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非致敏性表皮皮肤试验可防止随后诱导免疫耐受。

Non-sensitizing epicutaneous skin tests prevent subsequent induction of immune tolerance.

作者信息

van Hoogstraten I M, von Blomberg B M, Boden D, Kraal G, Scheper R J

机构信息

Department of Pathology, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

J Invest Dermatol. 1994 Jan;102(1):80-3. doi: 10.1111/1523-1747.ep12371736.

DOI:10.1111/1523-1747.ep12371736
PMID:7507154
Abstract

Oral administration of nickel or chromium to naive guinea pigs results in immune unresponsiveness to subsequent induction of allergic contact hypersensitivity. Such "oral tolerance" depends on the oral dose, is antigen specific, T-suppressor-cell mediated, and very persistent. In contrast, oral antigen administration to sensitized animals results at best in transient desensitization. Here we report that even non-sensitizing epicutaneous skin contacts prevented the subsequent induction of oral tolerance. These data support the view that primed T cells are less sensitive to suppressor T-cell function than naive T cells.

摘要

给未接触过镍或铬的豚鼠口服镍或铬会导致其对随后诱导的过敏性接触超敏反应产生免疫无反应性。这种“口服耐受”取决于口服剂量,具有抗原特异性,由T抑制细胞介导,且非常持久。相比之下,给致敏动物口服抗原最多只能导致短暂的脱敏。我们在此报告,即使是非致敏性的经皮皮肤接触也能阻止随后口服耐受的诱导。这些数据支持这样一种观点,即已致敏的T细胞比未接触过抗原的T细胞对抑制性T细胞功能的敏感性更低。

相似文献

1
Non-sensitizing epicutaneous skin tests prevent subsequent induction of immune tolerance.非致敏性表皮皮肤试验可防止随后诱导免疫耐受。
J Invest Dermatol. 1994 Jan;102(1):80-3. doi: 10.1111/1523-1747.ep12371736.
2
Persistent immune tolerance to nickel and chromium by oral administration prior to cutaneous sensitization.
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Induction of immunological tolerance by oral administration of nickel and chromium.通过口服镍和铬诱导免疫耐受。
J Dent Res. 1984 Feb;63(2):124-8. doi: 10.1177/00220345840630020501.
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Effects of oral exposure to nickel or chromium on cutaneous sensitization.经口暴露于镍或铬对皮肤致敏的影响。
Curr Probl Dermatol. 1991;20:237-41. doi: 10.1159/000420029.
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Oral and epicutaneous desensitization in urushiol contact dermatitis in guinea pigs sensitized by 2 methods of different sensitizing potency.
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Oral induction of immunological tolerance to chromium in the guinea pig.豚鼠对铬的口服免疫耐受性诱导
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Nickel allergy versus nickel tolerance: can oral uptake of nickel protect from sensitization?镍过敏与镍耐受性:口服镍能预防致敏吗?
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引用本文的文献

1
[Tolerance induction towards nickel. From animal model to humans].[镍的耐受性诱导。从动物模型到人类]
Hautarzt. 2004 Nov;55(11):1052-9. doi: 10.1007/s00105-004-0815-3.
2
Pilot study to assess the effects of early flea exposure on the development of flea hypersensitivity in cats.评估早期接触跳蚤对猫蚤过敏性发展影响的试点研究。
J Feline Med Surg. 2003 Oct;5(5):287-94. doi: 10.1016/S1098-612X(03)00026-3.
3
Orthodontic appliances in relation to nickel hypersensitivity. A review.与镍过敏相关的正畸矫治器。综述。
J Orofac Orthop. 1997;58(2):100-8.
4
Reversal of mucosal tolerance by subcutaneous administration of interleukin-12 at the site of attempted sensitization.在致敏尝试部位皮下注射白细胞介素-12可逆转黏膜耐受性。
Immunology. 1996 Jul;88(3):363-7. doi: 10.1046/j.1365-2567.1996.d01-659.x.