z-logo
open-access-imgOpen Access
The adjuvant system AS01 up‐regulates neutrophil CD14 expression and neutrophil‐associated antigen transport in the local lymphatic network
Author(s) -
Neeland M. R.,
Shi W.,
Collig C.,
Meeusen E. N. T.,
Didierlaurent A. M.,
de Veer M. J.
Publication year - 2018
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.13088
Subject(s) - immunology , adjuvant , antigen , hbsag , vaccination , cd14 , medicine , biology , immune system , hepatitis b virus , virus
Summary The liposome‐based adjuvant system AS01 is under evaluation for use in several vaccines in clinical development. We have shown previously that AS01 injected with hepatitis B surface antigen (HBsAg) induces a distinct cellular signature within the draining lymphatics that enhances local lymphocyte recruitment and antigen‐specific humoral immunity. Here, we show that AS01‐induced neutrophil recruitment is associated with increased expression of CD14 and enhanced antigen uptake capacity in neutrophils from both afferent and efferent lymphatic compartments during the first 48 h after vaccination. Significant and transient increases in CD14 expression on systemic neutrophils were also observed following primary and boost vaccination with HBsAg‐AS01; however, they were not observed following additional encounter with HBsAg‐alone or HBsAg‐alum. These results show that following immunization with AS01, neutrophils expressing higher levels of CD14 are both more abundant and efficient at antigen uptake, warranting further investigation into the role of neutrophil‐associated CD14 in the adjuvanticity of AS01.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom