Evidence map›Paper›PMID 40244456›Full record

ReviewCellular and molecular life sciences : CMLS2025

Targeting inflammasomes as a therapeutic potential for HIV/AIDS.

Hongliang Zhang, Botao Tan, Tinbing Tang, Jinhui Tao, Tengchuan Jin, Songquan Wu

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. HIV-1 latency: From acquaintance to confidant.Journal of virus eradication · 2025
    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

6 authors.

Hongliang ZhangCenter of Disease Immunity and Intervention, College of Medicine, Lishui University, Lishui, 323000, China.ORCID http://orcid.org/0000-0002-9163-9592
Botao TanCenter of Disease Immunity and Intervention, College of Medicine, Lishui University, Lishui, 323000, China.
Tinbing TangCenter of Disease Immunity and Intervention, College of Medicine, Lishui University, Lishui, 323000, China.
Jinhui TaoDepartment of Rheumatology and Immunology, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, 230001, China. taojinhui@ustc.edu.cn.
Tengchuan JinCenter of Disease Immunity and Intervention, College of Medicine, Lishui University, Lishui, 323000, China. jint@ustc.edu.cn.
Songquan WuCenter of Disease Immunity and Intervention, College of Medicine, Lishui University, Lishui, 323000, China. lswsq163@163.com.

Funding

National Natural Science Foundation of China 82402072Natural Science Foundation of Zhejiang Province QN25H100002
6 · The paper itself

Abstract

Human immunodeficiency virus (HIV) infection in humans can cause a variety of symptoms. Among these, acquired immunodeficiency syndrome (AIDS) remains the most severe form. Current treatment of HIV/AIDS with antiretroviral drugs effectively inhibits HIV replication and infection and significantly extends the lifespan of HIV/AIDS patients. However, antiretroviral drugs cannot completely remove HIV from patients due to the high latency of HIV, and they possess side effects and can lead to drug resistance. HIV/AIDS remains to be an incurable disease, and new methods and drugs are still desirable. Inflammasomes were found to be activated during HIV infection and regulate AIDS progression. Previous reviews provide a simple summary of inflammasome activators and inhibitors during HIV infection without distinguishing the specific infection stage, this kind of summary does not provide any clinical target value. Here, we provide a comprehensive review of inflammasomes in HIV/AIDS according to the infection timeline and propose several inflammasome target strategies for clinical HIV/AIDS treatment. We systematacially summarized the activation and function of kinds inflammasomes during the different HIV infection stages, with the aim of providing new therapeutic targets and directions for HIV/AIDS and HIV-associated comorbidities.

Indexed as

Acquired Immunodeficiency SyndromeHIV InfectionsInflammasomesAnimalsAnti-HIV AgentsHIV-1HumansAnti-HIV AgentsInflammasomesAIDSCARD8HIVInflammasomeNLRP3

Identifiers

PMID40244456
PMCPMC12006635

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.