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针对来自烟曲霉f16变应原的HLA II类限制性表位产生Th1 T细胞应答。

Generation of Th1 T cell responses directed to a HLA Class II restricted epitope from the Aspergillus f16 allergen.

作者信息

Ramadan G, Davies B, Kurup V P, Keever-Taylor C A

机构信息

Medical College of Wisconsin, BMT Program, Milwaukee, WI 53226, USA.

出版信息

Clin Exp Immunol. 2005 Feb;139(2):257-67. doi: 10.1111/j.1365-2249.2005.02699.x.

Abstract

The Aspergillus allergen Asp f16 has been shown to confer protective Th1 T cell-mediated immunity against infection with Aspergillus conidia in murine models. Here, we use overlapping (11-aa overlap with preceding peptide) pentadecapeptides spanning the entire 427-aa coding region of Asp f16 presented on autologous dendritic cells (DC) to evaluate the ability of this antigen to induce Th1 responses in humans. Proliferative responses were induced in five out of five donors, and one line with a high frequency of interferon (IFN)-gamma-producing CD4(+) T cells in response to the complete peptide pool was characterized. This line was cytotoxic to autologous pool-pulsed and Aspergillus culture extract-pulsed targets. Limitation of cytotoxicity to the CD4(+) T cell subset was demonstrated by co-expression of the degranulation marker CD107a in response to peptide pool-pulsed targets. Cytotoxic T lymphocytes (CTL) killed Aspergillus hyphae and CTL culture supernatant killed Aspergillus conidia. By screening 21 smaller pools and individual peptides shared by positive pools we identified a single candidate sequence of TWSIDGAVVRT that elicited responses equal to the complete pool. The defined epitope was presented by human leucocyte antigen (HLA)-DRB1-0301. These data identify the first known Aspergillus-specific T cell epitope and support the use of Asp f16 in clinical immunotherapy protocols to prime protective immune responses to prevent or treat Aspergillus infection in immunocompromised patients.

摘要

在小鼠模型中,已证明烟曲霉变应原Asp f16可赋予保护性Th1 T细胞介导的免疫,以抵抗烟曲霉分生孢子感染。在此,我们使用跨越Asp f16整个427个氨基酸编码区域的重叠(与前一个肽有11个氨基酸重叠)十五肽,将其呈递于自体树突状细胞(DC)上,以评估该抗原在人类中诱导Th1反应的能力。在五名供体中的五名中均诱导出增殖反应,并对一条在响应完整肽库时产生干扰素(IFN)-γ的CD4(+) T细胞频率较高的细胞系进行了表征。该细胞系对自体库脉冲和烟曲霉培养提取物脉冲的靶细胞具有细胞毒性。通过脱颗粒标记物CD107a对肽库脉冲靶细胞的共表达,证明了细胞毒性仅限于CD4(+) T细胞亚群。细胞毒性T淋巴细胞(CTL)杀死烟曲霉菌丝,CTL培养上清液杀死烟曲霉分生孢子。通过筛选21个较小的库和阳性库共有的单个肽,我们鉴定出一个单一的候选序列TWSIDGAVVRT,其引发反应等同于完整库。确定的表位由人类白细胞抗原(HLA)-DRB1-0301呈递。这些数据确定了首个已知的烟曲霉特异性T细胞表位,并支持在临床免疫治疗方案中使用Asp f16来引发保护性免疫反应,以预防或治疗免疫功能低下患者的烟曲霉感染。

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