Induction of lymphocytes activated marker CD69 following exposure to chitosan and alginate biopolymers

被引:39
作者
Borges, Olga
Orchard, Gerrit B.
de Sousa, Adriano
Junginger, Hans E.
Cordeiro-da-Silva, Anabela
机构
[1] Univ Coimbra, Fac Pharm, Pharmaceut Technol Lab, Ctr Pharmaceut Studies, P-3000295 Coimbra, Portugal
[2] Univ Geneva, Sch Pharm Geneva Lausanne, CH-1211 Geneva, Switzerland
[3] Naresuan Univ, Fac Pharmaceut Sci, Phitsanulok 65000, Thailand
[4] Univ Porto, Fac Pharm, Inst Mol & Cell Biol, Biochem Lab, P-4050047 Oporto, Portugal
关键词
CD69; expression; chitosan; alginate; CpG ODN; lymphocyte activation;
D O I
10.1016/j.ijpharm.2007.01.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CD69 is a very early cell activation antigen expressed on the surface of activated immune cells. It can appear within 1-2 h of activation and exhibits maximal expression levels between 18 and 24 h after stimulation. In this work, the expression profile of CD69 in mice splenocytes was evaluated following exposure to the biopolymers, chitosan or alginate and the immunostimulatory factors, CpG ODN 1826 or concanavalin A. We have shown that both polymers are able to upregulate expression of CD69 on B cells and CD4+ T-lymphocytes, with alginate as the least potent stimulus. Moreover, the expression of the CD69 molecule on CD8+ T-lymphocytes was observed only in splenocytes cultured with chitosan. However, activation of lymphocytes, did not result in cell proliferation. On the other hand, CpG ODN proved to be a potent B cell stimulator, as evidenced by the upregulation of CD69, but had less effect on T-cells. These results, together with previous discoveries reported in scientific literature, may contribute to the clarification of the adjuvant effect, which has been attributed to chitosan and alginate formulations or to the biopolymers itself. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:254 / 264
页数:11
相关论文
共 39 条
[1]   Differential levels of dendritic cell maturation on different biomaterials used in combination products [J].
Babensee, JE ;
Paranjpe, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 74A (04) :503-510
[2]   Protective immune responses to meningococcal C conjugate vaccine after intranasal immunization of mice with the LTK63 mutant plus chitosan or trimethyl chitosan chloride as novel delivery platform [J].
Baudner, BC ;
Verhoef, JC ;
Giuliani, MM ;
Peppoloni, S ;
Rappuoli, R ;
Del Giudice, G ;
Junginger, HE .
JOURNAL OF DRUG TARGETING, 2005, 13 (8-9) :489-498
[3]   Chitosan-induced phospholipase A2 activation and arachidonic acid mobilization in P388D1 macrophages [J].
Bianco, ID ;
Balsinde, J ;
Beltramo, DM ;
Castagna, LF ;
Landa, CA ;
Dennis, EA .
FEBS LETTERS, 2000, 466 (2-3) :292-294
[4]   Preparation of coated nanoparticles for a new mucosal vaccine delivery system [J].
Borges, O ;
Borchard, G ;
Verhoef, JC ;
de Sousa, A ;
Junginger, HE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 299 (1-2) :155-166
[5]   Uptake studies in rat Peyer's patches, cytotoxicity and release studies of alginate coated chitosan nanoparticles for mucosal vaccination [J].
Borges, Olga ;
Cordeiro-da-Silva, Anabela ;
Romeijn, Stefan G. ;
Amidi, Maryam ;
de Sousa, Adriano ;
Borchard, Gerrit ;
Junginger, Hans E. .
JOURNAL OF CONTROLLED RELEASE, 2006, 114 (03) :348-358
[6]  
Davis HL, 1998, J IMMUNOL, V160, P870
[7]   Effect of chitosan on epithelial permeability and structure [J].
Dodane, V ;
Khan, MA ;
Merwin, JR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :21-32
[8]   Chitosan: A unique polysaccharide for drug delivery [J].
Felt, O ;
Buri, P ;
Gurny, R .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1998, 24 (11) :979-993
[9]   A potential role for CD69 in thymocyte emigration [J].
Feng, CG ;
Woodside, KJ ;
Vance, BA ;
El-Khoury, D ;
Canelles, M ;
Lee, J ;
Gress, R ;
Fowlkes, BJ ;
Shores, EW ;
Love, PE .
INTERNATIONAL IMMUNOLOGY, 2002, 14 (06) :535-544
[10]   Involvement of Toll-like receptor (TLR) 2 and TLR4 in cell activation by mannuronic acid polymers [J].
Flo, TH ;
Ryan, L ;
Latz, E ;
Takeuchi, O ;
Monks, BG ;
Lien, E ;
Halaas, O ;
Akira, S ;
Skjåk-Bræk, G ;
Golenbock, DT ;
Espevik, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (38) :35489-35495