Journal article icon

Journal article

Germinal centre B cell and T follicular helper cell responses to viral vector and protein-in-adjuvant vaccines

Abstract:

There is great interest in the development of antibody-inducing subunit vaccines targeting infections including HIV, malaria and Ebola. We previously reported that adenovirus vectored vaccines are potent in priming antibody responses, but uncertainty remains regarding the optimal approach for induction of humoral immune responses.

Here, using ovalbumin as a model antigen, we assessed the magnitude of the primary and anamnestic antigen-specific IgG responses of mice to four clinically-relevant vaccine formulations: replication-deficient adenovirus; modified vaccinia Ankara (MVA, a poxvirus); protein with alum; and protein in the squalene oil-in-water adjuvant Addavax. We then used flow cytometric assays capable of measuring total and antigen-specific germinal center (GC) B cell and follicular helper T cell (Tfh) responses to compare the induction of these responses by the different formulations.

We report that adenovirus vectored vaccines induce antigen insert-specific GC B cell and antibody responses of a magnitude comparable to those induced by a potent protein/ squalene oil-in-water formulation whereas- despite a robust overall GC response - the insertspecific GC B cell and antibody responses induced by MVA were extremely weak. Antigenspecific Tfh responses to adenovirus vectored responses exceeded those induced by other platforms at day 7 after immunization. We found little evidence that innate immune activation by adenovirus may act as an adjuvant in such a manner that the humoral response to a recombinant protein may be enhanced by co-administering with an adenovirus lacking a transgene of interest.

Overall, these studies provide further support for the use of replication-deficient adenoviruses to induce humoral responses.

Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Files:
Publisher copy:
10.4049/jimmunol.1502472

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author


More from this funder
Funder identifier:
https://ror.org/05kwhph67
Funding agency for:
Borrow, P
Draper, SJ
Grant:
NIAID, DAIDS grantUM1 AI00645 (Duke CHAVI-ID)
Career Development Fellowship (MRC/DFID Concordat G1000527)
More from this funder
Funder identifier:
https://ror.org/00k4n6c32
Funding agency for:
de Cassan, SC
Grant:
LSHP-CT-2007-037506
More from this funder
Funder identifier:
https://ror.org/03x94j517
Funding agency for:
Borrow, P
Draper, SJ
Grant:
NIAID, DAIDS grantUM1 AI00645 (Duke CHAVI-ID)
Career Development Fellowship (MRC/DFID Concordat G1000527)
More from this funder
Funding agency for:
Draper, SJ
Grant:
Career Development Fellowship (MRC/DFID Concordat G1000527)
More from this funder
Funding agency for:
Borrow, P
Grant:
NIAID, DAIDS grantUM1 AI00645 (Duke CHAVI-ID)


Publisher:
American Association of Immunologists
Journal:
Journal of Immunology More from this journal
Volume:
197
Issue:
4
Pages:
1242–1251
Publication date:
2016-08-15
Acceptance date:
2016-06-09
DOI:
EISSN:
1550-6606
ISSN:
0022-1767


Language:
English
Pubs id:
pubs:628251
UUID:
uuid:f18f9fbe-7404-4a6c-b146-2db1b11585b5
Local pid:
pubs:628251
Source identifiers:
628251
Deposit date:
2016-06-16
ARK identifier:

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP