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Detection of a human intracisternal retroviral particle associated with CD4+ T-cell deficiency.

作者信息

Gupta S, Ribak C E, Gollapudi S, Kim C H, Salahuddin S Z

机构信息

Department of Medicine, University of California, Irvine 92717.

出版信息

Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7831-5. doi: 10.1073/pnas.89.16.7831.

DOI:10.1073/pnas.89.16.7831
PMID:1380169
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC49805/
Abstract

A number of non-human-immunodeficiency-virus (HIV) type 1 disorders are associated with CD4+ T-cell deficiency and dysfunction. However, the etiopathogenesis of CD4+ T-cell immunodeficiency in these disease states remains unclear. Human intracisternal retroviral (HICRV) particles were detected in a lymphoblastoid cell line exposed to mononuclear cells from a patient with severe CD4+ T-cell deficiency without risk factors for HIV infection. Ultrastructurally, the HICRV is distinct from HIV-1, HIV-2, human T-lymphotropic virus (HTLV) type I, and HTLV-II. Supernatants of activated mononuclear cells showed significant reverse transcriptase activity that was predominantly Mn2+ dependent. The patient's mononuclear cells were negative for HIV-1, HIV-2, HTLV-I, and HTLV-II proviruses as demonstrated by the lack of amplification by PCR. Also, the patient's serum was negative for antibodies to HIV-1, HTLV-I, and HTLV-II and for HIV-1 p24 antigen; however, serum was positive for antibodies against the HICRV as demonstrated by Western blot. Similar HICRV particles were detected in a lymphoblastoid cell line exposed to mononuclear cells from the patient's daughter, who showed CD4+ T-cell dysfunction. The HICRV may be associated with CD4+ T-cell immunodeficiency and dysfunction in patients without risk for HIV-1, HIV-2, HTLV-I, and HTLV-II.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/8b9cb987bf2b/pnas01090-0557-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/02d4b771782d/pnas01090-0555-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/20cadf1ac572/pnas01090-0556-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/4b5069d3a372/pnas01090-0556-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/16cccb91d79e/pnas01090-0556-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/8b9cb987bf2b/pnas01090-0557-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/02d4b771782d/pnas01090-0555-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/20cadf1ac572/pnas01090-0556-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/4b5069d3a372/pnas01090-0556-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/16cccb91d79e/pnas01090-0556-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9809/49805/8b9cb987bf2b/pnas01090-0557-a.jpg

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