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Updated: Feb 1, 2026

Multifocal Electroretinograms
Published on: December 4, 2011
Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
Jérôme Hadjadj1, Aurélien Guffroy2, Christophe Delavaud3
1Department of Haematology, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, France et Université Paris Descartes, 149 rue de Sèvres, 75015, Paris, France.
Purpose:
Progressive multifocal leukoencephalopathy (PML) is a rare but severe demyelinating disease caused by the polyomavirus JC (JCV) in immunocompromised patients. We report a series of patients with primary immune deficiencies (PIDs) who developed PML.
Methods:
Retrospective observational study including PID patients with PML. Clinical, immunological, imaging features, and outcome are provided for each patient.
Results:
Eleven unrelated patients with PIDs developed PML. PIDs were characterized by a wide range of syndromic or genetically defined defects, mostly with combined B and T cell impairment. Genetic diagnosis was made in 7 patients. Before the development of PML, 10 patients had recurrent infections, 7 had autoimmune and/or inflammatory manifestations, and 3 had a history of malignancies. Immunologic investigations showed CD4+ lymphopenia (median 265, range 50-344) in all cases. Six patients received immunosuppressive therapy in the year before PML onset, including prolonged steroid therapy in 3 cases, rituximab in 5 cases, anti-TNF-α therapy, and azathioprine in 1 case each. Despite various treatments, all but 1 patient died after a median of 8 months following PML diagnosis.
Conclusion:
PML is a rare but fatal complication of PIDs. Many cases are secondary to immunosuppressive therapy warranting careful evaluation before initiation subsequent immunosuppression during PIDs.
Insights
Progressive multifocal leukoencephalopathy (PML) is a rare, fatal complication in patients with primary immune deficiencies (PIDs). Many cases result from immunosuppressive therapy, requiring careful consideration before its use in PIDs.
Area of Science:
- Neuroimmunology
- Infectious Diseases
- Genetics
Background:
- Progressive multifocal leukoencephalopathy (PML) is a severe demyelinating disease caused by JC virus (JCV) in immunocompromised individuals.
- Primary immune deficiencies (PIDs) represent a diverse group of genetic disorders affecting the immune system, increasing susceptibility to infections and autoimmune conditions.
Purpose of the Study:
- To report a series of patients with primary immune deficiencies (PIDs) who developed PML.
- To describe the clinical, immunological, imaging, and outcome features of PML in PID patients.
Main Methods:
- Retrospective observational study.
- Inclusion of eleven unrelated patients diagnosed with PIDs and PML.
- Analysis of clinical data, immunological investigations, imaging findings, and patient outcomes.
Main Results:
- Eleven PID patients developed PML, predominantly with combined B and T cell defects.
- Patients experienced recurrent infections, autoimmune manifestations, and malignancies prior to PML.
- All patients exhibited CD4+ lymphopenia; immunosuppressive therapies were common preceding PML.
- PML was fatal in all but one patient, with a median survival of 8 months post-diagnosis.
Conclusions:
- PML is a rare but frequently fatal complication in patients with PIDs.
- A significant proportion of PML cases in PIDs are linked to prior immunosuppressive therapy.
- Careful evaluation is crucial before initiating or continuing immunosuppressive treatments in PID patients to mitigate PML risk.
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