Yurovsky V V, Weersink E J, Meltzer S S, Moore W C, Postma D S, Bleecker E R, White B
Department of Medicine, University of Maryland, Baltimore, Maryland 21201, USA.
Am J Respir Cell Mol Biol. 1998 Mar;18(3):370-83. doi: 10.1165/ajrcmb.18.3.2935.
T cells play a pivotal role in initiating and orchestrating allergic responses in asthma. The goal of this work was to learn whether ragweed challenge in the lungs alters the T-cell repertoire expressed in the blood and lungs of atopic asthmatics. Analyses of cell numbers, differentials, and T-cell subsets in bronchoalveolar lavage (BAL) fluids showed that ragweed challenge was associated with preferential recruitment of CD4+ T cells into the lungs. A reverse transcriptase-polymerase chain reaction (RT-PCR) was used to amplify T-cell receptor (TCR) gene transcripts from unfractionated, CD4+, and CD8+ T cells in blood and BAL fluids. As judged by RT-PCR, the usage of TCR Valpha and Vbeta gene families in BAL fluids was similar to that in blood. Ragweed challenge did not change the levels of expression of these V gene families. The clonality of T cells was estimated by analyzing the diversity of TCR V-(D)-J junctional region nucleotide lengths associated with each Valpha and Vbeta gene family, using sequencing gel electrophoresis. Most V gene families in blood and BAL fluids were associated with multiple junctional region lengths before and after ragweed challenge, indicating polyclonal expression. Some V gene families were expressed in an oligoclonal manner in unfractionated, CD4+, and CD8+ T cells in BAL fluids before ragweed challenge, as indicated by a few predominant junctional region lengths. The majority of these V gene families became polyclonal after challenge, compatible with polyclonal T-cell influx during inflammation immediately after ragweed challenge. However, some V gene families became oligoclonal or developed a new oligoclonal pattern of junctional region lengths in BAL T cells after ragweed challenge. Surprisingly, this occurred in both CD4+ and CD8+ T cells. In one of these instances, DNA sequencing of Vbeta21 junctional regions in CD8+ T cells confirmed a change from polyclonal to oligoclonal expression after ragweed challenge. These findings show that ragweed challenge is associated with polyclonal influx and oligoclonal activation of both CD4+ and CD8+ T cells in the lungs.
T细胞在引发和协调哮喘中的过敏反应中起关键作用。这项研究的目的是了解肺部豚草激发是否会改变特应性哮喘患者血液和肺部中表达的T细胞库。对支气管肺泡灌洗(BAL)液中的细胞数量、分类以及T细胞亚群进行分析,结果显示豚草激发与CD4⁺T细胞向肺部的优先募集有关。采用逆转录聚合酶链反应(RT-PCR)从血液和BAL液中的未分离T细胞、CD4⁺T细胞和CD8⁺T细胞中扩增T细胞受体(TCR)基因转录本。通过RT-PCR判断,BAL液中TCR Vα和Vβ基因家族的使用情况与血液中的相似。豚草激发并未改变这些V基因家族的表达水平。通过测序凝胶电泳分析与每个Vα和Vβ基因家族相关的TCR V-(D)-J连接区核苷酸长度的多样性,来估计T细胞的克隆性。在豚草激发前后,血液和BAL液中的大多数V基因家族都与多个连接区长度相关,表明为多克隆表达。在豚草激发前,一些V基因家族在BAL液中的未分离T细胞、CD4⁺T细胞和CD8⁺T细胞中以寡克隆方式表达,表现为少数几个主要的连接区长度。这些V基因家族中的大多数在激发后变为多克隆,这与豚草激发后炎症期间多克隆T细胞流入相一致。然而,一些V基因家族在豚草激发后在BAL T细胞中变为寡克隆或形成了新的连接区长度寡克隆模式。令人惊讶的是,这种情况在CD4⁺和CD8⁺T细胞中均有发生。在其中一个实例中,对CD8⁺T细胞中Vβ21连接区进行DNA测序证实,豚草激发后从多克隆表达转变为寡克隆表达。这些发现表明,豚草激发与肺部CD4⁺和CD8⁺T细胞的多克隆流入和寡克隆激活有关。