A novel multicolor fluorescent spot assay for the functional assessment of chimeric antigen receptor (CAR) T-cell products

被引:2
|
作者
Atanackovic, Djordje [1 ,2 ,3 ,6 ]
Iraguha, Thierry [1 ,2 ]
Omili, Destiny [1 ,2 ]
Avila, Stephanie V. [1 ,2 ]
Fan, Xiaoxuan [3 ,4 ]
Kocoglu, Mehmet [1 ,2 ]
Gebru, Etse [1 ,2 ]
Baker, Jillian M. [3 ]
Dishanthan, Nishanthini [1 ,2 ]
Dietze, Kenneth A. [3 ]
Oluwafemi, Ayooluwakiitan [1 ,2 ,3 ]
Hardy, Nancy M. [1 ,2 ]
Yared, Jean A. [1 ,2 ]
Hankey, Kim [2 ]
Dahiya, Saurabh [1 ,2 ,5 ]
Rapoport, Aaron P. [1 ,2 ]
Luetkens, Tim
机构
[1] Univ Maryland, Sch Med, Dept Med, Baltimore, MD USA
[2] Univ Maryland, Greenebaum Comprehens Canc Ctr, Transplant & Cellular Therapy Program, Baltimore, MD USA
[3] Univ Maryland, Dept Microbiol & Immunol, Baltimore, MD USA
[4] Univ Maryland, Greenebaum Comprehens Canc Ctr, Baltimore, MD USA
[5] Stanford Univ, Stanford, CA USA
[6] Univ Maryland, Fannie Angelos Cellular Therapeut GMP Lab, Greenebaum Comprehens Canc Ctr, Canc Immunotherapy Med Director, Bressler Res Bldg,Room 9 011655,W Baltimore St, Baltimore, MD 21201 USA
关键词
biomarkers; CART cells; cellular immunotherapies; cytokines; T cells; GAMMA-ELISPOT ASSAY; B-CELL; PERIPHERAL-BLOOD; REMISSIONS; OUTCOMES; THERAPY;
D O I
10.1016/j.jcyt.2024.01.006
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims: Chimeric antigen receptor (CAR) T-cell (CAR-T) therapies have revolutionized the treatment of B-cell lymphomas. Unfortunately, relapses after CD19-targeted CAR-T are relatively common and, therefore, there is a critical need for assays able to assess the function and potency of CAR-T products preinfusion, which will hopefully help to optimize CAR-T therapies. We developed a novel multicolor fluorescent spot assay (MFSA) for the functional assessment of CAR-T products on a single-cell level, combining the numerical assessment of CAR-T products with their functional characterization. Methods: We first used a standard single-cell interferon (IFN)-g enzyme-linked immune absorbent spot assay to measure CD19-targeted CAR-T responses to CD19-coated beads. We then developed, optimized and validated an MFSA that simultaneously measures the secretion of combinations of different cytokines on a single CAR-T level. Results: We identified IFN-g/tumor necrosis factor-a/granzyme B as the most relevant cytokine combination, and we used our novel MFSA to functionally and numerically characterize two clinical-grade CAR-T products. Conclusions: In conclusion, we have developed a novel assay for the quantitative and functional potency assessment of CAR-T products. Our optimized MFSA is cost-effective, easy to perform, reliable, can be performed overnight, allowing for a fast delivery of the product to the patient, and requires relatively minimal maintenance and training. The clinical value of our novel assay will be assessed in studies correlating the pre-infusion assessment of CAR-T products with the patients' outcome in a prospective fashion. (c) 2024 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:318 / 324
页数:7
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