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小鼠巨细胞病毒感染和移植物抗宿主反应期间的间质性肺炎。支气管肺泡灌洗细胞的特征

Interstitial pneumonitis during murine cytomegalovirus infection and graft-versus-host reaction. Characterization of bronchoalveolar lavage cells.

作者信息

Shanley J D, Via C S, Sharrow S O, Shearer G M

机构信息

Veterans Administration Medical Center, University of Connecticut, Newington 06111.

出版信息

Transplantation. 1987 Nov;44(5):658-62.

PMID:2446406
Abstract

Acute murine cytomegalovirus (MCMV) infection alters the course of graft-vs-host (GVH) disease involving major histocompatibility (MHC) antigens and induces interstitial pneumonitis. F1 (B10 x B10.BR) mice given 20 x 10(6) B10.BR spleen cells and MCMV (1 x 10(5) plaque-forming units [PFU]) develop severe, diffuse pneumonitis not seen with either MCMV or GVH alone. As one index of the host immune processes operating in the lungs during MCMV/GVH pneumonitis, we examined the types of cells recovered from the lung by bronchoalveolar lavage (BAL) during pneumonitis. During MCMV/GVH pneumonitis, the total cells recovered significantly increased, due primarily to an influx of Thy 1.2 lymphocytes. Characterization of cells using multiparameter flow cytometric analysis revealed that greater than 80% of all BAL cells were Thy 1.2-positive lymphocytes of donor origin. In addition, donor Thy 1.2-positive cells were of both the L3T4+ (43% of BAL cells) and Lyt 2+ (38% of BAL cells) phenotype. Thus, MCMV infection during GVH to MHC antigens induces interstitial pneumonitis, characterized by an influx of T lymphocytes (both helper and suppressor/cytotoxic) from the donor. The antigenic specificity of these cells is not known.

摘要

急性小鼠巨细胞病毒(MCMV)感染会改变涉及主要组织相容性(MHC)抗原的移植物抗宿主(GVH)疾病进程,并诱发间质性肺炎。给F1(B10×B10.BR)小鼠注射20×10⁶个B10.BR脾细胞和MCMV(1×10⁵个空斑形成单位[PFU]),会引发严重的弥漫性肺炎,单独的MCMV或GVH均不会出现这种情况。作为MCMV/GVH肺炎期间肺部宿主免疫过程的一个指标,我们检查了肺炎期间通过支气管肺泡灌洗(BAL)从肺中回收的细胞类型。在MCMV/GVH肺炎期间,回收的总细胞显著增加,主要是由于Thy 1.2淋巴细胞的流入。使用多参数流式细胞术分析对细胞进行表征显示,所有BAL细胞中超过80%是供体来源的Thy 1.2阳性淋巴细胞。此外,供体Thy 1.2阳性细胞具有L3T4⁺(占BAL细胞的43%)和Lyt 2⁺(占BAL细胞的38%)两种表型。因此,GVH期间针对MHC抗原的MCMV感染会诱发间质性肺炎,其特征是供体的T淋巴细胞(辅助性和抑制性/细胞毒性)流入。这些细胞的抗原特异性尚不清楚。

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