POPULATION BIOLOGY OF LYMPHOCYTES: The flight for survival

被引:367
作者
Freitas, AA
Rocha, B
机构
[1] Inst Pasteur, Lymphocyte Populat Biol Unit, CNRS, URA 1961, F-75015 Paris, France
[2] Inst Necker, INSERM, U345, F-75015 Paris, France
关键词
lymphocyte survival and life spans; lymphocyte competition; lymphocyte homeostasis; naive and memory lymphocytes;
D O I
10.1146/annurev.immunol.18.1.83
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 this essay we suggest that the primary goal of the cells of the immune system is to ensure their own growth and survival. In adults, in steady-state conditions, the number and distribution of lymphocyte populations is under homeostatic control. New lymphocytes that are continuously produced in primary and secondary lymphoid organs must compete with resident cells for survival. We discuss recent findings supporting lymphocyte survival as a continuous active process and implicating cognate receptor engagement as fundamental survival signals for both T and B lymphocytes. The conflict of survival interests between different cell types gives rise to a pattern of interactions that mimics the behavior of complex ecological systems. In their flight for survival and in response to competition, lymphocytes use different survival signals within different ecological niches during cell differentiation. This is the case for T and B lymphocytes and also for naive and memory/activated T and B cells. We discuss how niche differentiation allows the co-existence of different cell types and guarantees both repertoire diversity and efficient immune responses.
引用
收藏
页码:83 / 111
页数:29
相关论文
共 162 条
[51]   Increased peptide promiscuity provides a rationale for the lack of N regions in the neonatal T cell repertoire [J].
Gavin, MA ;
Bevan, MJ .
IMMUNITY, 1995, 3 (06) :793-800
[52]   RECEPTOR EDITING - AN APPROACH BY AUTOREACTIVE B-CELLS TO ESCAPE TOLERANCE [J].
GAY, D ;
SAUNDERS, T ;
CAMPER, S ;
WEIGERT, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (04) :999-1008
[53]   Cell division regulates the T cell cytokine repertoire, revealing a mechanism underlying immune class regulation [J].
Gett, AV ;
Hodgkin, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9488-9493
[54]   The sequential role of lymphotoxin and B cells in the development of splenic follicles [J].
Gonzalez, M ;
Mackay, F ;
Browning, JL ;
Kosco-Vilbois, MH ;
Noelle, RJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (07) :997-1007
[55]   SELF-TOLERANCE CHECKPOINTS IN B-LYMPHOCYTE DEVELOPMENT [J].
GOODNOW, CC ;
CYSTER, JG ;
HARTLEY, SB ;
BELL, SE ;
COOKE, MP ;
HEALY, JI ;
AKKARAJU, S ;
RATHMELL, JC ;
POGUE, SL ;
SHOKAT, KP .
ADVANCES IN IMMUNOLOGY, VOL 59, 1995, 59 :279-368
[56]   B-CELL MEMORY IS SHORT-LIVED IN THE ABSENCE OF ANTIGEN [J].
GRAY, D ;
SKARVALL, H .
NATURE, 1988, 336 (6194) :70-73
[57]   The fate of thymocytes labeled in vivo with CFSE [J].
Graziano, M ;
St-Pierre, Y ;
Beauchemin, C ;
Desrosiers, M ;
Potworowski, EF .
EXPERIMENTAL CELL RESEARCH, 1998, 240 (01) :75-85
[59]   ADAPTIVE CELLULAR INTERACTIONS IN THE IMMUNE-SYSTEM - THE TUNABLE ACTIVATION THRESHOLD AND THE SIGNIFICANCE OF SUBTHRESHOLD RESPONSES [J].
GROSSMAN, Z ;
PAUL, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10365-10369
[60]   MOST PERIPHERAL B-CELLS IN MICE ARE LIGAND SELECTED [J].
GU, H ;
TARLINTON, D ;
MULLER, W ;
RAJEWSKY, K ;
FORSTER, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (06) :1357-1371