The same well-characterized T cell epitope SIINFEKL expressed in the context of a cytoplasmic or secreted protein in BCG induces different CD8+ T cell responses

被引:9
作者
Hulseberg, Paul D. [1 ]
Zozulya, Alla [1 ]
Chu, Hamlet H. [1 ]
Triccas, James A. [2 ]
Fabry, Zsuzsanna [1 ]
Sandor, Matyas [1 ]
机构
[1] Univ Wisconsin, Dept Pathol & Lab Sci, Madison, WI 53706 USA
[2] Univ Sydney, Centenary Inst Canc Med & Cell Biol, Sydney, NSW 2006, Australia
关键词
Mycobacterium; CD8(+) T cell responses; Antigen location; CLASS-I PRESENTATION; MYCOBACTERIUM-TUBERCULOSIS INFECTION; DENDRITIC CELLS; CROSS-PRESENTATION; ANTIGEN PRESENTATION; EXOGENOUS ANTIGENS; LISTERIA-MONOCYTOGENES; PARTICULATE ANTIGENS; PROCESSING PATHWAY; TAP-DEFICIENT;
D O I
10.1016/j.imlet.2009.12.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mycobacterium bovis BCG is still the most widely used vaccine against tuberculosis and CD8(+) T cells play important roles in fighting infection. We investigated how well antigen is processed and presented to CD8(+) T cells using the same well-characterized CD8(+) T cell epitope SIINFEKL expressed in either a cytoplasmic (GFP-OVA) or secreted (85B-OVA) context from BCG. We report that secreted SIINFEKL from 85B-OVA BCG is presented better than cytoplasmic SIINFEKL expressed by GFP-OVA BCG. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:36 / 42
页数:7
相关论文
共 49 条
[1]  
*2009 WR, 2009, GLOB TUB CONTR
[2]   Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12889-12894
[3]   A role for the endoplasmic reticulum protein retrotranslocation machinery during crosspresentation by dendritic cells [J].
Ackerman, Anne L. ;
Giodini, Alessandra ;
Cresswell, Peter .
IMMUNITY, 2006, 25 (04) :607-617
[4]   The success and failure of BCG - implications for a novel tuberculosis vaccine [J].
Andersen, P ;
Doherty, TM .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (08) :656-662
[5]   MHC Class I Endosomal and Lysosomal Trafficking Coincides with Exogenous Antigen Loading in Dendritic Cells [J].
Basha, Genc ;
Lizee, Gregory ;
Reinicke, Anna T. ;
Seipp, Robyn P. ;
Omilusik, Kyla D. ;
Jefferies, Wilfred A. .
PLOS ONE, 2008, 3 (09)
[6]   Trafficking and release of mycobacterial lipids from infected macrophages [J].
Beatty, WL ;
Rhoades, ER ;
Ullrich, HJ ;
Chatterjee, D ;
Heuser, JE ;
Russell, DG .
TRAFFIC, 2000, 1 (03) :235-247
[7]   Mycobacterial surface moieties are released from infected macrophages by a constitutive exocytic event [J].
Beatty, WL ;
Ullrich, HJ ;
Russell, DG .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2001, 80 (01) :31-40
[8]   Identification of mycobacterial surface proteins released into subcellular compartments of infected macrophages [J].
Beatty, WL ;
Russell, DG .
INFECTION AND IMMUNITY, 2000, 68 (12) :6997-7002
[9]   Bacterial proteins can be processed by macrophages in a transporter associated with antigen processing-independent, cysteine protease-dependent manner for presentation by MHC class I molecules [J].
Campbell, DJ ;
Serwold, T ;
Shastri, N .
JOURNAL OF IMMUNOLOGY, 2000, 164 (01) :168-175
[10]   Alternative processing for MHC class I presentation by immature and CpG-activated dendritic cells [J].
Chen, LY ;
Jondal, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (04) :952-960