MINI-REVIEW

How to manage chimeric antigen receptor T cell recipients upon encountering COVID-19 infection?

Tingting Zhang1,2† Ganggang Wang1,2† Boyan Zhang3† Shuling Hou1,2* Dong Song1,2* Li Li1,2*
Show Less
1 Department of lymphoma, Cancer Center, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan, Shanxi, China
2 Sino-German Joint Oncological Research Laboratory, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Taiyuan, Shanxi, China
3 Department of Pharmaceutics, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China
CP, 3742
Submitted: 23 May 2024 | Accepted: 12 July 2024 | Published: 26 December 2024
© 2024 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
Abstract

Chimeric antigen receptor (CAR) T cell recipients are considered at higher risk of SARS-CoV-2 infection, more severe COVID-19 illness, and poorer outcomes compared to the general population due to their impaired humoral immunity. Managing COVID-19 in these vulnerable patients is particularly challenging. In this review, we provide a brief overview of the characteristics of COVID-19 infection in CAR-T cell recipients, including the pre-treatment assessments and the timing for initiating CAR-T cell therapy, the treatment of COVID-19 during CAR-T cell therapy, and considerations for SARS-CoV-2 vaccination. Our aim is to offer practical strategies to help clinicians conduct safer and more effective CAR-T cell therapies in the post-COVID-19 pandemic era. The therapeutic approach to COVID-19 in this patient population must be individualized. In regions affected by the SARS-CoV-2 outbreak, CAR-T cell therapy is recommended to be conducted at well-established medical centers with expertise in CAR-T. This approach ensures optimal, comprehensive care throughout the treatment process, with the involvement of a multidisciplinary team being essential to the patient’s care.

Keywords
SARS-CoV-2
COVID-19
CAR-T
Hematological malignancies
Treatment
Vaccine
Funding
This work was supported by grants from the National Natural Science Foundation of China (No. 82300227 to Dr. Tingting Zhang) and Fundamental Research Program of Shanxi Province (No. 202303021222318 to Dr. Tingting Zhang and No.202203021221246 to Dr. Dong Song).
Conflict of interest
The authors declare that they have no competing interests.
References
  1. Callaway E. COVID’s future: Mini-waves rather than seasonal surges. Nature. 2023;617(7960):229-230. doi: 10.1038/d41586-023-01437-8

 

  1. Zhang T, Tian W, Wei S, et al. Multidisciplinary recommendations for the management of CAR-T recipients in the post-COVID-19 pandemic era. Exp Hematol Oncol. 2023;12(1):66. doi: 10.1186/s40164-023-00426-x

 

  1. Li X, Dai H, Wang Y, et al. Regional empowerment through decentralised governance under a centralised regulatory system facilitates the development of cellular therapy in China. Lancet Haematol. 2022;9(12):e942-e954. doi: 10.1016/S2352-3026(22)00331-3

 

  1. Luque-Paz D, Sesques P, Wallet F, Bachy E, Ader F. The burden of SARS-CoV-2 in patients receiving chimeric antigen receptor T cell immunotherapy: Everything to lose. Expert Rev Anti Infect Ther. 2022;20(9):1155-1162. doi: 10.1080/14787210.2022.2101448

 

  1. Xiao X, Chen P, Zhong Y, et al. Outcomes and risk factors of SARS-CoV-2 omicron variant in B-cell lymphoma patients following CD19 targeted CAR-T therapy. Cancer Med. 2023;12(22):20838-20846. doi: 10.1002/cam4.6657

 

  1. Pagano L, Salmanton-Garcia J, Marchesi F, et al. COVID-19 infection in adult patients with hematological malignancies: A European Hematology Association Survey (EPICOVIDEHA). J Hematol Oncol. 2021;14(1):168. doi: 10.1186/s13045-021-01177-0

 

  1. Wat J, Barmettler S. Hypogammaglobulinemia after Chimeric Antigen Receptor (CAR) T-Cell therapy: Characteristics, management, and future directions. J Allergy Clin Immunol Pract. 2022;10(2):460-466. doi: 10.1016/j.jaip.2021.10.037

 

  1. Hao S, Lian J, Lu Y, et al. Decreased B cells on admission associated with prolonged viral RNA shedding from the respiratory tract in coronavirus disease 2019: A case-control study. J Infect Dis. 2020;222(3):367-371. doi: 10.1093/infdis/jiaa311

 

  1. Shah GL, DeWolf S, Lee YJ, et al. Favorable outcomes of COVID-19 in recipients of hematopoietic cell transplantation. J Clin Invest. 2020;130(12):6656-6667. doi: 10.1172/JCI141777

 

  1. Tarhini H, Recoing A, Bridier-Nahmias A, et al. Long-term severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infectiousness among three immunocompromised patients: From prolonged viral shedding to SARS-CoV-2 superinfection. J Infect Dis. 2021;223(9):1522-1527. doi: 10.1093/infdis/jiab075

 

  1. Wei J, Zhao J, Han M, Meng F, Zhou J. SARS-CoV-2 infection in immunocompromised patients: Humoral versus cell-mediated immunity. J Immunother Cancer. 2020;8(2):e000862. doi: 10.1136/jitc-2020-000862

 

  1. Lynch M, Macori G, Fanning S, et al. Genomic evolution of SARS-CoV-2 virus in immunocompromised patient, Ireland. Emerg Infect Dis. 2021;27(9):2499-2501. doi: 10.3201/eid2709.211159

 

  1. Kupferschmidt K. Where did ‘weird’ Omicron come from? Science. 2021;374(6572):1179. doi: 10.1126/science.acx9738

 

  1. Ortega R, Gonzalez M, Nozari A, Canelli R. Personal protective equipment and Covid-19. N Engl J Med. 2020;382(26):e105. doi: 10.1056/NEJMvcm2014809

 

  1. Cao W, Wei J, Wang N, et al. Entecavir prophylaxis for hepatitis B virus reactivation in patients with CAR T-cell therapy. Blood. 2020;136(4):516-519. doi: 10.1182/blood.2020004907

 

  1. Hill JA, Li D, Hay KA, et al. Infectious complications of CD19-targeted chimeric antigen receptor-modified T-cell immunotherapy. Blood. 2018;131(1):121-130. doi: 10.1182/blood-2017-07-793760

 

  1. World Health Organization. WHO guidelines approved by the guidelines review committee. In: Therapeutics and COVID-19: Living Guideline. Geneva: World Health Organization; 2022.

 

  1. Lemaitre F, Budde K, Van Gelder T, et al. Therapeutic drug monitoring and dosage adjustments of immunosuppressive drugs when combined with nirmatrelvir/ritonavir in patients with COVID-19. Ther Drug Monit. 2022;45:191-199. doi: 10.1097/ftd.0000000000001014

 

  1. Li G, Hilgenfeld R, Whitley R, De Clercq E. Therapeutic strategies for COVID-19: Progress and lessons learned. Nat Rev Drug Discov. 2023;22(6):449-475. doi: 10.1038/s41573-023-00672-y

 

  1. RECOVERY Collaborative Group, Horby P, Lim WS, et al. Dexamethasone in hospitalized patients with Covid-19. N Engl J Med. 2021;384(8):693-704. doi: 10.1056/NEJMoa2021436

 

  1. Nie J, Yang L, Huang L, et al. Infection complications in febrile chimeric antigen receptor (CAR)-T recipients during the peri-CAR-T cell treatment period examined using metagenomic next-generation sequencing (mNGS). Cancer Commun (Lond). 2022;42(5):476-480. doi: 10.1002/cac2.12260

 

  1. Bowe B, Xie Y, Al-Aly Z. Postacute sequelae of COVID-19 at 2 years. Nat Med. 2023;29:2347-2357. doi: 10.1038/s41591-023-02521-2

 

  1. Pinana JL, Lopez-Corral L, Martino R, et al. SARS-CoV-2 vaccine response and rate of breakthrough infection in patients with hematological disorders. J Hematol Oncol. 2022;15(1):54. doi: 10.1186/s13045-022-01275-7

 

  1. Wang Y, Li C, Xia J, et al. Humoral immune reconstitution after anti-BCMA CAR T-cell therapy in relapsed/refractory multiple myeloma. Blood Adv. 2021;5(23):5290-5299. doi: 10.1182/bloodadvances.2021004603

 

  1. Sakuraba A, Luna A, Micic D. Serologic response following SARS-COV2 vaccination in patients with cancer: A systematic review and meta-analysis. J Hematol Oncol. 2022;15(1):15. doi: 10.1186/s13045-022-01233-3

 

  1. Cappell KM, Kochenderfer JN. Long-term outcomes following CAR T cell therapy: What we know so far. Nat Rev Clin Oncol. 2023;20(6):359-371. doi: 10.1038/s41571-023-00754-1

 

  1. Zheng C, Shao W, Chen X, Zhang B, Wang G, Zhang W. Real-world effectiveness of COVID-19 vaccines: A literature review and meta-analysis. Int J Infect Dis. 2022;114:252-260. doi: 10.1016/j.ijid.2021.11.009

 

  1. Rehabilitation Committee of Hematological Diseases, Chinese Association of Rehabilitation Medicine, Chinese Society of Hematology, Chinese Medical Association. Chinese consensus on severe acute respiratory syndrome coronavirus-2 vaccination in adult patients with hematological diseases (2023). Zhonghua Xue Ye Xue Za Zhi. 2023;44(1):19-25. doi: 10.3760/cma.j.issn.0253-2727.2023.01.004

 

  1. Pinana JL, Vazquez L, Martino R, et al. Spanish Society of Hematology and Hemotherapy expert consensus opinion for SARS-CoV-2 vaccination in onco-hematological patients. Leuk Lymphoma. 2022;63(3):538-550. doi: 10.1080/10428194.2021.1992619

 

  1. Aleissa MM, Little JS, Davey S, et al. Severe acute respiratory syndrome coronavirus 2 vaccine immunogenicity among chimeric antigen receptor T cell therapy recipients. Transplant Cell Ther. 2023;29:398.e1-398.e5. doi: 10.1016/j.jtct.2023.03.005

 

  1. Dyer O. Covid-19: Infections climb globally as EG.5 variant gains ground. BMJ. 2023;382:1900. doi: 10.1136/bmj.p1900

 

  1. Vangeel L, Chiu W, De Jonghe S, et al. Remdesivir, molnupiravir and nirmatrelvir remain active against SARS-CoV-2 omicron and other variants of concern. Antiviral Res. 2022;198:105252. doi: 10.1016/j.antiviral.2022.10525
Share
Back to top
Cancer Plus, Electronic ISSN: 2661-3840 Print ISSN: 2661-3832, Published by AccScience Publishing