SELECTIVE KILLING OF HEPATITIS-B ENVELOPE ANTIGEN-SPECIFIC B-CELLS BY CLASS-I-RESTRICTED, EXOGENOUS ANTIGEN-SPECIFIC LYMPHOCYTES-T

被引:191
作者
BARNABA, V [1 ]
FRANCO, A [1 ]
ALBERTI, A [1 ]
BENVENUTO, R [1 ]
BALSANO, F [1 ]
机构
[1] IST MED CLIN,MED CLIN 2,I-35126 PADUA,ITALY
关键词
D O I
10.1038/345258a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
SPECIFIC B lymphocytes can act as very efficient antigen-presenting cells. They bind antigen with high affinity via their immunoglobulin receptors, process it through the class II major histocompatibility complex (MHC) pathway, and present its fragments to class II-restricted T lymphocytes1. In general, exogenous antigens and noninfectious viral particles enter the class II pathway and are selectively associated with class II MHC molecules2-4. The presentation of an exogenous antigen in association with class I molecules has been reported for only a few antigens, including the hepatitis B envelope antigen (HBenvAg)5-8. Here we demonstrate that antigen-specific B cells can efficiently deliver HBenvAg to the class I pathway, presenting its fragments to class I-restricted cytotoxic T lymphocytes (CTLs) which kill the specific B cells. This could represent a mechanism of suppression of neutralizing anti-hepatitis B virus (HBV) antibody response, a phenomenon that accompanies the development of the chronic HBV-carrier state. © 1990 Nature Publishing Group.
引用
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页码:258 / 260
页数:3
相关论文
共 24 条
[1]  
ALBERTI A, 1988, LANCET, V1, P1421
[2]  
BARNABA V, 1989, J IMMUNOL, V143, P2650
[3]   USE OF SYNTHETIC PEPTIDES OF INFLUENZA NUCLEOPROTEIN TO DEFINE EPITOPES RECOGNIZED BY CLASS-I-RESTRICTED CYTOTOXIC LYMPHOCYTES-T [J].
BASTIN, J ;
ROTHBARD, J ;
DAVEY, J ;
JONES, I ;
TOWNSEND, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (06) :1508-1523
[4]   CLASS DISCRIMINATION IN THE WORLD OF IMMUNOLOGY [J].
BEVAN, MJ .
NATURE, 1987, 325 (6101) :192-194
[5]   INVIVO PRIMING OF VIRUS-SPECIFIC CYTO-TOXIC LYMPHOCYTES-T WITH SYNTHETIC LIPOPEPTIDE VACCINE [J].
DERES, K ;
SCHILD, H ;
WIESMULLER, KH ;
JUNG, G ;
RAMMENSEE, HG .
NATURE, 1989, 342 (6249) :561-564
[6]   HEPATITIS-B SURFACE-ANTIGEN - AN UNUSUAL SECRETED PROTEIN INITIALLY SYNTHESIZED AS A TRANSMEMBRANE POLYPEPTIDE [J].
EBLE, BE ;
LINGAPPA, VR ;
GANEM, D .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1454-1463
[7]   THE INS AND OUTS OF ANTIGEN PROCESSING AND PRESENTATION [J].
GERMAIN, RN .
NATURE, 1986, 322 (6081) :687-689
[8]  
GOLDING H, 1985, J IMMUNOL, V135, P1610
[9]   HUMAN T-CELL RESPONSE TO THE SURFACE-ANTIGEN OF HEPATITIS-B VIRUS (HBSAG) - ENDOSOMAL AND NONENDOSOMAL PROCESSING PATHWAYS ARE ACCESSIBLE TO BOTH ENDOGENOUS AND EXOGENOUS ANTIGEN [J].
JIN, Y ;
SHIH, JWK ;
BERKOWER, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (01) :293-306
[10]   IS SUPPRESSION A FUNCTION OF CLASS-II RESTRICTED CYTO-TOXIC T-CELLS [J].
LANZAVECCHIA, A .
IMMUNOLOGY TODAY, 1989, 10 (05) :157-159