Evidence map›Paper›PMID 25755905›Full record

ReviewAmerican journal of blood research2014

Towards an off-the-shelf vaccine therapy targeting shared B-cell tumor idiotypes.

Flavio E Baio, Larry W Kwak, Jinsheng Weng

Open access · greenAbstract readReview
In one paragraph

Review in American journal of blood research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Frontiers in immunology · 2018
    Article
  2. 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

3 authors at 1 institution in 1 country.

Flavio E BaioDepartment of Lymphoma and Myeloma, M.D. Anderson Cancer Center Houston, TX, USA ; Center for Cancer Immunology Research, M.D. Anderson Cancer Center Houston, TX, USA.
Larry W KwakDepartment of Lymphoma and Myeloma, M.D. Anderson Cancer Center Houston, TX, USA ; Center for Cancer Immunology Research, M.D. Anderson Cancer Center Houston, TX, USA.
Jinsheng WengDepartment of Lymphoma and Myeloma, M.D. Anderson Cancer Center Houston, TX, USA ; Center for Cancer Immunology Research, M.D. Anderson Cancer Center Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ideal tumor antigen is one expressed selectively by the tumor, present in all cancer patients, essential for tumor survival and nonetheless able to induce both humoral and cellular immune response. The personalized idiotype (Id) of the surface immunoglobulin is a tumor specific antigen in that it is expressed on clonal B-cell tumors, mediates B-cell survival, and induces tumor specific immunity in both human and animal models. With the availability of monoclonal antibodies against B cells, such as rituximab, the cellular immune response mediated by specific T cells has gained more importance as a combination therapy for the complete elimination of residual tumor cells in lymphoma and myeloma.

Indexed as

allogeneic T cellsimmunotherapyMyeloma

Identifiers

PMID25755905
PMCPMC4348793
OpenAlexW175413086

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.