Vγ2 TCR repertoire overlap in different anatomical compartments of healthy, unrelated rhesus macaques

被引:12
作者
MacDougall, AV
Enders, P
Hatfield, G
Pauza, DC
Rakasz, E
机构
[1] Univ Wisconsin, Wisconsin Reg Primate Res Ctr, Madison, WI 53715 USA
[2] Univ Wisconsin, Dept Pathol & Lab Med, Madison, WI 53715 USA
关键词
D O I
10.4049/jimmunol.166.4.2296
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
gamma delta T cells show preferential homing that is characterized by biased TCR repertoire at different anatomical locations. The processes that regulate this compartmentalization are largely unknown, A model that allows repeated multiple sample procurement under different conditions and enables with relatively straightforward extrapolation to a human situation will facilitate our understanding. The peripheral blood V gamma2 T cell population is the best-characterized human gamma delta T cell subset. To determine its diversity at multiple immunocompartments matching blood, colon, and vagina samples from rhesus macaques were investigated. Four joining segments used in V gamma2-J gamma transcripts were identified, including one segment with no human counterpart. Like in humans, the rhesus peripheral blood V gamma2 TCR repertoire was limited and contained common sequences that were shared by genetically heterogeneous animals, Furthermore, this subset comprised several phylogenetically conserved V gamma2 complementarity-determining region 3 (CDR3) motifs between rhesus and humans. Common sequences were also found within the colon and vagina of the same animal, and,within the peripheral blood and intestine of different unrelated animals. These results validate rhesus macaques as a useful model for gamma delta TCR repertoire and homing studies, Moreover, they provide evidence that the concept of limited but overlapping V gamma TCR repertoire between unrelated individuals can be extended including the mucosa of the digestive and reproductive tract.
引用
收藏
页码:2296 / 2302
页数:7
相关论文
共 55 条
  • [31] REGULATION OF THE MATURE HUMAN-T CELL RECEPTOR-GAMMA REPERTOIRE BY BIASED V-J GENE REARRANGEMENT
    KOHSAKA, H
    CHEN, PP
    TANIGUCHI, A
    OLLIER, WER
    CARSON, DA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) : 171 - 178
  • [32] STRUCTURALLY DIVERGENT HUMAN T-CELL RECEPTOR GAMMA-PROTEINS ENCODED BY DISTINCT C-GAMMA GENES
    KRANGEL, MS
    BAND, H
    HATA, S
    MCLEAN, J
    BRENNER, MB
    [J]. SCIENCE, 1987, 237 (4810) : 64 - 67
  • [33] DIVERSITY AND REARRANGEMENT OF THE HUMAN T-CELL REARRANGING GAMMA-GENES - 9 GERM-LINE VARIABLE GENES BELONGING TO 2 SUBGROUPS
    LEFRANC, MP
    FORSTER, A
    BAER, R
    STINSON, MA
    RABBITTS, TH
    [J]. CELL, 1986, 45 (02) : 237 - 246
  • [34] GENETIC-POLYMORPHISM AND EXON CHANGES OF THE CONSTANT REGIONS OF THE HUMAN T-CELL REARRANGING GENE-GAMMA
    LEFRANC, MP
    FORSTER, A
    RABBITTS, TH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) : 9596 - 9600
  • [35] Structure of the Vδ domain of a human γδ T-cell antigen receptor
    Li, HM
    Lebedeva, MI
    Llera, AS
    Fields, BA
    Brenner, MB
    Mariuzza, RA
    [J]. NATURE, 1998, 391 (6666) : 502 - 506
  • [36] Systemic activation and antigen-driven oligoclonal expansion of T cells in a mouse model of colitis
    Matsuda, JL
    Gapin, L
    Sydora, BC
    Byrne, F
    Binder, S
    Kronenberg, M
    Aranda, R
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 164 (05) : 2797 - 2806
  • [37] McVay LD, 1998, J IMMUNOL, V160, P5851
  • [38] McVay LD, 1996, J IMMUNOL, V157, P2873
  • [39] MinchevaNilsson L, 1997, J IMMUNOL, V159, P3266
  • [40] MORITA CT, 1994, J IMMUNOL, V153, P3979