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局部用氮芥通过靶向浸润淋巴细胞,恢复患有斑秃样疾病小鼠中自身免疫性停滞的毛囊活性。

Topical mechlorethamine restores autoimmune-arrested follicular activity in mice with an alopecia areata-like disease by targeting infiltrated lymphocytes.

作者信息

Tang Liren, Cao Liping, Bernardo Olga, Chen Yongliang, Sundberg John P, Lui Harvey, Chung Stephen, Shapiro Jerry

机构信息

Division of Dermatology, Department of Surgery, University of British Columbia and Vancouver General Hospital, Vancouver, Canada.

出版信息

J Invest Dermatol. 2003 Mar;120(3):400-6. doi: 10.1046/j.1523-1747.2003.12059.x.

DOI:10.1046/j.1523-1747.2003.12059.x
PMID:12603852
Abstract

Alopecia areata is an autoimmune disease targeted at hair follicles with infiltrated T lymphocytes probably playing an important role in the pathogenesis. It was reported in 1985 that mechlorethamine was effective on alopecia areata patients. This has never been confirmed since. The aims of the study were to investigate the effects of mechlorethamine on balding C3H/HeJ mice affected with an alopecia-areata-like disease and to study the underlying mechanisms. Mice were treated on half of the dorsal skin with mechlorethamine and the contralateral side was treated with the vehicle ointment. After 10 wk of mechlorethamine therapy, a full pelage of hair covered the treated side in all the mice and was maintained during the study, whereas the vehicle-treated sides showed either no change or continued hair loss. Immunohistochemistry revealed that infiltrated CD4+ and CD8+ lymphocytes were eliminated from the treated side. In vitro cell viability assay showed that lymphocytes were much more sensitive to the cytotoxic effects of mechlorethamine than skin and hair follicular cells. RNase protection assay and real-time reverse transcription polymerase chain reaction showed that tumor necrosis factor alpha/beta, interleukin-12, and interferon-gamma were inhibited by mechlorethamine upon successful treatment. Our findings support that mechlorethamine restores follicular activity by selectively targeting infiltrated lymphocytes in vivo in alopecia-areata-affected mice.

摘要

斑秃是一种针对毛囊的自身免疫性疾病,浸润的T淋巴细胞可能在发病机制中起重要作用。1985年有报道称氮芥对斑秃患者有效。但此后从未得到证实。本研究的目的是研究氮芥对患有斑秃样疾病的C3H/HeJ秃毛小鼠的影响,并探讨其潜在机制。用氮芥处理小鼠背部皮肤的一半,对侧用赋形剂软膏处理。氮芥治疗10周后,所有小鼠治疗侧均被完整的毛发覆盖,且在研究期间保持不变,而赋形剂处理侧则无变化或持续脱发。免疫组织化学显示,治疗侧浸润的CD4+和CD8+淋巴细胞被清除。体外细胞活力测定表明,淋巴细胞对氮芥的细胞毒性作用比皮肤和毛囊细胞更敏感。核糖核酸酶保护试验和实时逆转录聚合酶链反应表明,成功治疗后,氮芥可抑制肿瘤坏死因子α/β、白细胞介素-12和干扰素-γ。我们的研究结果支持氮芥通过在体内选择性地靶向斑秃小鼠中浸润的淋巴细胞来恢复毛囊活性。

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Topical mechlorethamine restores autoimmune-arrested follicular activity in mice with an alopecia areata-like disease by targeting infiltrated lymphocytes.局部用氮芥通过靶向浸润淋巴细胞,恢复患有斑秃样疾病小鼠中自身免疫性停滞的毛囊活性。
J Invest Dermatol. 2003 Mar;120(3):400-6. doi: 10.1046/j.1523-1747.2003.12059.x.
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Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-affected skin from C3H/HeJ mice.Fas缺陷的C3.MRL-Tnfrsf6(lpr)小鼠和Fas配体缺陷的C3H/HeJ-Tnfsf6(gld)小鼠,通过移植来自C3H/HeJ小鼠的斑秃病变皮肤,相对不易被诱导发生斑秃。
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The C3H/HeJ mouse and DEBR rat models for alopecia areata: review of preclinical drug screening approaches and results.斑秃的C3H/HeJ小鼠和DEBR大鼠模型:临床前药物筛选方法及结果综述
Exp Dermatol. 2008 Oct;17(10):793-805. doi: 10.1111/j.1600-0625.2008.00773.x.
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Alopecia areata, primary sclerosing cholangitis, and ulcerative colitis: autoimmunity and apoptosis as common links?
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Dig Dis Sci. 2007 May;52(5):1288-92. doi: 10.1007/s10620-006-9265-3. Epub 2007 Mar 20.