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Cited by 525

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Macrophages as a Source of HIV During Opportunistic Infections

Orenstein, Jan M., Fox, Cecil, Wahl, Sharon M.·1997·Science

Abstract

The source of increasing viremia that characterizes the latter stages of human immunodeficiency virus (HIV) disease has remained a paradox because it occurs at a time when lymphoid tissue is quantitatively and qualitatively impaired, and the patients' CD4 T lymphocytes are steadily declining. Here, macrophages, both infected and uninfected with common opportunistic pathogens of HIV disease such as Mycobacterium avium complex and Pneumocystis carinii , were identified as highly productive sources of HIV in coinfected lymph nodes. These observations indicate that tissue macrophages are not only infected with HIV, but that common pathogens of HIV disease can dramatically increase their production of virus. Thus, prevention or successful treatment of opportunistic coinfections, or both, potentially benefits the patient twofold by limiting the pathology caused by opportunistic infection and by controlling induction of HIV replication.

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Metadata

Authors
Orenstein, J. M., Fox, C., & Wahl, S. M.
Venue
Science
Published
1997-06-20
Volume
276
Issue
5320
Pages
1857-1861
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2004319639
Cited by
525
References
1
FWCI
12.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Macrophages as a Source of HIV During Opportunistic Infections. https://app.cochat.ai/papers/10.1126/science.276.5320.1857
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Orenstein, J. M., Fox, C., & Wahl, S. M. (1997). Macrophages as a Source of HIV During Opportunistic Infections. Science. https://doi.org/10.1126/science.276.5320.1857

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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.