A novel luciferase-based assay for the detection of Chimeric Antigen Receptors

• Published in: Scientific reports Vol. 9; no. 1; p. 1957
• Main Authors: Gopalakrishnan, Ramakrishnan, Matta, Hittu, Choi, Sunju, Natarajan, Venkatesh, Prins, Ruben, Gong, Songjie, Zenunovic, Arta, Narasappa, Nell, Patel, Fatima, Prakash, Rekha, Chaudhary, Vishan, Sikri, Varun, Chitnis, Saurabh Deepak, Kochegarov, Andrei, Wang, Dan, Falat, Magdalena, Kahn, Michael, Keerthipati, Pooja Smruthi, Sharma, Naman, Lenka, Jyotirmayee, Stieben, Tomas Meza, Braun, Jason, Batra, Ankita, Purvis, Katelyn, Ito, Kenta, Lee, Jae Han, Jeronimo, Alberto, Zamora, Hannalei Mae, Membreno, Allen, Qiu, Queenie, Peshin, Supriya, Namburu, Lalith, Chaudhary, Preet M
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 13.02.2019; Nature Publishing Group UK
• Subjects: Antigens; Chimeric antigen receptors; Effector cells; Epitopes; Flow cytometry; Fusion protein; Immunoglobulins; Immunotherapy; Luminescence; Protein purification
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-38258-z

Chimeric Antigen Receptor-T (CAR-T) cell immunotherapy has produced dramatic responses in hematologic malignancies. One of the challenges in the field is the lack of a simple assay for the detection of CARs on the surface of immune effector cells. In this study, we describe a novel luciferase-based assay, termed Topanga Assay, for the detection of CAR expression. The assay utilizes a recombinant fusion protein, called Topanga reagent, generated by joining the extra-cellular domain of a CAR-target in frame with one of the marine luciferases or their engineered derivatives. The assay involves incubation of CAR expressing cells with the Topanga reagent, a few washes and measurement of luminescence. The assay can detect CARs comprising either immunoglobulin- or non-immunoglobulin-based antigen binding domains. We further demonstrate that addition of epitope tags to the Topanga reagent not only allows its convenient one step purification but also extends its use for detection of CAR cells using flow cytometry. However, crude supernatant containing the secreted Topanga reagent can be directly used in both luminescence and flow-cytometry based assays without prior protein purification. Our results demonstrate that the Topanga assay is a highly sensitive, specific, convenient, economical and versatile assay for the detection of CARs.