B-CELL DEVELOPMENT IN MAN

被引:20
作者
BURROWS, PD
COOPER, MD
机构
[1] UNIV ALABAMA,DEPT PEDIAT,DIV DEV & CLIN IMMUNOL,BIRMINGHAM,AL 35294
[2] UNIV ALABAMA,DEPT MICROBIOL,DIV DEV & CLIN IMMUNOL,BIRMINGHAM,AL 35294
[3] HOWARD HUGHES MED INST,BIRMINGHAM,AL 35294
关键词
D O I
10.1016/0952-7915(93)90005-D
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 development of B-lineage cells requires a series of complex interactions with hemopoietic stromal cell elements during the generative phase, and with antigen and T lymphocytes during the subsequent proliferative/differentiative phases in lymphoid tissues. Recent advances have been made in defining developmental changes in structure and assembly of the antigen receptors and in identifying protein kinases involved in signal transduction via these receptors. The mechanism of T-cell help has also come into much clearer focus through elucidation of the interaction between CD40 on B cells and the CD40 ligand on activated T cells. Finally, progress has been made with the recent identification of defects in a cytoplasmic protein tyrosine kinase and in the CD40 ligand as causes of two B-cell immunodeficiencies in man.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 47 条
  • [1] CD40 LIGAND GENE DEFECTS RESPONSIBLE FOR X-LINKED HYPER-IGM SYNDROME
    ALLEN, RC
    ARMITAGE, RJ
    CONLEY, ME
    ROSENBLATT, H
    JENKINS, NA
    COPELAND, NG
    BEDELL, MA
    EDELHOFF, S
    DISTECHE, CM
    SIMONEAUX, DK
    FANSLOW, WC
    BELMONT, J
    SPRIGGS, MK
    [J]. SCIENCE, 1993, 259 (5097) : 990 - 993
  • [2] MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF A MURINE LIGAND FOR CD40
    ARMITAGE, RJ
    FANSLOW, WC
    STROCKBINE, L
    SATO, TA
    CLIFFORD, KN
    MACDUFF, BM
    ANDERSON, DM
    GIMPEL, SD
    DAVISSMITH, T
    MALISZEWSKI, CR
    CLARK, EA
    SMITH, CA
    GRABSTEIN, KH
    COSMAN, D
    SPRIGGS, MK
    [J]. NATURE, 1992, 357 (6373) : 80 - 82
  • [3] THE CD40 LIGAND, GP39, IS DEFECTIVE IN ACTIVATED T-CELLS FROM PATIENTS WITH X-LINKED HYPER-IGM SYNDROME
    ARUFFO, A
    FARRINGTON, M
    HOLLENBAUGH, D
    LI, X
    MILATOVICH, A
    NONOYAMA, S
    BAJORATH, J
    GROSMAIRE, LS
    STENKAMP, R
    NEUBAUER, M
    ROBERTS, RL
    NOELLE, RJ
    LEDBETTER, JA
    FRANCKE, U
    OCHS, HD
    [J]. CELL, 1993, 72 (02) : 291 - 300
  • [4] ORGANIZATION AND EXPRESSION OF THE LAMBDA-LIKE GENES THAT CONTRIBUTE TO THE MU-PSI LIGHT CHAIN COMPLEX IN HUMAN PRE-B-CELLS
    BOSSY, D
    MILILI, M
    ZUCMAN, J
    THOMAS, G
    FOUGEREAU, M
    SCHIFF, C
    [J]. INTERNATIONAL IMMUNOLOGY, 1991, 3 (11) : 1081 - 1090
  • [5] ANTIIMMUNOGLOBULIN STIMULATION OF LYMPHOCYTES-B ACTIVATES SRC-RELATED PROTEIN-TYROSINE KINASES
    BURKHARDT, AL
    BRUNSWICK, M
    BOLEN, JB
    MOND, JJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7410 - 7414
  • [6] ASSOCIATION BETWEEN LYMPHOCYTE-B MEMBRANE IMMUNOGLOBULIN AND MULTIPLE MEMBERS OF THE SRC FAMILY OF PROTEIN TYROSINE KINASES
    CAMPBELL, MA
    SEFTON, BM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) : 2315 - 2321
  • [7] CD19 - LOWERING THE THRESHOLD FOR ANTIGEN RECEPTOR STIMULATION OF LYMPHOCYTES-B
    CARTER, RH
    FEARON, DT
    [J]. SCIENCE, 1992, 256 (5053) : 105 - 107
  • [8] CLARK EA, 1991, ANNU REV IMMUNOL, V149, P2857
  • [9] PREDOMINANT EXPRESSION AND ACTIVATION-INDUCED TYROSINE PHOSPHORYLATION OF PHOSPHOLIPASE C-GAMMA-2 IN LYMPHOCYTES-B
    COGGESHALL, KM
    MCHUGH, JC
    ALTMAN, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) : 5660 - 5664
  • [10] INTERLEUKIN-10 AND TRANSFORMING GROWTH-FACTOR-BETA COOPERATE TO INDUCE ANTI-CD40 ACTIVATED NAIVE HUMAN B-CELLS TO SECRETE IMMUNOGLOBULIN-A
    DEFRANCE, T
    VANBERVLIET, B
    BRIERE, F
    DURAND, I
    ROUSSET, F
    BANCHEREAU, J
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (03) : 671 - 682