CD8+ T cells secreting type 2 lymphokines are defective in protection against viral infection

被引:23
作者
Wirth, S
van den Broek, M
Frossard, CP
Hügin, AW
Leblond, I
Pircher, H
Hauser, C
机构
[1] Hop Cantonal Geneva, Div Immunol & Allergy, Allergy Unit, CH-1211 Geneva 14, Switzerland
[2] Hop Cantonal Geneva, Dept Dermatol, CH-1211 Geneva, Switzerland
[3] Univ Zurich, Inst Expt Immunol, CH-8091 Zurich, Switzerland
[4] Univ Freiburg, Dept Immunol, Inst Med Microbiol & Hyg, Freiburg, Germany
关键词
D O I
10.1006/cimm.2000.1639
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Effector T cells secreting type 1 and/or type 2 lymphokines (Tc1, Tc0, Tc2) were generated in vitro from CD8(+) T cells of mice with a transgenic TCR recognizing lymphocytic choriomeningitis virus (LCMV) glycoprotein to compare their effector function in vitro and in vivo, Tc1, Tc2, and Tc0 showed similar Fas- and perforin-mediated cytotoxicity in vitro. Upon adoptive transfer, Tc2 and Tc0 effecters were less efficient than Tc1 at controlling LCMV or recombinant vaccinia virus expressing the LCMV glycoprotein in vivo, Tc2 and Tc0 had decreased surface VLA-4 density and deficient activation-induced LFA-1/ICAM-1-dependent homotypic adhesion in vitro, Therefore, the reduced antiviral activity in vivo of Tc2 and Tc0 compared with Tc1 is not due to reduced cytotoxic activity or IFN-gamma secretion but may be explained by defective homing to the target organ due to decreased expression and/or lower activity of adhesion molecules. (C) 2000 Academic Press.
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页码:13 / 22
页数:10
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