T(H)2-TYPE INFILTRATING T-CELLS IN NICKEL-INDUCED CONTACT-DERMATITIS

被引:64
作者
PROBST, P
KUNTZLIN, D
FLEISCHER, B
机构
[1] Department of Medical Microbiology and Immunology, Bernhard-Nocht Institute for Tropical Medicine, Hamburg
关键词
D O I
10.1006/cimm.1995.1196
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The T cell response to nickel-modified endogenous peptides is involved in the immunopathogenesis of nickel-induced contact dermatitis. Nickel-reactive T cells described so far display a T(H)1 lymphokine secretion pattern characterized by high amounts of IFN gamma, but Little or no IL-4 and IL-5. In this paper we demonstrate that nickel-reactive T cells can belong to the THO and even to the T(H)2 CD4(+) T cell subset. Nickel-reactive T cell clones (TCC) were derived from the lesion of a patient with nickel contact dermatitis. These TCC responded to nickel with the production of high levels of IL-5 and variable amounts of IFN-gamma and IL-4 resembling a T(H)2- or T(H)0-like cytokine secretion pattern. None of the nickel-reactive TCC showed a clear cut T(H)1 profile. We show that IL-4 was a growth factor for the T(H)2 and some of the T(H)0 TCC. We conclude that nickel is able to induce T(H)2 cells and that in this patient with a typical nickel-induced contact dermatitis T(H)2 cells are prevalent and might contribute to the immunopathogenesis of contact dermatitis. (C) 1995 Academic Press, Inc.
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页码:134 / 140
页数:7
相关论文
共 27 条
[1]   STABLE GROWTH TRANSFORMATION OF HUMAN LYMPHOCYTES-T BY HERPESVIRUS SAIMIRI [J].
BIESINGER, B ;
MULLERFLECKENSTEIN, I ;
SIMMER, B ;
LANG, G ;
WITTMANN, S ;
PLATZER, E ;
DESROSIERS, RC ;
FLECKENSTEIN, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :3116-3119
[2]  
CHANG TL, 1990, J IMMUNOL, V145, P2803
[3]  
DECARLI M, 1993, J IMMUNOL, V151, P5022
[4]  
DIELI F, 1994, J IMMUNOL, V152, P2698
[5]  
GOCINSKI BL, 1990, J IMMUNOL, V144, P4121
[6]   DEVELOPMENT OF TH1 CD4+ T-CELLS THROUGH IL-12 PRODUCED BY LISTERIA-INDUCED MACROPHAGES [J].
HSIEH, CS ;
MACATONIA, SE ;
TRIPP, CS ;
WOLF, SF ;
OGARRA, A ;
MURPHY, KM .
SCIENCE, 1993, 260 (5107) :547-549
[7]  
HSIEH CS, 1993, INT IMMUNOL, V5, P371
[8]   CD4+ T-CELLS - SPECIFICITY AND FUNCTION [J].
JANEWAY, CA ;
CARDING, S ;
JONES, B ;
MURRAY, J ;
PORTOLES, P ;
RASMUSSEN, R ;
ROJO, J ;
SAIZAWA, K ;
WEST, J ;
BOTTOMLY, K .
IMMUNOLOGICAL REVIEWS, 1988, 101 :39-80
[9]   NICKEL-SPECIFIC LYMPHOCYTE-T CLONES DERIVED FROM ALLERGIC NICKEL-CONTACT DERMATITIS LESIONS IN MAN - HETEROGENEITY BASED ON REQUIREMENT OF DENDRITIC ANTIGEN-PRESENTING CELL SUBSETS [J].
KAPSENBERG, ML ;
RES, P ;
BOS, JD ;
SCHOOTEMIJER, A ;
TEUNISSEN, MBM ;
VANSCHOOTEN, W .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (06) :861-865
[10]   TH1 LYMPHOKINE PRODUCTION PROFILES OF NICKEL-SPECIFIC CD4+ LYMPHOCYTE-T CLONES FROM NICKEL CONTACT ALLERGIC AND NONALLERGIC INDIVIDUALS [J].
KAPSENBERG, ML ;
WIERENGA, EA ;
STIEKEMA, FEM ;
TIGGELMAN, AMBC ;
BOS, JD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 98 (01) :59-63