Activation‐Associated Necrosis in Human Immunodeficiency Virus Infection
Author(s) -
Nicola Borthwick,
R. Gitendra Wickremasinghe,
Jackie Lewin,
Lynette D. Fairbanks,
Margarita Bofill
Publication year - 1999
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314594
Subject(s) - necrosis , apoptosis , tumor necrosis factor alpha , programmed cell death , biology , dna fragmentation , tunel assay , virus , fas receptor , virology , fas ligand , stimulation , interferon , immunology , endocrinology , biochemistry , genetics
Mitogenic stimulation of lymphocytes from persons infected with human immunodeficiency virus (HIV) resulted in massive cell death. In addition to early apoptosis, a second wave of cell death occurred 48-72 h after stimulation. At that time, the cells were enlarged, leaked content, and had plasma membrane damage-all indicative of necrosis. Furthermore, DNA fragmentation as determined by TUNEL assay was virtually absent. This activation-associated necrosis could not be prevented by interfering with CD95/CD95-ligand interactions or by blocking caspase activity and was unaffected by neutralizing antibodies to tumor necrosis factor-alpha or interferon-gamma. Necrosis was also induced by activation of normal lymphocytes in the presence of ribavirin, which inhibits the de novo pathway of nucleotide synthesis. Lymphocytes from HIV-infected persons are defective in their ability to synthesize nucleotides via this pathway, indicating one possible mechanism for the activation-associated necrosis seen in HIV infection.
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