Evidence map›Paper›PMID 19667089›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

In vivo sensitized and in vitro activated B cells mediate tumor regression in cancer adoptive immunotherapy.

Qiao Li, Seagal Teitz-Tennenbaum, Elizabeth J Donald, Mu Li, Alfred E Chang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

69 citing papers in PubMed, 131 citations in OpenAlex.

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  20. B cells in pancreatic cancer stroma.World journal of gastroenterology · 2022
    Review

9 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Qiao LiDivision of Surgical Oncology, University of Michigan, Ann Arbor, MI 48109, USA. qiaoli@umich.edu
Seagal Teitz-Tennenbaum
Elizabeth J Donald
Mu Li
Alfred E Chang
University of Michigan · US

Funding

T CELL ACTIVATION FOR CANCER IMMUNOTHERAPYR01CA082529 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, ALFRED E · 1999 to 2008
$2.8M
T and B cell Activation of Cancer ImmunotherapyR56CA082529 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, ALFRED E · 2009 to 2009
$340k
NCI NIH HHS CA82529NCI NIH HHS R01 CA082529NCI NIH HHS R56 CA082529
6 · The paper itself

Abstract

Adoptive cellular immunotherapy utilizing tumor-reactive T cells has proven to be a promising strategy for cancer treatment. However, we hypothesize that successful treatment strategies will have to appropriately stimulate not only cellular immunity, but also humoral immunity. We previously reported that B cells in tumor-draining lymph nodes (TDLNs) may function as APCs. In this study, we identified TDLN B cells as effector cells in an adoptive immunotherapy model. In vivo primed and in vitro activated TDLN B cells alone mediated effective (p < 0.05) tumor regression after adoptive transfer into two histologically distinct murine pulmonary metastatic tumor models. Prior lymphodepletion of the host with either chemotherapy or whole-body irradiation augmented the therapeutic efficacy of the adoptively transferred TDLN B cells in the treatment of s.c. tumors as well as metastatic pulmonary tumors. Furthermore, B cell plus T cell transfers resulted in substantially more efficient antitumor responses than B cells or T cells alone (p < 0.05). Activated TDLN B cells conferred strong humoral responses to tumor. This was evident by the production of IgM, IgG, and IgG2b, which bound specifically to tumor cells and led to specific tumor cell lysis in the presence of complement. Collectively, these data indicate that in vivo primed and in vitro activated B cells can be employed as effector cells for cancer therapy. The synergistic antitumor efficacy of cotransferred activated B effector cells and T effector cells represents a novel approach for cancer adoptive immunotherapy.

Indexed as

Immunotherapy, AdoptiveAnimalsAntibodies, NeoplasmB-Lymphocyte SubsetsCell Line, TumorFemaleFibrosarcomaImmunoglobulin GImmunoglobulin MInjections, SubcutaneousLung NeoplasmsLymph NodesLymphocyte ActivationMelanoma, ExperimentalMiceMice, Inbred C57BLAntibodies, NeoplasmImmunoglobulin GImmunoglobulin M

Identifiers

PMID19667089
PMCPMC3740231
OpenAlexW1542537947

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.