tetano
Editor, Senior Moderator
Hum Vaccin Immunother. 2014 Jul 3:e29695. [Epub ahead of print]
Nine ?g intradermal influenza vaccine and 15 ?g intramuscular influenza vaccine induce similar cellular and humoral immune responses in adults.
Nolwenn N1, Bisceglia H, Rozi?res A, Goujon C, Boudet F, Laurent P, Vanbervliet B, Rodet K, Hennino A, Nicolas JF.
Author information
Abstract
Intanza? 9 ?g (Sanofi Pasteur), a trivalent split-virion vaccine administered by intradermal (ID) injection, was approved in Europe in 2009 for the prevention of seasonal influenza in adults 18 to 59 years. Here, we examined the immune responses induced in adults by the ID 9 ?g vaccine and the standard trivalent intramuscular (IM) vaccine (Vaxigrip? 15 ?g, Sanofi Pasteur). This trial was a randomized, controlled, single-center, open-label study in healthy adults 18 to 40 years of age during the 2007/8 influenza season. Subjects received a single vaccination with the ID 9 ?g (n = 38) or IM 15 ?g (n = 42) vaccine. Serum, saliva, and peripheral blood mononuclear cells were collected up to 180 days post-vaccination. Geometric mean hemagglutination inhibition titers, seroprotection rates, seroconversion rates, and pre-vaccination-to-post-vaccination ratios of geometric mean hemagglutination inhibition titers did not differ between the two vaccines. Compared with pre-vaccination, the vaccines induced similar increases in vaccine-specific circulating B cells at day 7 but did not induce significant increases in vaccine-specific memory B cells at day 180. Cell-mediated immunity to all three vaccine strains, measured in peripheral blood mononuclear cells, was high at baseline and not increased by either vaccine. Neither vaccine induced a mucosal immune response. These results show that the humoral and cellular immune responses to the ID 9 ?g vaccine are similar to those to the standard IM 15 ?g vaccine.
KEYWORDS:
adult; immunogenicity; intradermal influenza vaccine; intramuscular vaccination; trivalent influenza vaccine
PMID:
25483667
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/25483667
Nine ?g intradermal influenza vaccine and 15 ?g intramuscular influenza vaccine induce similar cellular and humoral immune responses in adults.
Nolwenn N1, Bisceglia H, Rozi?res A, Goujon C, Boudet F, Laurent P, Vanbervliet B, Rodet K, Hennino A, Nicolas JF.
Author information
Abstract
Intanza? 9 ?g (Sanofi Pasteur), a trivalent split-virion vaccine administered by intradermal (ID) injection, was approved in Europe in 2009 for the prevention of seasonal influenza in adults 18 to 59 years. Here, we examined the immune responses induced in adults by the ID 9 ?g vaccine and the standard trivalent intramuscular (IM) vaccine (Vaxigrip? 15 ?g, Sanofi Pasteur). This trial was a randomized, controlled, single-center, open-label study in healthy adults 18 to 40 years of age during the 2007/8 influenza season. Subjects received a single vaccination with the ID 9 ?g (n = 38) or IM 15 ?g (n = 42) vaccine. Serum, saliva, and peripheral blood mononuclear cells were collected up to 180 days post-vaccination. Geometric mean hemagglutination inhibition titers, seroprotection rates, seroconversion rates, and pre-vaccination-to-post-vaccination ratios of geometric mean hemagglutination inhibition titers did not differ between the two vaccines. Compared with pre-vaccination, the vaccines induced similar increases in vaccine-specific circulating B cells at day 7 but did not induce significant increases in vaccine-specific memory B cells at day 180. Cell-mediated immunity to all three vaccine strains, measured in peripheral blood mononuclear cells, was high at baseline and not increased by either vaccine. Neither vaccine induced a mucosal immune response. These results show that the humoral and cellular immune responses to the ID 9 ?g vaccine are similar to those to the standard IM 15 ?g vaccine.
KEYWORDS:
adult; immunogenicity; intradermal influenza vaccine; intramuscular vaccination; trivalent influenza vaccine
PMID:
25483667
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/25483667