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Clinical and Vaccine Immunology, February 2008, p. 253-259, Vol. 15, No. 2
1071-412X/08/$08.00+0 doi:10.1128/CVI.00316-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
Safety and Immunogenicity of Two Influenza Virus Subunit Vaccines, with or without MF59 Adjuvant, Administered to Human Immunodeficiency Virus Type 1-Seropositive and -Seronegative Adults
P. Durando,1*
D. Fenoglio,2
A. Boschini,3
F. Ansaldi,1
G. Icardi,1
L. Sticchi,1
A. Renzoni,1
P. Fabbri,3
A. Ferrera,2
A. Parodi,4
B. Bruzzone,1
G. Gabutti,5
A. Podda,6
G. Del Giudice,6
E. Fragapane,6
F. Indiveri,2
P. Crovari,1 and
R. Gasparini1
Department of Health Sciences,1 Stem Cell Center, Pathologic Anatomy Unit, San Martino Hospital,4 Centre of Excellence for Biomedical Research, Department of Internal Medicine, University of Genoa, 16132 Genoa,2 San Patrignano Medical Centre, 47852 Coriano, Rimini,3 Department of Clinical and Experimental Medicine, University of Ferrara, 44100 Ferrara,5 Novartis Vaccines S.r.l., 53100 Siena, Italy6
Received 31 July 2007/ Returned for modification 31 August 2007/ Accepted 1 November 2007
The objective of this study was to evaluate and compare both the safety and tolerability and the humoral and cell-mediated immune responses for two influenza virus subunit vaccines, one with MF59 adjuvant (Fluad) and one without an adjuvant (Agrippal), in healthy and in human immunodeficiency virus type 1 (HIV-1)-infected adult individuals. To achieve this aim, an open, randomized, comparative clinical trial was performed during the 2005-2006 season. A total of 256 subjects were enrolled to receive one dose of vaccine intramuscularly. Blood samples were taken at the time of vaccination and at 1 and 3 months postvaccination. A good humoral antibody response was detected for both vaccines, meeting all the criteria of the Committee for Medical Products for Human Use. After Beyer's correction for prevaccination status, Fluad exhibited better immunogenicity than Agrippal, as shown from the analysis of the geometric mean titers, with significant differences for some virus strains; however, no definitive conclusions on the clinical significance of such results can be drawn, because the method used to estimate antibody response is currently nonstandard for influenza virus vaccines. Significant induction of an antigen-specific CD4+ T-lymphocyte proliferative response was detected at all time points after immunization, for both the vaccines, among HIV-1-seronegative subjects. This was different from what was observed for HIV-1-infected individuals. In this group, significance was not reached at 30 days postvaccination (T30) for those immunized with Agrippal. Also when data were compared between treatment groups, a clear difference in the response at T30 was observed in favor of Fluad (P = 0.0002). The safety profiles of both vaccines were excellent. For HIV-1-infected individuals, no significant changes either in viremia or in the CD4+ cell count were observed at any time point. The results showed good safety and immunogenicity for both vaccines under study for both uninfected and HIV-1-infected adults, confirming current recommendations for immunization of this high-risk category.
* Corresponding author. Mailing address: Department of Health Sciences, Section of Hygiene and Preventive Medicine, University of Genoa, Via A. Pastore, 1, 16132 Genoa, Italy. Phone: 39 347 4454082. Fax: 39 010 505618. E-mail: durando{at}unige.it
Published ahead of print on 14 November 2007.
Clinical and Vaccine Immunology, February 2008, p. 253-259, Vol. 15, No. 2
1071-412X/08/$08.00+0 doi:10.1128/CVI.00316-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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