Human cytomegalovirus pp65-and immediate early 1 antigen-specific HLA class I-restricted cytotoxic T cell responses induced by cross-presentation of viral antigens

被引:76
作者
Tabi, Z [1 ]
Moutaftsi, M [1 ]
Borysiewicz, LK [1 ]
机构
[1] Univ Wales Coll Cardiff, Coll Med, Dept Med, Cardiff CF14 4XX, S Glam, Wales
关键词
D O I
10.4049/jimmunol.166.9.5695
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) play a pivotal role in the development of anti-viral CD8(+) CTL responses. This is straightforward if they are directly infected with virus, but is less clear in response to viruses that cannot productively infect DCs. Human CMV (HCMV) shows strain-specific cell tropism: fibroblast (Fb)-adapted laboratory strains (AD169) and recent clinical isolates do not infect DCs, whereas endothelial cell-adapted strains (TB40/E) result in productive lytic DC infection. However, we show here that uninfected DCs induce CD8(+) T cell cytotoxicity and IFN-gamma production against HCMV pp65 and immediate early 1 Ags following in vitro coculture with HCMV-AD169-infected Fbs, regardless of the HLA type of these Fbs. CD8(+) T cell stimulation was inhibited by pretreatment of DCs with cytochalasin B or brefeldin A, indicating a phagosome/endosome to cytosol pathway. HCMV-infected Fbs were not apoptotic as measured by annexin V binding, and induction of apoptosis of infected Fbs in vitro did not augment CTL induction by DCs, suggesting a mechanism other than apoptosis in the initiation of cross-presentation. Furthermore, HCMV-infected Fbs provided a maturation signal for immature DCs during coculture, as evidenced by increased CD83 and HLA class II expression. Cross-presentation of HCMV Ags by host DCs enables these professional APCs to bypass some of the evasion mechanisms HCMV has developed to avoid T cell recognition. It may also serve to explain the presence of immediate early 1 Ag-specific CTLs in the face of pp65-induced inhibition of Ag presentation at the level of the infected cell.
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页码:5695 / 5703
页数:9
相关论文
共 57 条
[1]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[2]   Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes [J].
Albert, ML ;
Pearce, SFA ;
Francisco, LM ;
Sauter, B ;
Roy, P ;
Silverstein, RL ;
Bhardwaj, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) :1359-1368
[3]   FINE SPECIFICITY OF CELLULAR IMMUNE-RESPONSES IN HUMANS TO HUMAN CYTOMEGALOVIRUS IMMEDIATE-EARLY 1-PROTEIN [J].
ALP, NJ ;
ALLPORT, TD ;
VANZANTEN, J ;
RODGERS, B ;
SISSONS, JGP ;
BORYSIEWICZ, LK .
JOURNAL OF VIROLOGY, 1991, 65 (09) :4812-4820
[4]  
Arnold-Schild D, 1999, J IMMUNOL, V162, P3757
[5]   Incoming human cytomegalovirus pp65 (UL83) contained in apoptotic infected fibroblasts is cross-presented to CD8+ T cells by dendritic cells [J].
Arrode, G ;
Boccaccio, C ;
Lule, J ;
Allart, S ;
Moinard, N ;
Abastado, JP ;
Alam, A ;
Davrinche, C .
JOURNAL OF VIROLOGY, 2000, 74 (21) :10018-10024
[6]   Dendritic cells process exogenous viral proteins and virus-like particles for class I presentation to CD8(+) cytotoxic T lymphocytes [J].
Bachmann, MF ;
Lutz, MB ;
Layton, GT ;
Harris, SJ ;
Fehr, T ;
Rescigno, M ;
RicciardiCastagnoli, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (11) :2595-2600
[7]   Apoptosis regulators from DNA viruses [J].
Barry, M ;
McFadden, G .
CURRENT OPINION IN IMMUNOLOGY, 1998, 10 (04) :422-430
[8]   Chemokine sequestration by viral chemoreceptors as a novel viral escape strategy: Withdrawal of chemokines from the environment of cytomegalovirus-infected cells [J].
Bodaghi, B ;
Jones, TR ;
Zipeto, D ;
Vita, C ;
Sun, L ;
Laurent, L ;
Arenzana-Seisdedos, F ;
Virelizier, JL ;
Michelson, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (05) :855-866
[9]   Recognition of human cytomegalovirus gene products by HCMV-specific cytotoxic T cells [J].
Boppana, SB ;
Britt, WJ .
VIROLOGY, 1996, 222 (01) :293-296
[10]   HUMAN CYTOMEGALOVIRUS-SPECIFIC CYTO-TOXIC T-CELLS - RELATIVE FREQUENCY OF STAGE-SPECIFIC CTL RECOGNIZING THE 72-KD IMMEDIATE EARLY PROTEIN AND GLYCOPROTEIN-B EXPRESSED BY RECOMBINANT VACCINIA VIRUSES [J].
BORYSIEWICZ, LK ;
HICKLING, JK ;
GRAHAM, S ;
SINCLAIR, J ;
CRANAGE, MP ;
SMITH, GL ;
SISSONS, JGP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :919-931