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Pregled bibliografske jedinice broj: 1051579

Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection?


Lay, M. D. H.; Petravic, J.; Gordon, S. N.; Engram, J.; Silvestri, G.; Davenport, M. P.
Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection? // Journal of Virology, 83 (2009), 15; 7517-7523 doi:10.1128/jvi.00552-09 (međunarodna recenzija, članak, znanstveni)


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Naslov
Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection?

Autori
Lay, M. D. H. ; Petravic, J. ; Gordon, S. N. ; Engram, J. ; Silvestri, G. ; Davenport, M. P.

Izvornik
Journal of Virology (0022-538X) 83 (2009), 15; 7517-7523

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
HIV ; CD4 depletion ; gut

Sažetak
The acute phases of human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infection are characterized by rapid and profound depletion of CD4+ T cells from the guts of infected individuals. The large number of CD4+ T cells in the gut (a large fraction of which are activated and express the HIV/SIV coreceptor CCR5), the high level of infection of these cells, and the temporal coincidence of this CD4+ T-cell depletion with the peak of virus in plasma in acute infection suggest that the intestinal mucosa may be the major source of virus driving the peak viral load. Here, we used data on CD4+ T-cell proportions in the lamina propria of the rectums of SIV-infected rhesus macaques (which progress to AIDS) and sooty mangabeys (which do not progress) to show that in both species, the depletion of CD4+ T cells from this mucosal site and its maximum loss rate are often observed several days before the peak in viral load, with few CD4+ T cells remaining in the rectum by the time of peak viral load. In contrast, the maximum loss rate of CD4+ T cells from bronchoalveolar lavage specimens and lymph nodes coincides with the peak in virus. Analysis of the kinetics of depletion suggests that, in both rhesus macaques and sooty mangabeys, CD4+ T cells in the intestinal mucosa are a highly susceptible population for infection but not a major source of plasma virus in acute SIV infection.

Izvorni jezik
Engleski

Znanstvena područja
Matematika, Biologija



POVEZANOST RADA


Profili:

Avatar Url Janka Petravić (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Lay, M. D. H.; Petravic, J.; Gordon, S. N.; Engram, J.; Silvestri, G.; Davenport, M. P.
Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection? // Journal of Virology, 83 (2009), 15; 7517-7523 doi:10.1128/jvi.00552-09 (međunarodna recenzija, članak, znanstveni)
Lay, M., Petravic, J., Gordon, S., Engram, J., Silvestri, G. & Davenport, M. (2009) Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection?. Journal of Virology, 83 (15), 7517-7523 doi:10.1128/jvi.00552-09.
@article{article, author = {Lay, M. D. H. and Petravic, J. and Gordon, S. N. and Engram, J. and Silvestri, G. and Davenport, M. P.}, year = {2009}, pages = {7517-7523}, DOI = {10.1128/jvi.00552-09}, keywords = {HIV, CD4 depletion, gut}, journal = {Journal of Virology}, doi = {10.1128/jvi.00552-09}, volume = {83}, number = {15}, issn = {0022-538X}, title = {Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection?}, keyword = {HIV, CD4 depletion, gut} }
@article{article, author = {Lay, M. D. H. and Petravic, J. and Gordon, S. N. and Engram, J. and Silvestri, G. and Davenport, M. P.}, year = {2009}, pages = {7517-7523}, DOI = {10.1128/jvi.00552-09}, keywords = {HIV, CD4 depletion, gut}, journal = {Journal of Virology}, doi = {10.1128/jvi.00552-09}, volume = {83}, number = {15}, issn = {0022-538X}, title = {Is the Gut the Major Source of Virus in Early Simian Immunodeficiency Virus Infection?}, keyword = {HIV, CD4 depletion, gut} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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