Development of tbe antibody repertoire in rabbit: gut-associated lymphoid tissue, microbes, and selection

被引:53
作者
Lanning, D [1 ]
Zhu, XC [1 ]
Zhai, SK [1 ]
Knight, KL [1 ]
机构
[1] Loyola Univ, Stritch Sch Med, Dept Microbiol & Immunol, Maywood, IL 60153 USA
关键词
D O I
10.1111/j.1600-065X.2000.imr017516.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Rabbits generate their antibody repertoire in three stages, First, a neonatal repertoire is generated by B lymphopoiesis in fetal liver and bone marrow and is limited by preferential V-H gene segment usage. Between 4 and 8 weeks after birth a complex primary antibody repertoire is developed by somatically diversifying the neonatal repertoire through somatic hypermutation and a somatic gene conversion-like mechanism in gut-associated lymphoid tissue (GALT). In rabbits, unlike other species. the development of the primary antibody repertoire through somatic diversification of Ig genes appears to be dependent on intestinal microbial nora. The primary antibody repertoire is subsequently modified during antigen-dependent immune responses in which VDJ genes further diversify both by somatic hypermutation and by a gene conversion-like mechanism (the secondary repertoire). During the various stages of development, the antibody repertoire is modified and shaped by selective processes. In this review. we discuss the roles of GALT, microbes, and B-cell selection in generating antibody diversity in rabbits.
引用
收藏
页码:214 / 228
页数:15
相关论文
共 109 条
[1]   CHARACTERIZATION OF DONOR-DERIVED LYMPHOCYTES IN CHIMERIC RABBITS [J].
ADLER, LT ;
LEBEAU, MM ;
ADLER, FL .
TRANSPLANTATION, 1983, 35 (06) :530-534
[2]   PREFERENTIAL REARRANGEMENT IN NORMAL RABBITS OF THE 3' VHA ALLOTYPE GENE THAT IS DELETED IN ALICIA MUTANTS - SOMATIC HYPERMUTATION CONVERSION MAY PLAY A MAJOR ROLE IN GENERATING THE HETEROGENEITY OF RABBIT HEAVY-CHAIN VARIABLE REGION SEQUENCES [J].
ALLEGRUCCI, M ;
YOUNGCOOPER, GO ;
ALEXANDER, CB ;
NEWMAN, BA ;
MAGE, RG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (02) :411-417
[3]   APPENDIX OF RABBIT - A HOMOLOGUE OF BURSA IN CHICKEN [J].
ARCHER, OK ;
SUTHERLAND, DE ;
GOOD, RA .
NATURE, 1963, 200 (490) :337-+
[4]   RESTRICTED UTILIZATION OF VH AND DH GENES IN LEUKEMIC RABBIT B-CELLS [J].
BECKER, RS ;
SUTER, M ;
KNIGHT, KL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (02) :397-402
[5]   SOMATIC DIVERSIFICATION OF IMMUNOGLOBULIN HEAVY-CHAIN VDJ GENES - EVIDENCE FOR SOMATIC GENE CONVERSION IN RABBITS [J].
BECKER, RS ;
KNIGHT, KL .
CELL, 1990, 63 (05) :987-997
[6]   STOCHASTIC REARRANGEMENT OF IMMUNOGLOBULIN VARIABLE-REGION GENES IN CHICKEN B-CELL DEVELOPMENT [J].
BENATAR, T ;
TKALEC, L ;
RATCLIFFE, MJH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7615-7619
[7]   IMMUNOGLOBULIN-V(H)3 GENE-PRODUCTS - NATURAL LIGANDS FOR HIV GP120 [J].
BERBERIAN, L ;
GOODGLICK, L ;
KIPPS, TJ ;
BRAUN, J .
SCIENCE, 1993, 261 (5128) :1588-1591
[8]   FUNCTIONAL HISTOLOGY OF APPENDIX [J].
BOCKMAN, DE .
ARCHIVUM HISTOLOGICUM JAPONICUM, 1983, 46 (03) :271-292
[9]   PANETH CELL-DIFFERENTIATION IN THE DEVELOPING INTESTINE OF NORMAL AND TRANSGENIC MICE [J].
BRY, L ;
FALK, P ;
HUTTNER, K ;
OUELLETTE, A ;
MIDTVEDT, T ;
GORDON, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10335-10339
[10]   A model of host-microbial interactions in an open mammalian ecosystem [J].
Bry, L ;
Falk, PG ;
Midtvedt, T ;
Gordon, JI .
SCIENCE, 1996, 273 (5280) :1380-1383