Protein arrays for studying blood cells and their secreted products

被引:35
作者
Utz, PJ [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
关键词
D O I
10.1111/j.0105-2896.2005.00251.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
Protein microarrays have been developed and partially validated for studying blood cells, which play a role in many human diseases. Arrays of capture antibodies are commercially available for analyzing cytokines and intracellular signaling proteins. Several academic laboratories have developed antigen microarrays for characterizing autoimmune and allergic diseases, with a goal toward using such arrays to profile antibodies found in blood or other biological fluids. Arrays composed of major histocompatibility complex tetramers have been constructed and validated for analysis of immune responses in mice, paving the way toward studying antigen-specific T-lymphocyte responses. Finally, reverse-phase protein lysate microarray technology, first developed for analyzing cancer cells from tissue sections, has now been demonstrated for studying living cells, including knockout cells, cells treated with drugs such as kinase inhibitors, and rare populations of lymphocytes such as regulatory T cells. The goal of this review is to focus on advances in and future uses of arrays of proteins that can be printed on glass microscope slides using traditional microarray robots that are commonly found at academic medical centers. Dissemination of protein array technology will occur in the next decade and will markedly change how immunology research, particularly in the fields of autoimmunity and inflammation, is conducted.
引用
收藏
页码:264 / 282
页数:19
相关论文
共 85 条
  • [31] Joos TO, 2000, ELECTROPHORESIS, V21, P2641, DOI 10.1002/1522-2683(20000701)21:13<2641::AID-ELPS2641>3.3.CO
  • [32] 2-X
  • [33] Kaliyaperumal A, 1999, J IMMUNOL, V162, P5775
  • [34] Biomarker discovery by comprehensive phenotyping for autoimmune diseases
    Kantor, AB
    Wang, WX
    Lin, H
    Govindarajan, H
    Anderle, M
    Perrone, A
    Becker, C
    [J]. CLINICAL IMMUNOLOGY, 2004, 111 (02) : 186 - 195
  • [35] Kellar KL, 2001, CYTOMETRY, V45, P27, DOI 10.1002/1097-0320(20010901)45:1<27::AID-CYTO1141>3.0.CO
  • [36] 2-I
  • [37] Genomics in the immune system
    Kraan, TCMTV
    Kasperkovitz, PV
    Verbeet, N
    Verweij, CL
    [J]. CLINICAL IMMUNOLOGY, 2004, 111 (02) : 175 - 185
  • [38] Rheumatoid arthritis is a heterogeneous disease - Evidence for differences in the activation of the STAT-1 pathway between rheumatoid tissues
    Kraan, TCTMV
    van Gaalen, FA
    Kasperkovitz, PV
    Verbeet, NL
    Smeets, TJM
    Kraan, MC
    Fero, M
    Tak, PP
    Huizinga, TWJ
    Pieterman, E
    Breedveld, FC
    Alizadeh, AA
    Verweij, CL
    [J]. ARTHRITIS AND RHEUMATISM, 2003, 48 (08): : 2132 - 2145
  • [39] KRAAN TCV, 2003, GENES IMMUNITY, V0004
  • [40] Detection of multiple cytokines by protein arrays from cell lysate and tissue lysate
    Lin, Y
    Huang, RC
    Cao, X
    Wang, SM
    Shi, Q
    Huang, RP
    [J]. CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2003, 41 (02) : 139 - 145