Generation of dendritic cells from rabbit bone marrow mononuclear cell cultures supplemented with hGM-CSF and hIL-4

被引:14
作者
Cody, V
Shen, H
Shlyankevich, M
Tigelaar, RE
Brandsma, JL
Hanlon, DJ
机构
[1] Yale Univ, Dept Dermatol, Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Dept Biomed Engn, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Comparat Med Sect, New Haven, CT 06520 USA
关键词
dendritic cell; rabbit; bone inarrow; GM-CSF; IL-4;
D O I
10.1016/j.vetimm.2004.08.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The in vitro generation of dendritic cells (DCs) from either blood or bone marrow has been accomplished for humans and a number of other species. This ability has facilitated the opportunity to test the efficacy of DC vaccines in various tumor models. The cottontail rabbit papillomavirus (CRPV) model is the most clinically relevant animal model for human papillomavirus (HPV)-associated carcinogenesis. The CRPV model has been used to test various preventative and therapeutic vaccination strategies, and the availability of rabbit DCs would further expand its utility, However. to date, rabbit DCs have not been phenotypically and/or functionally characterized. Here we show that DCs can be generated in vitro from rabbit bone marrow mononuclear cells (BMMCs) cultured in the presence of the human cytokines GM-CSF and IL-4 and matured with lipopolysaccharide (LPS). These cells show upregulation of MHC class II and CD86. as well as downregulation of CD14. do not have non-specific esterase activity, are able to perform receptor-mediated endocytosis. and are potent stimulators of allogeneic T cell proliferation in mixed lymphocyte reactions. The ability to generate rabbit DCs makes it possible to test the efficacy of DC vaccination in the prevention and treatment of CRPV-induced lesions. which may provide useful preclinical data regarding the use of DC vaccines for HPV-associated lesions, including cervical cancer. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 172
页数:10
相关论文
共 38 条
[1]  
Bai L, 2002, INT J ONCOL, V20, P247
[2]   Chimpanzee dendritic cells with potent immunostimulatory function can be propagated from peripheral blood [J].
BarrattBoyes, SM ;
Henderson, RA ;
Finn, OJ .
IMMUNOLOGY, 1996, 87 (04) :528-534
[3]   Immunophenotype and functional properties of feline dendritic cells derived from blood and bone marrow [J].
Bienzle, D ;
Reggeti, F ;
Clark, ME ;
Chow, C .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2003, 96 (1-2) :19-30
[4]   Vaccination of rabbits with an adenovirus vector expressing the papillomavirus E2 protein leads to clearance of papillomas and infection [J].
Brandsma, JL ;
Shlyankevich, M ;
Zhang, LX ;
Slade, MD ;
Goodwin, EC ;
Peh, W ;
Deisseroth, AB .
JOURNAL OF VIROLOGY, 2004, 78 (01) :116-123
[5]  
BRANDSMA JL, 1996, PAPILLOMAVIRUS REV C, P69
[6]   Origin, maturation and antigen presenting function of dendritic cells [J].
Cella, M ;
Sallusto, F ;
Lanzavecchia, A .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :10-16
[7]   Active immunization using dendritic cells mixed with tumor cells inhibits the growth of primary breast cancer [J].
Coveney, E ;
Wheatley, GH ;
Lyerly, HK .
SURGERY, 1997, 122 (02) :228-234
[8]   Dendritic cells charged with apoptotic tumor cells induce long-lived protective CD4+ and CD8+ T cell immunity against B16 melanoma [J].
Goldszmid, RS ;
Idoyaga, J ;
Bravo, AI ;
Steinman, R ;
Mordoh, J ;
Wainstok, R .
JOURNAL OF IMMUNOLOGY, 2003, 171 (11) :5940-5947
[9]   Ex vivo expansion of canine dendritic cells from CD34+ bone marrow progenitor cells [J].
Hägglund, HG ;
McSweeney, PA ;
Mathioudakis, G ;
Bruno, B ;
Georges, GE ;
Gass, MJ ;
Moore, P ;
Sale, GE ;
Storb, R ;
Nash, RA .
TRANSPLANTATION, 2000, 70 (10) :1437-1442
[10]   Functional characterization of equine dendritic cells propagated ex vivo using recombinant human GM-CSF and recombinant equine IL-4 [J].
Hammond, SA ;
Horohov, D ;
Montelaro, RC .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1999, 71 (3-4) :197-214