Tocilizumab not associated with increased infection risk after CAR T-cell therapy: implications for COVID-19?

As of 28 April 2020, COVID-19 has been confirmed in 2.9 million people worldwide, with an estimated overall global mortality of up to 6.9%; it is even higher (up to 50%) in older populations with comorbidities. Healthcare systems around the world are stretched to the point of collapse, with no treatment proven to be effective. There is an urgent need for therapeutic interventions that can reduce the rate of respiratory failure, the leading cause of mortality. The current focus is on the development of novel antiviral therapeutics, as well as vaccines. Accumulating evidence suggests that a subgroup of patients with COVID-19 develops a severe inflammatory response akin to macrophage activation syndrome (MAS)/hemophagocytic lympho-histiocytosis (HLH), orchimeric antigen receptor (CAR) T-cell–mediated cytokine release syndrome (CRS), which may contribute to the acute respiratory distress syndrome (ARDS) seen in up to 20% of patient. Antibody therapies to block cytokines are used in the management of CRS in other settings and are highly effective. This approach may be useful to decrease pulmonary inflammation in patients suffering from COVID-19, but there is concern about the potential for increasing direct infection-related morbidity and mortality

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Publication Details

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UNC Libraries
Published
2024-08-31
DOI
https://doi.org/10.17615/h0gs-sd07
Citations
1
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Tocilizumab not associated with increased infection risk after CAR T-cell therapy: implications for COVID-19?

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1 citations
UNC Libraries
CAR-T cell therapy research
article

Tocilizumab not associated with increased infection risk after CAR T-cell therapy: implications for COVID-19?

Sarah Nikiforow, Michael K. Mansour, Marcie Riches, Zhen‐Huan Hu, Peiman Hematti, Matthew J. Frigault, Miguel‐Angel Perales, Marcelo C. Pasquini, Cameron J. Turtle, Mary M. Horowitz, Mei-Jie Zhang
article en
1 citations

Abstract

As of 28 April 2020, COVID-19 has been confirmed in 2.9 million people worldwide, with an estimated overall global mortality of up to 6.9%; it is even higher (up to 50%) in older populations with comorbidities. Healthcare systems around the world are stretched to the point of collapse, with no treatment proven to be effective. There is an urgent need for therapeutic interventions that can reduce the rate of respiratory failure, the leading cause of mortality. The current focus is on the development of novel antiviral therapeutics, as well as vaccines. Accumulating evidence suggests that a subgroup of patients with COVID-19 develops a severe inflammatory response akin to macrophage activation syndrome (MAS)/hemophagocytic lympho-histiocytosis (HLH), orchimeric antigen receptor (CAR) T-cell–mediated cytokine release syndrome (CRS), which may contribute to the acute respiratory distress syndrome (ARDS) seen in up to 20% of patient. Antibody therapies to block cytokines are used in the management of CRS in other settings and are highly effective. This approach may be useful to decrease pulmonary inflammation in patients suffering from COVID-19, but there is concern about the potential for increasing direct infection-related morbidity and mortality

UNC Libraries
University of North Carolina at Chapel Hill (US)
National Institutes of Health, Kite Pharma, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 75%
CAR-T cell therapy research
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