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Human Vaccines & Immunotherapeutics • June 2014<br />

Thimerosal compromises human dendritic cell<br />

maturation, IL-12 production, chemokine release,<br />

and T-helper polarization<br />

by Emily Loison & Marie-Lise Gougeon<br />

Abstract<br />

In conclusion, our study indicates that ex-vivo exposure of human immature dendritic<br />

cells to very low nontoxic concentrations of thimerosal alters the LPS-induced<br />

maturation process and dampens their proinflammatory response, in particular the<br />

production of the T-helper polarizing cytokine IL-12. Moreover, thimerosal exposure<br />

of DCs corrupts their interaction with naïve CD4+ T cells, leading to a decreased production<br />

of IFN-γ IP10 and GM-CSF and increased levels of IL-8, IL-9, and MIP-1α.<br />

Today, except for some flu vaccines in multi-dose vials, no recommended childhood<br />

vaccines contain thimerosal as a preservative. It must be stressed that the toxicity and<br />

immunomodulatory effects of thimerosal that we report ex-vivo on human monocytederived<br />

DCs may occur in vivo and induce an alteration of the immune response to<br />

the vaccine. These observations highlight the need to use this preservative with caution<br />

and avoid it if possible.<br />

“These observations<br />

highlight the need to use<br />

this preservative with caution<br />

and avoid it if possible.”<br />

Full Report<br />

https://app.box.com/s/0dg5ksp3f377qes3m5qsp16rl1gxws8l

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