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1
The antigen-presenting activities of Ia+ dendritic cells shift dynamically from lung to lymph node after an airway challenge with soluble antigen.在用可溶性抗原进行气道刺激后,Ia+树突状细胞的抗原呈递活性从肺动态转移至淋巴结。
J Exp Med. 1995 Apr 1;181(4):1275-83. doi: 10.1084/jem.181.4.1275.
2
The mode of protein antigen administration determines preferential presentation of peptide-class II complexes by lymph node dendritic or B cells.蛋白质抗原的给药方式决定了淋巴结树突状细胞或B细胞对肽-Ⅱ类复合物的优先呈递。
Int Immunol. 1997 Jan;9(1):9-15. doi: 10.1093/intimm/9.1.9.
3
Lung dendritic cells are primed by inhaled particulate antigens, and retain MHC class II/antigenic peptide complexes in hilar lymph nodes for a prolonged period of time.肺树突状细胞由吸入的颗粒性抗原致敏,并在肺门淋巴结中长期保留II类主要组织相容性复合体/抗原肽复合物。
Immunology. 2002 Apr;105(4):488-98. doi: 10.1046/j.1365-2567.2002.01382.x.
4
Pulmonary response to inhaled antigen: neuroimmune interactions promote the recruitment of dendritic cells to the lung and the cellular immune response to inhaled antigen.肺部对吸入抗原的反应:神经免疫相互作用促进树突状细胞向肺部募集以及对吸入抗原的细胞免疫反应。
Am J Pathol. 1997 May;150(5):1735-43.
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Sequestration of inhaled particulate antigens by lung phagocytes. A mechanism for the effective inhibition of pulmonary cell-mediated immunity.肺吞噬细胞对吸入颗粒性抗原的隔离。一种有效抑制肺细胞介导免疫的机制。
Am J Pathol. 1996 Feb;148(2):657-66.
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Antigen-unspecific B cells and lymphoid dendritic cells both show extensive surface expression of processed antigen-major histocompatibility complex class II complexes after soluble protein exposure in vivo or in vitro.在体内或体外暴露于可溶性蛋白质后,抗原非特异性B细胞和淋巴样树突状细胞均显示出加工后的抗原 - 主要组织相容性复合体II类复合物的广泛表面表达。
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7
Dendritic cells but not B cells present antigenic complexes to class II-restricted T cells after administration of protein in adjuvant.在佐剂中给予蛋白质后,树突状细胞而非B细胞将抗原复合物呈递给II类限制性T细胞。
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Following immunization antigen becomes concentrated in a limited number of APCs including B cells.免疫接种后,抗原会集中在包括B细胞在内的少数抗原呈递细胞中。
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FcR+/- subsets of Ia+ pulmonary dendritic cells in the rat display differences in their abilities to provide accessory co-stimulation for naive (OX-22+) and sensitized (OX-22-) T cells.大鼠肺部Ia+肺树突状细胞的FcR+/-亚群在为未致敏(OX-22+)和致敏(OX-22-)T细胞提供辅助共刺激的能力上存在差异。
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Microbial and T cell-derived stimuli regulate antigen presentation by dendritic cells in vivo.微生物和T细胞衍生的刺激物在体内调节树突状细胞的抗原呈递。
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Apoptotic cells activate NKT cells through T cell Ig-like mucin-like-1 resulting in airway hyperreactivity.凋亡细胞通过 T 细胞免疫球蛋白样黏蛋白-1 激活 NKT 细胞,导致气道高反应性。
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T cell responses are required for protection from clinical disease and for virus clearance in severe acute respiratory syndrome coronavirus-infected mice.T 细胞应答对于严重急性呼吸综合征冠状病毒感染小鼠的临床疾病保护和病毒清除是必需的。
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Aryl hydrocarbon receptor activation reduces dendritic cell function during influenza virus infection.芳烃受体激活可降低流感病毒感染期间树突状细胞的功能。
Toxicol Sci. 2010 Aug;116(2):514-22. doi: 10.1093/toxsci/kfq153. Epub 2010 May 23.

本文引用的文献

1
FcR+/- subsets of Ia+ pulmonary dendritic cells in the rat display differences in their abilities to provide accessory co-stimulation for naive (OX-22+) and sensitized (OX-22-) T cells.大鼠肺部Ia+肺树突状细胞的FcR+/-亚群在为未致敏(OX-22+)和致敏(OX-22-)T细胞提供辅助共刺激的能力上存在差异。
Am J Pathol. 1993 Mar;142(3):811-9.
2
T cell priming in situ by intratracheally instilled antigen-pulsed dendritic cells.经气管内注入抗原脉冲树突状细胞在原位引发T细胞反应。
Am J Respir Cell Mol Biol. 1993 Mar;8(3):319-24. doi: 10.1165/ajrcmb/8.3.319.
3
Downregulation of the antigen presenting cell function(s) of pulmonary dendritic cells in vivo by resident alveolar macrophages.驻留肺泡巨噬细胞在体内下调肺树突状细胞的抗原呈递细胞功能。
J Exp Med. 1993 Feb 1;177(2):397-407. doi: 10.1084/jem.177.2.397.
4
Antigen specific T cell priming in vivo by intratracheal injection of antigen presenting cells.通过气管内注射抗原呈递细胞在体内进行抗原特异性T细胞致敏。
Adv Exp Med Biol. 1993;329:571-5. doi: 10.1007/978-1-4615-2930-9_95.
5
Origin and steady-state turnover of class II MHC-bearing dendritic cells in the epithelium of the conducting airways.传导气道上皮中携带II类主要组织相容性复合体的树突状细胞的起源和稳态更新。
J Immunol. 1994 Jul 1;153(1):256-61.
6
Rapid dendritic cell recruitment is a hallmark of the acute inflammatory response at mucosal surfaces.快速的树突状细胞募集是黏膜表面急性炎症反应的一个标志。
J Exp Med. 1994 Apr 1;179(4):1331-6. doi: 10.1084/jem.179.4.1331.
7
Pulmonary dendritic cell populations.肺树突状细胞群体
Adv Exp Med Biol. 1993;329:557-62. doi: 10.1007/978-1-4615-2930-9_93.
8
The local and systemic IgA and IgG antibody responses of rabbits to a soluble inhaled antigen: measurement of responses in a model of acute hypersensitivity pneumonitis.兔对可溶性吸入性抗原的局部和全身IgA及IgG抗体反应:急性过敏性肺炎模型中反应的测定
Am Rev Respir Dis. 1982 Jul;126(1):80-5. doi: 10.1164/arrd.1982.126.1.80.
9
Human alveolar macrophages suppress the proliferative response of peripheral blood lymphocytes.人肺泡巨噬细胞抑制外周血淋巴细胞的增殖反应。
Chest. 1982 Sep;82(3):266-71. doi: 10.1378/chest.82.3.266.
10
Immune responses in rats sensitized with aerosolized antigen. Antibody formation, lymphoblastic responses and mast cell and mucous cell development related to bronchial reactivity.经雾化抗原致敏的大鼠的免疫反应。抗体形成、淋巴细胞反应以及与支气管反应性相关的肥大细胞和黏液细胞发育。
Int Arch Allergy Appl Immunol. 1983;72(1):71-8. doi: 10.1159/000234843.

在用可溶性抗原进行气道刺激后,Ia+树突状细胞的抗原呈递活性从肺动态转移至淋巴结。

The antigen-presenting activities of Ia+ dendritic cells shift dynamically from lung to lymph node after an airway challenge with soluble antigen.

作者信息

Xia W, Pinto C E, Kradin R L

机构信息

Department of Pathology, Massachusetts General Hospital, Boston 02114, USA.

出版信息

J Exp Med. 1995 Apr 1;181(4):1275-83. doi: 10.1084/jem.181.4.1275.

DOI:10.1084/jem.181.4.1275
PMID:7699319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2191960/
Abstract

Dendritic cells (DC) are widely distributed in the lung where they are distinguished by their morphology and class II major histocompatibility complex (Ia) antigen expression. Although a role for DC as pulmonary antigen-presenting cell (APC) has been suggested, little is currently known concerning how these cells respond to inhaled antigens in vivo. Hen-egg lysozyme (HEL) was injected intratracheally into Lewis rats; DC were subsequently purified from the lung and regional lymph nodes (LN) at intervals of up to 14 d and examined for their ability to stimulate the proliferation of HEL-immune T cells in vitro in the absence of added HEL. Pulmonary DC displayed APC activities at 3 h and for up to 7 d after the injection of antigen. Dendritic cells in the draining hilar LN showed APC activities that appeared at 24 h, peaked at day 3, and then diminished progressively. After the primary sensitization, HEL-immune T cells were detected in hilar LN but not in the lung. A second airway challenge with HEL at day 14 yielded an antigen-specific pulmonary immune response, characterized histologically by the accumulation of mononuclear cells around lung venules. We conclude that APC activities shift from lung to lymph node during the response to inhaled antigen.

摘要

树突状细胞(DC)广泛分布于肺中,其形态和II类主要组织相容性复合体(Ia)抗原表达使其得以区分。尽管已有人提出DC作为肺部抗原呈递细胞(APC)的作用,但目前对于这些细胞在体内如何对吸入抗原作出反应知之甚少。将鸡卵溶菌酶(HEL)经气管内注射到Lewis大鼠体内;随后每隔14天从肺和局部淋巴结(LN)中纯化DC,并检测其在不添加HEL的情况下体外刺激HEL免疫T细胞增殖的能力。注射抗原后3小时至7天内,肺部DC表现出APC活性。引流肺门LN中的树突状细胞显示出APC活性,在24小时出现,第3天达到峰值,然后逐渐减弱。初次致敏后,在肺门LN中检测到HEL免疫T细胞,但在肺中未检测到。在第14天用HEL进行第二次气道激发产生了抗原特异性肺部免疫反应,组织学特征为肺小静脉周围单核细胞积聚。我们得出结论,在对吸入抗原的反应过程中,APC活性从肺转移至淋巴结。