RESEARCH ON HUMAN AIRWAY EPITHELIUM ACTING AS ALLOANTIGEN-PRESENTING CELLS
RESEARCH ON HUMAN AIRWAY EPITHELIUM ACTING AS ALLOANTIGEN-PRESENTING CELLS
批准号:
06454397
负责人:
NAKAJIMA Jun
金额:
$3.97万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995
中文摘要
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英文摘要
In lung allotransplantation, circulating leukocytes and vascular endothelial cells have been considered to be antigen-presenting cells (APCs). First in this research, we determined whether airway epithelial cells function as APCs.An immortal human epithelial cell line, BEAS-2B (B2B,1*10^5 cells/ml), which constitutively expresses both HLA-class I and class II antigens along with costimulatory molecules, ICAM-1, LFA-3, and B7 on its surface, was irradiated (50Gy) and transferred to 10ml of complete culture medium with allogeneic human peripheral blood lymphocyte (PBL) (1*10^6 cells/ml) from a healthy volunteer. The mixed lymphocyte-epithelial cell line culture (ML-AECL) was then incubated for 3 days, and harvested. As a control study, a one-way mixed lymphocyte culture (MLC) was also made up. Concentration of interleukin (IL) -10 in each supeynatant were assayd using an EASIA method. The concentration of IL-10 was not elevatedin MLC (9.3<plus-minus>11.8pg/ml, N=5) but significantly elev … More atedin ML-AECL (128<plus-minus>110pg/ml, N=5, p=0.043). Stimulation of B2B induceda population of allogeneic lymphocytes to proliferate and secrete IL-10. It has been reported that Th2, a subset of helper-T cells, secretes IL-10, which in turn inhibits both Th1 and cytotoxic T cells (CTLs) from proliferating and becoming active. We suggest that airway epithelial cells stimulate Th2, and, as a result, may play a role is suppressiing the allospecific reaction in acute rejection.Second, we investigated the role of costimulatory molecules on B2B.B2B were pretreated with either anti-HLA class I,anti-HLA class II,anti : ICAM-1, anti-LFA-3, or anti-B7 monoclonal antibody, Then the ML-AECL culture was then incubated, and harvested. Cell proliferation assay was performed using the colorimetric (MTT) assay. The MTT indeces (percentages relative to the control) were found to be significantly lower than the control when HLA class I,class II or LFA-3 on B2B was masked. In mixed culture consisting of B2B cells as stimulators and allogeneic lymphocytes, the lymphocytes recognized MHC-class I and II antigens expressed on the BEAS-2B.LFA-3 on BEAS-2B also contributed to the activation of lymphocyte alloreactivity. Less
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Nakajima J, Furuse A, et al: "Hemoptysis from emphysematous bulla following open heart surgery." Surgery Today. (in press). (1996)
Nakajima J、Furuse A 等人:“心脏直视手术后肺气肿大疱导致咯血。”
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中島 淳,他: "結節性硬化症に合併した過誤腫性肺脈管筋腫症-特異な臨床修飾が加えられた1例-" 日本胸部疾患学会雑誌. 33. 80-84 (1995)
Jun Nakajima 等人:“错构瘤性肺血管肌瘤病并发结节性硬化症 - 具有独特临床修改的病例”日本胸科疾病学会杂志 33. 80-84 (1995)。
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Hiroshi Oiwa, Jun Nakajima, Akira Furuse, et al: "[The distribution of FK506 in the blood and other organs on a non-human primate model of lung transplantation] (Japanese manuscript with English abstract)" Japanese Journal of Transplantation. 29. 144-148
Hiroshi Oiwa、Jun Nakajima、Akira Furuse 等人:“[FK506 在非人灵长类肺移植模型的血液和其他器官中的分布](日文手稿,英文摘要)”《日本移植杂志》。
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Jun Nakajima: "Problems in xenografted lung of the primates.(in Update clinical immunology,Molecular Science in Organ Transplantation)" Pabst Science Publishers,Lengerich,Germany(出版中), 20 (1996)
Jun Nakajima:“灵长类异种移植肺的问题。(更新临床免疫学,器官移植中的分子科学)”Pabst Science Publishers,Lengerich,德国(印刷中),20(1996)
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Jun Nakajima, Akira Furuse, Teruaki Oka, et al: "Excellent Survival in a subgroup of patients with intrapulmonary metastasis of lung cancer." Annals of Thoracis Surgery. 61. 158-163 (1996)
Jun Nakajima、Akira Furuse、Teruaki Oka 等人:“肺癌肺内转移患者亚组的存活率极好。”
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