Evidence map›Paper›PMID 37110545›Full record

ArticleMolecules (Basel, Switzerland)2023

Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells.

Dong Wei, Kristin L Horton, John Chen, Linlin Dong, Susan Chen, Kojo Abdul-Hadi, Ting Ting Zhang, Cierra N Casson, Michael Shaw, Tsubasa Shiraishi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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  5. Article
  6. Proteomic Investigation of Immune Checkpoints and Some of Their Inhibitors.International journal of molecular sciences · 2024
    Review
  7. 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

13 authors at 1 institution in 1 country.

Dong WeiTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.ORCID 0009-0008-0935-1065
Kristin L HortonTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
John ChenNovaBioAssays LLC, 52 Dragon Ct, Suite 3B, Woburn, MA 01801, USA.
Linlin DongTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Susan ChenTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Kojo Abdul-HadiTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Ting Ting ZhangTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Cierra N CassonTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Michael ShawTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Tsubasa ShiraishiTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.
Brandon WilkinsonTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.ORCID 0009-0000-9440-4855
Chengjie JiNovaBioAssays LLC, 52 Dragon Ct, Suite 3B, Woburn, MA 01801, USA.
Mark G QianTakeda Pharmaceutical Company International Co., 35 Landsdowne Street, Cambridge, MA 02139, USA.ORCID 0000-0001-6140-973X
Takeda (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a check point protein expressed on the surface of T cells and plays a central role in regulating the immune response. In recent years, CTLA-4 has become a popular target for cancer immunotherapy in which blocking CTLA-4 can restore T-cell function and enhance the immune response against cancer. Currently, there are many CTLA-4 inhibitors in a variety of modalities, including cell therapies, which are being developed in both preclinical and clinical stages to further harness the potential of the target for the treatment of certain types of cancer. In drug discovery research, measuring the level of CTLA-4 in T cells is important for drug discovery and development because it provides key information for quantitative assessment of the pharmacodynamics, efficacy, and safety of the CTLA-4-based therapies. However, to our best knowledge, there is still no report of a sensitive, specific, accurate, and reliable assay for CTLA-4 measurement. In this work, an LC/MS-based method was developed to measure CTLA-4 in human T cells. The assay demonstrated high specificity with an LLOQ of 5 copies of CTLA-4 per cell when using 2.5 million T cells for analysis. As shown in the work, the assay was successfully used to measure CTLA-4 levels in subtype T-cell samples from individual healthy subjects. The assay could be applied in supporting the studies of CTLA-4-based cancer therapies.

Indexed as

NeoplasmsCTLA-4 AntigenHumansImmunotherapyT-LymphocytesCTLA-4 Antigenhuman T cellsLC/MSquantificationT-lymphocyte-associated protein 4 (CTLA-4)

Identifiers

PMID37110545
PMCPMC10142971
OpenAlexW4363648056

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.