LYMPHOCYTE-T RESPONSE TO HEPATITIS-C VIRUS IN DIFFERENT CLINICAL COURSES OF INFECTION

被引:308
作者
BOTARELLI, P
BRUNETTO, MR
MINUTELLO, MA
CALVO, P
UNUTMAZ, D
WEINER, AJ
CHOO, QL
SHUSTER, JR
KUO, G
BONINO, F
HOUGHTON, M
ABRIGNANI, S
机构
[1] IRIS,VIA FIORENTINA 1,I-53100 SIENA,ITALY
[2] CIBA GEIGY AG,DEPT ALLERGY IMMUNOL,DIV RES,CH-4002 BASEL,SWITZERLAND
[3] OSPED MOLINETTE,DIV GASTROENTEROL,TURIN,ITALY
[4] CHIRON CORP,EMERYVILLE,CA
关键词
D O I
10.1016/0016-5085(93)90430-K
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: To assess the role played by the immune response in the outcome of hepatitis C virus infection, the CD4+ T-lymphocyte response to viral antigens was studied in infected individuals with different clinical courses. Methods: Using six recombinant proteins of hepatitis C virus, the study assessed the proliferative responses of peripheral blood mononuclear cells from 41 patients with chronic hepatitis C, 11 patients whose chronic hepatitis was successfully treated with interferon alfa and 11 healthy HCV seropositive individuals. Results: (1) Sixty-five percent of hepatitis C virus-seropositive individuals had CD4+ T-cell responses to viral proteins. (2) All viral proteins were immunogenic for T cells, although NS4 was the most immunogenic. (3) There was a significant correlation between the presence of CD4+ T cell responses to Core and a benign course of infection in healthy seropositives, most of whom were viremic. Conclusions: CD4+ T-cell responses to Core, although they do not coincide with virus clearance, are associated with a benign course of infection and may be required to maintain humoral and cellular responses protective against the disease. © 1993.
引用
收藏
页码:580 / 587
页数:8
相关论文
共 22 条
[1]   PRIMING OF CD4+ T-CELLS SPECIFIC FOR CONSERVED REGIONS OF HUMAN-IMMUNODEFICIENCY-VIRUS GLYCOPROTEIN GP120 IN HUMANS IMMUNIZED WITH A RECOMBINANT ENVELOPE PROTEIN [J].
ABRIGNANI, S ;
MONTAGNA, D ;
JEANNET, M ;
WINTSCH, J ;
HAIGWOOD, NL ;
SHUSTER, JR ;
STEIMER, KS ;
CRUCHAUD, A ;
STAEHELIN, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6136-6140
[2]  
ALTER HJ, 1988, VIRAL HEPATITIS LIVE, P537
[3]   SELECTIVE KILLING OF HEPATITIS-B ENVELOPE ANTIGEN-SPECIFIC B-CELLS BY CLASS-I-RESTRICTED, EXOGENOUS ANTIGEN-SPECIFIC LYMPHOCYTES-T [J].
BARNABA, V ;
FRANCO, A ;
ALBERTI, A ;
BENVENUTO, R ;
BALSANO, F .
NATURE, 1990, 345 (6272) :258-260
[5]   INFLUENCES OF ANTIGEN PROCESSING ON THE EXPRESSION OF THE T-CELL REPERTOIRE - EVIDENCE FOR MHC-SPECIFIC HINDERING STRUCTURES ON THE PRODUCTS OF PROCESSING [J].
BRETT, SJ ;
CEASE, KB ;
BERZOFSKY, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (01) :357-373
[6]   BIOLOGY OF CLONED CYTO-TOXIC LYMPHOCYTES-T SPECIFIC FOR LYMPHOCYTIC CHORIOMENINGITIS VIRUS - CLEARANCE OF VIRUS INVIVO [J].
BYRNE, JA ;
OLDSTONE, MBA .
JOURNAL OF VIROLOGY, 1984, 51 (03) :682-686
[7]   GENETIC ORGANIZATION AND DIVERSITY OF THE HEPATITIS-C VIRUS [J].
CHOO, QL ;
RICHMAN, KH ;
HAN, JH ;
BERGER, K ;
LEE, C ;
DONG, C ;
GALLEGOS, C ;
COIT, D ;
MEDINASELBY, A ;
BARR, PJ ;
WEINER, AJ ;
BRADLEY, DW ;
KUO, G ;
HOUGHTON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2451-2455
[8]   HEPATITIS NON-A, NON-B - C AT LAST [J].
DIENSTAG, JL .
GASTROENTEROLOGY, 1990, 99 (04) :1177-1180
[9]   A LONG-TERM STUDY OF HEPATITIS-C VIRUS-REPLICATION IN NON-A, NON-B HEPATITIS [J].
FARCI, P ;
ALTER, HJ ;
WONG, D ;
MILLER, RH ;
SHIH, JW ;
JETT, B ;
PURCELL, RH .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (02) :98-104
[10]   CHARACTERIZATION OF THE TERMINAL REGIONS OF HEPATITIS-C VIRAL-RNA - IDENTIFICATION OF CONSERVED SEQUENCES IN THE 5' UNTRANSLATED REGION AND POLY(A) TAILS AT THE 3' END [J].
HAN, JH ;
SHYAMALA, V ;
RICHMAN, KH ;
BRAUER, MJ ;
IRVINE, B ;
URDEA, MS ;
TEKAMPOLSON, P ;
KUO, G ;
CHOO, QL ;
HOUGHTON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1711-1715