# Hypomagnesemia in lymphoma patients receiving CAR T therapy correlates with immune dysfunction and decreased survival

**Authors:** Jennifer J. Gile, Patrizia Mondello, Zixing Wang, Ying Li, Radhika Bansal, Sangeetha Gandhi, Henan Zhang, Elham Babadi, Kodi Martinez, Gabrielle McCoy, Zuoyi Shao, Kevin Regan, Matthew A. Hathcock, Panwen Wang, Junwen Wang, Abdullah S. Al Saleh, Gordon Ruan, Stephen M. Ansell, N. Nora Bennani, Patrick B. Johnston, Jonas Paludo, Jose C. Villasboas-Bisneto, Arushi Khurana, Urshila Durani, Yucai Wang, Paul J. Hampel, Allison Rosenthal, Javier Munoz, Eider Moreno, Januario E. Castro, Hemant S. Murthy, Mohamed Kharfan-Dabaja, Saad S. Kenderian, Jenny J. Kim, Rhine Shen, Mike Mattie, Yi Lin, Thomas E. Witzig

PMC · DOI: 10.1186/s40164-025-00623-w · 2025-04-30

## TL;DR

Low magnesium levels in lymphoma patients before CAR T therapy are linked to worse survival and immune dysfunction.

## Contribution

This study identifies hypomagnesemia as a novel prognostic factor for CAR T therapy outcomes in lymphoma patients.

## Key findings

- Hypomagnesemia before treatment predicted worse progression-free and overall survival in ZUMA-1 and Mayo Clinic cohorts.
- Low magnesium correlated with elevated inflammatory markers and altered immune cell interactions.
- scRNAseq revealed an immune suppressive transcriptome associated with hypomagnesemia.

## Abstract

Hypomagnesemia has been correlated with inferior outcomes in patients with large B cell lymphoma (LBCL) undergoing stem cell transplants. As T-cell and myeloid cell dysfunction have been associated with low magnesium conditions, we investigated whether serum magnesium (Mg) levels could predict clinical outcomes in LBCL patients who received chimeric antigen receptor T-cell therapy.

Patients with LBCL who received axi-cel under the ZUMA-1 trial or as FDA approved therapy at Mayo Clinic were examined. Serum samples were obtained at specified time points and cytokine analysis was performed. Single cell RNA sequencing was performed on peripheral blood mononuclear cells. The Student T-test, Kruskal Wallis, or Fisher's Exact Tests were used to compare differences in demographics across Mg levels. Survival curves were plotted using the Kaplan–Meier methodology and compared using the Wilcoxon test.

We found that hypomagnesemia before lymphodepletion chemotherapy predicted inferior progression-free and overall survival in the pivotal study ZUMA-1 (NCT02348216). These results were validated in an independent cohort of LBCL patients receiving axicabtagene ciloleucel (axi-cel) at Mayo Clinic. Hypomagnesemia correlated with increased inflammatory serum markers and cytokine levels including ferritin, IL-6, IL1Ra, IL-8, and MIP1a. scRNAseq analysis unveiled altered immune interactions between monocytes and T cells with a concordant immune suppressive transcriptome.

Hypomagnesemia at the time of CAR-T infusion is associated with an unfavorable inflammatory profile and decreased response and survival in LBCL patients receiving axi-cel. These findings suggest a potentially actionable prognostic factor for patients with large cell lymphoma undergoing CAR-T.

The online version contains supplementary material available at 10.1186/s40164-025-00623-w.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL1R1 (interleukin 1 receptor type 1), CXCL8 (C-X-C motif chemokine ligand 8), CCL3 (C-C motif chemokine ligand 3)
- **Chemicals:** magnesium (PubChem CID 5462224)
- **Diseases:** large B cell lymphoma (MONDO:0968974), lymphoma (MONDO:0003659)

## Full-text entities

- **Genes:** CCL3 (C-C motif chemokine ligand 3) [NCBI Gene 6348] {aka G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI}, IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** cell and myeloid cell dysfunction (MESH:D002292), large cell lymphoma (MESH:D016403), lymphoma (MESH:D008223), inflammatory (MESH:D007249), immune dysfunction (MESH:D007154), LBCL (MESH:D016393), Hypomagnesemia (OMIM:613882)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12044716/full.md

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Source: https://tomesphere.com/paper/PMC12044716