Evidence map›Paper›PMID 32731512›Full record

ReviewJournal of clinical medicine2020

Inflammatory Cells in Diffuse Large B Cell Lymphoma.

Roberto Tamma, Girolamo Ranieri, Giuseppe Ingravallo, Tiziana Annese, Angela Oranger, Francesco Gaudio, Pellegrino Musto, Giorgina Specchia, Domenico Ribatti

Abstract readReview
In one paragraph

Review in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
–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

35 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Macrophages and angiogenesis in human lymphomas.Clinical and experimental medicine · 2024
    Review
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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

9 authors.

Roberto TammaDepartment of Basic Medical Sciences, Neurosciences, and Sensory Organs, University of Bari Medical School, 70124 Bari, Italy.ORCID 0000-0003-4623-5406
Girolamo RanieriIRCCS Istituto Tumori 'Giovanni Paolo II', 70124 Bari, Italy.
Giuseppe IngravalloPathology Section, Department of Emergency and Transplantation, University of Bari Medical School, 70124 Bari, Italy.ORCID 0000-0002-4792-3545
Tiziana AnneseDepartment of Basic Medical Sciences, Neurosciences, and Sensory Organs, University of Bari Medical School, 70124 Bari, Italy.ORCID 0000-0002-7752-0368
Angela OrangerSection of Human Anatomy and Histology, Department of Emergency and Organ Transplantation, University of Bari, 70124 Bari, Italy.
Francesco GaudioHematology Section, Department of Emergency and Transplantation, University of Bari Medical School, 70124 Bari, Italy.
Pellegrino MustoHematology Section, Department of Emergency and Transplantation, University of Bari Medical School, 70124 Bari, Italy.ORCID 0000-0003-3277-6594
Giorgina SpecchiaHematology Section, Department of Emergency and Transplantation, University of Bari Medical School, 70124 Bari, Italy.
Domenico RibattiDepartment of Basic Medical Sciences, Neurosciences, and Sensory Organs, University of Bari Medical School, 70124 Bari, Italy.ORCID 0000-0003-4768-8431

Funding

Association against non- Hodgkin lymphomas "Il Sorriso di Antonio", Corato, Italy
6 · The paper itself

Abstract

Diffuse large B cell lymphoma (DLBCL), known as the most common non-Hodgkin lymphoma (NHL) subtype, is characterized by high clinical and biological heterogeneity. The tumor microenvironment (TME), in which the tumor cells reside, is crucial in the regulation of tumor initiation, progression, and metastasis, but it also has profound effects on therapeutic efficacy. The role of immune cells during DLBCL development is complex and involves reciprocal interactions between tumor cells, adaptive and innate immune cells, their soluble mediators and structural components present in the tumor microenvironment. Different immune cells are recruited into the tumor microenvironment and exert distinct effects on tumor progression and therapeutic outcomes. In this review, we focused on the role of macrophages, Neutrophils, T cells, natural killer cells and dendritic cells in the DLBCL microenvironment and their implication as target for DLBCL treatment. These new therapies, carried out by the induction of adaptive immunity through vaccination or passive of immunologic effectors delivery, enhance the ability of the immune system to react against the tumor antigens inducing the destruction of tumor cells.

Indexed as

dendritic cellsDLBCLmacrophagesneutrophilsNK cellsT cellstumor cellstumor microenvironment

Identifiers

PMID32731512
PMCPMC7463675

What OpenQuestion holds

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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.