4.2 Review

Adjuvants for HIV vaccines

Journal

CURRENT OPINION IN HIV AND AIDS
Volume 11, Issue 6, Pages 585-592

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/COH.0000000000000315

Keywords

adjuvant; Army Liposome Formulation; HIV; liposomes; monophosphoryl lipid A; vaccine

Funding

  1. Henry M. Jackson Foundation for the Advancement of Military Medicine [W81XWH-07-2-067]
  2. US Army Medical Research and Materiel Command (MRMC)

Ask authors/readers for more resources

Purpose of reviewAdvances in the understanding of the structural biology of HIV-1 proteins, and in the vulnerabilities of HIV-1 at various points in the infectious process have led to innovative approaches for vaccine constructs for clinical trials. Lessons from the successful Retrovirology study 144 (RV144) phase III Thai trial have revealed the need for novel and more potent adjuvant formulations. Fortunately, the vaccine adjuvant field is experiencing an emergence of innovative new adjuvants and strategies that may lead to improved formulations.Recent findingsThe review highlights the status of currently used and available new adjuvant formulations for HIV antigens. Adjuvants used in preclinical or in human clinical trials using HIV-1 protein antigens will be discussed along with adjuvant improvements for vectors and DNA immunization.SummaryThe HIV-1 immunogen and the design of the adjuvant formulations are both equally important for the development of an effective HIV vaccine. Adjuvants work by numerous different mechanisms, many of which are quite complex and often not well comprehended. Understanding the interplay of innate and adaptive immune responses that can be harnessed by adjuvant formulations would aid in the rational design of a well tolerated and effective vaccine formulation that can block HIV at the site of transmission.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available