Immunogenicity and safety of the 2009 non-adjuvanted influenza A/H1N1 vaccine in a large cohort of autoimmune rheumatic diseases


Autoria(s): SAAD, Carla G. S.; BORBA, Eduardo F.; AIKAWA, Nadia E.; SILVA, Clovis A.; PEREIRA, Rosa M. R.; CALICH, Ana Luisa; MORAES, Julio C. B.; RIBEIRO, Ana C. M.; VIANA, Vilma S. T.; PASOTO, Sandra G.; CARVALHO, Jozelio F.; FRANCA, Ivan L. A.; GUEDES, Lissiane K. N.; SHINJO, Samuel K.; SAMPAIO-BARROS, Percival D.; CALEIRO, Maria T.; GONCALVES, Celio R.; FULLER, Ricardo; LEVY-NETO, Mauricio; TIMENETSKY, Maria do Carmo S.; PRECIOSO, Alexander R.; BONFA, Eloisa
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Background Despite the WHO recommendation that the 2010-2011 trivalent seasonal flu vaccine must contain A/California/7/2009/H1N1-like virus there is no consistent data regarding its immunogenicity and safety in a large autoimmune rheumatic disease (ARD) population. Methods 1668 ARD patients (systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), ankylosing spondylitis (AS), systemic sclerosis, psoriatic arthritis (PsA), Behcet`s disease (BD), mixed connective tissue disease, primary antiphospholipid syndrome (PAPS), dermatomyositis (DM), primary Sjogren`s syndrome, Takayasu`s arteritis, polymyositis and Granulomatosis with polyangiitis (Wegener`s) (GPA)) and 234 healthy controls were vaccinated with a non-adjuvanted influenza A/California/7/2009(H1N1) virus-like strain flu. Subjects were evaluated before vaccination and 21 days post-vaccination. The percentage of seroprotection, seroconversion and the factor increase in geometric mean titre (GMT) were calculated. Results After immunisation, seroprotection rates (68.5% vs 82.9% p < 0.0001), seroconversion rates (63.4% vs 76.9%, p < 0.001) and the factor increase in GMT (8.9 vs 13.2 p < 0.0001) were significantly lower in ARD than controls. Analysis of specific diseases revealed that seroprotection significantly reduced in SLE (p < 0.0001), RA (p < 0.0001), PsA (p=0.0006), AS (p=0.04), BD (p=0.04) and DM (p=0.04) patients than controls. The seroconversion rates in SLE (p < 0.0001), RA (p < 0.0001) and PsA (p=0.0006) patients and the increase in GMTs in SLE (p < 0.0001), RA (p < 0.0001) and PsA (p < 0.0001) patients were also reduced compared with controls. Moderate and severe side effects were not reported. Conclusions The novel recognition of a diverse vaccine immunogenicity profile in distinct ARDs supports the notion that a booster dose may be recommended for diseases with suboptimal immune responses. This large study also settles the issue of vaccine safety. (ClinicalTrials.gov #NCT01151644)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[2010/10749-0]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ)[303165/2008-1]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ)[300248/2008-3]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ)[300559/2009-7]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ)[300665/2009-1]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ)[301411/2009-3]

Federico Foundation

Butantan Foundation

Identificador

ANNALS OF THE RHEUMATIC DISEASES, v.70, n.6, p.1068-1073, 2011

0003-4967

http://producao.usp.br/handle/BDPI/21669

10.1136/ard.2011.150250

http://dx.doi.org/10.1136/ard.2011.150250

Idioma(s)

eng

Publicador

B M J PUBLISHING GROUP

Relação

Annals of the Rheumatic Diseases

Direitos

restrictedAccess

Copyright B M J PUBLISHING GROUP

Palavras-Chave #SYSTEMIC-LUPUS-ERYTHEMATOSUS #MEDIATED IMMUNE-RESPONSES #CLASSIFICATION CRITERIA #ANTIBODY-RESPONSES #REVISED CRITERIA #SPLIT-VIRION #ARTHRITIS #GRANULOMATOSIS #MULTICENTER #RITUXIMAB #Rheumatology
Tipo

article

original article

publishedVersion