LYMPHOCYTE MEMBRANE MODIFICATIONS INDUCED BY HIV-INFECTION

被引:11
作者
KASHIWAGI, N
GILL, MJ
ADACHI, M
CHURCH, D
WONG, SJ
POON, MC
HAKOMORI, S
TAMAOKI, T
SHIOZAWA, C
机构
[1] UNIV CALGARY, FOOTHILLS PROV GEN HOSP, DEPT MED BIOCHEM, CALGARY T2N 4N1, AB, CANADA
[2] UNIV CALGARY, FOOTHILLS PROV GEN HOSP, DEPT MED & MICROBIOL, CALGARY T2N 4N1, AB, CANADA
[3] UNIV CALGARY, FOOTHILLS PROV GEN HOSP, DEPT INFECT DIS, CALGARY T2N 4N1, AB, CANADA
[4] UNIV CALGARY, FOOTHILLS PROV GEN HOSP, DIV IMMUNOL, CALGARY T2N 4N1, AB, CANADA
[5] JIMRO, TAKASAKI, GUMMA 370, JAPAN
[6] UNIV WASHINGTON, SEATTLE, WA 98195 USA
[7] BIOMEMBRANE INST, SEATTLE, WA 98119 USA
关键词
HUMAN IMMUNODEFICIENCY VIRUS; CARBOHYBRATE ANTIGEN; T LYMPHOCYTES; MONOCLONAL ANTIBODIES; LE(Y) ANTIGEN;
D O I
10.1620/tjem.173.115
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Novel carbohydrate antigen expressions were observed on T lymphocytes from HIV infected patients using flowcytometric analysis with four mAbs; BM-1, ACFH-18, PH-2 and C-6. These carbohydrate antigens were also expressed on oncogenic transformed cells but mere either not expressed or were weakly expressed in lymphocyte populations from healthy subjects. A dramatic change in glycosylation was induced on CD8(+)T cells from HIV infected patients. The glycosylation change correlated with the progression of the disease. The incidence of Le(y) antigen expression on CD8(+)T cells increased as the disease progressed with the ongoing impairment of immune function. The phenotype change that occurred with Le(Y) antigen expression might reflect the abnormal activation of T lymphocytes of some specific, but unknown, population of CD8(+)T cells. Thus, carbohydrate changes on the cell surface may induce immunological abnormality and accelerate the damage within the CD4(+)T cell subset, resulting in an impairment of the antigen specific immune system.
引用
收藏
页码:115 / 131
页数:17
相关论文
共 19 条
  • [1] ABE K, 1983, J BIOL CHEM, V258, P1793
  • [2] EXPRESSION OF LEY ANTIGEN IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED HUMAN T-CELL LINES AND IN PERIPHERAL LYMPHOCYTES OF PATIENTS WITH ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS) AND AIDS-RELATED COMPLEX (ARC)
    ADACHI, M
    HAYAMI, M
    KASHIWAGI, N
    MIZUTA, T
    OHTA, Y
    GILL, MJ
    MATHESON, DS
    TAMAOKI, T
    SHIOZAWA, C
    HAKOMORI, SI
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (02) : 323 - 331
  • [3] DETECTION OF 3 DISTINCT PATTERNS OF T-HELPER CELL DYSFUNCTION IN ASYMPTOMATIC, HUMAN IMMUNODEFICIENCY VIRUS-SEROPOSITIVE PATIENTS - INDEPENDENCE OF CD4+ CELL NUMBERS AND CLINICAL STAGING
    CLERICI, M
    STOCKS, NI
    ZAJAC, RA
    BOSWELL, RN
    LUCEY, DR
    VIA, CS
    SHEARER, GM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) : 1892 - 1899
  • [4] COSTER L, 1986, J BIOL CHEM, V261, P2079
  • [5] EGGENS I, 1989, J BIOL CHEM, V264, P9476
  • [6] A MONOCLONAL-ANTIBODY DEFINING A BINARY N-ACETYLLACTOSAMINYL STRUCTURE IN LACTOISOOCTAOSYLCERAMIDE (IV6GALBETA-1-]4GLCNACNLC6) - A USEFUL PROBE FOR DETERMINING DIFFERENTIAL GLYCOSYLATION PATTERNS BETWEEN NORMAL AND TRANSFORMED HUMAN-FIBROBLASTS
    FENDERSON, BA
    NICHOLS, EJ
    CLAUSEN, H
    HAKOMORI, S
    [J]. MOLECULAR IMMUNOLOGY, 1986, 23 (07) : 747 - 754
  • [7] EVIDENCE FOR HTLV-III/LAV EXPRESSION BY PRIMARY CULTURES OF T8 CELLS
    FOUCHARD, M
    REVEIL, B
    MBAYO, K
    LURHUMA, A
    SARIN, PS
    GALLO, RC
    ZAGURY, D
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1986, 38 (05) : 657 - 659
  • [8] FUKUSHI Y, 1984, J BIOL CHEM, V259, P4681
  • [9] KOJIMA N, 1989, J BIOL CHEM, V264, P20159
  • [10] PHENOTYPIC DISTRIBUTION OF T-CELLS OF PATIENTS WHO HAVE SUBSEQUENTLY DEVELOPED AIDS
    NICHOLSON, JKA
    JONES, BM
    ECHENBERG, DF
    SPIRA, TJ
    MCDOUGAL, JS
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1987, 43 (01): : 82 - 87