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Published on: June 30, 2013
Triple Central Nervous System Pathogen Infections and Vascular Events in Advanced Human Immunodeficiency
Sakshi Puri1, Rupak Chatterjee2, Insha Aleena3
1Consultant, Department of Neurology, Apollo Multispeciality Hospital, Kolkata, West Bengal, India, Corresponding Author.
Insights
Central nervous system infections in people living with HIV (PLHIV) are complex. This study found triple-pathogen CNS infections are challenging, often linked to immune reconstitution inflammatory syndrome (IRIS) after starting antiretroviral therapy (ART).
Area of Science:
- Neurology
- Infectious Diseases
- HIV Medicine
Background:
- Central nervous system (CNS) infections are a significant cause of illness and death in people living with HIV (PLHIV).
- Opportunistic CNS infections are known, but simultaneous infections with multiple pathogens are rare and difficult to diagnose.
- Advanced immunosuppression and recent initiation of antiretroviral therapy (ART) increase risk.
Purpose of the Study:
- To describe a case series of HIV-positive individuals with multiple CNS pathogens.
- To highlight diagnostic and therapeutic challenges in managing these complex infections.
- To underscore the role of immune reconstitution inflammatory syndrome (IRIS) in unmasking coinfections.
Main Methods:
- Retrospective case series of 11 HIV-positive patients presenting with meningitis symptoms within 3 months of ART initiation.
- Involved cerebrospinal fluid (CSF) analysis, PCR testing, neuroimaging, and comprehensive microbiological workup.
- Data collected over a 2-year period from two tertiary centers.
Main Results:
- All 11 patients were diagnosed with triple-pathogen CNS infections.
- Common pathogens included *Mycobacterium tuberculosis*, *Cryptococcus neoformans*, and HSV-1; others included *Toxoplasma gondii*, *Treponema pallidum*, and CMV.
- Median CD4 count was <70 cells/µL, and coinfections often appeared with ART initiation, suggesting IRIS. Mortality rate was 45%.
Conclusions:
- Managing CNS coinfections in PLHIV, especially with IRIS, presents significant diagnostic and therapeutic challenges.
- A high index of suspicion, early multiplex diagnostic testing, and multidisciplinary care are essential.
- Noninfectious complications like stroke and thromboembolism highlight the broad spectrum of HIV-related neurological disease.
Background:
Central nervous system (CNS) infections remain a major cause of morbidity and mortality in people living with HIV (PLHIV), particularly in the setting of advanced immunosuppression and recent initiation of antiretroviral therapy (ART). While individual opportunistic CNS infections are well-documented, simultaneous infections with multiple pathogens are rare and diagnostically challenging.
Methods:
We report a case series of 11 HIV-positive individuals aged 25-50 years, presenting within 3 months of ART initiation to two tertiary centers over a 2-year period. All patients exhibited clinical features of meningitis and underwent cerebrospinal fluid (CSF) analysis, PCR testing, neuroimaging, and comprehensive microbiological workup.
Results:
All 11 patients were diagnosed with triple-pathogen CNS infections. The most common combination was Mycobacterium tuberculosis, Cryptococcus neoformans, and herpes simplex virus type 1 (HSV-1). Additional pathogens included Toxoplasma gondii, Treponema pallidum, and CMV. Median CD4 count was <70 cells/µL. Coinfections were frequently unmasked shortly after ART initiation, suggestive of immune reconstitution inflammatory syndrome (IRIS). Despite aggressive treatment, mortality was 45%. One complex case included CNS vasculitis, ischemic stroke, pulmonary embolism, and multiple systemic infections.
Conclusion:
This series underscores the diagnostic and therapeutic complexities of managing CNS coinfections in PLHIV, especially in the context of IRIS. A high index of suspicion, early multiplex diagnostic testing, and multidisciplinary management are crucial. Furthermore, the presence of noninfectious complications such as stroke and thromboembolism highlights the broader spectrum of HIV-related neurological disease. Early recognition and targeted treatment can improve outcomes in this high-risk population.
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