ACTIVATION OF HUMAN CD4+ AND CD8+ CELLS BY SARCOCYSTIS-GIGANTEA LECTIN

被引:4
|
作者
TIETZ, HJ
MONTAG, T
VOLK, HD
BROSE, E
GANTENBERG, R
WEICHOLD, FF
HIEPE, T
机构
[1] PAUL EHRLICH INST,LANGEN,GERMANY
[2] HUMBOLDT UNIV,FAK VET MED,INST PARASITOL,O-1086 BERLIN,GERMANY
[3] HUMBOLDT UNIV,BEREICH MED CHARITE,INST MIKROBIOL,O-1040 BERLIN,GERMANY
[4] HUMBOLDT UNIV,BEREICH MED CHARITE,INST MED IMMUNOL,O-1040 BERLIN,GERMANY
来源
PARASITOLOGY RESEARCH | 1991年 / 77卷 / 07期
关键词
D O I
10.1007/BF00931016
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
As recently reported, Sarcocystis gigantea lectin (SGL) is a powerful mitogen and a polyclonal activator (Syn. S. ovifelis) of human peripheral B-cells. In the present study we investigated the reactivity of human T-helper (CD4) and T-suppressor (CD8) cells to SGL. Mononuclear cells (MNCs) from five newborns and six adults were examined cytofluorometrically for the expression of cell-surface differentiation and activation antigens using a set of seven monoclonal antibodies. In all, 96% of cord-blood and 81% of adult CD4 cells expressed receptors for interleukin-2 (Tac+) after 64 and 164 h incubation, respectively, in the presence of SGL (50-mu-g/ml). The percentages of neonatal and adult Tac+ CD8 cells amounted to 67% and 59%, respectively. Major histocompatibility complex (MHC) class II antigens identified using the monoclonal anti-human leukocyte antigen (HLA)-DR antibody L243 were expressed on 30% (CD4) and 44% (CD8) of adult T-cells. Neonatal HLA-DR+ T-lymphocytes were not detectable. In parallel, functional tests were performed to examine cell proliferation and MNC antibody production.
引用
收藏
页码:577 / 580
页数:4
相关论文
共 50 条
  • [1] Acthar Gel Inhibits the Activation of CD4+ and CD8+ T Cells
    Wright, Dale
    Hayes, Kyle
    JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2023, 43 (04): : 182 - 187
  • [2] Heterogeneity of CD4+ and CD8+ T cells
    Woodland, DL
    Dutton, RW
    CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (03) : 336 - 342
  • [3] CD4+ and CD8+ T Cell Activation Are Associated with HIV DNA in Resting CD4+ T Cells
    Cockerham, Leslie R.
    Siliciano, Janet D.
    Sinclair, Elizabeth
    O'Doherty, Una
    Palmer, Sarah
    Yukl, Steven A.
    Strain, Matt C.
    Chomont, Nicolas
    Hecht, Frederick M.
    Siliciano, Robert F.
    Richman, Douglas D.
    Deeks, Steven G.
    PLOS ONE, 2014, 9 (10):
  • [4] Differentiation of human alloreactive CD4+ and CD8+ T cells in vitro
    Nikolaeva, N
    Uss, E
    van Leeuwen, EMM
    van Lier, RAW
    ten Berge, IJM
    TRANSPLANTATION, 2004, 78 (06) : 815 - 824
  • [5] Canine CD4+ CD8+ double-positive T cells can develop from CD4+ and CD8+ T cells
    Bismarck, Doris
    Moore, Peter F.
    Alber, Gottfried
    von Buttlar, Heiner
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2014, 162 (3-4) : 72 - 82
  • [6] Differentiation of subsets of CD4+ and CD8+ T cells
    Mosmann, TR
    Sad, S
    Krishnan, L
    Wegmann, TG
    Guilbert, LJ
    Belosevic, M
    T CELL SUBSETS IN INFECTIOUS AND AUTOIMMUNE DISEASES, 1995, 195 : 42 - 50
  • [7] Human fetal retinal pigment epithelium suppresses the activation of CD4+ and CD8+ T-cells
    L. Farrokh-Siar
    K. A. Rezai
    R. T. Semnani
    S. C. Patel
    J. T. Ernest
    G.A. van Seventer
    Graefe's Archive for Clinical and Experimental Ophthalmology, 1999, 237 : 934 - 939
  • [8] Human fetal retinal pigment epithelium suppresses the activation of CD4+ and CD8+ T-cells
    Farrokh-Siar, L
    Rezai, KA
    Semnani, RT
    Patel, SC
    Ernest, JT
    van Seventer, GA
    GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1999, 237 (11) : 934 - 939
  • [9] THE ROLES OF CD8+ AND CD4+ CELLS IN TUMOR REJECTION
    UDONO, H
    MIENO, M
    SHIKU, H
    NAKAYAMA, E
    JAPANESE JOURNAL OF CANCER RESEARCH, 1989, 80 (07): : 649 - 654
  • [10] Characteristics of differentiated CD8+ and CD4+ T cells present in the human brain
    Smolders, Joost
    Remmerswaal, Ester B. M.
    Schuurman, Karianne G.
    Melief, Jeroen
    van Eden, Corbert G.
    van Lier, Rene A. W.
    Huitinga, Inge
    Hamann, Jorg
    ACTA NEUROPATHOLOGICA, 2013, 126 (04) : 525 - 535