Persistence of Human Immunodeficiency Virus–Associated Cerebral Toxoplasmosis Lesions in Successfully Treated Patients Receiving Combination Antiretroviral Therapy

Author:

Coleman Benjamin1,Smith Bryan R1,Kapoor Rama2,Proschan Michael A3,Sereti Irini2,Hammoud Dima A4,Kovacs Joseph A5ORCID

Affiliation:

1. Section of Infections of the Nervous System, National Institute of Neurological Disorders and Stroke, National Institutes of Health , Bethesda, Maryland , USA

2. Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland , USA

3. Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland , USA

4. Center for Infectious Disease Imaging, Radiology and Imaging Sciences, NIH Clinical Center, National Institutes of Health , Bethesda, Maryland , USA

5. Critical Care Medicine Department, NIH Clinical Center, National Institutes of Health , Bethesda, Maryland , USA

Abstract

Abstract Background Toxoplasmic encephalitis (TE) is a life-threatening complication of people with human immunodeficiency virus (PWH) with severe immunodeficiency, especially those with a CD4+ T-cell count <100 cells/µL. Following a clinical response to anti-Toxoplasma therapy, and immune reconstitution after initiation of combination antiretroviral therapy (ART), anti-Toxoplasma therapy can be discontinued with a low risk of relapse. Methods To better understand the evolution of magnetic resonance imaging (MRI)–defined TE lesions in PWH receiving ART, we undertook a retrospective study of PWH initially seen at the National Institutes of Health between 2001 and 2012, who had at least 2 serial MRI scans. Lesion size and change over time were calculated and correlated with clinical parameters. Results Among 24 PWH with TE and serial MRI scans, only 4 had complete clearance of lesions at the last MRI (follow-up, 0.09–5.8 years). Of 10 PWH off all anti-Toxoplasma therapy (median, 3.2 years after TE diagnosis), 6 had persistent MRI enhancement. In contrast, all 5 PWH seen in a pre–ART era study who were followed for >6 months had complete clearance of lesions. TE lesion area at diagnosis was associated with the absolute change in area (P < .0001). Conclusions Contrast enhancement can persist even when TE has been successfully treated and anti-Toxoplasma therapy has been stopped, highlighting the need to consider diagnostic alternatives in successfully treated patients with immune reconstitution presenting with new neurologic symptoms.

Funder

Intramural Research Program of the National Institutes of Health Clinical Center

National Institute of Allergy and Infectious Diseases

National Institute of Neurological Disorders and Stroke

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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