Jimenez-Finkel B E, Murphy J W
Department of Botany/Microbiology, University of Oklahoma, Norman 73019.
Infect Immun. 1988 Apr;56(4):744-50. doi: 10.1128/iai.56.4.744-750.1988.
Previously, we reported that Paracoccidioides brasiliensis culture filtrate antigen (Pb.Ag) when injected i.v. into mice induces antigen-specific suppressor cells which down-regulate the anti-P. brasiliensis delayed-type hypersensitivity (DTH) response. The suppressor cells are present in both spleens and lymph nodes of Pb.Ag-treated animals and suppress the afferent limb but not the efferent limb of the DTH response to P. brasiliensis. The suppressor cells induced by Pb.Ag are L3T4+ Lyt-1+2- I-J+ T cells and are considered to be equivalent to the Ts1 cells described for other antigen-specific suppressor cell pathways. This report provides data which show that Ts1 cells induced by Pb.Ag or a soluble factor derived from Ts1 cells (TsF1) stimulates the production of second-order or efferent suppressor cells. The second-order suppressor cells are detectable in spleens and lymph nodes of mice 7 days after injection of Ts1 cells or TsF1 and are specific in suppressing the paracoccidioidal DTH response. In addition, the second-order suppressor cells are T cells with an L3T4- Lyt-2+ I-J+ phenotype and are effective in suppressing only the efferent limb of the P. brasiliensis DTH response. On the basis of the characteristics defined in this study, the paracoccidioidal second-order suppressor cells are equivalent to the Ts2 cells described for other antigen-specific suppressor-cell pathways. Thus, the suppressive circuit induced by Pb.Ag is similar to the suppressor-cell pathways that regulate the DTH responses to azobenzenearsonate, 4-hydroxy-3-nitrophenyl acetyl, lysozyme, and Cryptococcus neoformans antigen. We propose that such a suppressor-cell circuit as defined here with the murine model could be responsible for the depressed cell-mediated immune responses observed in paracoccidioidomycosis patients who have antigen circulating in their sera.
此前,我们报道巴西副球孢子菌培养滤液抗原(Pb.Ag)经静脉注射到小鼠体内时,可诱导抗原特异性抑制细胞,这些细胞会下调抗巴西副球孢子菌迟发型超敏反应(DTH)。抑制细胞存在于接受Pb.Ag处理动物的脾脏和淋巴结中,抑制对巴西副球孢子菌DTH反应的传入支而非传出支。由Pb.Ag诱导的抑制细胞是L3T4 + Lyt-1 + 2 - I-J + T细胞,被认为等同于针对其他抗原特异性抑制细胞途径所描述的Ts1细胞。本报告提供的数据表明,由Pb.Ag或源自Ts1细胞的可溶性因子(TsF1)诱导的Ts1细胞可刺激二阶或传出抑制细胞的产生。在注射Ts1细胞或TsF1后7天,可在小鼠的脾脏和淋巴结中检测到二阶抑制细胞,它们特异性抑制副球孢子菌DTH反应。此外,二阶抑制细胞是具有L3T4 - Lyt-2 + I-J +表型的T细胞,仅有效抑制巴西副球孢子菌DTH反应的传出支。基于本研究中定义的特征,副球孢子菌二阶抑制细胞等同于针对其他抗原特异性抑制细胞途径所描述的Ts2细胞。因此,由Pb.Ag诱导的抑制回路类似于调节对偶氮苯胂酸盐、4-羟基-3-硝基苯基乙酰、溶菌酶和新型隐球菌抗原的DTH反应的抑制细胞途径。我们提出,此处用小鼠模型定义的这种抑制细胞回路可能是导致血清中存在抗原的副球孢子菌病患者细胞介导免疫反应低下的原因。