Chemokine regulation of normal and pathologic immune responses

被引:104
作者
Christopherson, K
Hromas, R
机构
[1] Indiana Univ, Ctr Canc, Indianapolis, IN 46202 USA
[2] Indiana Univ, Walther Oncol Inst, Indianapolis, IN 46202 USA
关键词
chemokine; chemotaxis; homing; hematopoiesis; T cell;
D O I
10.1634/stemcells.19-5-388
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Chemokines are small basic proteins that are the major mediators of all leukocyte migration. There are at least 46 distinct chemokines, and 19 chemokine receptors, making it easily the largest cytokine family. Chemokines can be both beneficial and harmful, by either stimulating an appropriate immune response to microbial invasion, or by mediating pathologic tissue destruction in many types of human disease. Chemokines have been implicated in the tissue destruction seen in autoimmune diseases, atherosclerosis, allograft rejection, and neoplasia. Chemokines. also play essential roles in normal lymphocyte trafficking to primary and secondary lymphoid organs for antigen presentation and lymphocyte maturation. Chemokines also regulate hematopoietic stem and progenitor cell homing and proliferation. Therefore, it is likely that chemokines; will become important targets for pharmacologic intervention in a wide variety of human diseases in the future.
引用
收藏
页码:388 / 396
页数:9
相关论文
共 89 条
[51]
Chemokines and chemokine receptors: Biology and clinical relevance in inflammation and AIDS [J].
Locati, M ;
Murphy, PM .
ANNUAL REVIEW OF MEDICINE, 1999, 50 :425-440
[52]
LORD BI, 1992, BLOOD, V79, P2605
[53]
Coexpression of the chemokines ELC and SLC by T zone stromal cells and deletion of the ELC gene in the plt/plt mouse [J].
Luther, SA ;
Tang, HL ;
Hyman, PL ;
Farr, AG ;
Cyster, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12694-12699
[54]
Impaired B-lymphopoiesis, myelopoiesis, and derailed cerebellar neuron migration in CXCR4- and SDF-1-deficient mice [J].
Ma, Q ;
Jones, D ;
Borghesani, PR ;
Segal, RA ;
Nagasawa, T ;
Kishimoto, T ;
Bronson, RT ;
Springer, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9448-9453
[55]
MANOME Y, 1995, CANCER IMMUNOL IMMUN, V41, P227
[56]
CARDIAC MYOCYTES RELEASE LEUKOCYTE-STIMULATING FACTORS [J].
MASSEY, KD ;
STRIETER, RM ;
KUNKEL, SL ;
DANFORTH, JM ;
STANDIFORD, TJ .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (03) :H980-H987
[57]
Mice lacking expression of the chemokines CCL21-Ser and CCL19 (plt mice) demonstrate delayed but enhanced T cell immune responses [J].
Mori, S ;
Nakano, H ;
Aritomi, K ;
Wang, CR ;
Gunn, MD ;
Kakiuchi, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (02) :207-217
[58]
Involvement of chemokine receptors in breast cancer metastasis [J].
Müller, A ;
Homey, B ;
Soto, H ;
Ge, NF ;
Catron, D ;
Buchanan, ME ;
McClanahan, T ;
Murphy, E ;
Yuan, W ;
Wagner, SN ;
Barrera, JL ;
Mohar, A ;
Verástegui, E ;
Zlotnik, A .
NATURE, 2001, 410 (6824) :50-56
[59]
Viral exploitation and subversion of the immune system through chemokine mimicry [J].
Murphy, PM .
NATURE IMMUNOLOGY, 2001, 2 (02) :116-122
[60]
Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1 [J].
Nagasawa, T ;
Hirota, S ;
Tachibana, K ;
Takakura, N ;
Nishikawa, S ;
Kitamura, Y ;
Yoshida, N ;
Kikutani, H ;
Kishimoto, T .
NATURE, 1996, 382 (6592) :635-638