90
Views
7
CrossRef citations to date
0
Altmetric
Review

Potential utility of GB virus type C as a preventive vaccine for HIV-1

, , &
Pages 335-347 | Published online: 09 Jan 2014

References

  • Baggio-Zappia GL, Hernandes Granato CF. HIV-GB virus C co-infection: an overview. Clin. Chem. Lab Med. 47(1), 12–19 (2009).
  • Reshetnyak VI, Karlovich TI, Ilchenko LU. Hepatitis G virus. World J. Gastroenterol. 14(30), 4725–4734 (2008).
  • Björkman P, Widell A. HIV and GB virus C infections seen from the perspective of the vertically coexposed infant. J. Infect. Dis. 197(10), 1358–1360 (2008).
  • Maidana MT, Sabino EC, Kallas EG. GBV-C/HGV and HIV-1 coinfection. Braz. J. Infect. Dis. (2), 122–125 (2005).
  • Kaiser T, Tillmann HL. GB virus C infection: is there a clinical relevance for patients infected with the human immunodeficiency virus? AIDS Rev. 7(1), 3–12 (2005).
  • Leary TP, Muerhoff AS, Simons JN et al. Sequence and genomic organization of GBV-C: a novel member of the Flaviviridae associated with human non-A-E hepatitis. J. Med. Virol. 48, 60–67 (1996).
  • Naito H, Abe K. Genotyping system of GBV-C/HGV type 1 to type 4 by the polymerase chain reaction using typespecific primers and geographical distribution of viral genotypes. J. Virol. Methods 1, 3–9 (2001).
  • Smith DB, Cuceanu N, Davidson F, Jarvis LM, Mokili JL, Hamid S et al. Discrimination of hepatitis G virus/GBVC geographical variants by analysis of the 5′ non-coding region. J. Gen. Virol. 78, 1533–1542 (1997).
  • Muerhoff AS, Smith DB, Leary TP, Erker JC, Desai Mushahwar IK. Identification of GB virus C variants bb phylogenetic analysis of 5′-untranslated and coding region sequences. J. Virol. 71, 6501–6508 (1997).
  • Sathar MA, York DF, Gouws E, Coutsoudis A, Coovadia HM. GB virus type C coinfection in HIV-infected African mothers and their infants, KwaZulu Natal, South Africa. Clin. Infect. Dis. 38, 405–409 (2004).
  • Mohr EL, Murthy KK, McLinden JH, Xiang J, Stapleton JT. The natural history of nonhuman GB Virus C (GBV-Ccpz) in captive chimpanzees. J. Gen. Virol. 92, 91–100 (2011).
  • Abu Odeh RO. Detection and genotyping of GB virus-C in dromedary camels in the United Arab Emirates. Vet. Microbiol. 147, 226–230 (2011).
  • Stapleton JT, Williams CF, Xiang J. GB virus type C: a beneficial infection? J. Clin. Microbiol. 42, 915–3919 (2004).
  • George SL, Varmaz D, Stapleton JT. GB virus C replicates in primary T and B lymphocytes. J. Infect. Dis. 193, 451–454 (2006).
  • Lefrere JJ, Roudot-Thoraval F, Morand-Joubert L et al. Carriage of GB virus C/hepatitis G virus RNA is associated with a slower immunologic, virologic, and clinical progression of human immunodeficiency virus disease in coinfected persons. J. Infect. Dis. 179, 783–789 (1999).
  • Xiang J, Wunschmann S, Diekema DJ et al. Effect of coinfection with GB virus C on survival among patients with HIV infection. N. Engl. J. Med. 345, 707–714 (2001).
  • Tillmann HL, Heiken H, Knapik-Botor A et al. Infection with GB virus C and reduced mortality among HIV-infected patients. N. Engl. J. Med. 345, 715–724 (2001).
  • Van der Bij AK, Kloosterboer N, Prins M et al. GB virus C coinfection and HIV-1 disease progression: the Amsterdam Cohort Study. J. Infect. Dis. 191, 678–685 (2005).
  • Zhang W, Chaloner K, Tillmann HL, Williams CF, Stapleton JT. Effect of early and late GB virus C viraemia on survival of HIV-infected individuals: a meta-analysis. HIV Med. 7, 173–180 (2006).
  • Tillmann HL, Manns MP. GB virus-C infection in patients infected with the human immunodeficiency virus. Antiviral Res. 52, 83–90 (2001).
  • Toyoda H, Fukuda Y, Hayakawa T, Takamatsu J, Saito H. Effect of GB virus C/hepatitis G virus coinfection on the course of HIV infection in hemophilia patients in Japan. J. Acquir. Immune Defic. Syndr. Hum. Retrovirol. 17, 209–213 (1998).
  • Heringlake S, Ockenga J, Tillmann HL et al. GB virus C/hepatitis G virus infection: a favorable prognostic factor in human immunodeficiency virus infected patients? J. Infect. Dis. 177, 1723–1726 (1998).
  • Birk M, Lindback S, Lidman C. No influence of GB virus C replication on the prognosis in a cohort of HIV-1-infected patients. AIDS 16, 2482–2485 (2002).
  • Bjorkman P, Naucler A, Winqvist N, Mushahwar I, Widell A. A case-control study of the transmission routes for GB virus C/hepatitis G virus in Swedish blood donors lacking markers for hepatitis C virus infection. Vox Sang. 81, 148–153 (2001).
  • Bjorkman P, Flamholc L, Naucler A, Molnegren V, Wallmark E, Widell A. GB virus C during the natural course of HIV-1 infection: viremia at diagnosis does not predict mortality. AIDS 18, 877–886 (2004).
  • Gómara MJ, Fernández L, Pérez T, Ercilla G, Haro I. Assessment of synthetic chimeric multiple antigenic peptides for diagnosis of GB virus C infection. Anal. Biochem. 396(1), 51–48 (2010).
  • Gómara MJ, Fernández L, Pérez T et al. Diagnostic value of anti-GBV-C antibodies in HIV-infected patients. Chem. Biol. Drug. Des. 78(2), 277–282 (2011).
  • Bagasra O, Sheraz M. Role of GBV-C specific miRNAs in HIV-1 inhibition. Presented at: 111th ASM Annual Conference. New Orleans, LA, USA, 21–25 May 2011.
  • Stapleton JT. GB virus type C/Hepatitis G virus. Semin. Liver Dis. 23, 137–148 (2003).
  • Mohr EL, Xiang J, McLinden JH et al. GB virus type C envelope protein E2 elicits antibodies that react with a cellular antigen on HIV-1 particles and neutralize diverse HIV-1 isolates. J. Immunol. 185(7), 4496–4505 (2010).
  • Mohr EL, Stapleton JT. GB virus type C interactions with HIV: the role of envelope glycoproteins. J. Viral. Hepat. 16(11), 757–768 (2009).
  • Herrera E, Tenckhoff S, Gómara MJ et al. Effect of synthetic peptides belonging to E2 envelope protein of GB virus C on human immunodeficiency virus type 1 infection. J. Med. Chem. 53(16), 6054–6063 (2010).
  • Bagasra O. A unified concept of HIV-1 latency. Expert Opin. Biol. Ther. 6, 1135–1149 (2006).
  • Bagasra O, Stir AE, Pirisi-Creek L, Creek KE, Bagasra Au, Lee JS. Role of miRNAs in regulation of lentiviral latency and persistence. Appl. Immunochem. Mol. Morphol. 14, 276–290 (2006).
  • Kanak MA, Alseiari MA, Addanki KC et al. Triplex forming microRNAs form stable complexes with HIV-1 provirus and inhibit its replication. Appl. Immunohistochem. Mol. Morphol. 18(6), 532–545 (2010).
  • Medzhitov R, Littman D. HIV immunology needs a new direction. Nature 455, 591 (2008).
  • Walker BD, Goulder PJ. AIDS. Escape from the immune system. Nature 407, 313–314 (2000).
  • Korber BT, Letvin NL, Haynes BF. T-cell vaccine strategies for human immunodeficiency virus, the virus with a thousand faces. J. Virol. 83(17), 8300–8314 (2009).
  • Houzet L, Yeung ML, de Lame V, Desai D, Smith SM, Jeang KT. MicroRNA profile changes in human immunodeficiency virus type 1 (HIV-1) seropositive individuals. Retrovirology. 5, 118 (2008).
  • Lama J. The physiological relevance of CD4 receptor down-modulation during HIV infection. Curr. HIV Res. 1(2), 167–184 (2003).
  • The International HIV Controllers Study. The major genetic determinants of HIV-1 control affect HLA Class I peptide presentation. Science 330, 1551–1557 (2010).
  • Krajden M, Yu A, Braybrook H et al. GBV-C/ hepatitis G virus infection and non-Hodgkin lymphoma: a case control study. Int. J. Cancer 126(12), 2885–2892 (2010).
  • Horvilleur E, Wilson LA, Willis AE. Translation deregulation in B-cell lymphomas. Biochem. Soc. Trans. 38(6), 1593–1597 (2010).
  • Kotani A, Harnprasopwat R, Toyoshima T, Kawamata T, Tojo A. miRNAs in normal and malignant B cells. Int. J. Hematol. 92(2), 255–261 (2010).
  • Stapleton JT, Chaloner K. GB virus C infection and non-Hodgkin lymphoma: important to know but the jury is out. Int. J. Cancer 126(12), 2759–2761 (2010)
  • Bagasra O, Prilliman KP. RNA interference: the molecular immune system. J. Mol. Histol. 35, 545–553 (2004).
  • Zhang GL, Li YX, Zheng SQ, Liu M, Li X, Tang H. Suppression of hepatitis B virus replication by microRNA-199a-3p and microRNA-210. Antiviral Res. 88(2), 169–175 (2010).
  • Hakim ST, Alsayari M, McLean DC et al. A large number of the primate microRNAs target lentiviruses, RE and endogenous retroviruses. Biochem. Biophys. Res. Commun. 369, 357–362 (2008).
  • Bagasra O, Pace DG. Back to the soil: retroviruses and transposons. In: Biocommunication of Soil-Bacteria and Viruses. Springer, 161–188 (2010).
  • Lecellier CH, Dunoyer P, Arar K et al. A cellular microRNA mediates antiviral defense in human cells. Science 308(5721), 557–560 (2005).
  • Pfeffer S, Baumert TF. Impact of microRNAs for pathogenesis and treatment of hepatitis C virus minfection. Gastroenterol. Clin. Biol. 2034(8–9), 431–435 (2010).
  • Morita K, Taketomi A, Shirabe K et al. Clinical significance and potential of hepatic microRNA-122 expression in hepatitis C. Liver Int. 31(4), 474–484 (2010).
  • Qiu L, Fan H, Jin W et al. miR-122-induced down-regulation of HO-1 negatively affects miR-122-mediated suppression of HBV. Biochem. Biophys. Res. Commun. 398(4), 771–777 (2010).
  • Schwarze-Zander C, Neibecker M, Othman S et al. GB virus C coinfection in advanced HIV type-1 disease is associated with low CCR5 and CXCR4 surface expression on CD4(+) T-cells. Antivir. Ther. 15(5), 745–752 (2010).
  • Sánchez-Martín MJ, Urbán P, Pujol M, Haro I, Alsina MA, Busquets MA. Biophysical investigations of GBV-C E1 peptides as potential inhibitors of HIV-1 fusion peptide. Chemphyschem. 2(15), 2816–2822 (2011).
  • Zhou T, Xu L, Dey B et al. Structural definition of a conserved neutralization epitope on HIV-1 gp120. Nature 445(7129), 732–737 (2007).
  • Kwong PD. Human immunodeficiency virus: refolding the envelope. Nature 433(7028), 815–816 (2005).
  • Moenkemeyer M, Schmidt RE, Wedemeyer H, Tillmann HL, Heiken H. GBV-C coinfection is negatively correlated to Fas expression and Fas-mediated apoptosis in HIV-1 infected patients. J. Med. Virol. 80(11), 1933–1940 (2008).
  • Sánchez-Martín MJ, Busquets MA, Girona V, Haro I, Alsina MA, Pujol M. Effect of E1(64–81) hepatitis G peptide on the in vitro interaction of HIV-1 fusion peptide with membrane models. Biochim. Biophys. Acta. 1808(9), 2178–2188 (2011).
  • Haro I, Gómara MJ, Galatola R et al. Study of the inhibition capacity of an 18-mer peptide domain of GBV-C virus on gp41-FP HIV-1 activity. Biochim. Biophys. Acta. 1808(6), 1567–1573 (2011).
  • Berzsenyi MD, Woollard DJ, McLean CA et al. Down-regulation of intra-hepatic T-cell signaling associated with GB virus C in a HCV/HIV co-infected group with reduced liver disease. J. Hepatol. 55(3), 536–544 (2011).
  • Koedel Y, Eissmann K, Wend H, Fleckenstein B, Reil H. Peptides derived from a distinct region of GB virus C glycoprotein E2 mediate strain-specific HIV-1 entry inhibition. J. Virol. 85(14), 7037–7047 (2011).
  • Herrera E, Gomara MJ, Mazzini S, Ragg E, Haro I. Synthetic peptides of hepatitis G virus (GBV-C/HGV) in the selection of putative peptide inhibitors of the HIV-1 fusion peptide. J. Phys. Chem. B. 113(20), 7383–7391 (2009).
  • Fenizia C, Keele BF, Nichols D et al. TRIM5α does not affect simian immunodeficiency virus SIVmac251 replication in vaccinated or unvaccinated Indian Rhesus Macaques following intrarectal challenge exposure. J. Virol. 85(23), 12399–12409 (2011).
  • Lauring AS, Jones JO, Andino R. Rationalizing the development of live attenuated virus vaccines. Nat. Biotechnol. 28(6), 573–579 (2010).
  • Xiang J, George SL, Wunschmann S, Chang Q, Klinzman D, Stapleton JT. Inhibition of HIV-1 replication by GB virus C infection through increases in RANTES, MIP-1a, MIP-1b, and SDF-1. Lancet 363, 2040–2046 (2004).
  • Suresh P, Wanchu A, Bhatnagar A, Sachdeva RK, Sharma M. Spontaneous and antigen-induced chemokine production in exposed but uninfected partners of HIV type 1-infected individuals in North India. AIDS Res. Hum. Retroviruses 23(2), 261–268 (2007).
  • Luciw PA, Shaw KE, Unger RE et al. Genetic and biological comparisons of pathogenic and nonpathogenic molecular clones of simian immunodeficiency virus (SIVmac). AIDS Res. Hum. Retroviruses. 8(3), 395–402 (1992).
  • Bagasra O. Retroviruses and AIDS: birth of a new epidemic. HIV and Molecular Immunity: Prospect for AIDS Vaccine. Eaton Publishing, MA, 9–59 (1999).
  • Bosinger SE, Sodora DL, Silvestri G. Generalized immune activation and innate immune responses in simian immunodeficiency virus infection. Curr. Opin. HIV AIDS. 6(5), 411–418. (2011).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.