Orally administered OVA/CpG-ODN induces specific mucosal and systemic immune response in young and aged mice

被引:55
作者
Alignani, D [1 ]
Maletto, B [1 ]
Liscovsky, M [1 ]
Rópolo, A [1 ]
Morón, G [1 ]
Pistoresi-Palencia, MC [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, CONICET, CIBICI,Dept Bioquim Clin, RA-5000 Cordoba, Argentina
关键词
adjuvants; aging;
D O I
10.1189/jlb.0604330
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously demonstrated that subcutaneously administered ovalbumin (OVA) plus synthetic oligodeoxynucleotides containing immunostimulatory CpG motifs (CpG-ODN) as adjuvant stimulate cellular and humoral immunity and promote T helper cell type I differentiation in aged mice. The present study assessed the ability of CpG-ODN to induce an OVA-specific immune respouse after oral immunization in young (3-month-old) and aged (18-month-old) BALB/c mice. Oral OVA/CpG-ODN immunization induces a similar OVA-specific T cell-proliferative response (in mucosal and systemic tissues), immunoglobulin G (IgG) in plasma, and IgA in intestinal washes in both groups of ages. The OVA-specific humoral immune response observed in aged mice was similar to the one observed in young mice, peaking at day 7 after the last oral immunization and was present over 40 days after the last oral immunization. The pattern of cytokines released in culture supernatants in both groups of mice was similar, with specific interferon-gamma secretion in the absence of interleukin-5 responses. These results provide evidence that orally administered OVA/CpG-ODN induces a young-like, specific, immune response against OVA in aged mice, showing that CpG-ODN might be used as a mucosal adjuvant during aging.
引用
收藏
页码:898 / 905
页数:8
相关论文
共 42 条
[1]   Bacterial CpG-DNA triggers activation and maturation of human CD11c-, CD123+ dendritic cells [J].
Bauer, M ;
Redecke, V ;
Ellwart, JW ;
Scherer, B ;
Kremer, JP ;
Wagner, H ;
Lipford, GB .
JOURNAL OF IMMUNOLOGY, 2001, 166 (08) :5000-5007
[2]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[3]   Bacterial DNA-induced NK cell IFN-gamma production is dependent on macrophage secretion of IL-12 [J].
Chace, JH ;
Hooker, NA ;
Mildenstein, KL ;
Krieg, AM ;
Cowdery, JS .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 84 (02) :185-193
[4]   Affinity of anti-GM1 antibodies in Guillain-Barre syndrome patients [J].
Deisenhammer, F ;
Keir, G ;
Pfausler, B ;
Thompson, EJ .
JOURNAL OF NEUROIMMUNOLOGY, 1996, 66 (1-2) :85-93
[5]   Recent advances in mucosal vaccines and adjuvants [J].
Eriksson, K ;
Holmgren, J .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (05) :666-672
[6]   Peyer's patches are required for oral tolerance to proteins [J].
Fujihashi, K ;
Dohi, T ;
Rennert, PD ;
Yamamoto, M ;
Koga, T ;
Kiyono, H ;
McGhee, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3310-3315
[7]   Immunosenescence and infectious diseases [J].
Ginaldi, L ;
Loreto, MF ;
Corsi, MP ;
Modesti, M ;
De Martinis, M .
MICROBES AND INFECTION, 2001, 3 (10) :851-857
[8]   Ageing of lymphocytes and lymphocytes in the aged [J].
Globerson, A ;
Effros, RB .
IMMUNOLOGY TODAY, 2000, 21 (10) :515-521
[9]   The aging of the immune system [J].
Grubeck-Loebenstein, B ;
Wick, G .
ADVANCES IN IMMUNOLOGY, VOL 80, 2002, 80 :243-284
[10]   INDUCTION OF SPECIFIC IMMUNOGLOBULIN-A IN THE SMALL-INTESTINE, COLON-RECTUM, AND VAGINA MEASURED BY A NEW METHOD FOR COLLECTION OF SECRETIONS FROM LOCAL MUCOSAL SURFACES [J].
HANEBERG, B ;
KENDALL, D ;
AMERONGEN, HM ;
APTER, FM ;
KRAEHENBUHL, JP ;
NEUTRA, MR .
INFECTION AND IMMUNITY, 1994, 62 (01) :15-23