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本文引用的文献

1
Pathophysiology of fixed drug eruption: the role of skin-resident T cells.固定性药疹的病理生理学:皮肤驻留T细胞的作用。
Curr Opin Allergy Clin Immunol. 2002 Aug;2(4):317-23. doi: 10.1097/00130832-200208000-00005.
2
Cellular and molecular pathophysiology of cutaneous drug reactions.皮肤药物反应的细胞和分子病理生理学
Am J Clin Dermatol. 2002;3(4):229-38. doi: 10.2165/00128071-200203040-00001.
3
Delayed reactions to drugs show levels of perforin, granzyme B, and Fas-L to be related to disease severity.药物的延迟反应显示穿孔素、颗粒酶B和Fas-L的水平与疾病严重程度相关。
J Allergy Clin Immunol. 2002 Jan;109(1):155-61. doi: 10.1067/mai.2002.120563.
4
Behçet's disease: infectious aetiology, new autoantigens, and HLA-B51.白塞病:感染病因、新自身抗原与HLA - B51
Ann Rheum Dis. 2001 Nov;60(11):996-1002. doi: 10.1136/ard.60.11.996.
5
T cell involvement in cutaneous drug eruptions.T细胞在皮肤药物疹中的作用。
Clin Exp Allergy. 2001 Sep;31(9):1398-408. doi: 10.1046/j.1365-2222.2001.01164.x.
6
T-cell involvement in drug-induced acute generalized exanthematous pustulosis.T细胞参与药物性急性泛发性脓疱病。
J Clin Invest. 2001 Jun;107(11):1433-41. doi: 10.1172/JCI12118.
7
Pathogenesis of drug-induced exanthema.药物性皮疹的发病机制。
Int Arch Allergy Immunol. 2001 Jan-Mar;124(1-3):336-8. doi: 10.1159/000053750.
8
Acute generalized exanthematous pustulosis (AGEP)--a clinical reaction pattern.急性泛发性脓疱性皮病(AGEP)——一种临床反应模式。
J Cutan Pathol. 2001 Mar;28(3):113-9. doi: 10.1034/j.1600-0560.2001.028003113.x.
9
Neutrophilic drug eruptions.嗜中性粒细胞性药物疹
Clin Dermatol. 2000 May-Jun;18(3):331-7. doi: 10.1016/s0738-081x(99)00124-8.
10
Infiltration of cytotoxic T cells in drug-induced cutaneous eruptions.细胞毒性T细胞在药物性皮肤疹中的浸润。
Clin Exp Allergy. 2000 Jun;30(6):847-55. doi: 10.1046/j.1365-2222.2000.00847.x.

急性泛发性脓疱性皮病:细胞毒性T细胞在脓疱形成中的作用

Acute generalized exanthematous pustulosis: role of cytotoxic T cells in pustule formation.

作者信息

Schmid Simone, Kuechler Petra C, Britschgi Markus, Steiner Urs C, Yawalkar Nikhil, Limat Alain, Baltensperger Kurt, Braathen Lasse, Pichler Werner J

机构信息

Clinic of Rheumatology and Clinical Immunology/Allergology, Inselspital, CH-3010 Bern, Switzerland.

出版信息

Am J Pathol. 2002 Dec;161(6):2079-86. doi: 10.1016/S0002-9440(10)64486-0.

DOI:10.1016/S0002-9440(10)64486-0
PMID:12466124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1850901/
Abstract

Extensive formation of nonfollicular sterile pustules on erythematous background combined with fever and peripheral blood leukocytosis are the characteristics of acute generalized exanthematous pustulosis. This uncommon eruption most often is an allergic reaction because of drugs such as aminopenicillins and sulfonamides inter alia. We recently demonstrated the important role of drug-specific T cells in the pathogenesis of this disease, showing that they produce high amounts of the neutrophil-attracting chemokine interleukin-8 and therefore stand out as a special subgroup of T cells, differing from the usual Th1 and Th2 subsets. In this study we use immunohistochemistry as well as cytotoxicity assays (4- and 18-hour assays) and fluorescence-activated cell-sorting analysis of drug-specific circulating T cells and of cells eluted from the skin of five patients with acute generalized exanthematous pustulosis, to analyze whether cytotoxic T-cell functions are important in the pathogenesis of this disease, in particular for the formation of vesicles. The data reveal that drug-specific CD4(+) as well as CD8(+) T cells both are activated and cytotoxic; perforin/granzyme B and to a variable degree the Fas/FasL-killing mechanism is involved in tissue destruction. These features allow the formation of vesicles. Additional secretion of interleukin-8 by T cells and keratinocytes attracts neutrophils that fill the vesicles and transform them into pustules.

摘要

在红斑背景上广泛形成非毛囊性无菌脓疱,并伴有发热和外周血白细胞增多,是急性泛发性发疹性脓疱病的特征。这种不常见的皮疹最常见的是由氨基青霉素和磺胺类等药物引起的过敏反应。我们最近证明了药物特异性T细胞在该疾病发病机制中的重要作用,表明它们产生大量吸引中性粒细胞的趋化因子白细胞介素-8,因此作为T细胞的一个特殊亚群脱颖而出,不同于常见的Th1和Th2亚群。在本研究中,我们使用免疫组织化学以及细胞毒性测定(4小时和18小时测定),并对5例急性泛发性发疹性脓疱病患者的药物特异性循环T细胞和从皮肤洗脱的细胞进行荧光激活细胞分选分析,以分析细胞毒性T细胞功能在该疾病发病机制中是否重要,特别是对于水疱的形成。数据显示,药物特异性CD4(+)以及CD8(+) T细胞均被激活且具有细胞毒性;穿孔素/颗粒酶B以及不同程度的Fas/FasL杀伤机制参与组织破坏。这些特征使得水疱得以形成。T细胞和角质形成细胞额外分泌白细胞介素-8会吸引中性粒细胞,中性粒细胞填充水疱并将其转化为脓疱。