Evidence map›Paper›PMID 33765210›Full record

ArticleCancer immunology, immunotherapy : CII2021

Activated B lymphocytes and tumor cell lysate as an effective cellular cancer vaccine.

Kyp L Oxley, Brett M Hanson, Ashley N Zani, Gail A Bishop

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. 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
0.4field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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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

4 authors at 1 institution in 1 country.

Kyp L OxleyDepartment of Microbiology and Immunology, The University of Iowa Bishop, 2296 Carver Biomedical Research Bldg., 340 Newton Rd, Iowa City, IA, 52242, USA.
Brett M HansonDepartment of Microbiology and Immunology, The University of Iowa Bishop, 2296 Carver Biomedical Research Bldg., 340 Newton Rd, Iowa City, IA, 52242, USA.
Ashley N ZaniDepartment of Microbiology and Immunology, The University of Iowa Bishop, 2296 Carver Biomedical Research Bldg., 340 Newton Rd, Iowa City, IA, 52242, USA.
Gail A BishopDepartment of Microbiology and Immunology, The University of Iowa Bishop, 2296 Carver Biomedical Research Bldg., 340 Newton Rd, Iowa City, IA, 52242, USA. gail-bishop@uiowa.edu.ORCID http://orcid.org/0000-0002-1291-5078
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Understanding and applying innate and adaptive immune signal interactionsI01BX001702 · VA · IOWA CITY VA MEDICAL CENTER · PI BISHOP, GAIL A. · 2013 to 2020
–
BLRD VA I01 BX001702National Science Foundation REU grant 1559927NIEHS NIH HHS P30 ES005605U.S. Department of Veterans Affairs I01BX001702
6 · The paper itself

Abstract

Cancer vaccines that utilize patient antigen-presenting cells to fight their own tumors have shown exciting promise in many preclinical studies, but have proven quite challenging to translate to clinical feasibility. Dendritic cells have typically been the cell of choice for such vaccine platforms, due to their ability to endocytose antigens nonspecifically, and their expression of multiple surface molecules that enhance antigen presentation. However, dendritic cells are present in low numbers in human peripheral blood and must be matured in culture before use in vaccines. Mature B lymphocytes, in contrast, are relatively abundant in peripheral blood, and can be quickly activated and expanded in overnight cultures. We devised an optimal stimulation cocktail that engages the B cell antigen receptor, CD40, TLR4 and TLR7, to activate B cells to present antigens from lysates of the recipient's tumor cells, precluding the need for known tumor antigens. This B cell vaccine (Bvac) improved overall survival from B16F1 melanoma challenge, as well as reduced tumor size and increased time to tumor appearance. Bvac upregulated B cell antigen presentation molecules, stimulated activation of both CD4

Indexed as

AnimalsAntigen PresentationAntigens, NeoplasmB-LymphocytesCancer VaccinesChemotaxis, LeukocyteFemaleLymphocyte ActivationMaleMelanoma, ExperimentalMiceMice, Inbred C57BLSkin NeoplasmsT-LymphocytesAntigens, NeoplasmCancer VaccinesAntigen presentationB cellCancerCellular vaccineT cell

Identifiers

PMID33765210
PMCPMC8720267
OpenAlexW3139523165

What OpenQuestion holds

Textmetadata
LicenceTDM
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.