Advances in the design and delivery of peptide subunit vaccines with a focus on Toll-like receptor agonists

被引:39
作者
Black, Matthew [2 ]
Trent, Amanda [2 ]
Tirrell, Matthew [2 ,3 ]
Olive, Colleen [1 ]
机构
[1] Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[2] Univ Calif Santa Barbara, Santa Barbara, CA 93106 USA
[3] Univ Calif Berkeley, Berkeley, CA 94720 USA
关键词
adjuvant; antigen delivery system; liposome; micelle; nanoparticle; peptide; subunit vaccine; Toll-like receptor; virus-like particle; T-CELL RESPONSES; VIRUS-LIKE PARTICLES; DNA/CATIONIC LIPOSOME COMPLEX; PLASMACYTOID DENDRITIC CELLS; ANTIGEN-CONTAINING LIPOSOMES; BINDING PREDICTION SERVERS; HEPATITIS-B-VACCINE; MHC CLASS-I; IMMUNE-RESPONSE; SYNTHETIC LIPOPEPTIDES;
D O I
10.1586/ERV.09.160
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Considerable success has been made with many peptide antigen formulations, and peptide-based vaccines are emerging as the next generation of prophylactic and remedial immunotherapy. However, finding an optimal platform balancing all of the requirements for an effective, specific and safe immune response remains a major challenge for many infectious and chronic diseases. This review outlines how peptide immunogenicity is influenced by the way in which peptides are presented to the immune system, underscoring the need for multifunctional delivery systems that couple antigen and adjuvant into a single construct. Particular attention is given to the ability of Toll-like receptor agonists to act as adjuvants. A survey of recent approaches to developing peptide antigen delivery systems is given, many of which incorporate Toll-like receptor agonists into the design.
引用
收藏
页码:157 / 173
页数:17
相关论文
共 193 条
[1]   Structure-activity relationship of a series of synthetic lipopeptide self-adjuvanting group A streptococcal vaccine candidates [J].
Abdel-Aal, Abu-Baker M. ;
Batzloff, Michael R. ;
Fujita, Yoshio ;
Barozzi, Nadia ;
Faria, Andres ;
Simerska, Pavia ;
Moyle, Peter M. ;
Good, Michael F. ;
Toth, Istvan .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (01) :167-172
[2]   Toll-like receptors: critical proteins linking innate and acquired immunity [J].
Akira, S ;
Takeda, K ;
Kaisho, T .
NATURE IMMUNOLOGY, 2001, 2 (08) :675-680
[3]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[4]   Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T gondii infection [J].
Aline, F ;
Bout, D ;
Amigorena, S ;
Roingeard, P ;
Dimier-Poisson, I .
INFECTION AND IMMUNITY, 2004, 72 (07) :4127-4137
[5]   Exosomes as potent cell-free peptide-based vaccine.: I.: Dendritic cell-derived exosomes transfer functional MHC class I/peptide complexes to dendritic cells [J].
André, F ;
Chaput, N ;
Schartz, NEC ;
Flament, C ;
Aubert, N ;
Bernard, J ;
Lemonnier, F ;
Raposo, G ;
Escudier, B ;
Hsu, DH ;
Tursz, T ;
Amigorena, S ;
Angevin, E ;
Zitvogel, L .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :2126-2136
[6]  
Aucouturier Jerome, 2002, Expert Rev Vaccines, V1, P111, DOI 10.1586/14760584.1.1.111
[7]   Broadening the approaches to developing more effective vaccines [J].
Babiuk, LA .
VACCINE, 1999, 17 (13-14) :1587-1595
[8]   Neutralizing antiviral B cell responses [J].
Bachmann, MF ;
Zinkernagel, RM .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :235-270
[9]   TLR9 regulates Th1 responses and cooperates with TLR2 in mediating optimal resistance to Mycobacterium tuberculosis [J].
Bafica, A ;
Scanga, CA ;
Feng, CG ;
Leifer, C ;
Cheever, A ;
Sher, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (12) :1715-1724
[10]   MyD88-dependent and MyD88-independent pathways in synergy, priming, and tolerance between TLR agonists [J].
Bagchi, Aranya ;
Herrup, Elizabeth A. ;
Warren, H. Shaw ;
Trigilio, James ;
Shin, Hae-Sook ;
Valentine, Catherine ;
Hellman, Judith .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :1164-1171