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
相关论文
共 50 条
  • [21] Chimeric Antigen Receptor (CAR) T-Cell Products for Pediatric Cancers: Why Alternative Development Paths Are Needed
    Rossig, Claudia
    Pearson, Andrew D.
    Vassal, Gilles
    Scobie, Nicole
    Bird, Nick
    Blanc, Patricia
    Vormoor, H. Josef
    Calkoen, Friso G.
    Locatelli, Franco
    del Bufalo, Francesca
    Rives, Susana
    Jacoby, Elad
    Balduzzi, Adriana
    Bourquin, Jean-Pierre
    Baruchel, Andre
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (03)
  • [22] Chimeric Antigen Receptor T Cell (CAR - T) Therapy - A Novel Treatment in Cancer
    Baskaran, Priyadarsini
    Karthikeayan, Venkatraman
    Natarajan, Anusha
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2018, 23 (04)
  • [23] Cardiotoxicity of Chimeric Antigen Receptor T-Cell (CAR-T) Therapy: Pathophysiology, Clinical Implications, and Echocardiographic Assessment
    Nenna, Antonio
    Carpenito, Myriam
    Chello, Camilla
    Nappi, Pierluigi
    Annibali, Ombretta
    Vincenzi, Bruno
    Grigioni, Francesco
    Chello, Massimo
    Nappi, Francesco
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (15)
  • [24] Chimeric antigen receptor T-cell therapy - assessment and management of toxicities
    Neelapu, Sattva S.
    Tummala, Sudhakar
    Kebriaei, Partow
    Wierda, William
    Gutierrez, Cristina
    Locke, Frederick L.
    Komanduri, Krishna V.
    Lin, Yi
    Jain, Nitin
    Daver, Naval
    Westin, Jason
    Gulbis, Alison M.
    Loghin, Monica E.
    de Groot, John F.
    Adkins, Sherry
    Davis, Suzanne E.
    Rezvani, Katayoun
    Hwu, Patrick
    Shpall, Elizabeth J.
    NATURE REVIEWS CLINICAL ONCOLOGY, 2018, 15 (01) : 47 - 62
  • [25] Chimeric antigen receptor T-cell therapy — assessment and management of toxicities
    Sattva S. Neelapu
    Sudhakar Tummala
    Partow Kebriaei
    William Wierda
    Cristina Gutierrez
    Frederick L. Locke
    Krishna V. Komanduri
    Yi Lin
    Nitin Jain
    Naval Daver
    Jason Westin
    Alison M. Gulbis
    Monica E. Loghin
    John F. de Groot
    Sherry Adkins
    Suzanne E. Davis
    Katayoun Rezvani
    Patrick Hwu
    Elizabeth J. Shpall
    Nature Reviews Clinical Oncology, 2018, 15 : 47 - 62
  • [26] Innovations in cancer immunotherapy: chimeric antigen receptor T-cell therapy (CAR-T)
    Brown, Kevin
    Seftel, Matthew D.
    Hay, Kevin A.
    CANADIAN MEDICAL ASSOCIATION JOURNAL, 2021, 193 (33) : E1300 - E1302
  • [27] Chimeric antigen receptor T-cell therapy
    Burge, Cale
    Vanguru, Vinay
    Ho, Phoebe Joy
    AUSTRALIAN PRESCRIBER, 2023, 46 (02) : 36 - 39
  • [28] Chimeric antigen receptor T-cell toxicity
    Baymon, DaMarcus E.
    Boyer, Edward W.
    CURRENT OPINION IN PEDIATRICS, 2019, 31 (02) : 251 - 255
  • [29] Patterns of Failure Following Chimeric Antigen Receptor T-cell (CAR-T) Therapy
    Figura, N. B.
    Jain, M. D.
    Sim, A. J.
    Chavez, J. C.
    Shah, B. D.
    Khimani, F.
    Lazaryan, A.
    Liu, H. D.
    Kim, S.
    Locke, F. L.
    Robinson, T. J.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2019, 105 (01): : S66 - S67
  • [30] Chimeric Antigen Receptor T-Cell Therapy
    Ogba, Ndiya
    Arwood, Nicole M.
    Bartlett, Nancy L.
    Bloom, Mara
    Brown, Patrick
    Brown, Christine
    Budde, Elizabeth Lihua
    Carlson, Robert
    Farnia, Stephanie
    Fry, Terry J.
    Garber, Morgan
    Gardner, Rebecca A.
    Gurschick, Lauren
    Kropf, Patricia
    Reitan, Jeff J.
    Sauter, Craig
    Shah, Bijal
    Shpall, Elizabeth J.
    Rosen, Steven T.
    JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2018, 16 (09): : 1093 - 1106