Evidence mapPaperPMID 38883270Full record

ArticleJournal of cellular immunology2024

Essentials of CAR-T Therapy and Associated Microbial Challenges in Long Run Immunotherapy.

Muhammad Kalim, Rui Jing, Xin Li, Zhiwu Jiang, Ningbo Zheng, Ziyu Wang, Guo Wei, Yong Lu

Abstract read
In one paragraph

Article in Journal of cellular immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Muhammad KalimHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Rui JingHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Xin LiHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Zhiwu JiangHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Ningbo ZhengDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Ziyu WangHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Guo WeiHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Yong LuHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.

Funding

Eradication of Escaped Variant Tumor Cells for Cancer ImmunotherapyR01CA248111 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · 2023 to 2025
$770k
Decoupling acute toxicities and antitumor efficacy in adoptive cell therapyR01CA288403 · METHODIST HOSPITAL RESEARCH INSTITUTE · 2025 to 2025
$594k
Induction of autosis to overcome resistance in adoptive cell therapy for solid tumorsR01CA278911 · METHODIST HOSPITAL RESEARCH INSTITUTE · 2025 to 2025
$569k
The Unique Roles of Tumor-Specific Th9 Cells for Solid Tumor EradicationR01CA258477 · METHODIST HOSPITAL RESEARCH INSTITUTE · 2025 to 2025
$397k
NCI NIH HHS R01 CA248111NCI NIH HHS R01 CA258477NCI NIH HHS R01 CA278911NCI NIH HHS R01 CA288403NCI NIH HHS R37 CA251318
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-T cell therapy has shown potential in improving outcomes for individuals with hematological malignancies. However, achieving long-term full remission for blood cancer remains challenging due to severe life-threatening toxicities such as limited anti-tumor efficacy, antigen escape, trafficking restrictions, and limited tumor invasion. Furthermore, the interactions between CAR-T cells and their host tumor microenvironments have a significant impact on CAR-T function. To overcome these considerable hurdles, fresh methodologies and approaches are needed to produce more powerful CAR-T cells with greater anti-tumor activity and less toxicity. Despite advances in CAR-T research, microbial resistance remains a significant obstacle. In this review, we discuss and describe the basics of CAR-T structures, generations, challenges, and potential risks of infections in CAR-T cell therapy.

Indexed as

Adoptive cellular therapyCAR-TCOVID-19ImmunotherapyInfection

Identifiers

PMID38883270
PMCPMC11172397

What Socratic 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 Socratic graph.