Skip to main content
Log in

Host cell antigenic profile acquired by HIV-1 is a marker of its cellular origin

  • Brief Report
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

HIV-1 acquires cell membrane proteins during budding. The cell membrane proteins (CMP) profile of laboratory HIV-1 strains grown in different host cells was established, by using an immobilized antibody capture (IAC), to verify whether CMPs present on HIV-1 correlate with its host cell origin. HIV-1 grown in different cell lines incorporates cell markers such as CD3, CD19, CD14, CD31 and IL 2-R, according to the distinctive expression of these antigens on the host cells. Furthermore, also T-tropic and monocytotropic HIV-1 strains display host cell specific markers, supporting the hypothesis that virus associated CMPs are a marker of host cell origin.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Pantaleo G, Graziosi C, Fauci AS (1993) The immunopathogenesis of human immunodeficiency virus infection. N Engl J Med 338: 327–334

    Google Scholar 

  2. Tamalet C, Lafeuillade A, Yahi N, Vignoli C, Tourres C, Pellegrino P, De Micco P (1994) Comparison of viral burden and phenotype of HIV-1 isolates from lymph nodes and blood. AIDS 8: 1083–1088

    PubMed  Google Scholar 

  3. Schuitemaker H, Koot M, Kootstra NA, Dercksen MW, De Golde REY, Von Streenwijk RP, Lange JMA, Schattenkerk JKM, Miedema F, Tersmette M (1992) Biological phenotype of human immunodeficiency virus type 1 clones at different stages of infection: progression of disease is associated with a shift from monocytotropic to T-cell-tropic virus populations. J Virol 66: 1354–1360

    PubMed  Google Scholar 

  4. Bozzette SA, McCutchan JA, Spector SA, Wright B, Richman DD (1993) A cross-sectional comparison of persons with syncytium- and non-syncytium-inducing human immunodeficiency virus. J Infect Dis 168: 1374–1379

    PubMed  Google Scholar 

  5. Hunter E (1994) Macromolecular interactions in the assembly of HIV and other retroviruses. Semin Virol 5: 71–83

    Google Scholar 

  6. Capobianchi MR, Fais S, Castilletti C, Gentile M, Ameglio F, Dianzani F (1994) A simple and reliable method to detect cell membrane proteins on infectious human immunodeficiency virus-1 particles. J Infect Dis 169: 886–889

    PubMed  Google Scholar 

  7. Orentas RM, Hildreth JEK (1993) Association of host cell surface adhesion receptors and other membrane proteins with HIV and SIV. AIDS Res Hum Retroviruses 9: 1157–1165

    PubMed  Google Scholar 

  8. Gelderblom H, Reupke H, Winkel T, Kunze R, Pauli G (1987) MHC-antigens: constituents of the envelopes of human and immunodeficiency viruses. Z Naturforsch [C] 42: 1328–1334

    Google Scholar 

  9. Arthur LO, Bess JW, Sowder II Jr R, Benveniste RE, Mann DL, Chermann JC, Henderson LE (1992) Cellular proteins bound to immunodeficiency viruses: implication for pathogenesis and vaccines. Science 258: 1935–1937

    PubMed  Google Scholar 

  10. Merloo T, Sheikh MA, Bloem AC, De Ronde A, Schutten M, Van Els CAC, Roholl PJM, Joling P, Goudsmit J, Schuurmann HJ (1993) Host cell membrane proteins on human immunodeficiency virus type 1 after in vitro infection of H9 cells and blood mononuclear cells. An immuno-electron microscopic study. J Gen Virol 74: 129–135

    PubMed  Google Scholar 

  11. Capobianchi MR, Serra C, Abbate I, Marongiu P, Castilletti C, Tilocca F, Dianzani F, Dolei A (1994) Treatment of HIV-1 infected fibroblasts with human leukocyte antigen (HLA)-DR-inductive cytokines leads to infectious virions with newly acquired HLA-DR. AIDS 8: 1731–1733

    PubMed  Google Scholar 

  12. Fais S, Capobianchi MR, Abbate I, Castilletti C, Gentile M, Cordiali Fei P, Ameglio F, Dianzani F (1995) Unidirectional budding of HIV-1 at the site of cell-to-cell contact is associated with co-polarization of intercellular adhesion molecules (ICAM)-1 and HIV-1 viral matrix protein. AIDS 9: 329–335

    PubMed  Google Scholar 

  13. Garzelli C, Puglisi C, Falcone G (1986) Human monoclonal antibody to purified protein derivative of tuberculin produced by hybrids constructed with Epstein-Barr virus transformed B lymphocytes and mouse myeloma cells. Eur J Immunol 16: 584–587

    PubMed  Google Scholar 

  14. Massari FE, Poli G, Schnittman SM, Psallidopoulos MC, Davey V, Fauci AS (1990) In vivo T lymphocyte origin of macrophage-tropic strains of HIV. J Immunol 144: 4628–4632

    PubMed  Google Scholar 

  15. Burgio VL, Zupo S, Zocchi M, Ruco LP, Baroni CD (1994) Characterization of EN4 monoclonal antibody; a reagent with CD31 specificity. Clin Exp Immunol 96: 170–176

    PubMed  Google Scholar 

  16. Collin M, Illei P, James W, Gordon S (1994) Definition of the range and distribution of human immunodeficiency virus macrophage tropism using PCR-based infectivity measurements. J Gen Virol 75: 1597–1603

    PubMed  Google Scholar 

  17. Ebenbichler C, Westervelt P, Carrillo A, Henkel T, Johnson D, Ratner L (1993) Structure-function relationships of the HIV-1 envelope V3 loop tropism determinant: evidence for two distinct conformations. AIDS 7: 639–646

    PubMed  Google Scholar 

  18. De Wolf F, Hogervorst E, Goudsmit J, Fenyo EM, Rubsamen-Waigmann H, Holmes H, Galvao-Castro B, Karita E, Wasi C, Sempola SDK, Baan E, Zorgdrager F, Lukashov V, Osmanov S, Kuiken C, Cornelissen M, The WHO Network for HIV Isolation and Characterization (1994) Syncytium-inducing and non-syncytium-inducing capacity of human immunodeficiency virus type 1 subtypes other than B: phenotypic characteristics. AIDS Res Hum Retroviruses 10: 1387–1400

    PubMed  Google Scholar 

  19. Cheng-Mayer C, Seto D, Levy JA (1991) Altered host range of HIV-1 after passage through various human cell types. Virology 181: 288–294

    PubMed  Google Scholar 

  20. Fecondo JV, Pavuk NC, Silburn KA, Read DMY, Mansell AS, Boyd AW, McPhee DA (1993) Synthetic peptide analogs of intercellular adhesion molecule 1 (ICAM-1) inhibit HIV-1 replication in MT-2 cells. AIDS Res Hum Retroviruses 9: 733–740

    PubMed  Google Scholar 

  21. Castilletti C, Capobianchi MR, Fais S, Abbate I, Ficociello B, Ameglio F, Cordiali Fei P, Santini SM, Dianzani F (1995) HIV-1 grown on IFN gamma-treated U937 cells shows selective increase of virion associated ICAM-1 and HLA-DR and enhanced infectivity for CD4-negative cells. AIDS Res Hum Retroviruses 11: 547–553

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Abbate, I., Capobianchi, M.R., Fais, S. et al. Host cell antigenic profile acquired by HIV-1 is a marker of its cellular origin. Archives of Virology 140, 1849–1854 (1995). https://doi.org/10.1007/BF01384347

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01384347

Keywords

Navigation