TY - JOUR
T1 - Design of a protective single-dose intranasal nanoparticle-based vaccine platform for respiratory infectious diseases
AU - Ulery, Bret D.
AU - Kumar, Devender
AU - Ramer-Tait, Amanda E.
AU - Metzger, Dennis W.
AU - Wannemuehler, Michael J.
AU - Narasimhan, Balaji
PY - 2011
Y1 - 2011
N2 - Despite the successes provided by vaccination, many challenges still exist with respect to controlling new and re-emerging infectious diseases. Innovative vaccine platforms composed of adaptable adjuvants able to appropriately modulate immune responses, induce long-lived immunity in a single dose, and deliver immunogens in a safe and stable manner via multiple routes of administration are needed. This work describes the development of a novel biodegradable polyanhydride nanoparticle-based vaccine platform administered as a single intranasal dose that induced long-lived protective immunity against respiratory disease caused by Yesinia pestis, the causative agent of pneumonic plague. Relative to the responses induced by the recombinant protein F1-V alone and MPLA-adjuvanted F1-V, the nanoparticle-based vaccination regimen induced an immune response that was characterized by high titer and high avidity IgG1 anti-F1-V antibody that persisted for at least 23 weeks post-vaccination. After challenge, no Y. pestis were recovered from the lungs, livers, or spleens of mice vaccinated with the nanoparticle-based formulation and histopathological appearance of lung, liver, and splenic tissues from these mice post-vaccination was remarkably similar to uninfected control mice.
AB - Despite the successes provided by vaccination, many challenges still exist with respect to controlling new and re-emerging infectious diseases. Innovative vaccine platforms composed of adaptable adjuvants able to appropriately modulate immune responses, induce long-lived immunity in a single dose, and deliver immunogens in a safe and stable manner via multiple routes of administration are needed. This work describes the development of a novel biodegradable polyanhydride nanoparticle-based vaccine platform administered as a single intranasal dose that induced long-lived protective immunity against respiratory disease caused by Yesinia pestis, the causative agent of pneumonic plague. Relative to the responses induced by the recombinant protein F1-V alone and MPLA-adjuvanted F1-V, the nanoparticle-based vaccination regimen induced an immune response that was characterized by high titer and high avidity IgG1 anti-F1-V antibody that persisted for at least 23 weeks post-vaccination. After challenge, no Y. pestis were recovered from the lungs, livers, or spleens of mice vaccinated with the nanoparticle-based formulation and histopathological appearance of lung, liver, and splenic tissues from these mice post-vaccination was remarkably similar to uninfected control mice.
UR - http://www.scopus.com/inward/record.url?scp=79952285914&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79952285914&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0017642
DO - 10.1371/journal.pone.0017642
M3 - Article
C2 - 21408610
AN - SCOPUS:79952285914
SN - 1932-6203
VL - 6
JO - PloS one
JF - PloS one
IS - 3
M1 - e17642
ER -