Evidence map›Paper›PMID 40386721›Full record

ArticleTranslational lung cancer research2025

Characterization of the xeno-GVHD response generated by advanced lung cancer patient peripheral blood mononuclear cells in NSG-SGM3 mice.

Vered Fuchs, Laila Roisman, Maha Msamra, Yael Refaely, Aharon Yehonatan Cohen, Angel Porgador, Nir Peled, Ariel Sobarzo

Abstract read
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Article in Translational lung cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Vered Fuchs *The Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Laila Roisman *Helmsley Cancer Center, Shaare Zedek Medical Center, Jerusalem, Israel.
Maha MsamraThe Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Yael RefaelyDepartment of Cardiothoracic Surgery, Soroka University Medical Center, Beer-Sheva, Israel.
Aharon Yehonatan CohenThe Oncology Institute, Soroka University Medical Center, Beer-Sheva, Israel.
Angel PorgadorThe Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Nir PeledHelmsley Cancer Center, Shaare Zedek Medical Center, Jerusalem, Israel.
Ariel SobarzoThe Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Peripheral blood mononuclear cell (PBMC) humanized mouse models are essential for researching non-small cell lung cancer (NSCLC) treatments. However, these models are prone to xeno-graft versus host disease (xeno-GVHD), hampering their utility and requiring further investigation. This study examined xeno-GVHD responses from PBMCs of advanced-stage NSCLC patients compared to healthy donors (HDs) in a humanized peripheral blood lymphocyte (hu-PBL) model. Methods: PBMCs from NSCLC patients and HDs were injected into immunocompromised NSG-SGM3 mice and monitored for eight weeks. xeno-GVHD progression was assessed through clinical examinations and flow cytometry of human T-cell levels in various tissues. Results: Mice injected with PBMCs from HDs showed xeno-GVHD signs as early as 28 days post-injection, whereas those from NSCLC patients exhibited minimal signs, with only one model showing delayed responses by day 42. Clinical symptoms in mice included weight loss, anemia, low platelet counts, fur changes, and behavioral modifications. Flow cytometry of human PBMCs in mice indicated dominant CD8 Conclusions: This study demonstrates significant differences in xeno-GVHD progression between advance-stage NSCLC patients and HDs, likely influenced by the patient's treatment histories. These findings improve our understanding of hu-PBL models for NSCLC research and may inform future treatment studies and strategies.

Indexed as

humanized micehumanized peripheral blood lymphocyte model (hu-PBL model)non-small cell lung cancer (NSCLC)peripheral blood mononuclear cells (PBMCs)Xeno-graft versus host disease (xeno-GVHD)

Identifiers

PMID40386721
PMCPMC12082230

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