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. 2013 Feb;29(2):365–370. doi: 10.1089/aid.2012.0138

Table 1.

Study Subjects, HIV-1 Isolates, and Summary of Long Terminal Repeat Clones

Subject Risk factor Last CD4 count (cells/μl) Antiretroviral(s) HIV-1 encephalitis Tissues yielding HIV-1 isolates Name of virus isolate LTRs cloned from virus isolate (n) Unique LTRs (n)
CB1 MH 10 ddI (prior AZT) Severe Brain CB1-BR 5 2
          CSF CB1-CSF 6 3
          PBMC CB1-PBMC 6 3
CB3 MH 5 ddI (prior AZT and ddC) Severe S.Cord CB3-SC 6 4
          CSF CB3-CSF 6 3
          PBMC CB3-PBMC 6 3
MACS1 MH 2 None Severe Brain MACS1-BR 6 3
          Spleen MACS1-SP 6 4
MACS2 MH 52 AZT Moderate Brain MACS2-BR 6 5
          L.Node MACS2-LN 6 4
MACS3 MH 95 None Moderate Brain MACS3-BR 6 6
          L.Node MACS3-LN 6 4
UK1 IVDU 87 ddC (1 mo) Moderate Brain UK1-BR 6 2
UK7 IVDU 90 AZT Severe Brain UK7-BR 5 4

The clinical and neuropathological details of the study subjects and the derivation and characterization of the primary tissue-derived HIV-1 isolates have been published previously21,23,26 and are summarized again here to assist in the interpretation of the data derived from the cloned long terminal repeats (LTRs). LTRs were amplified from primary virus isolates by PCR and cloned into the pGL3-Basic vector to act as a promoter for the luciferase gene. The LTRs described here have been assigned GenBank accession numbers JX289943 to JX290024. MH, male homosexual; IVDU, intravenous drug user; mo, month; ddI, didanosine; AZT, zidovudine; ddC, zalcitabine; CSF, cerebrospinal fluid; PBMC, peripheral blood mononuclear cells; S.Cord, spinal cord; L.Node, lymph node.