CD8+ T cells in atopic disease

被引:21
作者
Kemeny, DM [1 ]
机构
[1] Univ London Kings Coll, Guys Kings & St Thomas Sch Med, Dept Immunol, London SE5 9NU, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0952-7915(98)80080-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In recent years there has been a tremendous expansion in our understanding about CD8(+) T cells. We now know that, as for CD4(+) T cells, they can be divided into subsets (Tc1 and Tc2) according to the cytokines they secrete. These subsets may differ in their capacity to kill and may even, in some cases, provide help for B cell antibody production or be involved in the induction of inflammatory responses. In addition, there is a host of cross-regulatory networks between different CD4(+) and CD8(+) subsets that control the magnitude and duration of immune responses. The observation that some antigens that are normally presented by MHC class II and seen by CD4(+) T cells can be presented by MHC class I and stimulate CD8(+) T cells increases the possibility for such interactions. During the next few years we can expect that our understanding of the biology of CD8(+) T cells and their role in immunity will increase.
引用
收藏
页码:628 / 633
页数:6
相关论文
共 76 条
[41]   TH2-LIKE CD8+ T-CELLS SHOWING B-CELL HELPER FUNCTION AND REDUCED CYTOLYTIC ACTIVITY IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
MAGGI, E ;
GIUDIZI, MG ;
BIAGIOTTI, R ;
ANNUNZIATO, F ;
MANETTI, R ;
PICCINNI, MP ;
PARRONCHI, P ;
SAMPOGNARO, S ;
GIANNARINI, L ;
ZUCCATI, G ;
ROMAGNANI, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (02) :489-495
[42]   The role of CD8+ Th2 lymphocytes in the development of smoking-related lung damage [J].
Mattoli, S ;
Kleimberg, J ;
Stacey, MA ;
Bellini, A ;
Sun, G ;
Marini, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 239 (01) :146-149
[43]   REGULATION OF IGE RESPONSES TO INHALED ANTIGEN IN MICE BY ANTIGEN-SPECIFIC GAMMA-DELTA T-CELLS [J].
MCMENAMIN, C ;
PIMM, C ;
MCKERSEY, M ;
HOLT, PG .
SCIENCE, 1994, 265 (5180) :1869-1871
[44]   THE NATURAL IMMUNE-RESPONSE TO INHALED SOLUBLE-PROTEIN ANTIGENS INVOLVES MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) CLASS-I RESTRICTED CD8+ T-CELL MEDIATED BUT MHC CLASS-II RESTRICTED CD4+ T-CELL-DEPENDENT IMMUNE DEVIATION RESULTING IN SELECTIVE SUPPRESSION OF IMMUNOGLOBULIN-E PRODUCTION [J].
MCMENAMIN, C ;
HOLT, PG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) :889-899
[45]  
Meissner N, 1997, CLIN EXP ALLERGY, V27, P1402, DOI 10.1111/j.1365-2222.1997.tb02984.x
[46]   SUPPRESSOR T-CELLS GENERATED BY ORAL TOLERIZATION TO MYELIN BASIC-PROTEIN SUPPRESS BOTH INVITRO AND INVIVO IMMUNE-RESPONSES BY THE RELEASE OF TRANSFORMING GROWTH-FACTOR-BETA AFTER ANTIGEN-SPECIFIC TRIGGERING [J].
MILLER, A ;
LIDER, O ;
ROBERTS, AB ;
SPORN, MB ;
WEINER, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) :421-425
[47]  
MOSMANN TR, 1986, J IMMUNOL, V136, P2348
[48]  
Noble A, 1998, J IMMUNOL, V160, P559
[49]  
NOBLE A, 1995, J IMMUNOL, V155, P2928
[50]  
Noble A, 1998, J IMMUNOL, V160, P566