Clinical and Immunological Insights on Severe, Adverse Neurotropic and Viscerotropic Disease following 17D Yellow Fever Vaccination


Autoria(s): SILVA, Maria Luiza; ESPIRITO-SANTO, Lucandra Ramos; MARTINS, Marina Angela; SILVEIRA-LEMOS, Denise; PERUHYPE-MAGALHAES, Vanessa; CAMINHA, Ricardo Carvalho; MARANHAO-FILHO, Pericles de Andrade; AUXILIADORA-MARTINS, Maria; MARTINS, Reinaldo de Menezes; GALLER, Ricardo; FREIRE, Marcos da Silva; MARCOVISTZ, Rugimar; HOMMA, Akira; TEUWEN, Dirk E.; ELOI-SANTOS, Silvana Maria; ANDRADE, Marileia Chaves; TEIXEIRA-CARVALHO, Andrea; MARTINS-FILHO, Olindo Assis
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Yellow fever (YF) vaccines (17D-204 and 17DD) are well tolerated and cause very low rates of severe adverse events (YEL-SAE), such as serious allergic reactions, neurotropic adverse diseases (YEL-AND), and viscerotropic diseases (YEL-AVD). Viral and host factors have been postulated to explain the basis of YEL-SAE. However, the mechanisms underlying the occurrence of YEL-SAE remain unknown. The present report provides a detailed immunological analysis of a 23-year-old female patient. The patient developed a suspected case of severe YEL-AVD with encephalitis, as well as with pancreatitis and myositis, following receipt of a 17D-204 YF vaccination. The patient exhibited a decreased level of expression of Fc-gamma R in monocytes (CD16, CD32, and CD64), along with increased levels of NK T cells (an increased CD3(+) CD16(+/-) CD56(+/-)/CD3(+) ratio), activated T cells (CD4(+) and CD8(+) cells), and B lymphocytes. Enhanced levels of plasmatic cytokines (interleukin-6 [IL-6], IL-17, IL-4, IL-5, and IL-10) as well as an exacerbated ex vivo intracytoplasmic cytokine pattern, mainly observed within NK cells (gamma interferon positive [IFN-gamma(+)], tumor necrosis factor alpha positive [TNF-alpha(+)], and IL-4 positive [IL-4(+)]), CD8(+) T cells (IL-4(+) and IL-5(+)), and B lymphocytes (TNF-alpha(+), IL-4(+), and IL-10(+)). The analysis of CD4(+) T cells revealed a complex profile that consisted of an increased frequency of IL-12(+) and IFN-gamma(+) cells and a decreased percentage of TNF-alpha(+), IL-4(+), and IL-5+ cells. Depressed cytokine synthesis was observed in monocytes (TNF-alpha(+)) following the provision of antigenic stimuli in vitro. These results support the hypothesis that a strong adaptive response and abnormalities in the innate immune system may be involved in the establishment of YEL-AND and YEL-AVD.

Biomaguinhos[CC 05/2005]

FAPEMIG[13962/2008]

Centro de Pesquisas Rene Rachou-FIOCRUZ-Minas

CNPq

Identificador

CLINICAL AND VACCINE IMMUNOLOGY, v.17, n.1, p.118-126, 2010

1556-6811

http://producao.usp.br/handle/BDPI/24877

10.1128/CVI.00369-09

http://dx.doi.org/10.1128/CVI.00369-09

Idioma(s)

eng

Publicador

AMER SOC MICROBIOLOGY

Relação

Clinical and Vaccine Immunology

Direitos

restrictedAccess

Copyright AMER SOC MICROBIOLOGY

Palavras-Chave #1ST-TIME VACCINATION #SIMULTANEOUS RAISE #EVENTS #FAILURE #BRAZIL #DEATH #SPAIN #Immunology #Infectious Diseases #Microbiology
Tipo

article

original article

publishedVersion