The effect of age on the B-Cell repertoire

被引:139
作者
Weksler, ME [1 ]
Szabo, P [1 ]
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
aging; B cells; B cell repertoire; clonal B cell expansions;
D O I
10.1023/A:1006659401385
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antibody repertoire changes with age. This change reflects, in part, the age-associated impairment in the production of a diverse population of naive B cells in the bone marrow and, in parr, by the decreased diversification of B cells in the germinal center where affinity maturation and isotype switching takes place. B cell number is strictly regulated and despite the decreased output of B cells by the bone marrow does not decline during aging. Self-renewal of peripheral B cells is sufficient to assure the stability of peripheral B cell number. However, when B cell production is stressed as, for example, Following drug-induced lymphopenia, the rate of recovery of B cell number as well as of B cell diversity is compromised in old compared to young mice. Finally, aging is associated with the appearance of B cell clonal expansions which not only limit the diversity of the B cell repertoire but very likely give rise to monoclonal serum immunoglobulins and B cell neoplasms.
引用
收藏
页码:240 / 249
页数:10
相关论文
共 49 条
[1]  
ARREAZA EE, 1993, CLIN EXP IMMUNOL, V92, P169
[2]  
Baumgartner L, 1934, J IMMUNOL, V27, P407
[3]   Increased VH 11 and VH Q52 gene use by splenic B cells in old mice associated with oligoclonal expansions of CD5+B cells [J].
Ben-Yehuda, A ;
Szabo, P ;
LeMaoult, J ;
Manavalan, JS ;
Weksler, ME .
MECHANISMS OF AGEING AND DEVELOPMENT, 1998, 103 (02) :111-121
[4]   BONE-MARROW DECLINES AS A SITE OF B-CELL PRECURSOR DIFFERENTIATION WITH AGE - RELATIONSHIP TO THYMUS INVOLUTION [J].
BENYEHUDA, A ;
SZABO, P ;
DYALL, R ;
WEKSLER, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :11988-11992
[5]   CROSS-WIRING OF THE IMMUNE-RESPONSE IN OLD MICE - INCREASED AUTOANTIBODY RESPONSE DESPITE REDUCED ANTIBODY-RESPONSE TO NOMINAL ANTIGEN [J].
BOVBJERG, DH ;
KIM, YT ;
SCHWAB, R ;
SCHMITT, K ;
DEBLASIO, T ;
WEKSLER, ME .
CELLULAR IMMUNOLOGY, 1991, 135 (02) :519-525
[6]  
Crisi GM, 1996, INT IMMUNOL, V8, P387
[7]   Aging of the recipients but not of the bone marrow donors enhances autoimmunity In syngeneic radiation chimeras [J].
Doria, G ;
Mancini, C ;
Utsuyama, M ;
Frasca, D ;
Hirokawa, K .
MECHANISMS OF AGEING AND DEVELOPMENT, 1997, 95 (1-2) :131-142
[8]   Changes in thymic function with age and during the treatment of HIV infection [J].
Douek, DC ;
McFarland, RD ;
Keiser, PH ;
Gage, EA ;
Massey, JM ;
Haynes, BF ;
Polis, MA ;
Haase, AT ;
Feinberg, MB ;
Sullivan, JL ;
Jamieson, BD ;
Zack, JA ;
Picker, LJ ;
Koup, RA .
NATURE, 1998, 396 (6712) :690-695
[9]  
Fagerberg J, 1999, INT J CANCER, V80, P671, DOI 10.1002/(SICI)1097-0215(19990301)80:5<671::AID-IJC7>3.0.CO
[10]  
2-E