Related Experiment Video
Updated: Jul 15, 2026

Assessing the Innate Sensing of HIV-1 Infected CD4+ T Cells by Plasmacytoid Dendritic Cells Using an Ex vivo Co-culture System.
Published on: September 1, 2015
Cryptococcosis and idiopathic CD4 lymphocytopenia
Dimitrios I Zonios1, Judith Falloon, Chiung-Yu Huang
1From Clinical Mycology Section, Laboratory of Clinical Infectious Diseases (DIZ, JEB); Laboratory of Immunoregulation (JF); and Biostatistics Research Branch (C-YH), National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland; and Critical Care Medicine Department (DC), Warren G. Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland.
Insights
Idiopathic CD4 lymphocytopenia (ICL) patients with cryptococcosis show a male predominance and a median age of 41. Identification of ICL predicts a favorable outcome and increased risk of dermatomal zoster.
Area of Science:
- Infectious Diseases
- Immunology
- Neurology
Background:
- Cryptococcosis is a serious fungal infection, particularly in immunocompromised individuals.
- Idiopathic CD4 lymphocytopenia (ICL) is a condition characterized by a low CD4+ T-cell count without an identifiable cause.
- Understanding the interplay between cryptococcosis and ICL is crucial for patient management.
Purpose of the Study:
- To characterize the clinical features of cryptococcosis in patients with idiopathic CD4 lymphocytopenia (ICL).
- To compare the presentation and outcomes of cryptococcosis in ICL patients with those in immunocompetent individuals.
- To assess the prognostic value of identifying ICL in patients with cryptococcal infections.
Main Methods:
- A retrospective review of 11 patients with cryptococcosis and ICL at a single institution.
- Inclusion of 42 similar cases from existing literature for a total cohort of 53 patients.
- Analysis of demographic data, clinical presentation, cerebrospinal fluid findings, CD4 counts, and patient outcomes.
Main Results:
- The ICL cohort had a slight male predominance and a median age of 41 years.
- Cerebrospinal fluid analysis revealed common abnormalities, including low glucose and elevated protein.
- Patients with ICL experienced an increased incidence of dermatomal zoster, but Pneumocystis pneumonia was rare.
- A favorable outcome was observed more frequently in ICL patients compared to previously normal individuals with cryptococcal meningitis.
Conclusions:
- Identifying ICL in patients with cryptococcosis is valuable as it predicts a favorable prognosis.
- Patients with cryptococcosis and ICL have a higher likelihood of developing dermatomal zoster.
- Long-term follow-up suggests a generally favorable prognosis for cryptococcosis in the context of ICL.
Abstract:
We reviewed the cases of 11 patients with cryptococcosis and idiopathic CD4 lymphocytopenia (ICL) referred to our institution in the previous 12 years, as well as 42 similar cases reported in the literature, to assess the characteristics of the infection in this population. Cryptococcosis in 53 patients with ICL had features in common with cryptococcosis in previously normal patients. ICL patients had a slight male predominance (1.2:1) and a median age of presentation of 41 years (range, 4.5-85 yr). Initial cerebrospinal fluid findings showed glucose below 40 mg/dL in 60% of the patients, a median pleocytosis of 59 white blood cells/mm (range, 0-884), and protein of 156 mg/dL (range, 25-402 mg/dL). The median CD4 count at diagnosis of ICL and at the last available measurement was 82 (range, 7-292) and 132 (range, 13-892) cells/mm, respectively, for an average follow-up of 32 months in 46 patients. Unlike previously normal patients with cryptococcosis, those with ICL had an excess incidence of dermatomal zoster (7 episodes in 46 ICL cases). Pneumocystis pneumonia was rare (1 case), casting doubt on the need for prophylaxis in patients with ICL. A favorable outcome (cured or improved) may be more common in ICL patients than in previously normal patients with cryptococcal meningitis and no predisposing factors. Identification of ICL in patients who were apparently normal before the onset of cryptococcosis appears to be useful because it predicts a favorable outcome. Patients with cryptococcal infection and ICL have an increased likelihood of developing dermatomal zoster. The long-term follow-up of these patients offers some reassurance regarding favorable prognosis.
Related Concept Videos
Cryptococcal Meningitis
Immunodeficiency Diseases
There are three main causes of immunodeficiency disorders...
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Cytomegalovirus Disease
Fungal Phylum Microsporidia
Toxoplasmosis