Evidence map›Paper›PMID 29250325›Full record

ArticleBiomedical reports2017

Modern biotechnology-based therapeutic approaches against HIV infection.

Muhammad Imran, Yasir Waheed, Ayesha Ghazal, Sajjad Ullah, Sher Zaman Safi, Muhsin Jamal, Muhammad Ali, Muhammad Atif, Muhammad Imran, Farman Ullah

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Current and Future Therapeutic Strategies for Lentiviral Eradication from Macrophage Reservoirs.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Review
  2. Review
  3. 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

10 authors at 8 institutions in 2 countries.

Muhammad ImranDepartment of Microbiology, University of Health Sciences, Lahore 54600, Pakistan.
Yasir WaheedFoundation University Medical College, Foundation University, Islamabad 44000, Pakistan.
Ayesha GhazalDepartment of Microbiology, University of Health Sciences, Lahore 54600, Pakistan.
Sajjad UllahDepartment of Medical Laboratory Sciences, Imperial College of Business Studies, Lahore 53720, Pakistan.
Sher Zaman SafiInterdisciplinary Research Center in Biomedical Materials (IRCBM), COMSATS Institute of Information Technology, Lahore 54000, Pakistan.
Muhsin JamalDepartment of Microbiology, Abdul Wali Khan University, Garden Campus, Mardan 23200, Pakistan.
Muhammad AliDepartment of Life Sciences, University of Management Technology, Lahore 54600, Pakistan.
Muhammad AtifDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Aljouf University, Sakaka, Saudi Arabia.
Muhammad ImranDepartment of Diet and Nutrition, Imperial College of Business Studies, Lahore 54600, Pakistan.
Farman UllahDepartment of Physiology, Shaheed Zulfiqar Ali Bhutto Medical university Islamabad, Islamabad 44000, Pakistan.
Imperial College of Business Studies · PKUniversity of Health Sciences Lahore · PKAbdul Wali Khan University Mardan · PKAl Jouf University · SACOMSATS University Islamabad · PKFoundation University Islamabad · PKShaheed Zulfiqar Ali Bhutto Institute of Science and Technology · PKUniversity of Management and Technology · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The causative agent of acquired immune deficiency syndrome (AIDS) is human immunodeficiency virus (HIV). Since its discovery before 30 years, a number of drugs known as highly active antiretroviral therapy have been developed to suppress the life cycle of the virus at different stages. With the current therapeutic approaches, ending AIDS means providing treatment to 35 million individuals living with HIV for the rest of their lives or until a cure is developed. Additionally, therapy is associated with various other challenges such as potential of drug resistance, toxicity and presence of latent viral reservoir. Therefore, it is imperative to search for treatments and to identify new therapeutic approaches against HIV infection to avoid daily intake of drugs. The aim of the current review was to summarize different therapeutic strategies against HIV infection, including stem cell therapy, RNA interference, CRISPR/Cas9 pathways, antibodies, intrabodies and nanotechnology. Silencing RNA against chemokine receptor 5 and other HIV RNAs have been tested and found to elicit homology-based, post-transcriptional silencing. The CRISPR/Cas9 is a gene editing technology that produces a double-stranded nick in the virus DNA, which is repaired by the host machinery either by non-homology end joining mechanism or via homology recombination leading to insertion, deletion mutation which further leads to frame shift mutation and non-functional products. Intrabodies are intracellular-expressed antibodies that are directed towards the targets inside the cell unlike the naturally expressed antibodies which target outside the cell. Different nanotechnology-based therapeutic approaches are also in progress against HIV. HIV eradication is not feasible without deploying a cure or vaccine alongside the treatment.

Indexed as

antibodiesCRISPR/Cas9drugsHIVnanomedicineRNAistem celltherapy

Identifiers

PMID29250325
PMCPMC5727756
OpenAlexW2765164063

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.