DETECTION OF THE CARRIER STATE OF AIDS
DETECTION OF THE CARRIER STATE OF AIDS
批准号:
3343780
负责人:
EDGAR G. ENGLEMAN
金额:
$17.24万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-04-01 至 1987-03-31
关键词:
AIDS antiviral antibody blood donor cell population study communicable disease diagnosis disease carrier state enzyme linked immunosorbent assay flow cytometry helper T lymphocyte homosexuals human T cell lymphotropic virus type 1 human T cell lymphotropic virus type 2 human subject immunofluorescence technique immunohematology leukocyte count longitudinal human study male mass screening monoclonal antibody serology /serodiagnosis suppressor T lymphocyte virus classification
中文摘要
艾滋病可通过输血传播的证据
艾滋病高危人群的无症状成员促使人们寻找一种
一种筛查测试,可用于识别
无序。我们建议对精选的替代检测方法进行评估
预测艾滋病或持续性淋巴结病发展的能力
一组罹患疾病风险增加的同性恋者的综合症
这些障碍。我们还将研究两组志愿献血者
实验室检查结果在我们的普通捐献者库中很少见,但是
已知在艾滋病和艾滋病患者中更为普遍
相关障碍。将在三年内连续研究的种群将
包括150名看起来很健康男同性恋者
性伴侣,100名自愿献血者持续倒置
辅助性/诱导性T淋巴细胞与抑制性/细胞毒性T淋巴细胞的比值(Th:TS),
100名人类T细胞抗体阳性的志愿献血者
白血病/淋巴瘤病毒(HTLV)和50名Th:TS自愿献血者
在正常范围内。5名完全表达艾滋病的患者分组
50名患有持续性全身性淋巴结病的患者将在
仅限于研究的开始。除了临床随访外,
以下化验将在研究开始时和
此后6个月的间隔:使用A/D分析T淋巴细胞亚群
一组单抗,包括几种新试剂;
血清中可溶性淋巴细胞表面分子的测定;
检测三种已识别的人类T细胞抗体的试验
白血病淋巴瘤病毒;循环免疫复合物试验;
血清β-2-微球蛋白和胸腺素α-1的水平;以及
乙肝核心抗原(HBcAb)抗体的存在。这些化验
在鼓励初步研究的基础上被选为研究对象
以及潜在的方法论简便性。临床与临床的相关性分析
艾滋病高危人群和献血人群的实验室发现可能会有所帮助
确定最能预测的程序或程序组合
艾滋病或相关疾病的后续发展,有可能
应用程序筛查捐献的血液以检测艾滋病携带者状态。
英文摘要
Evidence that AIDS may be transmitted by transfusion of blood from
asymptomatic members of AIDS high risk groups has prompted a search for a
screening test that can be used to identify a carrier state for the
disorder. We propose to assess selected alternative assays for their
ability to predict the development of AIDS or persistent lymphadenopathy
syndrome in a group of homosexual men at increased risk for developing
these disorders. We will also study two groups of volunteer blood donors
with laboratory findings seen uncommonly in our general donor pool, but
known to be significantly more prevalent in patients with AIDS and AIDS
related disorder. The populations to be studied serially over 3 years will
include 150 apparently healthy homosexual men with multiple anonymous
sexual partners, 100 volunteer blood donors with persistent inversions of
the ratio of helper/inducer to suppressor/cytotoxic T lymphocytes (Th:Ts),
100 volunteer blood donors with antibodies to the human T cell
leukemia/lymphoma viruses (HTLV), and 50 volunteer blood donors with Th:Ts
within the normal range. Groups of 5 patients with fully expressed AIDS
and 50 with persistent generalized lymphadenopathy will be tested at the
beginning of the study only. In addition to clinical follow-up, the
following assays will be performed at the initiation of the study and at
six month intervals thereafter: analysis of T lymphocyte subsets using a
panel of monoclonal antibodies, including several novel reagents;
measurement in serum of soluble forms of lympohcyte surface molecules;
tests to detect antibodies to the three identified types of human T cell
leukemia lymphoma viruses (HTLV); tests of circulating immune complexes;
serum levels of beta-2-microglobulin and thymosin alpha-1; and tests for
the presence of antibody to hepatitis B core antigen (HBcAb). These assays
have been chosen for study on the basis of encouraging preliminary studies
and potential ease of methodology. Correlation of the clinical and
laboratory findings in the AIDS hight risk and blood donor groups may help
to identify the procedure or combination of procedures best able to predict
subsequent development of AIDS or related disorders, with potential
applications to screening donated blood to detect an AIDS carrier state.
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海外基金