scholarly journals Immunogenicity and safety of influenza vaccination in children with inflammatory bowel disease

2012 ◽  
Vol 18 (1) ◽  
pp. 25-33 ◽  
Author(s):  
Jennifer C.C. deBruyn ◽  
Robert Hilsden ◽  
Kevin Fonseca ◽  
Margaret L. Russell ◽  
Gilaad G. Kaplan ◽  
...  
2019 ◽  
Vol 156 (6) ◽  
pp. S-616
Author(s):  
Jamie Mathew ◽  
Sharon Thomas ◽  
Randa Samaha ◽  
Erealda Prendaj ◽  
Gitit Tomer

2021 ◽  
Vol 160 (6) ◽  
pp. S-391
Author(s):  
Sharmistha Rudra ◽  
Andrew B. Grossman ◽  
Maura Downing ◽  
Jillian Hillman ◽  
Kerry A. Ashcroft ◽  
...  

2014 ◽  
Vol 8 (4) ◽  
pp. 431-435 ◽  
Author(s):  
Aleksandra Banaszkiewicz ◽  
Beata Klincewicz ◽  
Izabella Łazowska-Przeorek ◽  
Urszula Grzybowska-Chlebowczyk ◽  
Paulina Kąkol ◽  
...  

2013 ◽  
Vol 144 (5) ◽  
pp. S-644-S-645
Author(s):  
Yoshie Hagihara ◽  
Kenji Watanabe ◽  
Hirokazu Yamagami ◽  
Takuya Tsukahara ◽  
Kenichi Morimoto ◽  
...  

2012 ◽  
Vol 153 (47) ◽  
pp. 1870-1874 ◽  
Author(s):  
Klaudia Farkas ◽  
Gabriella Terhes ◽  
Judit Deák ◽  
Anita Bálint ◽  
Ferenc Nagy ◽  
...  

Introduction: Inactivated influenza vaccination is recommended yearly for patients with inflammatory bowel disease on immunosuppressive therapy. Aim: The aim of our study was to evaluate the immune response to seasonal influenza vaccination in patients with inflammatory bowel disease treated with immunosuppressants. Patients and methods: Thirty patients were enrolled in this prospective study. Each patient was diagnosed with inflammatory bowel disease and treated with immunosuppressants. Blood samples were obtained from patients before and one month after influenza vaccination (A/California/7/2009(H1N1), A/Perth/16/2009(H3N2) B/Brisbane/60/2008) to assess the pre-and postimmunization antibody titers. Virus-specific antibodies were measured by ELISA. Results: The vaccine acceptance rate was 53.3%. Local adverse effect occurred in 5 patients. Seven patients developed systemic adverse events. Influenza-like symptoms occurred in 2 patients, although their antibody titers failed to increase significantly. Antibodies to influenza viruses were detected in each patient before the vaccination. Conclusion: The results confirmed that each patient had appropriate antibody titer as correlation of protection even before the immunisation. Seroprotection rates were not influenced by the vaccination. The vaccine seemed to be safe. Orv. Hetil., 2012, 153, 1870–1874.


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