TY - JOUR
T1 - Novel concepts for HIV vaccine vector design
AU - Alayo, Quazim A.
AU - Provine, Nicholas M.
AU - Penaloza-MacMaster, Pablo
N1 - Funding Information:
This work was supported by grants from the Chicago Centers for AIDS Research (P30 AI117943) and the NIH (1K22AI118421) to P.P.-M
PY - 2017/11/1
Y1 - 2017/11/1
N2 - The unprecedented challenges of developing effective vaccines against intracellular pathogens such as HIV, malaria, and tuberculosis have resulted in more rational approaches to vaccine development. Apart from the recent advances in the design and selection of improved epitopes and adjuvants, there are also ongoing efforts to optimize delivery platforms. Viral vectors are the best-characterized delivery tools because of their intrinsic adjuvant capability, unique cellular tropism, and ability to trigger robust adaptive immune responses. However, a known limitation of viral vectors is preexisting immunity, and ongoing efforts are aimed at developing novel vector platforms with lower seroprevalence. It is also becoming increasingly clear that different vectors, even those derived from phylogenetically similar viruses, can elicit substantially distinct immune responses, in terms of quantity, quality, and location, which can ultimately affect immune protection. This review provides a summary of the status of viral vector development for HIV vaccines, with a particular focus on novel viral vectors and the types of adaptive immune responses that they induce.
AB - The unprecedented challenges of developing effective vaccines against intracellular pathogens such as HIV, malaria, and tuberculosis have resulted in more rational approaches to vaccine development. Apart from the recent advances in the design and selection of improved epitopes and adjuvants, there are also ongoing efforts to optimize delivery platforms. Viral vectors are the best-characterized delivery tools because of their intrinsic adjuvant capability, unique cellular tropism, and ability to trigger robust adaptive immune responses. However, a known limitation of viral vectors is preexisting immunity, and ongoing efforts are aimed at developing novel vector platforms with lower seroprevalence. It is also becoming increasingly clear that different vectors, even those derived from phylogenetically similar viruses, can elicit substantially distinct immune responses, in terms of quantity, quality, and location, which can ultimately affect immune protection. This review provides a summary of the status of viral vector development for HIV vaccines, with a particular focus on novel viral vectors and the types of adaptive immune responses that they induce.
KW - Antibodies
KW - Human immunodeficiency virus
KW - T cells
KW - Vaccines
UR - http://www.scopus.com/inward/record.url?scp=85041545660&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85041545660&partnerID=8YFLogxK
U2 - 10.1128/mSphere.00415-17
DO - 10.1128/mSphere.00415-17
M3 - Short survey
C2 - 29242831
AN - SCOPUS:85041545660
VL - 2
JO - mSphere
JF - mSphere
SN - 2379-5042
IS - 6
M1 - e00415-17
ER -