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In vivo dendritic cell targeting cellular vaccine induces CD4+ Tfh cell-dependent antibody against influenza virus.


ABSTRACT: An induction of long-term cellular and humoral immunity is for the goal of vaccines, but the combination of antigens and adjuvant remain unclear. Here, we show, using a cellular vaccine carrying foreign protein antigen plus iNKT cell glycolipid antigen, designated as artificial adjuvant vector cells (aAVCs), that mature XCR1- DCs in situ elicit not only ordinal antigen-specific CD4+T cells, but also CD4+ Tfh and germinal center, resulted in inducing long-term antibody production. As a mechanism for leading the long-term antibody production by aAVC, memory CD4+ Tfh cells but not iNKTfh cells played an important role in a Bcl6 dependent manner. To develop it for influenza infection, we established influenza hemagglutinin-carrying aAVC (aAVC-HA) and found that all the mice vaccinated with aAVC-HA were protected from life-threatening influenza infection. Thus, the in vivo DC targeting therapy by aAVC would be useful for protection against viral infection.

SUBMITTER: Yamasaki S 

PROVIDER: S-EPMC5064395 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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In vivo dendritic cell targeting cellular vaccine induces CD4<sup>+</sup> Tfh cell-dependent antibody against influenza virus.

Yamasaki Satoru S   Shimizu Kanako K   Kometani Kohei K   Sakurai Maki M   Kawamura Masami M   Fujii Shin-Ichiro SI  

Scientific reports 20161014


An induction of long-term cellular and humoral immunity is for the goal of vaccines, but the combination of antigens and adjuvant remain unclear. Here, we show, using a cellular vaccine carrying foreign protein antigen plus iNKT cell glycolipid antigen, designated as artificial adjuvant vector cells (aAVCs), that mature XCR1<sup>-</sup> DCs in situ elicit not only ordinal antigen-specific CD4<sup>+</sup>T cells, but also CD4<sup>+</sup> Tfh and germinal center, resulted in inducing long-term ant  ...[more]

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