Booth Jayaum S, Patil Seema A, Ghazi Leyla, Barnes Robin, Fraser Claire M, Fasano Alessio, Greenwald Bruce D, Sztein Marcelo B
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland.
Department of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland.
Cell Mol Gastroenterol Hepatol. 2017 Aug 16;4(3):419-437. doi: 10.1016/j.jcmgh.2017.08.002. eCollection 2017 Nov.
BACKGROUND & AIMS: Systemic cellular immunity elicited by the Ty21a oral typhoid vaccine has been extensively characterized. However, very limited data are available in humans regarding mucosal immunity at the site of infection (terminal ileum [TI]). Here we investigated the host immunity elicited by Ty21a immunization on terminal ileum-lamina propria mononuclear cells (LPMC) and peripheral blood in volunteers undergoing routine colonoscopy.
We characterized LPMC-T memory (T) subsets and assessed serovar Typhi ( Typhi)-specific responses by multichromatic flow cytometry.
No differences were observed in cell yields and phenotypes in LPMC CD8-T subsets following Ty21a immunization. However, Ty21a immunization elicited LPMC CD8 T cells exhibiting significant Typhi-specific responses (interferon-γ, tumor necrosis factor-α, interleukin-17A, and/or CD107a) in all major T subsets (T-effector/memory [T], T-central/memory, and T-CD45RA), although each T subset exhibited unique characteristics. We also investigated whether Ty21a immunization elicited Typhi-specific multifunctional effectors in LPMC CD8 T. We observed that LPMC CD8 T responses were mostly multifunctional, except for those cells exhibiting the characteristics associated with cytotoxic responses. Finally, we compared mucosal with systemic responses and made the important observation that LPMC CD8 Typhi-specific responses were unique and distinct from their systemic counterparts.
This study provides the first demonstration of Typhi-specific responses in the human terminal ileum mucosa and provides novel insights into the generation of mucosal immune responses following oral Ty21a immunization.
Ty21a口服伤寒疫苗引发的全身细胞免疫已得到广泛研究。然而,关于感染部位(回肠末端[TI])的黏膜免疫,人类的数据非常有限。在此,我们调查了接受常规结肠镜检查的志愿者经Ty21a免疫后,回肠固有层单核细胞(LPMC)和外周血所引发的宿主免疫。
我们对LPMC-T记忆(T)亚群进行了特征分析,并通过多色流式细胞术评估了伤寒杆菌(Typhi)特异性反应。
Ty21a免疫后,LPMC CD8-T亚群的细胞产量和表型未观察到差异。然而,Ty21a免疫引发LPMC CD8 T细胞在所有主要T亚群(效应/记忆T细胞[T]、中枢/记忆T细胞和T-CD45RA)中均表现出显著的伤寒杆菌特异性反应(干扰素-γ、肿瘤坏死因子-α、白细胞介素-17A和/或CD107a),尽管每个T亚群都有独特的特征。我们还研究了Ty21a免疫是否在LPMC CD8 T细胞中引发伤寒杆菌特异性多功能效应细胞。我们观察到,LPMC CD8 T细胞反应大多是多功能的,但那些表现出与细胞毒性反应相关特征的细胞除外。最后,我们比较了黏膜反应和全身反应,并得出重要观察结果,即LPMC CD8伤寒杆菌特异性反应是独特的,与全身反应不同。
本研究首次证明了人类回肠末端黏膜中存在伤寒杆菌特异性反应,并为口服Ty21a免疫后黏膜免疫反应的产生提供了新见解。