生物
肉芽肿
免疫系统
免疫学
肺结核
结核分枝杆菌
多细胞生物
肺
免疫
炎症
病理
细胞
医学
遗传学
内科学
作者
Hannah P. Gideon,Travis K. Hughes,Constantine N. Tzouanas,Marc H. Wadsworth,Ang A. Tu,Todd M. Gierahn,Joshua M. Peters,Forrest Hopkins,Jun-Rong Wei,Conner Kummerlowe,Nicole L. Grant,Kievershen Nargan,Jia Yao Phuah,H. Jacob Borish,Pauline Maiello,Alexander G. White,Caylin G. Winchell,Sarah K. Nyquist,Sharie Keanne C. Ganchua,Amy Myers
出处
期刊:Immunity
[Cell Press]
日期:2022-04-27
卷期号:55 (5): 827-846.e10
被引量:176
标识
DOI:10.1016/j.immuni.2022.04.004
摘要
Mycobacterium tuberculosis lung infection results in a complex multicellular structure: the granuloma. In some granulomas, immune activity promotes bacterial clearance, but in others, bacteria persist and grow. We identified correlates of bacterial control in cynomolgus macaque lung granulomas by co-registering longitudinal positron emission tomography and computed tomography imaging, single-cell RNA sequencing, and measures of bacterial clearance. Bacterial persistence occurred in granulomas enriched for mast, endothelial, fibroblast, and plasma cells, signaling amongst themselves via type 2 immunity and wound-healing pathways. Granulomas that drove bacterial control were characterized by cellular ecosystems enriched for type 1-type 17, stem-like, and cytotoxic T cells engaged in pro-inflammatory signaling networks involving diverse cell populations. Granulomas that arose later in infection displayed functional characteristics of restrictive granulomas and were more capable of killing Mtb. Our results define the complex multicellular ecosystems underlying (lack of) granuloma resolution and highlight host immune targets that can be leveraged to develop new vaccine and therapeutic strategies for TB.
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