Hoover, Jocelyn Voell, H. Clifford Lane, Venn Natarajan, B. Omotosho, Nicole Engen, J. Scott, John Tierney, Robin Dewar, Timothy M. Uyeki, Barbara Standridge, James D. Neaton, Stacey A. Rizza, Eileen Denning, Richard T. Davey, L. Harlow, Abdel Babiker, Deborah Wentworth, H Preston Holley, Gordon E. Thompson, John D. Baxter, L. L. Faber, Raquel Nahra, M. Harrison, R. Mcconnell, Zelalem Temesgen, Hari Polenakovik |
Rok vydání: |
2015 |
Předmět: |
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Zdroj: |
The Journal of infectious diseases. 213(4) |
ISSN: |
1537-6613 |
Popis: |
Hemagglutination inhibition (HAI) antibody responses to anti–influenza virus hyperimmune intravenous immunoglobulin (hIVIG) were characterized. Thirty-one patients with influenza during the 2013–2014 season were randomly assigned to receive 0.25 g/kg of hIVIG (n = 16) or placebo (n = 15). For hIVIG recipients, the ratio of geometric mean titers (1 hour after infusion/before infusion) was 4.00 (95% confidence interval [CI], 2.61–6.13) for 2009 pandemic influenza A(H1N1) and 1.76 (95% CI, 1.33–2.32) for influenza A(H3N2) and influenza B. Among patients with 2009 pandemic influenza A(H1N1), ratios for hIVIG (n = 9) versus placebo (n = 8) were higher 1 hour after infusion (3.9 [95% CI, 2.3–6.7]) and sustained through day 3 (2.0 [95% CI, 1.0–4.0]). hIVIG administration significantly increases HAI titer levels among patients with influenza, supporting the need to perform a clinical outcomes study. Clinical trials registration: NCT02008578. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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