Approximately 20% of COVID-19 patients develop severe disease that can evolve into acute respiratory distress syndrome (ARDS), leading to respiratory or multiorgan failure with an overall mortality of up to 4%. Older age and comorbidities such as obesity, hypertension, diabetes and coronary heart disease, and immune deficiency have been associated with poor prognosis [2,3]. For example, in immunocompromised patients who received a haematopoietic stem-cell transplantation (HSCT), mortality rates as high as 20% have been reported [4].
Protective role of SARS-CoV-2-specific T cells
Growing evidence suggests that T cells have a protective role in combating COVID-19. Reduced counts and dysregulation are observed more prominently in individuals with severe compared with mild COVID-19 [5].
Dr Spyridoula Vasileiou (Baylor College of Medicine, USA) and colleagues have previously demonstrated the feasibility, safety, and clinical efficacy of administering allogeneic ex vivo expanded multivirus-specific T cells for the treatment of other viral infections in immunocompromised individuals. Given the lack of preventative or therapeutic agents and the emerging evidence of the pivotal protective role of SARS-CoV-2-specific CD4-postive and CD8-positive T cells, they explored the feasibility of developing a banked, SARS-CoV-2-specific virus-specific T cell product to treat individuals at highest risk of severe COVID-19 disease, such as HSCT recipients, elderly individuals, and patients with comorbidities [1].
The investigators are rapidly advancing this product to the clinic for administration in a randomised clinical trial to prevent the development of severe disease in high-risk hospitalised patients.
- Vasileiou S, et al. Using Allogeneic, Off-the-Shelf, Sars-Cov-2-Specific T Cells to Treat High Risk Patients with COVID-19. 62nd ASH Annual Meeting, 5-8 December 2020. Abstract 612.
- Yang Y, et al. Virol J. 2020;17:117
- Samudrala PK, et al. Eur J Pharmacol. 2020;883:173375.
- COVID-19 Reported Data as of 1/11/21. cibmtr.org/COVID19.
- Diao B, et al. Front Immunol. 2020;11:827
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Table of Contents: ASH 2020
Featured articles
COVID-19
More complicated course of COVID-19 in leukaemia patients
Older age and imatinib treatment associated with COVID-19 mortality in CML
Allogeneic SARS-CoV-2-specific T cells to treat COVID-19
More severe COVID-19 outcomes for patients with haematologic malignancies
Acute Lymphoblastic Leukaemia
Improved outcomes, but still substantial part experiences relapses
Strong correlation between peripheral blood and bone marrow NGS MRD
Encouraging outcomes after autoHCT in patients with ALL
Acute Myeloid Leukaemia
Prognostic validity of AML composite model in predicting mortality
Venetoclax plus hypomethylating agents in favourable-risk AML
Encouraging clinical activity of decitabine plus ipilimumab in R/R or secondary MDS/AML
AML patients with specific mutations are unlikely to achieve MRD
Comparable outcomes with gilteritinib or quizartinib in R/R AML
First-in-class macrophage immune checkpoint inhibitor in AML
Bispecific DART® as salvage therapy for primary induction failure and early relapse
Gilteritinib in R/R AML patients priorly treated with midostaurin or sorafenib
Addition of venetoclax provides an effective, lower-intensity regimen
Chronic Leukaemia
Bosutinib effective and well tolerated in newly diagnosed CP-CML
Efficacy and safety of ponatinib in patients with CP-CML who failed second-generation TKIs
First-in-class STAMP inhibitor versus bosutinib in resistant or intolerant CML
PFS and ORR benefits of first-line ibrutinib-based treatment in CLL
Multiple Myeloma
Validation of MY-RADS response assessment category criteria
High symptom burden in transplant-ineligible patients with newly diagnosed MM
Added value of ixazomib to lenalidomide plus dexamethasone in transplant-ineligible newly diagnosed MM
Survival of transplant-eligible newly diagnosed MM in FORTE trial
Better survival with upfront autoSCT versus bortezomib-based intensification
Subcutaneous daratumumab plus pomalidomide and dexamethasone in R/R MM
Melflufen well tolerated with encouraging activity in heavily pretreated R/R MM
Initial data of FcRH5/CD3 T-cell-engaging bispecific antibody
Lymphoma
CD58 aberrations limit durable responses to CD19 CAR T-cell therapy
Anti-CD19 CAR T-cell therapy in relapsed/refractory indolent NHL
Myeloproliferative Neoplasms
MPN disease burden, quality of life, and treatment patterns
Interventions in JAK/STAT signalling pathway
Novel, orally available inhibitor of BCL-XL/BCL-2
New insights into genetics of MPN
Immune Thrombocytopenia
Mycophenolate efficacious and tolerable, even in elderly patients
First-in-class antibody sutimlimab selectively inhibits classical complement pathway
BTK inhibition provides clinically active and durable platelet response
Haemophilia, Sickle Cell Disease, Thalassaemia
First results from gene therapy trial in haemophilia B
Impact of haemophilia on children and their caregivers
Promising CRISPR gene editing results in β-thalassaemia and sickle cell disease
Erythroid maturation agent in patients with β-thalassaemia requiring regular RBC transfusions
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