McArthur Monica A, Sztein Marcelo B
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
PLoS One. 2012;7(6):e38408. doi: 10.1371/journal.pone.0038408. Epub 2012 Jun 5.
Salmonella enterica serovar Typhi (S. Typhi), the causative agent of typhoid fever, continues to cause significant morbidity and mortality world-wide. CD8+ T cells are an important component of the cell mediated immune (CMI) response against S. Typhi. Recently, interleukin (IL)-17A has been shown to contribute to mucosal immunity and protection against intracellular pathogens. To investigate multifunctional IL-17A responses against S. Typhi antigens in T memory subsets, we developed multiparametric flow cytometry methods to detect up to 6 cytokines/chemokines (IL-10, IL-17A, IL-2, interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and macrophage inflammatory protein-1β (MIP-1β)) simultaneously. Five volunteers were immunized with a 4 dose regimen of live-attenuated S. Typhi vaccine (Ty21a), peripheral blood mononuclear cells (PBMC) were isolated before and at 11 time points after immunization, and CMI responses were evaluated. Of the 5 immunized volunteers studied, 3 produced detectable CD8+ T cell responses following stimulation with S. Typhi-infected autologous B lymphoblastoid cell lines (B-LCL). Additionally, 2 volunteers had detectable levels of intracellular cytokines in response to stimulation with S. Typhi-infected HLA-E restricted cells. Although the kinetics of the responses differed among volunteers, all of the responses were bi- or tri-phasic and included multifunctional CD8+ T cells. Virtually all of the IL-17A detected was derived from multifunctional CD8+ T cells. The presence of these multifunctional IL-17A+ CD8+ T cells was confirmed using an unsupervised analysis program, flow cytometry clustering without K (FLOCK). This is the first report of IL-17A production in response to S. Typhi in humans, indicating the presence of a Tc17 response which may be important in protection. The presence of IL-17A in multifunctional cells co-producing Tc1 cytokines (IL-2, IFN-γ and TNF-α) may also indicate that the distinction between Tc17 and Tc1 responses in humans is not as clearly delineated as suggested by in vitro experiments and animal models.
伤寒沙门氏菌血清型伤寒杆菌(伤寒杆菌)是伤寒热的病原体,在全球范围内继续导致大量发病和死亡。CD8 + T细胞是针对伤寒杆菌的细胞介导免疫(CMI)反应的重要组成部分。最近,白细胞介素(IL)-17A已被证明有助于黏膜免疫和抵抗细胞内病原体。为了研究T记忆亚群中针对伤寒杆菌抗原的多功能IL-17A反应,我们开发了多参数流式细胞术方法,可同时检测多达6种细胞因子/趋化因子(IL-10、IL-17A、IL-2、干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)和巨噬细胞炎性蛋白-1β(MIP-1β))。5名志愿者接种了4剂减毒活伤寒杆菌疫苗(Ty21a),在免疫前和免疫后的11个时间点分离外周血单核细胞(PBMC),并评估CMI反应。在研究的5名免疫志愿者中,3名在用伤寒杆菌感染的自体B淋巴母细胞系(B-LCL)刺激后产生了可检测到的CD8 + T细胞反应。此外,2名志愿者在用伤寒杆菌感染的HLA-E限制性细胞刺激后有可检测到的细胞内细胞因子水平。尽管志愿者之间的反应动力学不同,但所有反应均为双相或三相,且包括多功能CD8 + T细胞。几乎所有检测到的IL-17A都来自多功能CD8 + T细胞。使用无监督分析程序“无K流式细胞术聚类”(FLOCK)证实了这些多功能IL-17A + CD8 + T细胞的存在。这是人类中针对伤寒杆菌产生IL-17A的首次报告,表明存在可能在保护中起重要作用的Tc17反应。多功能细胞中IL-17A与共产生Tc1细胞因子(IL-2、IFN-γ和TNF-α)同时存在,这也可能表明人类中Tc17和Tc1反应之间的区别并不像体外实验和动物模型所表明的那样清晰。