2020National Science ReviewOpen access

Pathological changes in the lungs and lymphatic organs of 12 COVID-19 autopsy cases

Qian Liu, Yu Shi, Jun Cai, Yaqi Duan, Rongshuai Wang, Hongyan Zhang, Qiurong Ruan, Jiansha Li, Lei Zhao, Yi‐Fang Ping, Rong Chen, Liang Ren, Xiaochun Fei, Heng Zhang, Rui Tang, Xi Wang, Tao Luo, Xindong Liu, Xuequan Huang, Z H Liu, Qilin Ao, Yong Ren, Jing Xiong, Zhicheng He, Haibo Wu, Wenjuan Fu, Pengnan Zhao, Xinwei Chen, Guoqiang Qu, Yunyun Wang, Xi Wang, Jia Liu, Dongfang Xiang, Sanpeng Xu, Xiaowei Zhou, Qingrui Li, Jinghong Ma, Heng Li, Jie Zhang, Sizhe Huang, Xiaohong Yao, Yiwu Zhou, Chaofu Wang, Dingyu Zhang, Guoping Wang, Liang Liu, Xiu‐Wu Bian

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Abstract

Systematic autopsy and comprehensive pathological analyses of COVID-19 decedents should provide insights into the disease characteristics and facilitate the development of novel therapeutics. In this study, we report the autopsy findings from the lungs and lymphatic organs of 12 COVID-19 decedents-findings that evaluated histopathological changes, immune cell signature and inflammatory factor expression in the lungs, spleen and lymph nodes. Here we show that the major pulmonary alterations included diffuse alveolar damage, interstitial fibrosis and exudative inflammation featured with extensive serous and fibrin exudates, macrophage infiltration and abundant production of inflammatory factors (IL-6, IP-10, TNFα and IL-1β). The spleen and hilar lymph nodes contained lesions with tissue structure disruption and immune cell dysregulation, including lymphopenia and macrophage accumulation. These findings provide pathological evidence that links injuries of the lungs and lymphatic organs with the fatal systematic respiratory and immune malfunction in critically ill COVID-19 patients.

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Systematic autopsy and comprehensive pathological analyses of COVID-19 decedents should provide insights into the disease characteristics and facilitate the development of novel therapeutics. In this study, we report the autopsy findings from the lungs and lymphatic organs of 12 COVID-19 decedents-findings that evaluated histopathological changes, immune cell signature and inflammatory factor expression in the lungs, spleen and lymph nodes. Here we show that the major pulmonary alterations included diffuse alveolar damage, interstitial fibrosis and exudative inflammation featured with extensive serous and fibrin exudates, macrophage infiltration and abundant production of inflammatory factors (IL-6, IP-10, TNFα and IL-1β). The spleen and hilar lymph nodes contained lesions with tissue structure disruption and immune cell dysregulation, including lymphopenia and macrophage accumulation. These findings provide pathological evidence that links injuries of the lungs and lymphatic organs with the fatal systematic respiratory and immune malfunction in critically ill COVID-19 patients.

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Available abstract

Systematic autopsy and comprehensive pathological analyses of COVID-19 decedents should provide insights into the disease characteristics and facilitate the development of novel therapeutics. In this study, we report the autopsy findings from the lungs and lymphatic organs of 12 COVID-19 decedents-findings that evaluated histopathological changes, immune cell signature and inflammatory factor expression in the lungs, spleen and lymph nodes. Here we show that the major pulmonary alterations included diffuse alveolar damage, interstitial fibrosis and exudative inflammation featured with extensive serous and fibrin exudates, macrophage infiltration and abundant production of inflammatory factors (IL-6, IP-10, TNFα and IL-1β). The spleen and hilar lymph nodes contained lesions with tissue structure disruption and immune cell dysregulation, including lymphopenia and macrophage accumulation. These findings provide pathological evidence that links injuries of the lungs and lymphatic organs with the fatal systematic respiratory and immune malfunction in critically ill COVID-19 patients.

Key concepts: Lymphatic system, Autopsy, Pathology, Spleen, Lymph, Pathological, Diffuse alveolar damage, Immune system

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