CHARACTERIZATION OF 4AOHW CELL-LINE PANEL INCLUDING NEW DATA FOR THE 10IHW PANEL

被引:29
作者
DEGLIESPOSTI, MA
GRIFFITHS, MSJ
DALY, LN
WITT, CS
SIMONS, M
CARCASSI, C
ALBERT, ED
GIPHART, MJ
DAWKINS, RL
机构
[1] ROYAL PERTH HOSP,INST MOLEC GENET & IMMUNOL,DEPT CLIN IMMUNOL,PERTH,WA 6001,AUSTRALIA
[2] SIR CHARLES GAIRDNER HOSP,DEPT CLIN IMMUNOL,PERTH,WA,AUSTRALIA
[3] UNIV WESTERN AUSTRALIA,DEPT CLIN IMMUNOL,PERTH,WA,AUSTRALIA
[4] SIMONS GENE TYPE DIAGNOST PTY,FITZROY,VIC,AUSTRALIA
[5] UNIV CAGLIARI,INST CLIN MED,CAGLIARI,ITALY
[6] LMU,KINDERPOLIKLIN,IMMUNOGENET LAB,MUNICH,GERMANY
[7] UNIV HOSP LEIDEN,DEPT IMMUNOHEMATOL & BLOOD BANK,LEIDEN,NETHERLANDS
基金
英国医学研究理事会;
关键词
D O I
10.1016/0198-8859(93)90514-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There will be a continuing need for well characterized panels of EBV-transformed lymphoblastoid cell lines. Selection of the 4AOH panel was based on prior MHC typing and was intended to ensure representation of ancestral haplotypes from various racial groups. Cells from nonhuman primates, bone marrow donor-recipient pairs, and patients with IDDM were included. Selected cells from the 101HW were included to enable further characterization. Cells were distributed to participants in the 4AOHW and were typed at multiple loci by a variety of procedures. Non-HLA genes such as TNF were included. Since the cells were distributed ''blind'' with hidden replicates, it was possible to evaluate the quality of the typing data. An approach to data management is described. The best current estimates of the typing of these cells are presented. The panel will be useful since it provides standards for most alleles at most loci. Since the cells are so well characterized, they represent a useful resource for MHC sequencing and for the evaluation of new typing procedures.
引用
收藏
页码:3 / 16
页数:14
相关论文
共 12 条
  • [1] ABRAHAM LJ, 1991, IMMUNOGENETICS, V33, P50
  • [2] LYMPHOTOXIN-BETA, A NOVEL MEMBER OF THE TNF FAMILY THAT FORMS A HETEROMERIC COMPLEX WITH LYMPHOTOXIN ON THE CELL-SURFACE
    BROWNING, JL
    NGAMEK, A
    LAWTON, P
    DEMARINIS, J
    TIZARD, R
    CHOW, EPC
    HESSION, C
    OBRINEGRECO, B
    FOLEY, SF
    WARE, CF
    [J]. CELL, 1993, 72 (06) : 847 - 856
  • [3] CARRINGTON M, 1993, IMMUNOGENETICS, V37, P266
  • [4] EVIDENCE OF A NATURAL-KILLER (NK) CELL REPERTOIRE FOR (ALLO) ANTIGEN RECOGNITION - DEFINITION OF 5 DISTINCT NK-DETERMINED ALLOSPECIFICITIES IN HUMANS
    CICCONE, E
    PENDE, D
    VIALE, O
    DIDONATO, C
    TRIPODI, G
    ORENGO, AM
    GUARDIOLA, J
    MORETTA, A
    MORETTA, L
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (03) : 709 - 718
  • [5] SOME DISEASE-ASSOCIATED ANCESTRAL HAPLOTYPES CARRY A POLYMORPHISM OF TNF
    DAWKINS, RL
    LEAVER, A
    CAMERON, PU
    MARTIN, E
    KAY, PH
    CHRISTIANSEN, FT
    [J]. HUMAN IMMUNOLOGY, 1989, 26 (02) : 91 - 97
  • [6] DAWKINS RL, 1991, MOL EVOLUTION MAJOR, P391
  • [7] ANCESTRAL HAPLOTYPES - CONSERVED POPULATION MHC HAPLOTYPES
    DEGLIESPOSTI, MA
    LEAVER, AL
    CHRISTIANSEN, FT
    WITT, CS
    ABRAHAM, LJ
    DAWKINS, RL
    [J]. HUMAN IMMUNOLOGY, 1992, 34 (04) : 242 - 252
  • [8] NCOI RESTRICTION FRAGMENT LENGTH POLYMORPHISM (RFLP) OF THE TUMOR NECROSIS FACTOR (TNF-ALPHA) REGION IN 4 AUTOIMMUNE-DISEASES
    FUGGER, L
    MORLING, N
    RYDER, LP
    GEORGSEN, J
    JAKOBSEN, BK
    SVEJGAARD, A
    ANDERSEN, V
    OXHOLM, P
    PEDERSEN, FK
    FRIIS, J
    HALBERG, P
    [J]. TISSUE ANTIGENS, 1989, 34 (01): : 17 - 22
  • [9] POLYMORPHIC STRUCTURE OF THE TUMOR-NECROSIS-FACTOR (TNF) LOCUS - AN NCOI POLYMORPHISM IN THE 1ST INTRON OF THE HUMAN TNF-BETA GENE CORRELATES WITH A VARIANT AMINO-ACID IN POSITION-26 AND A REDUCED LEVEL OF TNF-BETA PRODUCTION
    MESSER, G
    SPENGLER, U
    JUNG, MC
    HONOLD, G
    BLOMER, K
    PAPE, GR
    RIETHMULLER, G
    WEISS, EH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (01) : 209 - 219
  • [10] PETERSDORF EW, 1993, HLA 1991, V1, P812