Pathology and Monkeypox virus Localization in Tissues From Immunocompromised Patients With Severe or Fatal Mpox

Author:

Ritter Jana M1,Martines Roosecelis B1,Bhatnagar Julu1,Rao Agam K2ORCID,Villalba Julian A1,Silva-Flannery Luciana1,Lee Elizabeth13,Bullock Hannah A1,Hutson Christina L2,Cederroth Terra4,Harris Cynthia K4,Hord Kristin4,Xu Ya56,Brown Cameron A56,Guccione Jack P7,Miller Matthew7,Paddock Christopher D8,Reagan-Steiner Sarah1, ,Carter Jasmine910,Seixas Josilene N9,Lee James9,Cash-Goldwasser Shama9,Bower William A9,Schrodt Caroline A9,Bamrah Morris Sapna9,Alarcón Jemma9,Evans Mark G11

Affiliation:

1. Infectious Diseases Pathology Branch

2. Poxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Diseases, Centers for Disease Control and Prevention , Atlanta, Georgia

3. Oak Ridge Institute for Science and Education , Oak Ridge, Tennessee

4. Office of Chief Medical Examiner , New York City, New York

5. Department of Pathology and Immunology, Baylor College of Medicine

6. Department of Pathology and Laboratory Medicine, Ben Taub Hospital, Harris Health System , Houston, Texas

7. Department of Medical Examiner-Coroner, Los Angeles County , Los Angeles, California

8. Rickettsial Zoonoses Branch, Division of Vector-Borne Diseases, National Center for Zoonotic and Emerging Diseases, Centers for Disease Control and Prevention , Atlanta, Georgia

9. Centers for Disease Control and Prevention , Atlanta, GA

10. Oak Ridge Institute for Science and Education (ORISE) , Oak Ridge, TN

11. Caris Life Sciences , Phoenix, AZ

Abstract

Abstract Background Pathology and Monkeypox virus (MPXV) tissue tropism in severe and fatal human mpox is not thoroughly described but can help elucidate the disease pathogenesis and the role of coinfections in immunocompromised patients. Methods We analyzed biopsy and autopsy tissues from 22 patients with severe or fatal outcomes to characterize pathology and viral antigen and DNA distribution in tissues by immunohistochemistry and in situ hybridization. Tissue-based testing for coinfections was also performed. Results Mucocutaneous lesions showed necrotizing and proliferative epithelial changes. Deceased patients with autopsy tissues evaluated had digestive tract lesions, and half had systemic tissue necrosis with thrombotic vasculopathy in lymphoid tissues, lung, or other solid organs. Half also had bronchopneumonia, and one-third had acute lung injury. All cases had MPXV antigen and DNA detected in tissues. Coinfections were identified in 5 of 16 (31%) biopsy and 4 of 6 (67%) autopsy cases. Conclusions Severe mpox in immunocompromised patients is characterized by extensive viral infection of tissues and viremic dissemination that can progress despite available therapeutics. Digestive tract and lung involvement are common and associated with prominent histopathological and clinical manifestations. Coinfections may complicate mpox diagnosis and treatment. Significant viral DNA (likely correlating to infectious virus) in tissues necessitates enhanced biosafety measures in healthcare and autopsy settings.

Publisher

Oxford University Press (OUP)

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