tetano
Editor, Senior Moderator
European Journal of Haematology
Adjuvanted Influenza A (H1N1) 2009 Vaccine in Patients With Hematological Diseases: Good Safety and Immunogenicity Even in Chemotherapy-Treated Patients
Honar Cherif1,*,
Martin H?glund1,
Karlis Pauksens2
DOI: 10.1111/ejh.12094
Abstract
Patients with hematological malignancies are more susceptible to viral infections including influenza. In 2009, the World Health Organization classified the novel influenza A (H1N1) viruses as pandemic. The potential impact of this pandemic for patients with hematological disorders was unknown. Institutional guidelines recommended two doses of AS03-adjuvanted influenza A (H1N1) 2009 pandemic vaccine for these patients.
Objectives
We aimed to determine the safety, immunogenicity and clinical efficacy of this vaccine in patients with hematological diseases. Furthermore, we compared the immunological responses to that obtained by the non-adjuvanted trivalent seasonal influenza vaccine (TIV). Methods
All included patients received adjuvanted pandemic vaccine and the majority received TIV. Serum for antibody analyses was collected at 5 time points.
Results
Thirty-one patients with different hematological diseases were included. After the second vaccine dose a total of 25 (81%) reached both protective levels of antibodies and seroconversion response. Antibody titers ≥1:40 persisted for 50% of responding patients at one year. Seroconversion was observed in 69% of 14 patients who had undergone hematopoietic stem cell transplantation and in all (9/9) myeloma patients (five with ongoing treatment including high dose corticosteroids). After vaccination with TIV, seroconversions against the three included strains were detected in 28%, 40% and 20%. Response to the adjuvanted pandemic vaccine was superior (p<0.009).
Conclusions
A substantial proportion of patients with hematological malignancies including patients undergoing chemotherapy mounted a good response to the adjuvanted pandemic vaccine. This vaccine had superior immonogenicity as compared to the non-adjuvanted TIV.
http://onlinelibrary.wiley.com/doi/10.1111/ejh.12094/abstract
Adjuvanted Influenza A (H1N1) 2009 Vaccine in Patients With Hematological Diseases: Good Safety and Immunogenicity Even in Chemotherapy-Treated Patients
Honar Cherif1,*,
Martin H?glund1,
Karlis Pauksens2
DOI: 10.1111/ejh.12094
Abstract
Patients with hematological malignancies are more susceptible to viral infections including influenza. In 2009, the World Health Organization classified the novel influenza A (H1N1) viruses as pandemic. The potential impact of this pandemic for patients with hematological disorders was unknown. Institutional guidelines recommended two doses of AS03-adjuvanted influenza A (H1N1) 2009 pandemic vaccine for these patients.
Objectives
We aimed to determine the safety, immunogenicity and clinical efficacy of this vaccine in patients with hematological diseases. Furthermore, we compared the immunological responses to that obtained by the non-adjuvanted trivalent seasonal influenza vaccine (TIV). Methods
All included patients received adjuvanted pandemic vaccine and the majority received TIV. Serum for antibody analyses was collected at 5 time points.
Results
Thirty-one patients with different hematological diseases were included. After the second vaccine dose a total of 25 (81%) reached both protective levels of antibodies and seroconversion response. Antibody titers ≥1:40 persisted for 50% of responding patients at one year. Seroconversion was observed in 69% of 14 patients who had undergone hematopoietic stem cell transplantation and in all (9/9) myeloma patients (five with ongoing treatment including high dose corticosteroids). After vaccination with TIV, seroconversions against the three included strains were detected in 28%, 40% and 20%. Response to the adjuvanted pandemic vaccine was superior (p<0.009).
Conclusions
A substantial proportion of patients with hematological malignancies including patients undergoing chemotherapy mounted a good response to the adjuvanted pandemic vaccine. This vaccine had superior immonogenicity as compared to the non-adjuvanted TIV.
http://onlinelibrary.wiley.com/doi/10.1111/ejh.12094/abstract