Cytokine Signatures of Innate and Adaptive Immunity in 17DD Yellow Fever Vaccinated Children and Its Association With the Level of Neutralizing Antibody
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2011
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Resumo |
Background. The live attenuated yellow fever (YF) vaccines have been available for decades and are considered highly effective and one of the safest vaccines worldwide. Methods. The impact of YF-17DD-antigens recall on cytokine profiles of YF-17DD-vaccinated children were characterized using short-term cultures of whole blood samples and single-cell flow cytometry. This study enrolled seroconverters and nonseroconverters after primovaccination (PV-PRNT(+) and PV-PRNT(-)), seroconverters after revaccination (RV-PRNT(+)), and unvaccinated volunteers (UV-PRNT(-)). Results. The analysis demonstrated in the PV-PRNT(+) group a balanced involvement of pro-inflammatory/regulatory adaptive immunity with a prominent participation of innate immunity pro-inflammatory events (IL-12(+) and TNF-alpha(+) NEU and MON). Using the PV-PRNT(+) cytokine signature as a reference profile, PV-PRNT(+) presented a striking lack of innate immunity proinflammatory response along with an increased adaptive regulatory profile (IL-4(+) CD4(+) T cells and IL-10(+) and IL-5(+) CD8(+) T cells). Conversely, the RV-PRNT(+) shifted the overall cytokine signatures toward an innate immunity pro-inflammatory profile and restored the adaptive regulatory response. Conclusions. The data demonstrated that the overall cytokine signature was associated with the levels of PRNT antibodies with a balanced innate/adaptive immunity with proinflammatory/regulatory profile as the hallmark of PV-PRNT(MEDIUM+), whereas a polarized regulatory response was observed in PV-PRNT(-) and a prominent proinflammatory signature was the characteristic of PV-PRNT(HIGH+). Bio-Manguinhos/Oswaldo Cruz Foundation (FIOCRUZ)[05/05] Bio-Manguinhos/Oswaldo Cruz Foundation (FIOCRUZ)[05/08] Bio-Manguinhos/Oswaldo Cruz Foundation (FIOCRUZ)[009/2010] Council for Scientific and Technological Development (CNPq)[479663/2004-1] Council for Scientific and Technological Development (CNPq)[308651/2006-5] Council for Scientific and Technological Development (CNPq)[472782/2009-6] Council for Scientific and Technological Development (CNPq)[303316/2009-8] Minas Gerais State Research Foundation (FAPEMIG)[APQ 01183-08] Minas Gerais State Research Foundation (FAPEMIG)[APQ 01877-10] Minas Gerais State Research Foundation (FAPEMIG)[PDJ 00265-09] National Council for Scientific and Technological Development (CNPq) |
Identificador |
JOURNAL OF INFECTIOUS DISEASES, v.204, n.6, p.873-883, 2011 0022-1899 http://producao.usp.br/handle/BDPI/25036 10.1093/infdis/jir439 |
Idioma(s) |
eng |
Publicador |
OXFORD UNIV PRESS INC |
Relação |
Journal of Infectious Diseases |
Direitos |
restrictedAccess Copyright OXFORD UNIV PRESS INC |
Palavras-Chave | #HERPES-SIMPLEX VIRUS #CD40 LIGAND #T-CELLS #FUNCTIONAL IMMATURITY #1ST-TIME VACCINATION #DENDRITIC CELLS #IMMUNIZATION #INFECTION #ACTIVATION #EXPRESSION #Immunology #Infectious Diseases #Microbiology |
Tipo |
article original article publishedVersion |