İmmün Yetmezlik veya İmmün Düzensizlik Hastalarının Deri Biyopsilerinden Fibroblast Kaynaklı Hücre Hatları Oluşturulması

Sade dilde özet

Bu çalışma, primer immün yetmezlik veya immün düzensizlik (immunodysregulation) hastalarının deri biyopsilerinden laboratuvarda araştırma amaçlı hücre hatları (fibroblast) oluşturmayı amaçlıyor. 2-85 yaş arası, bu tür tanısı olan hastalar ve akrabaları dahil edilir. Faz uygulanmayan gözlemsel bir çalışmadır; davetle katılım alınmaktadır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

N/A

Durum

Davetle katılım

Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Başlangıç

10.06.2009

Ülkeler

United States

İlgili genler

Merkezler

• Bethesda, United States

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

* INCLUSION CRITERIA:

Patients:

1. To be enrolled in this study, a patient must be \>=2 years of age but not \>85 years of age,
2. have a known diagnosis of primary immunodeficiency or immunodysregulation (or be a blood relative of such as patient),
3. be concurrently enrolled on an NIH IRB approved NIAID protocol that includes genetic testing for disease of the immune system, such as but not limited to 05-I-0213 or 06-I-0015

Patient Relative: To be enrolled in this study, a patient relative must be:

1. A biological relative of a participant being studied under this protocol. Relatives may be biological mother, father, sibling, children, grandparents, aunts, uncles and first cousins.

   a. A minor relative of the proban participant must demonstrate that they are asymptomatic carriers or are at risk for the disease
2. be concurrently enrolled on an NIH IRB approved protocol that includes genetic testing for disease of the immune system, such as but not limited to 05-I-0213 or 06-I-0015.
3. Greater than or equal to 8 years of age but not greater than 85 years of age,

Healthy Volunteers:

To be enrolled in this study, a normal volunteer must fulfill all of the following criteria:

1. Be enrolled on protocol 05-I-0213.
2. Be a healthy adult of either sex and between ages of 18 years and 85 years

EXCLUSION CRITERIA:

Patients or the Patient Relative are not eligible to be in this trial if::

1. Platelet count less than 20,000/microL
2. The individual is hemodynamically unstable because of acute bleeding.
3. Any condition that, in the investigator s opinion, places the patient at undue risk by participating in the study or limits the utility of the specimen to be obtained.
4. For Nasal Scraping: a history of turbinectomy or significant nasal pathology that would preclude obtaining mucosal scrape biopsies.

A Healthy Volunteer is not eligible to be in this trial if they:

1. Areless than 18 years old or older than 85 years
2. Weighs less than 110 pounds
3. Are pregnant or breastfeeding
4. Are receiving a chemotherapeutic agent(s) or has a malignancy
5. Cannot avoid taking aspirin or non-steroidal anti-inflammatory medications during the 7 days preceding skin biopsy
6. Have history of heart, lung, kidney disease, bleeding disorders, diabetes mellitus, chronic peripheral arterial or venous insufficiency, chronic diffuse skin conditions without uninvolved areas suitable for skin biopsy, poor skin healing, or keloid formation.
7. Have been diagnosed as having viral hepatitis (B or C), human immunodeficiency virus (HIV), or a carrier for methicillin-resistant Staphylococcus aureus (MRSA)
8. Hemoglobin measurement is less than 12.0 g/dL
9. Platelet count less than 150,000/(micro)L
10. PT greater than 15.0 seconds or PTT greater than 40 seconds
11. Have a history of intravenous injection drug use or of engaging in high-risk activities for exposure to the acquired immunodeficiency syndrome (AIDS) virus.