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A Single 17D Yellow Fever Vaccination Provides Lifelong Immunity; Characterization of Yellow-Fever-Specific Neutralizing Antibody and T-Cell Responses after Vaccination

Authors :
Perry J.J. van Genderen
Abraham Goorhuis
Godelieve J. de Bree
Emile F.F. Jonker
Ester B. M. Remmerswaal
Martin P. Grobusch
Ineke J. M. ten Berge
Ester M. M. van Leeuwen
Leo G. Visser
Adriëtte W. de Visser
Rosanne W. Wieten
Infectious diseases
AII - Amsterdam institute for Infection and Immunity
Experimental Immunology
Nephrology
APH - Amsterdam Public Health
Source :
PLoS ONE, PLoS ONE, 11(3). Public Library of Science, PLoS ONE, 11(3). PUBLIC LIBRARY SCIENCE, PLoS ONE, Vol 11, Iss 3, p e0149871 (2016)
Publication Year :
2016
Publisher :
PUBLIC LIBRARY SCIENCE, 2016.

Abstract

Introduction Prompted by recent amendments of Yellow Fever (YF) vaccination guidelines from boost to single vaccination strategy and the paucity of clinical data to support this adjustment, we used the profile of the YF-specific CD8+ T-cell subset profiles after primary vaccination and neutralizing antibodies as a proxy for potentially longer lasting immunity. Methods and Findings PBMCs and serum were collected in six individuals on days 0, 3, 5, 12, 28 and 180, and in 99 individuals >10 years after YF-vaccination. Phenotypic characteristics of YF- tetramer+ CD8+ T-cells were determined using class I tetramers. Antibody responses were measured using a standardized plaque reduction neutralization test (PRNT). Also, characteristics of YF-tetramer positive CD8+ T-cells were compared between individuals who had received a primary- and a booster vaccination. YF-tetramer+ CD8+ T-cells were detectable on day 12 (median tetramer+ cells as percentage of CD8+ T-cells 0.2%, range 0.07–3.1%). On day 180, these cells were still present (median 0.06%, range 0.02–0.78%). The phenotype of YF-tetramer positive CD8+ T-cells shifted from acute phase effector cells on day 12, to late differentiated or effector memory phenotype (CD45RA-/+CD27-) on day 28. Two subsets of YF-tetramer positive T-cells (CD45RA+CD27- and CD45RA+CD27+) persisted until day 180. Within all phenotypic subsets, the T-bet: Eomes ratio tended to be high on day 28 after vaccination and shifted towards predominant Eomes expression on day 180 (median 6.0 (day 28) vs. 2.2 (day 180) p = 0.0625), suggestive of imprinting compatible with long-lived memory properties. YF-tetramer positive CD8+ T-cells were detectable up to 18 years post vaccination, YF-specific antibodies were detectable up to 40 years after single vaccination. Booster vaccination did not increase titers of YF-specific antibodies (mean 12.5 vs. 13.1, p = 0.583), nor induce frequencies or alter phenotypes of YF-tetramer+ CD8+ T-cells. Conclusion The presence of a functionally competent YF-specific memory T-cell pool 18 years and sufficient titers of neutralizing antibodies 35–40 years after first vaccination suggest that single vaccination may be sufficient to provide long-term immunity.

Details

Language :
English
Database :
OpenAIRE
Journal :
PLoS ONE, PLoS ONE, 11(3). Public Library of Science, PLoS ONE, 11(3). PUBLIC LIBRARY SCIENCE, PLoS ONE, Vol 11, Iss 3, p e0149871 (2016)
Accession number :
edsair.doi.dedup.....53e9e0dd606839c004ddb523cb8d8937