Over 20% of 103 cancer patients studied had delayed clearance of the COVID-19 virus. Those with delayed clearance lost antibodies to viral proteins and instead developed compensatory T-cell responses with increased CD8+ effector T-cells but a poorly focused T-cell receptor repertoire. In contrast, patients with a dominant CD4+ T-cell response had a lower rate of prolonged disease and a more focused T-cell receptor repertoire against COVID, consistent with effective viral clearance and memory development. The results show the importance of coordinated B-cell and CD4+ T-cell immunity in durable viral clearance and long-term control of COVID-19.
Over 20% of 103 cancer patients studied had delayed clearance of the COVID-19 virus. Those with delayed clearance lost antibodies to viral proteins and instead developed compensatory T-cell responses with increased CD8+ effector T-cells but a poorly focused T-cell receptor repertoire. In contrast, patients with a dominant CD4+ T-cell response had a lower rate of prolonged disease and a more focused T-cell receptor repertoire against COVID, consistent with effective viral clearance and memory development. The results show the importance of coordinated B-cell and CD4+ T-cell immunity in durable viral clearance and long-term control of COVID-19.
Over 20% of 103 cancer patients studied had delayed clearance of the COVID-19 virus. Those with delayed clearance lost antibodies to viral proteins and instead developed compensatory T-cell responses with increased CD8+ effector T-cells but a poorly focused T-cell receptor repertoire. In contrast, patients with a dominant CD4+ T-cell response had a lower rate of prolonged disease and a more focused T-cell receptor repertoire against COVID, consistent with effective viral clearance and memory development. The results show the importance of coordinated B-cell and CD4+ T-cell immunity in durable viral clearance and long-term control of COVID-19.
COVID-19 infection in patients with cancer remains
unclear. We analyzed cellular and humoral immune responses in 103 patients with prior COVID-19 infection, over 20% of whom had delayed viral clearance. Delayed clearance was associated with loss of antibodies to nucleocapsid and spike proteins with a compensatory increase in functional T-cell responses. High-dimensional analysis of peripheral blood samples demonstrated increased CD8+ effector T-cell differentiation and a broad but poorly converged COVID-specific TCR repertoire in patients with prolonged disease. Conversely, patients with a CD4+ dominant immunophenotype had a lower incidence of prolonged disease and exhibited a deep and highly selected COVID-associated TCR repertoire, consistent with effective viral clearance and development of T-cell memory. These results highlight the importance of B-cells and CD4+ T- cells in promoting durable SARS-CoV-2 clearance and the significance of coordinated cellular and humoral immunity for long-term disease control.
CD4+ T Cell Recovery During Suppression of HIV Replication An International Comparison of The Immunological Efficacy of Antiretroviral Therapy in North America Asia and Africa 2015