Differential expression of cytokine mRNA in skin specimens from patients with erythema migrans or acrodermatitis chronica atrophicans

被引:65
作者
Müllegger, RR
McHugh, G
Ruthazer, R
Binder, B
Kerl, H
Steere, AC
机构
[1] Karl Franzens Univ Graz, Sch Med, Dept Dermatol, A-8036 Graz, Austria
[2] Tufts Univ, New England Med Ctr, Sch Med, Div Rheumatol Immunol, Boston, MA USA
[3] Tufts Univ, New England Med Ctr, Sch Med, Div Clin Care Res, Boston, MA USA
关键词
acrodermatitis chronica atrophicans; cytokines; erythema migrans; in situ hybridization;
D O I
10.1046/j.1523-1747.2000.00198.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Erythema migrans, the characteristic skin manifestation of acute Lyme borreliosis, is a self-limited lesion. In contrast, acrodermatitis chronica atrophicans, the typical cutaneous manifestation of late Lyme borreliosis, is a chronic skin condition. In an effort to understand pathogenic factors that lead to different outcomes in dermatoborrelioses, skin biopsy samples from 42 patients with erythema migrans and 27 patients with acrodermatitis chronica atrophicans were analyzed for mRNA expression of five pro-inflammatory cytokines (tumor necrosis factor alpha, interleukin-1 beta, interleukin-6, interferon-gamma, and interleukin-2) and two anti-inflammatory cytokines (interleukin-4 and interleukin-10) by in situ hybridization with cytokine-specific riboprobes. Among the 27 patients who had erythema migrans alone with no associated signs or symptoms, the major cytokines expressed in perivascular infiltrates of T cells and macrophages were the pro-inflammatory cytokine interferon-gamma and the anti-inflammatory cytokine interleukin-10. In the 15 erythema migrans patients who had associated signs and symptoms, including headache, elevated temperature, arthralgias, myalgias, or fatigue, a larger number of macrophages and greater expression of macrophage-derived pro-inflammatory cytokines, tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6, were also found. In comparison, infiltrates of T cells and macrophages in the skin lesions of acrodermatitis chronica atrophicans patients had very little or no interferon-gamma expression. Instead, they usually expressed only the pro-inflammatory cytokine tumor necrosis factor a and the anti-inflammatory cytokine interleukin-4. Thus, the activation of pro-inflammatory cytokines in erythema migrans lesions, particularly interferon-gamma, seems to be important in the control of the spirochetal infection. In contrast, the restricted pattern of cytokine expression in acrodermatitis chronica atrophicans, including the lack of interferon-gamma, may be less effective in spirochetal killing, resulting in the chronicity of this skin lesion.
引用
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页码:1115 / 1123
页数:9
相关论文
共 58 条
[1]  
ANDERSON S, 1994, DR DOBBS J, V19, P16
[2]   EVIDENCE FOR THE INVOLVEMENT OF DIFFERENT GENOSPECIES OF BORRELIA IN THE CLINICAL OUTCOME OF LYME-DISEASE IN BELGIUM [J].
ANTHONISSEN, FM ;
DEKESEL, M ;
HOET, PP ;
BIGAIGNON, GH .
RESEARCH IN MICROBIOLOGY, 1994, 145 (04) :327-331
[3]  
ASBRINK E, 1985, ACTA DERM-VENEREOL, V65, P43
[4]   EARLY AND LATE CUTANEOUS MANIFESTATIONS IN IXODES-BORNE BORRELIOSIS (ERYTHEMA MIGRANS BORRELIOSIS, LYME BORRELIOSIS) [J].
ASBRINK, E ;
HOVMARK, A .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 539 :4-15
[5]  
ASBRINK E, 1985, ACTA PATH MICRO IM B, V93, P161
[6]   DELINEATION OF BORRELIA-BURGDORFERI SENSU-STRICTO, BORRELIA-GARINII SP-NOV, AND GROUP VS461 ASSOCIATED WITH LYME BORRELIOSIS [J].
BARANTON, G ;
POSTIC, D ;
SAINTGIRONS, I ;
BOERLIN, P ;
PIFFARETTI, JC ;
ASSOUS, M ;
GRIMONT, PAD .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (03) :378-383
[7]   LYME BORRELIOSIS IN SELECTED STRAINS AND AGES OF LABORATORY MICE [J].
BARTHOLD, SW ;
BECK, DS ;
HANSEN, GM ;
TERWILLIGER, GA ;
MOODY, KD .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (01) :133-138
[8]   ERYTHEMA CHRONICUM MIGRANS OF LYME-DISEASE [J].
BERGER, BW .
ARCHIVES OF DERMATOLOGY, 1984, 120 (08) :1017-1021
[9]  
Boehm K D, 1995, Exp Dermatol, V4, P335, DOI 10.1111/j.1600-0625.1995.tb00057.x
[10]  
BOEHM KD, 1994, LYMPHOKINE CYTOK RES, V13, P9