Understanding immune responses in patients with cryptococcal infections
Official title: Cryptococcosis in Previously Healthy Adults
Run by National Institutes of Health Clinical Center (CC) · NCT00001352 · Data updated 2026-11-12
This study looks at how the immune system works in healthy adults with cryptococcal infections to see what makes them more likely to get sick.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 800 (estimated) |
| Sponsor | National Institutes of Health Clinical Center (CC) NIH |
| Drugs / interventions | radiation |
| Locations | 1 site (Bethesda, Maryland) |
| Status | Recruiting |
| Started | April 1, 1993 |
| Registry record updated | November 9, 2026 |
| Trial ID | NCT00001352 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults over 18 years old who have been diagnosed with cryptococcosis.
✕Probably not a fit
Patients with well-defined immune deficiencies or those who do not have cryptococcosis may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to investigate the immune deficits that predispose individuals to cryptococcosis, particularly in previously healthy adults. Participants diagnosed with cryptococcal infections will undergo various sampling procedures, including blood, saliva, and cerebrospinal fluid collection, to assess their immune responses. The study will also involve genetic testing to identify potential hereditary factors contributing to susceptibility. Throughout the study, participants will receive standard medical care to manage their condition effectively.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of cryptococcal infections, particularly in patients without identifiable immune defects.
How similar studies have gone: While the study focuses on a specific population and genetic factors, similar studies have shown promise in understanding immune responses to infections, suggesting potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
* INCLUSION CRITERIA: Patients Patients must: 1. Have cryptococcosis as determined by information collected from their medical records, telephone interviews, or from a referring physician: * histopathology showing cryptococci; or * culture of C. neoformans or C. gattii * a positive cryptococcal antigen in the serum and/or CSF, together with CSF cell count and chemistry consistent with cryptococcal meningitis. 2. Be over the age of 18 years old. 3. Have a primary physician outside of the NIH. 4. Agree to undergo genetic testing that will include WES and high density SNP arrays as appropriate for possible WES linkage studies. 5. Allow samples to be stored for future research. 6. Pregnant patients will not be excluded. However, research procedures greater than minimal risk including bone marrow biopsy and apheresis would not be performed on pregnant subjects. Otherwise, pregnant patients with cryptococcus would be treated with as per standard of care, minimizing teratogenic potential of drugs and ionizing radiation whenever possible. Blood Relatives of Patients Blood relatives must: 1. Be a genetic relative of a patient enrolled in this study 2. Be over the age of 18 years old 3. Agree to undergo genetic testing that may include WES and high density SNP analysis 4. Allow samples to be stored for future research Healthy Volunteers Healthy volunteers must: 1. Be between the ages of 18 and 70 years old 2. Allow samples to be stored for future research EXCLUSION CRITERIA: Patients Patients will be excluded for any of the following: 1. The presence of certain types of acquired abnormalities of immunity due to: * HIV * Cancer chemotherapeutic agent(s) * An underlying malignancy could be grounds for possible exclusion of a patient if, in the opinion of the investigator, the underlying disease predisposed the patient to the infection * Monoclonal antibody therapy directed against a patient s immune system 2. Any condition that in the opinion of the investigator may interfere with the evaluation of a co-existing abnormality of immunity that is the subject of study under this protocol. For example, we may exclude patients with Cushing s disease that have very high cortisol levels at the time of diagnosis of their cryptococcosis. Genetic Relatives of Patients Genetic relatives will be excluded for the following: -Any condition that in the opinion of the investigator may interfere with evaluation of an immune system abnormality that is the subject of study under this protocol. Healthy Volunteers Healthy volunteers will be excluded for any of the following: 1. HIV or viral hepatitis (B or C). 2. History of recurrent or severe infections. 3. History of intravenous drug use. 4. History of engaging in high-risk activities for exposure to HIV. 5. Receiving chemotherapeutic agent(s), immunosuppressants or have underlying malignancy. 6. Pregnancy. 7. Have history of heart, lung, kidney disease, or bleeding disorders. 8. Any condition that in the opinion of the investigator may interfere with evaluation of an immune system abnormality that is the subject of study under this protocol.
Where it's running
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National Institutes of Health Clinical Center
Bethesda, Maryland, United States Recruiting
Study contacts
- Principal investigator: Peter R Williamson, M.D. — National Institute of Allergy and Infectious Diseases (NIAID)
- Study coordinator: Peter R Williamson, M.D.
- Email: williamsonpr@mail.nih.gov
- Phone: (301) 443-8339
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Comparing antifungal treatment options for cryptococcal meningitis in people with HIV.
This will test several antifungal medicines to see which works best for adults with HIV who have cryptococcal meningitis.
-
Single dose treatment for asymptomatic cryptococcal antigenemia
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-
Long-term study of HIV patients in rural India
This study looks at how HIV affects people living in rural India over time to see how well different treatments work and to understand the disease better.
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Understanding Idiopathic CD4+ Lymphocytopenia and its Effects
This study is trying to understand how Idiopathic CD4+ lymphocytopenia affects people over time by looking at their immune system and any related health issues while they receive standard treatment for infections.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.