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
[31]  
Ke Y, 1997, J IMMUNOL, V158, P3610
[32]   Nonionic triblock copolymers facilitate delivery of exogenous proteins into the MHC class I and class II processing pathways [J].
Ke, Y ;
McGraw, CL ;
Hunter, RL ;
Kapp, JA .
CELLULAR IMMUNOLOGY, 1997, 176 (02) :113-121
[33]   Rush immunotherapy results in allergen-specific alterations in lymphocyte function and interferon-gamma productioni in CD4(+) T cells [J].
Lack, G ;
Nelson, HS ;
Amran, D ;
Oshiba, A ;
Jung, T ;
Bradley, KL ;
Giclas, PC ;
Gelfand, EW .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (04) :530-538
[34]   Inhibition of IgE antibody formation by plasmid DNA immunization is mediated by both CD4+ and CD8+ T cells [J].
Lee, DJ ;
Tighe, H ;
Corr, M ;
Roman, M ;
Carson, DA ;
Spiegelberg, HL ;
Raz, E .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1997, 113 (1-3) :227-230
[35]   NONCYTOTOXIC, IL-4, IL-5, IL-10 PRODUCING CD8+ T-CELLS - THEIR ACTIVATION AND EFFECTOR FUNCTIONS [J].
LEGROS, G ;
ERARD, F .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (03) :453-457
[36]   Immunological consequences of intervention in established immune responses by feeding protein antigens [J].
Leishman, AJ ;
Garside, P ;
Mowat, AM .
CELLULAR IMMUNOLOGY, 1998, 183 (02) :137-148
[37]   CYTOKINE PRODUCTION BY HIGHLY PURIFIED HUMAN CD8+T CELLS [J].
LI, Y ;
RICHARDS, D ;
NOBEL, A ;
KEMENY, DM .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (1-3) :354-355
[38]  
LUNDQVIST C, 1994, J IMMUNOL, V153, P2302
[39]  
MacAry PA, 1998, J IMMUNOL, V160, P580
[40]   PROFILES OF LYMPHOKINE ACTIVITIES AND HELPER FUNCTION FOR IGE IN HUMAN T-CELL CLONES [J].
MAGGI, E ;
DELPRETE, G ;
MACCHIA, D ;
PARRONCHI, P ;
TIRI, A ;
CHRETIEN, I ;
RICCI, M ;
ROMAGNANI, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (07) :1045-1050