Intraocular and Plasma HIV-1 RNA in HIV-infected Patients with CMV Retinitis and HIV-infected Controls

References

• Barré-Sinoussi F, Chermann JC, Rey F, Nugeyre MT, Chamaret S, Gruest J, et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 1983; 220: 868–71.
   Google Scholar
• Popovic M, Sarngadharan MG, Read E, Gallo RC. Detection, isolation and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 1984; 224: 497–500.
   PubMed Web of Science ®Google Scholar
• Gallo RC, Salahuddin SZ, Popovic M, Shearer GM, Kaplan M, Haynes BF, et al. Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS. Science 1984; 224: 500–3.
   PubMed Web of Science ®Google Scholar
• Zagury D, Bernard J, Leibowitch J, Safai B, Groopman JE, Feldman M, et al. HTLV-III in cells cultured from semen of two patients with AIDS. Science 1984; 226: 449–51.
   PubMed Web of Science ®Google Scholar
• Ho DD, Schooley RT, Rota TR, Kaplan JC, Flynn T, Salahuddin SZ, et al. HTLV-III in semen and blood of a healthy homosexual man. Science 1984; 226: 451–3.
   PubMed Web of Science ®Google Scholar
• Groopman JE, Salahuddin SZ, Sarngadharan MG, Markham PD, Gonda MA, Sliski A, et al. HTLV-III in saliva of people with AIDS-related complex and healthy homosexual men at risk for AIDS. Science 1984; 226: 447–9.
   PubMed Web of Science ®Google Scholar
• Ho DD, Rota TR, Schooley RT, Kaplan JC, Allan JD, Groopman JE, et al. Isolation of HTLV-III from cerebrospinal fluid and neural tissues of patients with neurologic syndromes related to the acquired immunodeficiency syndrome. N Engl J Med 1985; 313: 1493–7.
   PubMed Web of Science ®Google Scholar
• Fujikawa LS, Salahuddin SZ, Ablashi D, Palestine AG, Masur H, Nussenblatt RB, et al. HTLV-III in the tears of AIDS patients. Ophthalmology 1986; 93: 1479–81.
   PubMed Web of Science ®Google Scholar
• Garcia-Ferrer FJ, Laycock KA, Buerger DG, Flowers BE, Foos RY, Pepose JS. Screening corneas for human immunodeficiency virus type 1 proviral DNA by polymerase chain reaction. Am J Ophthalmol 1995; 119: 7–13.
   Google Scholar
• Ciulla TA, Schnizlein-Bick CT, Danis RP, Frank MO, Wheat LJ. Comparison of intraocular to plasma HIV-1 viral burden in patients with cytomegalovirus retinitis. Am J Ophthalmol 1999; 127: 221–3.
   PubMedGoogle Scholar
• Quinn TC, Wawer MJ, Sewankambo N, Serwadda D, Li C, Wabwire-Mangen F, et al. Viral load and heterosexual transmission of human immunodeficiency virus type 1. N Engl J Med 2000; 342: 921–9.
   Google Scholar
• Tovanabutra S, Robison V, Wongtrakul J, Sennum S, Suriyanon V, Kingkeow D, et al. Male viral load and heterosexual transmission of HIV-1 subtype E in northern Thailand. J Acquir Immune Defic Syndr Hum Retrovirol 2002; 29: 275–83.
   Google Scholar
• Ziegler JB, Cooper DA, Johnson RO, Gold J. Postnatal transmission of AIDS-associated retrovirus from mother to infant. Lancet 1985; i: 896–7.
   Google Scholar
• Mellors JW, Rinaldo Jr CR, Gupta P, White RM, Todd JA, Kingsley LA. Prognosis in HIV-1 infection predicted by the quantity of virus in plasma. Science 1996; 272: 1167–70.
   PubMed Web of Science ®Google Scholar
• O’Brien WA, Hartigen PM, Martin D, Esinhart J, Hill A, Benoit S, et al. Changes in plasma HIV-1 RNA and CD4 + lymphocyte counts and the risk of progression to AIDS. N Engl J Med 1996; 334: 426–31.
   Google Scholar
• Ho DD, Moudgil T, Alam M. Quantitation of human immunodeficiency virus type 1 in the blood of infected persons. N Engl J Med 1989; 321: 1621–5.
   Google Scholar
• Dunn DT, Brandt CD, Krivine A, Cassol SA, Roques P, Borkowsky W, et al. The sensitivity of HIV-1 DNA polymerase chain reaction in the neonatal period and the relative contributions of intra-uterine and intra-partum transmission. AIDS 1995; 9: F7–F11.
   PubMed Web of Science ®Google Scholar
• Pachl C, Todd JA, Kern DG, Sheridan PJ, Fong SJ, Stempien M, et al. Rapid and precise quantification of HIV-1 RNA in plasma using a branched DNA signal amplification assay. J Acquir Immune Defic Syndr Hum Retrovirol 1995; 8: 446–54.
   PubMedGoogle Scholar
• Robertson DL, Sharp PM, McCutchan FE, Hahn BH. Recombination in HIV-1. Nature 1995; 374: 124–6.
   PubMed Web of Science ®Google Scholar
• Michael NL, Herman SA, Kwok S, Dreyer K, Wang J, Christopherson C, et al. Development of calibrated viral load standards for group M subtypes of human immunodeficiency virus type 1 and performance of an improved AMPLICOR HIV-1 MONITOR test with isolates of diverse subtypes. J Clin Microbiol 1999; 37: 2557–63.
   PubMedGoogle Scholar
• Myers TW, Gelfand DH. Reverse transcription and DNA amplification by a Thermus thermophilus DNA polymerase. Biochemistry 1991; 30: 7661–6.
   PubMed Web of Science ®Google Scholar
• Longo MC, Berninger MS, Hartley JL. Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions. Gene 1990; 93: 125–8.
   Google Scholar
• Kwok S, Higuchi R. Avoiding false positives with PCR. Nature 1989; 339: 237–8.
   PubMed Web of Science ®Google Scholar
• Wiedbrauk DL, Werner JC, Drevon AM. Inhibition of PCR by aqueous and vitreous fluids. J Clin Microbiol 1995; 33: 2643–6.
   Google Scholar
• Smith IL, Macdonald C, Freemann WR, Shapiro AM, Spector SA. Cytomegalovirus (CMV) retinitis activity is accurately reflected by the presence and level of CMV DNA in aqueous humor and vitreous. J Infect Dis 1999; 179: 1249–53.
   Google Scholar
• Friedenwald JS. The formation of the intraocular fluids. Am J Ophthalmol 1949; 32: 9–27.
   PubMed Web of Science ®Google Scholar
• Fox GM, Crouse CA, Chuang EL, Pflugfelder SC, Cleary TJ, Nelson SJ, et al. Detection of herpesvirus DNA in vitreous and aqueous specimens by the polymerase chain reaction. Arch Ophthalmol 1991; 109: 266–71.
   PubMedGoogle Scholar
• Wright JG, McGeer AJ, Chyatte D, Ransohoff DF. Mechanisms of glove tears and sharp injuries among surgical personnel. JAMA 1991; 266: 1668–71.
   PubMed Web of Science ®Google Scholar