Evidence map›Paper›PMID 8016092›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

Combined intra- and extracellular immunization against human immunodeficiency virus type 1 infection with a human anti-gp120 antibody.

S Y Chen, Y Khouri, J Bagley, W A Marasco

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Gene therapy for HIV infections: Intracellular immunization.The Canadian journal of infectious diseases = Journal canadien des maladies infectieuses · 1999
    Article
  12. Article
  13. Article
  14. Phenotypic knockout of HIV type 1 chemokine coreceptor CCR-5 by intrakines as potential therapeutic approach for HIV-1 infection.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  15. Article
  16. Article
  17. Article
  18. Efficient infection of a human T-cell line and of human primary peripheral blood leukocytes with a pseudotyped retrovirus vector.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  19. Article
  20. A defective HIV-1 vector for gene transfer to human lymphocytes.Journal of molecular medicine (Berlin, Germany) · 1995
    Review
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

4 authors at 1 institution in 1 country.

S Y ChenDepartment of Medicine, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.
Y Khouri
J Bagley
W A Marasco
Dana-Farber Cancer Institute · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
DFCI-BIDMC-CH CENTER FOR AIDS RESEARCHP30AI028691 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SODROSKI, JOSEPH G · 1989 to 2003
$6.2M
MECHANISM OF ACTION OF THE TAT PRODUCT OF HIV-1R01AI028785 · NIAID · DANA-FARBER CANCER INSTITUTE · PI MARASCO, WAYNE A. · 1989 to 2002
$637k
NCI NIH HHS P30CA06516NIAID NIH HHS AI28785NIAID NIH HHS P30AI28691
6 · The paper itself

Abstract

In this study, a human CD4+ T lymphocyte line was transduced to secrete Fab fragments of a broadly neutralizing human monoclonal antibody F105 that reacts with the CD4-binding site of human immunodeficiency virus type 1 (HIV-1) envelope protein. In the transduced cells infected with HIV-1, the nascent Fab fragments bind intracellularly to the HIV-1 envelope protein and inhibit HIV-1 production. The secreted Fab fragments are able to neutralize cell-free HIV-1. In addition, the nascent Fab fragments can inhibit HIV-1 production by binding intracellularly to envelope mutants that escape neutralization by extracellular F105 antibody. The combined intra- and extracellular binding activities of the expressed Fab fragments result in the efficient blocking of cytopathic syncytium formation and infectious virus production. Thus, these antibody-producing T lymphocytes are not only resistant to HIV-1 infection but also can protect surrounding lymphocytes by secreting neutralizing antibodies. This novel strategy of combining intracellular and extracellular immunization may be useful for gene therapy of AIDS and other diseases.

Indexed as

AIDS VaccinesAnimalsAntibodies, MonoclonalBase SequenceCD4 AntigensCell LineChlorocebus aethiopsDNA PrimersFluorescent Antibody TechniqueGene ExpressionHIV-1HIV Envelope Protein gp120HumansImmunoglobulin Fab FragmentsImmunoglobulin Heavy ChainsImmunoglobulin kappa-ChainsAIDS VaccinesAntibodies, MonoclonalCD4 AntigensDNA PrimersHIV Envelope Protein gp120Immunoglobulin Fab FragmentsImmunoglobulin Heavy ChainsImmunoglobulin kappa-Chains

Identifiers

PMID8016092
PMCPMC44111
OpenAlexW1969845015

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.