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Cited by 300

The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.

Insufficient Production and Tissue Delivery of CD4+Memory T Cells in Rapidly Progressive Simian Immunodeficiency Virus Infection

Open access
Picker, Louis J., Hagen, Shoko I., Lum, Richard, Reed-Inderbitzin, Edward F., Daly, Lyn M., Sylwester, Andrew W., Walker, Joshua M., Siess, Don C., Piatak, Michael, Wang, Chenxi, Allison, David B., Maino, Vernon C., Lifson, Jeffrey D., Kodama, Toshiaki, Axthelm, Michael K.·2004·The Journal of Experimental Medicine

Abstract

The mechanisms linking human immunodeficiency virus replication to the progressive immunodeficiency of acquired immune deficiency syndrome are controversial, particularly the relative contribution of CD4+ T cell destruction. Here, we used the simian immunodeficiency virus (SIV) model to investigate the relationship between systemic CD4+ T cell dynamics and rapid disease progression. Of 18 rhesus macaques (RMs) infected with CCR5-tropic SIVmac239 (n = 14) or CXCR4-tropic SIVmac155T3 (n = 4), 4 of the former group manifested end-stage SIV disease by 200 d after infection. In SIVmac155T3 infections, naive CD4+ T cells were dramatically depleted, but this population was spared by SIVmac239, even in rapid progressors. In contrast, all SIVmac239-infected RMs demonstrated substantial systemic depletion of CD4+ memory T cells by day 28 after infection. Surprisingly, the extent of CD4+ memory T cell depletion was not, by itself, a strong predictor of rapid progression. However, in all RMs destined for stable infection, this depletion was countered by a striking increase in production of short-lived CD4+ memory T cells, many of which rapidly migrated to tissue. In all rapid progressors (P < 0.0001), production of these cells initiated but failed by day 42 of infection, and tissue delivery of new CD4+ memory T cells ceased. Thus, although profound depletion of tissue CD4+ memory T cells appeared to be a prerequisite for early pathogenesis, it was the inability to respond to this depletion with sustained production of tissue-homing CD4+ memory T cells that best distinguished rapid progressors, suggesting that mechanisms of the CD4+ memory T cell generation play a crucial role in maintaining immune homeostasis in stable SIV infection.

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Metadata

Authors
Picker, L. J., Hagen, S. I., Lum, R., Reed-Inderbitzin, E. F., Daly, L. M., Sylwester, A. W., Walker, J. M., Siess, D. C., Piatak, M., Wang, C., Allison, D. B., Maino, V. C., Lifson, J. D., Kodama, T., & Axthelm, M. K.
Venue
The Journal of Experimental Medicine
Published
2004-11-15
Volume
200
Issue
10
Pages
1299-1314
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2156616790
Cited by
300
References
50
FWCI
8.80
Type
journal article
Language
en
Open access
green

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Picker, L. J., Hagen, S. I., Lum, R., Reed-Inderbitzin, E. F., Daly, L. M., Sylwester, A. W., Walker, J. M., Siess, D. C., Piatak, M., Wang, C., Allison, D. B., Maino, V. C., Lifson, J. D., Kodama, T., & Axthelm, M. K. (2004). Insufficient Production and Tissue Delivery of CD4+Memory T Cells in Rapidly Progressive Simian Immunodeficiency Virus Infection. The Journal of Experimental Medicine. https://doi.org/10.1084/jem.20041049

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.