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临床试验/NCT00435201
NCT00435201已完成不适用

Characterization of Clonal B Cell Populations in HCV Infection

Rockefeller University2 个研究点 分布在 2 个国家目标入组 14 人开始时间: 2007年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2

研究概览

简要总结

The purpose of this study is to investigate the mechanism of autoantibody production during chronic hepatitis C virus (HCV) infection. 10-50% of individuals with HCV have symptoms of mixed cryoglobulinemia (MC). By studying the B cells from HCV-infected individuals with and without MC, as well as from healthy controls, we hope to gain insight into the mechanisms of autoantibody production and develop new strategies for treatment of MC.

详细描述

Hepatitis C virus (HCV) infects approximately 170 million people worldwide. About 10-50% of persons with HCV have MC. MC is associated with the development of autoimmune symptoms and B cell proliferative disorders. We plan to study B cells from individuals chronically infected with HCV as well as from healthy controls. We sort B cells into different types, and we analyze these types for differential levels of gene expression. We are testing the hypothesis that certain types of B cells from subjects with MC have increased expression of genes that allow for increased cell survival.

People interested in participating in this study will have a complete history and general medical examinations before beginning the study. Following the screening, you will have a procedure called leukapheresis, in which white blood cells are removed, but your own red blood cells are returned. The procedure takes approximately 3 hours and is similar to blood donation. The leukapheresis is done during a same day admission to the hospital by an outside blood collection company with trained nurses and certified equipment.

Some aspects of this study are experimental which means the fluid and cells collected will be studied and analyzed to determine more precisely how your body's immune system is responding to the virus. These tests are experimental in that they are not part of the usual routine care of patients.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • At least 18 years of age.
  • Ability to give informed consent.
  • WBC greater than 3,000/mm
  • Platelets greater than 80,000/mm
  • Hb at least 9.5 g/dl.
  • INR less than 1.
  • Biologic therapy: Greater than 6 months post-Rituximab therapy.
  • Greater than 6 months post IFN- alpha and Ribavirin therapy.

排除标准

  • Decompensated cirrhosis.
  • Serious uncontrolled medical illness.
  • Receipt of immune modulators or suppressors within 30 days prior to study entry, including, but not limited to, interferons and thalidomide.
  • Psychiatric illness or social condition that, in the opinion of the investigator, would interfere with adherence to study requirements.
  • Alcohol or drug use or dependence that, in the opinion of the investigator,would interfere with adherence to study requirements.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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