Zaidi Irfan, Diallo Hama, Conteh Solomon, Robbins Yvette, Kolasny Jacqueline, Orr-Gonzalez Sachy, Carter Dariyen, Butler Brandi, Lambert Lynn, Brickley Elizabeth, Morrison Robert, Sissoko Mahamadou, Healy Sara A, Sim B Kim Lee, Doumbo Ogobara K, Hoffman Stephen L, Duffy Patrick E
Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Malaria Research and Training Center, Mali-National Institute of Allergy and Infectious Diseases International Center for Excellence in Research, University of Science, Techniques and Technologies of Bamako, Bamako, Mali; and.
J Immunol. 2017 Dec 1;199(11):3781-3788. doi: 10.4049/jimmunol.1700314. Epub 2017 Oct 27.
Whole-sporozoite vaccines confer sterilizing immunity to malaria-naive individuals by unknown mechanisms. In the first PfSPZ Vaccine trial ever in a malaria-endemic population, Vδ2 γδ T cells were significantly elevated and Vγ9/Vδ2 transcripts ranked as the most upregulated in vaccinees who were protected from infection. In a mouse model, absence of γδ T cells during vaccination impaired protective CD8 T cell responses and ablated sterile protection. γδ T cells were not required for circumsporozoite protein-specific Ab responses, and γδ T cell depletion before infectious challenge did not ablate protection. γδ T cells alone were insufficient to induce protection and required the presence of CD8α dendritic cells. In the absence of γδ T cells, CD8α dendritic cells did not accumulate in the livers of vaccinated mice. Altogether, our results show that γδ T cells were essential for the induction of sterile immunity during whole-organism vaccination.
全子孢子疫苗可通过未知机制赋予未感染疟疾的个体无菌免疫力。在首次针对疟疾流行地区人群进行的PfSPZ疫苗试验中,Vδ2 γδ T细胞显著升高,在免受感染的疫苗接种者中,Vγ9/Vδ2转录本上调最为明显。在小鼠模型中,接种疫苗期间缺乏γδ T细胞会损害保护性CD8 T细胞反应并消除无菌保护。环子孢子蛋白特异性抗体反应不需要γδ T细胞,感染攻击前γδ T细胞耗竭不会消除保护作用。单独的γδ T细胞不足以诱导保护作用,需要CD8α树突状细胞的存在。在缺乏γδ T细胞的情况下,CD8α树突状细胞不会在接种疫苗小鼠的肝脏中积累。总之,我们的结果表明,γδ T细胞对于全生物体疫苗接种期间无菌免疫力的诱导至关重要。