Evidence map›Paper›PMID 27410493›Full record

ReviewAIDS patient care and STDs2016

Human Immunodeficiency Virus Immune Cell Receptors, Coreceptors, and Cofactors: Implications for Prevention and Treatment.

Andrew W Woodham, Joseph G Skeate, Adriana M Sanna, Julia R Taylor, Diane M Da Silva, Paula M Cannon, W Martin Kast

Open access · greenAbstract readReview
In one paragraph

Review in AIDS patient care and STDs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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  6. Review
  7. Article
  8. Molecular Engineering of Virus Tropism.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Identification and Implications of HIV-1 CRF01_AE Subtype in Hawai'i.Hawai'i journal of health & social welfare · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Andrew W Woodham1 Department of Molecular Microbiology and Immunology, University of Southern California , Los Angeles, California.
Joseph G Skeate1 Department of Molecular Microbiology and Immunology, University of Southern California , Los Angeles, California.
Adriana M Sanna2 Norris Comprehensive Cancer Center, University of Southern California , Los Angeles, California.
Julia R Taylor1 Department of Molecular Microbiology and Immunology, University of Southern California , Los Angeles, California.
Diane M Da Silva2 Norris Comprehensive Cancer Center, University of Southern California , Los Angeles, California.
Paula M Cannon1 Department of Molecular Microbiology and Immunology, University of Southern California , Los Angeles, California.
W Martin Kast1 Department of Molecular Microbiology and Immunology, University of Southern California , Los Angeles, California.
University of Southern California · US

Funding

VLP VACCINES AGAINST HPV INDUCED TUMORSR01CA074397 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAST, WIJBE MARTIN · 1997 to 2020
$5.5M
NCI NIH HHS R01 CA074397
6 · The paper itself

Abstract

In the last three decades, extensive research on human immunodeficiency virus (HIV) has highlighted its capability to exploit a variety of strategies to enter and infect immune cells. Although CD4(+) T cells are well known as the major HIV target, with infection occurring through the canonical combination of the cluster of differentiation 4 (CD4) receptor and either the C-C chemokine receptor type 5 (CCR5) or C-X-C chemokine receptor type 4 (CXCR4) coreceptors, HIV has also been found to enter other important immune cell types such as macrophages, dendritic cells, Langerhans cells, B cells, and granulocytes. Interestingly, the expression of distinct cellular cofactors partially regulates the rate in which HIV infects each distinct cell type. Furthermore, HIV can benefit from the acquisition of new proteins incorporated into its envelope during budding events. While several publications have investigated details of how HIV manipulates particular cell types or subtypes, an up-to-date comprehensive review on HIV tropism for different immune cells is lacking. Therefore, this review is meant to focus on the different receptors, coreceptors, and cofactors that HIV exploits to enter particular immune cells. Additionally, prophylactic approaches that have targeted particular molecules associated with HIV entry and infection of different immune cells will be discussed. Unveiling the underlying cellular receptors and cofactors that lead to HIV preference for specific immune cell populations is crucial in identifying novel preventative/therapeutic targets for comprehensive strategies to eliminate viral infection.

Indexed as

CD4 AntigensHIV-1HIV InfectionsHumansReceptors, CCR5Receptors, CXCR4Receptors, HIVCD4 AntigensCXCR4 protein, humanReceptors, CCR5Receptors, CXCR4Receptors, HIV

Identifiers

PMID27410493
PMCPMC4948215
OpenAlexW2469904508

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.