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
[11]  
Harwood CA, 2000, J MED VIROL, V61, P289, DOI 10.1002/1096-9071(200007)61:3&lt
[12]  
289::AID-JMV2&gt
[13]  
3.0.CO
[14]  
2-Z
[15]   GENERATION OF LARGE NUMBERS OF DENDRITIC CELLS FROM MOUSE BONE-MARROW CULTURES SUPPLEMENTED WITH GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR [J].
INABA, K ;
INABA, M ;
ROMANI, N ;
AYA, H ;
DEGUCHI, M ;
IKEHARA, S ;
MURAMATSU, S ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1693-1702
[16]   Human papillomavirus and skin cancer [J].
Jenson, AB ;
Geyer, S ;
Sundberg, JP ;
Ghim, SJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS, 2001, 6 (03) :203-206
[17]  
KEENEY M, 2003, J BIOL REGUL HOMEOST, V17, P267
[18]   Human CD14(+) leukocytes acquire the phenotype and function of antigen-presenting dendritic cells when cultured in GM-CSF and IL-4 [J].
Kiertscher, SM ;
Roth, MD .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 59 (02) :208-218
[19]   THE SHOPE PAPILLOMA-CARCINOMA COMPLEX OF RABBITS - A MODEL SYSTEM OF NEOPLASTIC PROGRESSION AND SPONTANEOUS REGRESSION [J].
KREIDER, JW ;
BARTLETT, GL .
ADVANCES IN CANCER RESEARCH, 1981, 35 :81-110
[20]   Granulocyte-macrophage colony-stimulating factor priming plus papillomavirus E6 DNA vaccination: Effects on papilloma formation and regression in the cottontail rabbit papillomavirus-rabbit model [J].
Leachman, SA ;
Tigelaar, RE ;
Shlyankevich, M ;
Slade, MD ;
Irwin, M ;
Chang, E ;
Wu, TC ;
Xiao, W ;
Pazhani, S ;
Zelterman, D ;
Brandsma, JL .
JOURNAL OF VIROLOGY, 2000, 74 (18) :8700-8708