Evidence map›Paper›PMID 40625531›Full record

ArticleHemaSphere2025

A spheroid model that recapitulates the protective role of the lymph node microenvironment and serves as a platform for drug testing in chronic lymphocytic leukemia.

Elisa Lenti, Edoardo Visentin, Engin Bojnik, Alessia Neroni, Martina Franchino, Daniela Talarico, Nicolò Sacchetti, Lydia Scarfò, Aurora Maurizio, Jose Manuel Garcia-Manteiga and 2 more

Abstract read
In one paragraph

Article in HemaSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors.

Elisa LentiLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Edoardo VisentinLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Engin BojnikB-Cell Neoplasia Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Alessia NeroniLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Martina FranchinoLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Daniela TalaricoLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Nicolò SacchettiLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Lydia ScarfòB-Cell Neoplasia Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Aurora MaurizioCenter for Omics Sciences, IRCCS San Raffaele Scientific Institute Milan Italy.
Jose Manuel Garcia-ManteigaCenter for Omics Sciences, IRCCS San Raffaele Scientific Institute Milan Italy.
Paolo GhiaB-Cell Neoplasia Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.ORCID https://orcid.org/0000-0003-3750-7342
Andrea BrendolanLymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.ORCID https://orcid.org/0000-0003-0109-6879

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) B cells are characterized by a propensity to undergo rapid apoptosis when cultured in vitro, underscoring the importance of the tissue microenvironment for disease survival. One of the major limitations in studying the role of the microenvironment in tumor development and drug response is the inadequacy of conventional two-dimensional (2D) in vitro assays to physiologically reconstruct the complex spatial organization and interactions of cells in their natural lymphoid niches. To overcome this limitation, we developed a novel in vitro 3D lymph node-like spheroid model of the leukemic microenvironment by culturing human CLL cells with fibroblastic reticular cells (FRCs). FRCs are a key structural component of secondary lymphoid organs and are emerging as crucial players in tissue homeostasis and immune responses. Our results demonstrate that CLL spheroids maintain the physiological cellular ratio between FRCs and leukemic cells over time and protect tumor cells from apoptosis by mimicking the protective effects of the microenvironment. This was further demonstrated by venetoclax treatment that showed reduced apoptosis in 3D compared to a 2D setting. Importantly, the spheroids promote a gene expression profile more aligned with that of CLL cells in lymphoid tissues. The spheroid model provides a straightforward, quick-to-use platform for investigating drug efficacy under conditions that better replicate the natural lymph node microenvironment. This 3D lymph node-like spheroid model could serve as a valuable tool for studying tumor biology and the protective effects of the stromal microenvironment, and for testing therapeutic strategies in a more clinically relevant setting.

Identifiers

PMID40625531
PMCPMC12233836

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Registered trials

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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.