The influence of mineral trioxide aggregate on adaptive immune responses to endodontic pathogens in mice

被引:14
作者
Berto Rezende, Taia Maria [1 ,2 ]
Veira, Leda Quercia [3 ]
Ribeiro Sobrinho, Antonio Paulino [2 ]
Oliveira, Ricardo Reis [2 ]
Taubman, Martin A. [1 ]
Kawai, Toshihisa [1 ]
机构
[1] Forsyth Inst, Dept Immunol, Boston, MA 02115 USA
[2] Univ Fed Minas Gerais, Fac Odontol, Dept Dent Restauradora, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
关键词
bacteria; cytokine; immunoglobulin antibody; mineral trioxide aggregate; T cells;
D O I
10.1016/j.joen.2008.06.006
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
This study assessed the influence of mineral trioxide aggregate (MTA) on adaptive immune responses. BALB/c mice were immunized with heat-killed Fusobacterium nucleatum (Fn) in MTA or other control adjuvants, and serum IgG responses to Fn were measured. Either Fn- or Peptostreptococcus anaerobius (Pa)-reactive memory T cells (Tm) were preincubated in vitro with/without MTA and restimulated with Fn or Pa. Tm proliferation and cytokine production were assessed. Compared with control groups, immunoglobulin G-antibody responses were upregulated in mice immunized with Fn in MTA in a similar manner to animals immunized with Fn in Freund's adjuvant or aluminum hydroxide adjuvant. Although MTA did not affect the upregulated expression of interleukin 10, tumor necrosis factor a, or RANKL by Tm, it suppressed the proliferation of Pa- or Fn-Tm and inhibited their production of Th1- or Th2-signature cytokines. MTA upregulated the adaptive humoral immune responses but had little or no effect on pro- or anti-inflammatory cytokine production by Tm.
引用
收藏
页码:1066 / 1071
页数:6
相关论文
共 20 条
[1]
Chemical differences between white and gray mineral trioxide aggregate [J].
Asgary, S ;
Parirokh, M ;
Eghbal, MJ ;
Brink, F .
JOURNAL OF ENDODONTICS, 2005, 31 (02) :101-103
[2]
Aluminum salts in vaccines - US perspective [J].
Baylor, NW ;
Egan, W ;
Richman, P .
VACCINE, 2002, 20 :S18-S23
[3]
Requirement of B7 costimulation for Th1-mediated inflammatory bone resorption in experimental periodontal disease [J].
Kawai, T ;
Eisen-Lev, R ;
Seki, M ;
Eastcott, JW ;
Wilson, ME ;
Taubman, MA .
JOURNAL OF IMMUNOLOGY, 2000, 164 (04) :2102-2109
[4]
Kinetics of macrophages and lymphoid cells during the development of experimentally induced periapical lesions in rat molars: A quantitative immunohistochemical study [J].
Kawashima, N ;
Okiji, T ;
Kosaka, T ;
Suda, H .
JOURNAL OF ENDODONTICS, 1996, 22 (06) :311-316
[5]
Microorganisms isolated from root canals presenting necrotic pulp and their drug susceptibility in vitro [J].
Lana, MA ;
Ribeiro-Sobrinho, AP ;
Stehling, R ;
Garcia, GD ;
Silva, BKC ;
Hamdan, JS ;
Nicoll, JR ;
Carvalho, MAR ;
Farias, LD .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2001, 16 (02) :100-105
[6]
In vitro evaluation of the cytotoxicity of two root canal sealers on macrophage activity [J].
Mendes, STD ;
Sobrinho, APR ;
de Carvalho, AT ;
Côrtes, MLD ;
Vieira, LQ .
JOURNAL OF ENDODONTICS, 2003, 29 (02) :95-99
[7]
Mechanisms of adjuvancy .1. metal oxides as adjuvants [J].
Naim, JO ;
vanOss, CJ ;
Wu, W ;
Giese, RF ;
Nickerson, PA .
VACCINE, 1997, 15 (11) :1183-1193
[8]
Vaccine adjuvants: Current state and future trends [J].
Petrovsky, N ;
Aguilar, JC .
IMMUNOLOGY AND CELL BIOLOGY, 2004, 82 (05) :488-496
[9]
IMMUNE COMPONENTS IN HUMAN DENTAL PERIAPICAL LESIONS [J].
PULVER, WH ;
TAUBMAN, MA ;
SMITH, DJ .
ARCHIVES OF ORAL BIOLOGY, 1978, 23 (06) :435-443
[10]
The effect of mineral trioxide aggregate on phagocytic activity and production of reactive oxygen, nitrogen species and arginase activity by M1 and M2 macrophages [J].
Rezende, T. M. B. ;
Vieira, L. Q. ;
Cardoso, F. P. ;
Oliveira, R. R. ;
de Oliveira Mendes, S. T. ;
Jorge, M. L. R. ;
Ribeiro Sobrinho, A. P. .
INTERNATIONAL ENDODONTIC JOURNAL, 2007, 40 (08) :603-611