The Utility of Poly(γ-glutamic acid) Nanoparticles as Antigen Delivery Carriers in Dendritic Cell-Based Cancer Immunotherapy

被引:16
作者
Matsuo, Keisuke [1 ]
Ishii, Yumiko [1 ]
Matsuo, Kazuhiko [1 ]
Yoshinaga, Tomoyo [1 ]
Akashi, Mitsuru [2 ,3 ]
Mukai, Yohei [1 ]
Yoshioka, Yasuo [1 ,2 ]
Okada, Naoki [1 ]
Nakagawa, Shinsaku [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Biotechnol & Therapeut, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Ctr Adv Med Engn & Informat, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
关键词
poly(gamma glutamic acid) nanoparticle; antigen delivery carrier; dendritic cell; AMPHIPHILIC GAMMA-PGA; CLASS-I PRESENTATION; MHC CLASS-I; TUMOR-VACCINE; T-CELLS; MATURATION; IMMUNITY; MOLECULES; RESPONSES; CD80;
D O I
10.1248/bpb.33.2003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cytotoxic T-lymphocytes (CTLs) specific for tumor-associated antigens (TAAs) act in the immune surveillance system as major effector cells to eliminate malignant cells Immunization with TAA-loaded dendritic cells (DCs) has great potential for treating cancer, because DCs are potent antigen-presenting cells capable of inducing antigen-specific CTLs by the primary activation of naive T-lymphocytes The establishment of a non-cyto-toxic and efficient antigen delivery method is required to Improve the efficacy of DC-based cancer immunotherapy We developed biodegradable poly(gamma-glutamic acid) nanoparticles (gamma-PGA NPs) that can efficiently entrap various proteins as antigen delivery carriers gamma-PGA NPs efficiently delivered entrapped antigenic proteins into DCs without cytotoxicity and presented antigens to DCs via major histocompatibility complex class I and II molecules Immunization with TAA-loaded DCs using gamma-PGA NPs inhibited tumor growth by inducing TAA-specific CTLs These findings indicate that gamma-PGA NPs can function as useful antigen delivery carriers in DC-based cancer Immunotherapy
引用
收藏
页码:2003 / 2007
页数:5
相关论文
共 23 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   Preparation and characterization of biodegradable nanoparticles based on poly(γ-glutamic acid) with L-phenylalanine as a protein carrier [J].
Akagi, T ;
Kaneko, T ;
Kida, T ;
Akashi, M .
JOURNAL OF CONTROLLED RELEASE, 2005, 108 (2-3) :226-236
[3]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[4]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[5]   Co-inhibitory molecules of the B7-CD28 family in the control of T-cell immunity [J].
Chen, LP .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (05) :336-347
[6]  
de Vries IJM, 2003, CLIN CANCER RES, V9, P5091
[7]   Regulation of dendritic cell numbers and maturation by lipopolysaccharide in vivo [J].
DeSmedt, T ;
Pajak, B ;
Muraille, E ;
Lespagnard, L ;
Heinen, E ;
DeBaetselier, P ;
Urbain, J ;
Leo, O ;
Moser, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (04) :1413-1424
[8]   Rapid generation of broad T-cell immunity in humans after a single injection of mature dendritic cells [J].
Dhodapkar, MV ;
Steinman, RM ;
Sapp, M ;
Desai, H ;
Fossella, C ;
Krasovsky, J ;
Donahoe, SM ;
Dunbar, PR ;
Cerundolo, V ;
Nixon, DF ;
Bhardwaj, N .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (02) :173-180
[9]  
Machy P, 2000, EUR J IMMUNOL, V30, P848, DOI 10.1002/1521-4141(200003)30:3<848::AID-IMMU848>3.0.CO
[10]  
2-Q